In [1]:
import requests
import json
import ssl

In [2]:
root_url = 'https://ega.crg.eu/metadata/v1/'

In [3]:
s = requests.session()

DAC


In [3]:
root_url+'dacs'


Out[3]:
'https://ega.crg.eu/metadata/v1/dacs'

In [19]:
dac_all = s.get(root_url+'dacs')

In [22]:
dac_all_json = json.loads(dac_all.text)

In [55]:
# List EGAC ids
[item['egaAccessionId'] for item in dac_all_json['response']['result']]


Out[55]:
['EGAC00001000031',
 'EGAC00001000263',
 'EGAC00001000426',
 'EGAC00001000078',
 'EGAC00001000153',
 'EGAC00001000045',
 'EGAC00001000413',
 'EGAC00001000100',
 'EGAC00001000337',
 'EGAC00001000176']

Does the list show the dacs available? 'EGAC00001000264' is not on the list, is it deleted?


In [47]:
dac_single = s.get(root_url+'dacs/EGAC00001000263')

In [48]:
# F
json.loads(dac_single.text)


Out[48]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'ena-DAC-LGLS-03-11-2014-06:00:03:431-602',
    'centerName': 'LGLS',
    'contacts': None,
    'creationTime': 1414991120000,
    'ebiId': 'EGAC00001000263',
    'ebiSubmissionDetailsIds': None,
    'editionTime': 1414991120000,
    'egaAccessionId': 'EGAC00001000263',
    'eraSubmissionId': 'ERA374356',
    'firstPublic': 1462896306844,
    'id': 'EGAC00001000263',
    'json': '""',
    'status': 'SUBMITTED',
    'submissionCommandIds': None,
    'submissionErrorMessages': None,
    'submissionId': 'ERA374356',
    'submissionInfoMessages': None,
    'submitterId': 'ega-box-326',
    'title': 'LG Life Sciences Data Access Committee',
    'userId': None,
    'validationErrorMessages': None,
    'validationResult': False,
    'version': 1,
    'xml': "<DAC_SET>  <DAC alias='ena-DAC-LGLS-03-11-2014-06:00:03:431-602' center_name='LGLS' accession='EGAC00001000263' broker_name='EGA'>    <IDENTIFIERS>      <PRIMARY_ID>EGAC00001000263</PRIMARY_ID>      <SUBMITTER_ID namespace='LGLS'>ena-DAC-LGLS-03-11-2014-06:00:03:431-602</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>LG Life Sciences Data Access Committee</TITLE>    <CONTACTS>      <CONTACT name='Eunji Shin' email='shineunji@lgls.com' telephone_number='82-42-870-6597' organisation='LG Life Sciences'/>    </CONTACTS>  </DAC></DAC_SET>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.DacData'}}

Analyses


In [49]:
analyses_all = s.get(root_url+'analyses')
analyses_all_json = json.loads(analyses_all.text)

In [54]:
analyses_all_json['response']['result']


Out[54]:
[{'alias': 'CompleteGenomics.GS000020189.ASM.GS02098.DNA.D06.MAP.GS61884.FS3.L07.reads.GS61884.FS3.L07.008.tsv.bz2.gpg',
  'analysisCenter': None,
  'analysisDate': None,
  'analysisFileType': 'other',
  'analysisType': 'SEQUENCE_VARIATION',
  'analysisTypeId': None,
  'attributes': None,
  'centerName': 'RUNMC',
  'chromosomeReferences': None,
  'chromosomeValues': None,
  'creationTime': 1447427971000,
  'description': '50 trios were whole genome sequenced with Complete Genomics to a depth of 80x. Each trio the child was affected with severe ID, and the parents were unaffected. All trios were negative for array, targeted gene and whole exome screening.',
  'ebiId': 'ERZ131905',
  'ebiSubmissionDetailsIds': None,
  'editionTime': 1447427971000,
  'egaAccessionId': 'EGAZ00001100051',
  'eraSubmissionId': 'ERA534960',
  'experimentType': ['Whole genome sequencing'],
  'experimentTypeId': None,
  'files': [{'checksum': None,
    'checksumMethod': None,
    'fileId': None,
    'fileName': 'CompleteGenomics/GS000020189-ASM/GS02098-DNA_D06/MAP/GS61884-FS3-L07/reads_GS61884-FS3-L07_008.tsv.bz2.gpg',
    'source': None,
    'unencryptedChecksum': None}],
  'firstPublic': 1462896990207,
  'genome': 'GRCh37',
  'genomeId': None,
  'id': 'ERZ131905',
  'json': '""',
  'platform': None,
  'sampleReferences': None,
  'status': 'SUBMITTED',
  'studyId': 'ERP005592',
  'submissionCommandIds': None,
  'submissionErrorMessages': None,
  'submissionId': 'ERA534960',
  'submissionInfoMessages': None,
  'submitterId': 'ega-box-126',
  'title': 'Whole genome sequencing of 50 trios, where the child is affected with ID, and the parents are unaffected',
  'userId': None,
  'validationErrorMessages': None,
  'validationResult': False,
  'version': 1,
  'xml': "<ANALYSIS_SET>  <ANALYSIS alias='CompleteGenomics.GS000020189.ASM.GS02098.DNA.D06.MAP.GS61884.FS3.L07.reads.GS61884.FS3.L07.008.tsv.bz2.gpg' center_name='RUNMC' broker_name='EGA' accession='ERZ131905'>    <IDENTIFIERS>      <PRIMARY_ID>ERZ131905</PRIMARY_ID>      <SUBMITTER_ID namespace='RUNMC'>CompleteGenomics.GS000020189.ASM.GS02098.DNA.D06.MAP.GS61884.FS3.L07.reads.GS61884.FS3.L07.008.tsv.bz2.gpg</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>Whole genome sequencing of 50 trios, where the child is affected with ID, and the parents are unaffected</TITLE>    <DESCRIPTION>50 trios were whole genome sequenced with Complete Genomics to a depth of 80x. Each trio the child was affected with severe ID, and the parents were unaffected. All trios were negative for array, targeted gene and whole exome screening.</DESCRIPTION>    <STUDY_REF accession='ERP005592' refcenter='RUNMC' refname='ena-STUDY-RUNMC-15-04-2014-16:49:54:970-106'>      <IDENTIFIERS>        <PRIMARY_ID>ERP005592</PRIMARY_ID>        <SUBMITTER_ID namespace='RUNMC'>ena-STUDY-RUNMC-15-04-2014-16:49:54:970-106</SUBMITTER_ID>      </IDENTIFIERS>    </STUDY_REF>    <SAMPLE_REF accession='ERS463443' refcenter='RUNMC' label='BvB1_F' refname='trio14_F'>      <IDENTIFIERS>        <PRIMARY_ID>ERS463443</PRIMARY_ID>        <SUBMITTER_ID namespace='RUNMC'>trio14_F</SUBMITTER_ID>      </IDENTIFIERS>    </SAMPLE_REF>    <ANALYSIS_TYPE>      <SEQUENCE_VARIATION>        <ASSEMBLY>          <STANDARD refname='GRCh37' accession='GCA_000001405.1'/>        </ASSEMBLY>        <SEQUENCE accession='NC_000001.9' label='chr1'/>        <SEQUENCE accession='NC_000002.10' label='chr2'/>        <SEQUENCE accession='NC_000003.10' label='chr3'/>        <SEQUENCE accession='NC_000004.10' label='chr4'/>        <SEQUENCE accession='NC_000005.8' label='chr5'/>        <SEQUENCE accession='NC_000006.10' label='chr6'/>        <SEQUENCE accession='NC_000007.12' label='chr7'/>        <SEQUENCE accession='NC_000008.9' label='chr8'/>        <SEQUENCE accession='NC_000009.10' label='chr9'/>        <SEQUENCE accession='NC_000010.9' label='chr10'/>        <SEQUENCE accession='NC_000011.8' label='chr11'/>        <SEQUENCE accession='NC_000012.10' label='chr12'/>        <SEQUENCE accession='NC_000013.9' label='chr13'/>        <SEQUENCE accession='NC_000014.7' label='chr14'/>        <SEQUENCE accession='NC_000015.8' label='chr15'/>        <SEQUENCE accession='NC_000016.8' label='chr16'/>        <SEQUENCE accession='NC_000017.9' label='chr17'/>        <SEQUENCE accession='NC_000018.8' label='chr18'/>        <SEQUENCE accession='NC_000019.8' label='chr19'/>        <SEQUENCE accession='NC_000020.9' label='chr20'/>        <SEQUENCE accession='NC_000021.7' label='chr21'/>        <SEQUENCE accession='NC_000022.9' label='chr22'/>        <SEQUENCE accession='NC_000023.9' label='chrX'/>        <SEQUENCE accession='NC_000024.8' label='chrY'/>        <SEQUENCE accession='NC_001807.4' label='chrM'/>        <EXPERIMENT_TYPE>Whole genome sequencing</EXPERIMENT_TYPE>      </SEQUENCE_VARIATION>    </ANALYSIS_TYPE>    <FILES>      <FILE filename='CompleteGenomics/GS000020189-ASM/GS02098-DNA_D06/MAP/GS61884-FS3-L07/reads_GS61884-FS3-L07_008.tsv.bz2.gpg' filetype='other' checksum_method='MD5' checksum='5f4ef194fbbe9d568671c1d4fe45625c' unencrypted_checksum='2935806147ecc169c18e5c2e1216af50'/>    </FILES>    <ANALYSIS_ATTRIBUTES>      <ANALYSIS_ATTRIBUTE>        <TAG>library_strategy</TAG>        <VALUE>WGS</VALUE>      </ANALYSIS_ATTRIBUTE>      <ANALYSIS_ATTRIBUTE>        <TAG>library_layout</TAG>        <VALUE>PAIRED</VALUE>      </ANALYSIS_ATTRIBUTE>    </ANALYSIS_ATTRIBUTES>  </ANALYSIS></ANALYSIS_SET>",
  'xmlRootElement': None},
 {'alias': 'uk10k_tamp5103528.rel-2013-04-20.vcf.gz-vcf_analysis-sc-20130524',
  'analysisCenter': None,
  'analysisDate': None,
  'analysisFileType': 'vcf',
  'analysisType': 'SEQUENCE_VARIATION',
  'analysisTypeId': None,
  'attributes': None,
  'centerName': 'SC',
  'chromosomeReferences': None,
  'chromosomeValues': None,
  'creationTime': 1369387705000,
  'description': 'UK10K_NEURO_ASD_TAMPERE.REL-2013-04-20.variant_calling',
  'ebiId': 'ERZ013530',
  'ebiSubmissionDetailsIds': None,
  'editionTime': 1369387705000,
  'egaAccessionId': 'EGAZ00001013168',
  'eraSubmissionId': 'ERA220624',
  'experimentType': [None],
  'experimentTypeId': None,
  'files': [{'checksum': None,
    'checksumMethod': None,
    'fileId': None,
    'fileName': 'UK10K_TAMP5103528.REL-2013-04-20.vcf.gz',
    'source': None,
    'unencryptedChecksum': None}],
  'firstPublic': 1462896990207,
  'genome': 'GRCh37',
  'genomeId': None,
  'id': 'ERZ013530',
  'json': '""',
  'platform': None,
  'sampleReferences': None,
  'status': 'SUBMITTED',
  'studyId': 'ERP000851',
  'submissionCommandIds': None,
  'submissionErrorMessages': None,
  'submissionId': 'ERA220624',
  'submissionInfoMessages': None,
  'submitterId': 'ega-box-03',
  'title': 'UK10K_NEURO_ASD_TAMPERE REL-2013-04-20 Variant Calls',
  'userId': None,
  'validationErrorMessages': None,
  'validationResult': False,
  'version': 1,
  'xml': "<ANALYSIS_SET>  <ANALYSIS alias='uk10k_tamp5103528.rel-2013-04-20.vcf.gz-vcf_analysis-sc-20130524' center_name='SC' broker_name='EGA' analysis_center='SC' accession='ERZ013530'>    <IDENTIFIERS>      <PRIMARY_ID>ERZ013530</PRIMARY_ID>      <SUBMITTER_ID namespace='SC'>uk10k_tamp5103528.rel-2013-04-20.vcf.gz-vcf_analysis-sc-20130524</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>UK10K_NEURO_ASD_TAMPERE REL-2013-04-20 Variant Calls</TITLE>    <DESCRIPTION>UK10K_NEURO_ASD_TAMPERE.REL-2013-04-20.variant_calling</DESCRIPTION>    <STUDY_REF refname='UK10K_exome_sequence__Tampere_samples-sc-2011-08-18T14:31:13Z-1789' refcenter='SC' accession='ERP000851'>      <IDENTIFIERS>        <PRIMARY_ID>ERP000851</PRIMARY_ID>        <SUBMITTER_ID namespace='SC'>UK10K_exome_sequence__Tampere_samples-sc-2011-08-18T14:31:13Z-1789</SUBMITTER_ID>      </IDENTIFIERS>    </STUDY_REF>    <SAMPLE_REF accession='ERS033022' refcenter='SC' label='UK10K_TAMP5103528' refname='UK10K_TAMP5103528-sc-2011-05-04T10:55:31Z-1127404'>      <IDENTIFIERS>        <PRIMARY_ID>ERS033022</PRIMARY_ID>        <SUBMITTER_ID namespace='SC'>UK10K_TAMP5103528-sc-2011-05-04T10:55:31Z-1127404</SUBMITTER_ID>      </IDENTIFIERS>    </SAMPLE_REF>    <ANALYSIS_TYPE>      <SEQUENCE_VARIATION>        <ASSEMBLY>          <STANDARD refname='GRCh37'/>        </ASSEMBLY>      </SEQUENCE_VARIATION>    </ANALYSIS_TYPE>    <FILES>      <FILE filename='UK10K_TAMP5103528.REL-2013-04-20.vcf.gz' filetype='vcf' checksum_method='MD5' checksum='539edae44f04a9de25b755ab38c3179f' unencrypted_checksum='d062b44357539d63bf514768895c7f83'/>    </FILES>  </ANALYSIS></ANALYSIS_SET>",
  'xmlRootElement': None},
 {'alias': 'CompleteGenomics.GS000021047.ASM.GS02099.DNA.E03.ASM.EVIDENCE.evidenceDnbs.chr9.GS000021047.ASM.tsv.bz2.gpg',
  'analysisCenter': None,
  'analysisDate': None,
  'analysisFileType': 'other',
  'analysisType': 'SEQUENCE_VARIATION',
  'analysisTypeId': None,
  'attributes': None,
  'centerName': 'RUNMC',
  'chromosomeReferences': None,
  'chromosomeValues': None,
  'creationTime': 1447431757000,
  'description': '50 trios were whole genome sequenced with Complete Genomics to a depth of 80x. Each trio the child was affected with severe ID, and the parents were unaffected. All trios were negative for array, targeted gene and whole exome screening.',
  'ebiId': 'ERZ167080',
  'ebiSubmissionDetailsIds': None,
  'editionTime': 1447431757000,
  'egaAccessionId': 'EGAZ00001135226',
  'eraSubmissionId': 'ERA535018',
  'experimentType': ['Whole genome sequencing'],
  'experimentTypeId': None,
  'files': [{'checksum': None,
    'checksumMethod': None,
    'fileId': None,
    'fileName': 'CompleteGenomics/GS000021047-ASM/GS02099-DNA_E03/ASM/EVIDENCE/evidenceDnbs-chr9-GS000021047-ASM.tsv.bz2.gpg',
    'source': None,
    'unencryptedChecksum': None}],
  'firstPublic': 1462896990207,
  'genome': 'GRCh37',
  'genomeId': None,
  'id': 'ERZ167080',
  'json': '""',
  'platform': None,
  'sampleReferences': None,
  'status': 'SUBMITTED',
  'studyId': 'ERP005592',
  'submissionCommandIds': None,
  'submissionErrorMessages': None,
  'submissionId': 'ERA535018',
  'submissionInfoMessages': None,
  'submitterId': 'ega-box-126',
  'title': 'Whole genome sequencing of 50 trios, where the child is affected with ID, and the parents are unaffected',
  'userId': None,
  'validationErrorMessages': None,
  'validationResult': False,
  'version': 1,
  'xml': "<ANALYSIS_SET>  <ANALYSIS alias='CompleteGenomics.GS000021047.ASM.GS02099.DNA.E03.ASM.EVIDENCE.evidenceDnbs.chr9.GS000021047.ASM.tsv.bz2.gpg' center_name='RUNMC' broker_name='EGA' accession='ERZ167080'>    <IDENTIFIERS>      <PRIMARY_ID>ERZ167080</PRIMARY_ID>      <SUBMITTER_ID namespace='RUNMC'>CompleteGenomics.GS000021047.ASM.GS02099.DNA.E03.ASM.EVIDENCE.evidenceDnbs.chr9.GS000021047.ASM.tsv.bz2.gpg</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>Whole genome sequencing of 50 trios, where the child is affected with ID, and the parents are unaffected</TITLE>    <DESCRIPTION>50 trios were whole genome sequenced with Complete Genomics to a depth of 80x. Each trio the child was affected with severe ID, and the parents were unaffected. All trios were negative for array, targeted gene and whole exome screening.</DESCRIPTION>    <STUDY_REF accession='ERP005592' refcenter='RUNMC' refname='ena-STUDY-RUNMC-15-04-2014-16:49:54:970-106'>      <IDENTIFIERS>        <PRIMARY_ID>ERP005592</PRIMARY_ID>        <SUBMITTER_ID namespace='RUNMC'>ena-STUDY-RUNMC-15-04-2014-16:49:54:970-106</SUBMITTER_ID>      </IDENTIFIERS>    </STUDY_REF>    <SAMPLE_REF accession='ERS463447' refcenter='RUNMC' label='BvB4_M' refname='trio15_M'>      <IDENTIFIERS>        <PRIMARY_ID>ERS463447</PRIMARY_ID>        <SUBMITTER_ID namespace='RUNMC'>trio15_M</SUBMITTER_ID>      </IDENTIFIERS>    </SAMPLE_REF>    <ANALYSIS_TYPE>      <SEQUENCE_VARIATION>        <ASSEMBLY>          <STANDARD refname='GRCh37' accession='GCA_000001405.1'/>        </ASSEMBLY>        <SEQUENCE accession='NC_000001.9' label='chr1'/>        <SEQUENCE accession='NC_000002.10' label='chr2'/>        <SEQUENCE accession='NC_000003.10' label='chr3'/>        <SEQUENCE accession='NC_000004.10' label='chr4'/>        <SEQUENCE accession='NC_000005.8' label='chr5'/>        <SEQUENCE accession='NC_000006.10' label='chr6'/>        <SEQUENCE accession='NC_000007.12' label='chr7'/>        <SEQUENCE accession='NC_000008.9' label='chr8'/>        <SEQUENCE accession='NC_000009.10' label='chr9'/>        <SEQUENCE accession='NC_000010.9' label='chr10'/>        <SEQUENCE accession='NC_000011.8' label='chr11'/>        <SEQUENCE accession='NC_000012.10' label='chr12'/>        <SEQUENCE accession='NC_000013.9' label='chr13'/>        <SEQUENCE accession='NC_000014.7' label='chr14'/>        <SEQUENCE accession='NC_000015.8' label='chr15'/>        <SEQUENCE accession='NC_000016.8' label='chr16'/>        <SEQUENCE accession='NC_000017.9' label='chr17'/>        <SEQUENCE accession='NC_000018.8' label='chr18'/>        <SEQUENCE accession='NC_000019.8' label='chr19'/>        <SEQUENCE accession='NC_000020.9' label='chr20'/>        <SEQUENCE accession='NC_000021.7' label='chr21'/>        <SEQUENCE accession='NC_000022.9' label='chr22'/>        <SEQUENCE accession='NC_000023.9' label='chrX'/>        <SEQUENCE accession='NC_000024.8' label='chrY'/>        <SEQUENCE accession='NC_001807.4' label='chrM'/>        <EXPERIMENT_TYPE>Whole genome sequencing</EXPERIMENT_TYPE>      </SEQUENCE_VARIATION>    </ANALYSIS_TYPE>    <FILES>      <FILE filename='CompleteGenomics/GS000021047-ASM/GS02099-DNA_E03/ASM/EVIDENCE/evidenceDnbs-chr9-GS000021047-ASM.tsv.bz2.gpg' filetype='other' checksum_method='MD5' checksum='139886f04f7c57d41d93fcbf3262914f' unencrypted_checksum='7d401eb0e82d55318096352b5dbb2a0c'/>    </FILES>    <ANALYSIS_ATTRIBUTES>      <ANALYSIS_ATTRIBUTE>        <TAG>library_strategy</TAG>        <VALUE>WGS</VALUE>      </ANALYSIS_ATTRIBUTE>      <ANALYSIS_ATTRIBUTE>        <TAG>library_layout</TAG>        <VALUE>PAIRED</VALUE>      </ANALYSIS_ATTRIBUTE>    </ANALYSIS_ATTRIBUTES>  </ANALYSIS></ANALYSIS_SET>",
  'xmlRootElement': None},
 {'alias': 'evidenceIntervals-chr6-GS000021173-ASM-2',
  'analysisCenter': None,
  'analysisDate': None,
  'analysisFileType': 'other',
  'analysisType': 'SEQUENCE_VARIATION',
  'analysisTypeId': None,
  'attributes': None,
  'centerName': 'TCAG',
  'chromosomeReferences': None,
  'chromosomeValues': None,
  'creationTime': 1420817650000,
  'description': 'Autism spectrum disorder (ASD) is genetically heterogeneous with &gt;100 susceptibility genes known. We used whole-genome sequencing (WGS) of 85 quartet families (two parents and two ASD-affected siblings) to comprehensively examine mutation characteristics. Our results emphasize using WGS to maximize the detection of all classes of mutations potentially involved in autism, and to enable the interpretation of that data in confirmatory and predictive diagnosis in different individuals in a family.',
  'ebiId': 'ERZ065346',
  'ebiSubmissionDetailsIds': None,
  'editionTime': 1440141039000,
  'egaAccessionId': 'EGAZ00001054658',
  'eraSubmissionId': 'ERA399700',
  'experimentType': ['Whole genome sequencing'],
  'experimentTypeId': None,
  'files': [{'checksum': None,
    'checksumMethod': None,
    'fileId': None,
    'fileName': 'EGAS00001001023/1-0479-006/ASM/EVIDENCE/evidenceIntervals-chr6-GS000021173-ASM.tsv.bz2.gpg',
    'source': None,
    'unencryptedChecksum': None}],
  'firstPublic': 1462896990207,
  'genome': 'GRCh37',
  'genomeId': None,
  'id': 'ERZ065346',
  'json': '""',
  'platform': None,
  'sampleReferences': None,
  'status': 'SUBMITTED',
  'studyId': 'ERP008564',
  'submissionCommandIds': None,
  'submissionErrorMessages': None,
  'submissionId': 'ERA399700',
  'submissionInfoMessages': None,
  'submitterId': 'ega-box-255',
  'title': 'Whole-genome sequencing of quartet families with Autism Spectrum Disorder',
  'userId': None,
  'validationErrorMessages': None,
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  'xml': "<ANALYSIS_SET>  <ANALYSIS alias='evidenceIntervals-chr13-GS000012485-ASM-2' center_name='TCAG' broker_name='EGA' accession='ERZ073249'>    <IDENTIFIERS>      <PRIMARY_ID>ERZ073249</PRIMARY_ID>      <SUBMITTER_ID namespace='TCAG'>evidenceIntervals-chr13-GS000012485-ASM-2</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>Whole-genome sequencing of quartet families with Autism Spectrum Disorder</TITLE>    <DESCRIPTION>Autism spectrum disorder (ASD) is genetically heterogeneous with &gt;100 susceptibility genes known. We used whole-genome sequencing (WGS) of 85 quartet families (two parents and two ASD-affected siblings) to comprehensively examine mutation characteristics. Our results emphasize using WGS to maximize the detection of all classes of mutations potentially involved in autism, and to enable the interpretation of that data in confirmatory and predictive diagnosis in different individuals in a family.</DESCRIPTION>    <STUDY_REF accession='ERP008564' refcenter='TCAG' refname='ena-STUDY-TCAG-31-10-2014-02:16:08:608-471'>      <IDENTIFIERS>        <PRIMARY_ID>ERP008564</PRIMARY_ID>        <SUBMITTER_ID namespace='TCAG'>ena-STUDY-TCAG-31-10-2014-02:16:08:608-471</SUBMITTER_ID>      </IDENTIFIERS>    </STUDY_REF>    <SAMPLE_REF refname='GS01451-DNA_D04' refcenter='TCAG' label='2-0171-004' accession='ERS637883'>      <IDENTIFIERS>        <PRIMARY_ID>ERS637883</PRIMARY_ID>        <SUBMITTER_ID namespace='TCAG'>GS01451-DNA_D04</SUBMITTER_ID>      </IDENTIFIERS>    </SAMPLE_REF>    <ANALYSIS_TYPE>      <SEQUENCE_VARIATION>        <ASSEMBLY>          <STANDARD refname='GRCh37' accession='GCA_000001405.1'/>        </ASSEMBLY>        <SEQUENCE accession='CM000663.1' label='chr1'/>        <SEQUENCE accession='CM000664.1' label='chr2'/>        <SEQUENCE accession='CM000665.1' label='chr3'/>        <SEQUENCE accession='CM000666.1' label='chr4'/>        <SEQUENCE accession='CM000667.1' label='chr5'/>        <SEQUENCE accession='CM000668.1' label='chr6'/>        <SEQUENCE accession='CM000669.1' label='chr7'/>        <SEQUENCE accession='CM000670.1' label='chr8'/>        <SEQUENCE accession='CM000671.1' label='chr9'/>        <SEQUENCE accession='CM000672.1' label='chr10'/>        <SEQUENCE accession='CM000673.1' label='chr11'/>        <SEQUENCE accession='CM000674.1' label='chr12'/>        <SEQUENCE accession='CM000675.1' label='chr13'/>        <SEQUENCE accession='CM000676.1' label='chr14'/>        <SEQUENCE accession='CM000677.1' label='chr15'/>        <SEQUENCE accession='CM000678.1' label='chr16'/>        <SEQUENCE accession='CM000679.1' label='chr17'/>        <SEQUENCE accession='CM000680.1' label='chr18'/>        <SEQUENCE accession='CM000681.1' label='chr19'/>        <SEQUENCE accession='CM000682.1' label='chr20'/>        <SEQUENCE accession='CM000683.1' label='chr21'/>        <SEQUENCE accession='CM000684.1' label='chr22'/>        <SEQUENCE accession='CM000685.1' label='chrX'/>        <SEQUENCE accession='CM000686.1' label='chrY'/>        <SEQUENCE accession='J01415.2' label='chrM'/>        <EXPERIMENT_TYPE>Whole genome sequencing</EXPERIMENT_TYPE>      </SEQUENCE_VARIATION>    </ANALYSIS_TYPE>    <FILES>      <FILE filename='EGAS00001001023/2-0171-004/ASM/EVIDENCE/evidenceIntervals-chr13-GS000012485-ASM.tsv.bz2.gpg' filetype='other' checksum_method='MD5' checksum='26f75adb06c48f923a5ac08631d92a76' unencrypted_checksum='46cfd24b8e92fdcfbe72b04ea4168afd'/>    </FILES>    <ANALYSIS_ATTRIBUTES>      <ANALYSIS_ATTRIBUTE>        <TAG>library_strategy</TAG>        <VALUE>WGS</VALUE>      </ANALYSIS_ATTRIBUTE>      <ANALYSIS_ATTRIBUTE>        <TAG>library_layout</TAG>        <VALUE>PAIRED</VALUE>      </ANALYSIS_ATTRIBUTE>    </ANALYSIS_ATTRIBUTES>  </ANALYSIS></ANALYSIS_SET>",
  'xmlRootElement': None},
 {'alias': 'highConfidenceSvEventsBeta-GS000011129-ASM-2',
  'analysisCenter': None,
  'analysisDate': None,
  'analysisFileType': 'other',
  'analysisType': 'SEQUENCE_VARIATION',
  'analysisTypeId': None,
  'attributes': None,
  'centerName': 'TCAG',
  'chromosomeReferences': None,
  'chromosomeValues': None,
  'creationTime': 1420818685000,
  'description': 'Autism spectrum disorder (ASD) is genetically heterogeneous with &gt;100 susceptibility genes known. We used whole-genome sequencing (WGS) of 85 quartet families (two parents and two ASD-affected siblings) to comprehensively examine mutation characteristics. Our results emphasize using WGS to maximize the detection of all classes of mutations potentially involved in autism, and to enable the interpretation of that data in confirmatory and predictive diagnosis in different individuals in a family.',
  'ebiId': 'ERZ084589',
  'ebiSubmissionDetailsIds': None,
  'editionTime': 1440140809000,
  'egaAccessionId': 'EGAZ00001073901',
  'eraSubmissionId': 'ERA399865',
  'experimentType': ['Whole genome sequencing'],
  'experimentTypeId': None,
  'files': [{'checksum': None,
    'checksumMethod': None,
    'fileId': None,
    'fileName': 'EGAS00001001023/2-1258-001/ASM/SV/highConfidenceSvEventsBeta-GS000011129-ASM.tsv.gpg',
    'source': None,
    'unencryptedChecksum': None}],
  'firstPublic': 1462896990207,
  'genome': 'GRCh37',
  'genomeId': None,
  'id': 'ERZ084589',
  'json': '""',
  'platform': None,
  'sampleReferences': None,
  'status': 'SUBMITTED',
  'studyId': 'ERP008564',
  'submissionCommandIds': None,
  'submissionErrorMessages': None,
  'submissionId': 'ERA399865',
  'submissionInfoMessages': None,
  'submitterId': 'ega-box-255',
  'title': 'Whole-genome sequencing of quartet families with Autism Spectrum Disorder',
  'userId': None,
  'validationErrorMessages': None,
  'validationResult': False,
  'version': 2,
  'xml': "<ANALYSIS_SET>  <ANALYSIS alias='highConfidenceSvEventsBeta-GS000011129-ASM-2' center_name='TCAG' broker_name='EGA' accession='ERZ084589'>    <IDENTIFIERS>      <PRIMARY_ID>ERZ084589</PRIMARY_ID>      <SUBMITTER_ID namespace='TCAG'>highConfidenceSvEventsBeta-GS000011129-ASM-2</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>Whole-genome sequencing of quartet families with Autism Spectrum Disorder</TITLE>    <DESCRIPTION>Autism spectrum disorder (ASD) is genetically heterogeneous with &gt;100 susceptibility genes known. We used whole-genome sequencing (WGS) of 85 quartet families (two parents and two ASD-affected siblings) to comprehensively examine mutation characteristics. Our results emphasize using WGS to maximize the detection of all classes of mutations potentially involved in autism, and to enable the interpretation of that data in confirmatory and predictive diagnosis in different individuals in a family.</DESCRIPTION>    <STUDY_REF accession='ERP008564' refcenter='TCAG' refname='ena-STUDY-TCAG-31-10-2014-02:16:08:608-471'>      <IDENTIFIERS>        <PRIMARY_ID>ERP008564</PRIMARY_ID>        <SUBMITTER_ID namespace='TCAG'>ena-STUDY-TCAG-31-10-2014-02:16:08:608-471</SUBMITTER_ID>      </IDENTIFIERS>    </STUDY_REF>    <SAMPLE_REF refname='GS01271-DNA_A01' refcenter='TCAG' label='2-1258-001' accession='ERS637816'>      <IDENTIFIERS>        <PRIMARY_ID>ERS637816</PRIMARY_ID>        <SUBMITTER_ID namespace='TCAG'>GS01271-DNA_A01</SUBMITTER_ID>      </IDENTIFIERS>    </SAMPLE_REF>    <ANALYSIS_TYPE>      <SEQUENCE_VARIATION>        <ASSEMBLY>          <STANDARD refname='GRCh37' accession='GCA_000001405.1'/>        </ASSEMBLY>        <SEQUENCE accession='CM000663.1' label='chr1'/>        <SEQUENCE accession='CM000664.1' label='chr2'/>        <SEQUENCE accession='CM000665.1' label='chr3'/>        <SEQUENCE accession='CM000666.1' label='chr4'/>        <SEQUENCE accession='CM000667.1' label='chr5'/>        <SEQUENCE accession='CM000668.1' label='chr6'/>        <SEQUENCE accession='CM000669.1' label='chr7'/>        <SEQUENCE accession='CM000670.1' label='chr8'/>        <SEQUENCE accession='CM000671.1' label='chr9'/>        <SEQUENCE accession='CM000672.1' label='chr10'/>        <SEQUENCE accession='CM000673.1' label='chr11'/>        <SEQUENCE accession='CM000674.1' label='chr12'/>        <SEQUENCE accession='CM000675.1' label='chr13'/>        <SEQUENCE accession='CM000676.1' label='chr14'/>        <SEQUENCE accession='CM000677.1' label='chr15'/>        <SEQUENCE accession='CM000678.1' label='chr16'/>        <SEQUENCE accession='CM000679.1' label='chr17'/>        <SEQUENCE accession='CM000680.1' label='chr18'/>        <SEQUENCE accession='CM000681.1' label='chr19'/>        <SEQUENCE accession='CM000682.1' label='chr20'/>        <SEQUENCE accession='CM000683.1' label='chr21'/>        <SEQUENCE accession='CM000684.1' label='chr22'/>        <SEQUENCE accession='CM000685.1' label='chrX'/>        <SEQUENCE accession='CM000686.1' label='chrY'/>        <SEQUENCE accession='J01415.2' label='chrM'/>        <EXPERIMENT_TYPE>Whole genome sequencing</EXPERIMENT_TYPE>      </SEQUENCE_VARIATION>    </ANALYSIS_TYPE>    <FILES>      <FILE filename='EGAS00001001023/2-1258-001/ASM/SV/highConfidenceSvEventsBeta-GS000011129-ASM.tsv.gpg' filetype='other' checksum_method='MD5' checksum='a073a60b640f8c7d1c63dedf830e0032' unencrypted_checksum='c6feb500c17b634b9fed08be646932b3'/>    </FILES>    <ANALYSIS_ATTRIBUTES>      <ANALYSIS_ATTRIBUTE>        <TAG>library_strategy</TAG>        <VALUE>WGS</VALUE>      </ANALYSIS_ATTRIBUTE>      <ANALYSIS_ATTRIBUTE>        <TAG>library_layout</TAG>        <VALUE>PAIRED</VALUE>      </ANALYSIS_ATTRIBUTE>    </ANALYSIS_ATTRIBUTES>  </ANALYSIS></ANALYSIS_SET>",
  'xmlRootElement': None},
 {'alias': 'SC_DDDP118448_EGAN00001293854.vcf.gz',
  'analysisCenter': None,
  'analysisDate': None,
  'analysisFileType': 'vcf',
  'analysisType': 'SEQUENCE_VARIATION',
  'analysisTypeId': None,
  'attributes': None,
  'centerName': 'SC',
  'chromosomeReferences': None,
  'chromosomeValues': None,
  'creationTime': 1449491738000,
  'description': 'DDD DATAFREEZE 2014-11-04: 4294 trios - VCF files',
  'ebiId': 'ERZ239074',
  'ebiSubmissionDetailsIds': None,
  'editionTime': 1449491738000,
  'egaAccessionId': 'EGAZ00001204192',
  'eraSubmissionId': 'ERA542321',
  'experimentType': ['Exome sequencing'],
  'experimentTypeId': None,
  'files': [{'checksum': None,
    'checksumMethod': None,
    'fileId': None,
    'fileName': 'DDDP118448_EGAN00001293854.vcf.gz.gpg',
    'source': None,
    'unencryptedChecksum': None}],
  'firstPublic': 1462896990207,
  'genome': None,
  'genomeId': None,
  'id': 'ERZ239074',
  'json': '""',
  'platform': None,
  'sampleReferences': None,
  'status': 'SUBMITTED',
  'studyId': 'ERP005661',
  'submissionCommandIds': None,
  'submissionErrorMessages': None,
  'submissionId': 'ERA542321',
  'submissionInfoMessages': None,
  'submitterId': 'ega-box-03',
  'title': 'DDD DATAFREEZE 2014-11-04: 4294 trios - VCF files',
  'userId': None,
  'validationErrorMessages': None,
  'validationResult': False,
  'version': 1,
  'xml': "<ANALYSIS_SET>  <ANALYSIS alias='SC_DDDP118448_EGAN00001293854.vcf.gz' accession='ERZ239074' center_name='SC' broker_name='EGA'>    <IDENTIFIERS>      <PRIMARY_ID>ERZ239074</PRIMARY_ID>      <SUBMITTER_ID namespace='SC'>SC_DDDP118448_EGAN00001293854.vcf.gz</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>DDD DATAFREEZE 2014-11-04: 4294 trios - VCF files</TITLE>    <DESCRIPTION>DDD DATAFREEZE 2014-11-04: 4294 trios - VCF files</DESCRIPTION>    <STUDY_REF accession='ERP005661' refname='ena-STUDY-SC-28-04-2014-15:21:11:982-94' refcenter='SC'>      <IDENTIFIERS>        <PRIMARY_ID>ERP005661</PRIMARY_ID>        <SUBMITTER_ID namespace='SC'>ena-STUDY-SC-28-04-2014-15:21:11:982-94</SUBMITTER_ID>      </IDENTIFIERS>    </STUDY_REF>    <SAMPLE_REF accession='ERS843839' refname='DDD_MAIN5684084-sc-1794594' refcenter='SC'>      <IDENTIFIERS>        <PRIMARY_ID>ERS843839</PRIMARY_ID>        <SUBMITTER_ID namespace='SC'>DDD_MAIN5684084-sc-1794594</SUBMITTER_ID>      </IDENTIFIERS>    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label='5'/>        <SEQUENCE accession='CM000668.1' label='6'/>        <SEQUENCE accession='CM000669.1' label='7'/>        <SEQUENCE accession='CM000670.1' label='8'/>        <SEQUENCE accession='CM000671.1' label='9'/>        <SEQUENCE accession='GL000191.1' label='GL000191.1'/>        <SEQUENCE accession='GL000192.1' label='GL000192.1'/>        <SEQUENCE accession='GL000193.1' label='GL000193.1'/>        <SEQUENCE accession='GL000194.1' label='GL000194.1'/>        <SEQUENCE accession='GL000195.1' label='GL000195.1'/>        <SEQUENCE accession='GL000196.1' label='GL000196.1'/>        <SEQUENCE accession='GL000197.1' label='GL000197.1'/>        <SEQUENCE accession='GL000198.1' label='GL000198.1'/>        <SEQUENCE accession='GL000199.1' label='GL000199.1'/>        <SEQUENCE accession='GL000200.1' label='GL000200.1'/>        <SEQUENCE accession='GL000201.1' label='GL000201.1'/>        <SEQUENCE accession='GL000202.1' label='GL000202.1'/>        <SEQUENCE accession='GL000203.1' label='GL000203.1'/>        <SEQUENCE accession='GL000204.1' label='GL000204.1'/>        <SEQUENCE accession='GL000205.1' label='GL000205.1'/>        <SEQUENCE accession='GL000206.1' label='GL000206.1'/>        <SEQUENCE accession='GL000207.1' label='GL000207.1'/>        <SEQUENCE accession='GL000208.1' label='GL000208.1'/>        <SEQUENCE accession='GL000209.1' label='GL000209.1'/>        <SEQUENCE accession='GL000210.1' label='GL000210.1'/>        <SEQUENCE accession='GL000211.1' label='GL000211.1'/>        <SEQUENCE accession='GL000212.1' label='GL000212.1'/>        <SEQUENCE accession='GL000213.1' label='GL000213.1'/>        <SEQUENCE accession='GL000214.1' label='GL000214.1'/>        <SEQUENCE accession='GL000215.1' label='GL000215.1'/>        <SEQUENCE accession='GL000216.1' label='GL000216.1'/>        <SEQUENCE accession='GL000217.1' label='GL000217.1'/>        <SEQUENCE accession='GL000218.1' label='GL000218.1'/>        <SEQUENCE accession='GL000219.1' label='GL000219.1'/>        <SEQUENCE accession='GL000220.1' label='GL000220.1'/>        <SEQUENCE accession='GL000221.1' label='GL000221.1'/>        <SEQUENCE accession='GL000222.1' label='GL000222.1'/>        <SEQUENCE accession='GL000223.1' label='GL000223.1'/>        <SEQUENCE accession='GL000224.1' label='GL000224.1'/>        <SEQUENCE accession='GL000225.1' label='GL000225.1'/>        <SEQUENCE accession='GL000226.1' label='GL000226.1'/>        <SEQUENCE accession='GL000227.1' label='GL000227.1'/>        <SEQUENCE accession='GL000228.1' label='GL000228.1'/>        <SEQUENCE accession='GL000229.1' label='GL000229.1'/>        <SEQUENCE accession='GL000230.1' label='GL000230.1'/>        <SEQUENCE accession='GL000231.1' label='GL000231.1'/>        <SEQUENCE accession='GL000232.1' label='GL000232.1'/>        <SEQUENCE accession='GL000233.1' label='GL000233.1'/>        <SEQUENCE accession='GL000234.1' label='GL000234.1'/>        <SEQUENCE accession='GL000235.1' label='GL000235.1'/>        <SEQUENCE 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label='X'/>        <SEQUENCE accession='CM000686.1' label='Y'/>        <EXPERIMENT_TYPE>Exome sequencing</EXPERIMENT_TYPE>      </SEQUENCE_VARIATION>    </ANALYSIS_TYPE>    <FILES>      <FILE filename='DDDP118448_EGAN00001293854.vcf.gz.gpg' filetype='vcf' checksum_method='MD5' checksum='2946b65d50273c0e8c7c43fc572b826d' unencrypted_checksum='e1026fd5be60aaebfa728c155739f52f'/>    </FILES>  </ANALYSIS></ANALYSIS_SET>",
  'xmlRootElement': None}]

In [56]:
# List analysis ids
[item['egaAccessionId'] for item in analyses_all_json['response']['result']]


Out[56]:
['EGAZ00001100051',
 'EGAZ00001013168',
 'EGAZ00001135226',
 'EGAZ00001054658',
 'EGAZ00001082732',
 'EGAZ00001175976',
 'EGAZ00001213204',
 'EGAZ00001062561',
 'EGAZ00001073901',
 'EGAZ00001204192']

In [57]:
analyses_single = s.get(root_url+'analyses/EGAZ00001013168')
json.loads(analyses_single.text)


Out[57]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'uk10k_tamp5103528.rel-2013-04-20.vcf.gz-vcf_analysis-sc-20130524',
    'analysisCenter': None,
    'analysisDate': None,
    'analysisFileType': 'vcf',
    'analysisType': 'SEQUENCE_VARIATION',
    'analysisTypeId': None,
    'attributes': None,
    'centerName': 'SC',
    'chromosomeReferences': None,
    'chromosomeValues': None,
    'creationTime': 1369387705000,
    'description': 'UK10K_NEURO_ASD_TAMPERE.REL-2013-04-20.variant_calling',
    'ebiId': 'ERZ013530',
    'ebiSubmissionDetailsIds': None,
    'editionTime': 1369387705000,
    'egaAccessionId': 'EGAZ00001013168',
    'eraSubmissionId': 'ERA220624',
    'experimentType': [None],
    'experimentTypeId': None,
    'files': [{'checksum': None,
      'checksumMethod': None,
      'fileId': None,
      'fileName': 'UK10K_TAMP5103528.REL-2013-04-20.vcf.gz',
      'source': None,
      'unencryptedChecksum': None}],
    'firstPublic': 1462897159940,
    'genome': 'GRCh37',
    'genomeId': None,
    'id': 'ERZ013530',
    'json': '""',
    'platform': None,
    'sampleReferences': None,
    'status': 'SUBMITTED',
    'studyId': 'ERP000851',
    'submissionCommandIds': None,
    'submissionErrorMessages': None,
    'submissionId': 'ERA220624',
    'submissionInfoMessages': None,
    'submitterId': 'ega-box-03',
    'title': 'UK10K_NEURO_ASD_TAMPERE REL-2013-04-20 Variant Calls',
    'userId': None,
    'validationErrorMessages': None,
    'validationResult': False,
    'version': 1,
    'xml': "<ANALYSIS_SET>  <ANALYSIS alias='uk10k_tamp5103528.rel-2013-04-20.vcf.gz-vcf_analysis-sc-20130524' center_name='SC' broker_name='EGA' analysis_center='SC' accession='ERZ013530'>    <IDENTIFIERS>      <PRIMARY_ID>ERZ013530</PRIMARY_ID>      <SUBMITTER_ID namespace='SC'>uk10k_tamp5103528.rel-2013-04-20.vcf.gz-vcf_analysis-sc-20130524</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>UK10K_NEURO_ASD_TAMPERE REL-2013-04-20 Variant Calls</TITLE>    <DESCRIPTION>UK10K_NEURO_ASD_TAMPERE.REL-2013-04-20.variant_calling</DESCRIPTION>    <STUDY_REF refname='UK10K_exome_sequence__Tampere_samples-sc-2011-08-18T14:31:13Z-1789' refcenter='SC' accession='ERP000851'>      <IDENTIFIERS>        <PRIMARY_ID>ERP000851</PRIMARY_ID>        <SUBMITTER_ID namespace='SC'>UK10K_exome_sequence__Tampere_samples-sc-2011-08-18T14:31:13Z-1789</SUBMITTER_ID>      </IDENTIFIERS>    </STUDY_REF>    <SAMPLE_REF accession='ERS033022' refcenter='SC' label='UK10K_TAMP5103528' refname='UK10K_TAMP5103528-sc-2011-05-04T10:55:31Z-1127404'>      <IDENTIFIERS>        <PRIMARY_ID>ERS033022</PRIMARY_ID>        <SUBMITTER_ID namespace='SC'>UK10K_TAMP5103528-sc-2011-05-04T10:55:31Z-1127404</SUBMITTER_ID>      </IDENTIFIERS>    </SAMPLE_REF>    <ANALYSIS_TYPE>      <SEQUENCE_VARIATION>        <ASSEMBLY>          <STANDARD refname='GRCh37'/>        </ASSEMBLY>      </SEQUENCE_VARIATION>    </ANALYSIS_TYPE>    <FILES>      <FILE filename='UK10K_TAMP5103528.REL-2013-04-20.vcf.gz' filetype='vcf' checksum_method='MD5' checksum='539edae44f04a9de25b755ab38c3179f' unencrypted_checksum='d062b44357539d63bf514768895c7f83'/>    </FILES>  </ANALYSIS></ANALYSIS_SET>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.AnalysisData'}}

Datasets


In [58]:
datasets_all = s.get(root_url+'datasets')
datasets_all_json = json.loads(datasets_all.text)

In [59]:
# List datasets ids
[item['egaAccessionId'] for item in datasets_all_json['response']['result']]


Out[59]:
['EGAD00001000667',
 'EGAD00001001382',
 'EGAD00001000293',
 'EGAD00001000025',
 'EGAD00001000044',
 'EGAD00001001740',
 'EGAD00001001566',
 'EGAD00001001458',
 'EGAD00001001952',
 'EGAD00001001813']

In [61]:
datasets_single = s.get(root_url+'datasets/EGAD00001000044')
json.loads(datasets_single.text)


Out[61]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'EGAS00000000092-ega-27092011',
    'analysisReferences': None,
    'attributes': [],
    'centerName': 'Hospital Clinic Barcelona',
    'creationTime': 1318490365000,
    'datasetLinks': [],
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Barcelona'>62BB5AAXX__exome_CNAG_CLL-323ND_paired</SUBMITTER_ID>      </IDENTIFIERS>    </RUN_REF>    <RUN_REF accession='EGAR00001004101' refname='100424_HWUSI-EAS1692_0001_CBOTC_61JJRAAXX__exome_CNAG_CLL-016ND_paired' refcenter='Hospital Clinic Barcelona'>      <IDENTIFIERS>        <PRIMARY_ID>EGAR00001004101</PRIMARY_ID>        <SUBMITTER_ID namespace='Hospital Clinic Barcelona'>100424_HWUSI-EAS1692_0001_CBOTC_61JJRAAXX__exome_CNAG_CLL-016ND_paired</SUBMITTER_ID>      </IDENTIFIERS>    </RUN_REF>    <RUN_REF accession='EGAR00001004102' refname='61UVHAAXX__exome_CNAG_CLL-049ND_paired' refcenter='Hospital Clinic Barcelona'>      <IDENTIFIERS>        <PRIMARY_ID>EGAR00001004102</PRIMARY_ID>        <SUBMITTER_ID namespace='Hospital Clinic Barcelona'>61UVHAAXX__exome_CNAG_CLL-049ND_paired</SUBMITTER_ID>      </IDENTIFIERS>    </RUN_REF>    <RUN_REF accession='EGAR00001004103' refname='62BB5AAXX__exome_CNAG_CLL-156ND_paired' refcenter='Hospital Clinic Barcelona'>      <IDENTIFIERS>        <PRIMARY_ID>EGAR00001004103</PRIMARY_ID>        <SUBMITTER_ID namespace='Hospital Clinic Barcelona'>62BB5AAXX__exome_CNAG_CLL-156ND_paired</SUBMITTER_ID>      </IDENTIFIERS>    </RUN_REF>    <RUN_REF accession='EGAR00001004104' refname='100701_HWUSI-EAS1684_0009_botA_62149AAXX__exome_CNAG_CLL-052ND_paired' refcenter='Hospital Clinic Barcelona'>      <IDENTIFIERS>        <PRIMARY_ID>EGAR00001004104</PRIMARY_ID>        <SUBMITTER_ID namespace='Hospital Clinic Barcelona'>100701_HWUSI-EAS1684_0009_botA_62149AAXX__exome_CNAG_CLL-052ND_paired</SUBMITTER_ID>      </IDENTIFIERS>    </RUN_REF>    <RUN_REF accession='EGAR00001006815' refname='exome_CNAG_CLL-018TD_paired_reverse' refcenter='Hospital Clinic Barcelona'>      <IDENTIFIERS>        <PRIMARY_ID>EGAR00001006815</PRIMARY_ID>        <SUBMITTER_ID namespace='Hospital Clinic Barcelona'>exome_CNAG_CLL-018TD_paired_reverse</SUBMITTER_ID>      </IDENTIFIERS>    </RUN_REF>    <RUN_REF accession='EGAR00001006816' refname='exome_CNAG_CLL-018TD_paired_forward' refcenter='Hospital Clinic Barcelona'>      <IDENTIFIERS>        <PRIMARY_ID>EGAR00001006816</PRIMARY_ID>        <SUBMITTER_ID namespace='Hospital Clinic Barcelona'>exome_CNAG_CLL-018TD_paired_forward</SUBMITTER_ID>      </IDENTIFIERS>    </RUN_REF>    <RUN_REF accession='EGAR00001006817' refname='exome_CNAG_CLL-018ND_paired_reverse' refcenter='Hospital Clinic Barcelona'>      <IDENTIFIERS>        <PRIMARY_ID>EGAR00001006817</PRIMARY_ID>        <SUBMITTER_ID namespace='Hospital Clinic Barcelona'>exome_CNAG_CLL-018ND_paired_reverse</SUBMITTER_ID>      </IDENTIFIERS>    </RUN_REF>    <RUN_REF accession='EGAR00001006818' refname='exome_CNAG_CLL-018ND_paired_forward' refcenter='Hospital Clinic Barcelona'>      <IDENTIFIERS>        <PRIMARY_ID>EGAR00001006818</PRIMARY_ID>        <SUBMITTER_ID namespace='Hospital Clinic Barcelona'>exome_CNAG_CLL-018ND_paired_forward</SUBMITTER_ID>      </IDENTIFIERS>    </RUN_REF>    <POLICY_REF accession='EGAP00001000036' refname='ICGC Data Access Agreements' refcenter='Hospital Clinic Barcelona'>      <IDENTIFIERS>        <PRIMARY_ID>EGAP00001000036</PRIMARY_ID>        <SUBMITTER_ID namespace='Hospital Clinic Barcelona'>ICGC Data Access Agreements</SUBMITTER_ID>      </IDENTIFIERS>    </POLICY_REF>    <DATASET_LINKS>      <DATASET_LINK>        <URL_LINK>          <LABEL>ICGC Data Portal</LABEL>          <URL>http://dcc.icgc.org</URL>        </URL_LINK>      </DATASET_LINK>      <DATASET_LINK>        <URL_LINK>          <LABEL>CLL Data Portal</LABEL>          <URL>http://www.cllgenome.es/</URL>        </URL_LINK>      </DATASET_LINK>    </DATASET_LINKS>  </DATASET></DATASETS>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.DatasetData'}}

Experiments


In [4]:
experiments_all = s.get(root_url+'experiments')
experiments_all_json = json.loads(experiments_all.text)


---------------------------------------------------------------------------
TypeError                                 Traceback (most recent call last)
C:\Users\cico\Anaconda3\lib\site-packages\requests\packages\urllib3\connectionpool.py in _make_request(self, conn, method, url, timeout, **httplib_request_kw)
    375             try:  # Python 2.7, use buffering of HTTP responses
--> 376                 httplib_response = conn.getresponse(buffering=True)
    377             except TypeError:  # Python 2.6 and older

TypeError: getresponse() got an unexpected keyword argument 'buffering'

During handling of the above exception, another exception occurred:

KeyboardInterrupt                         Traceback (most recent call last)
<ipython-input-4-535e6f0683e1> in <module>()
----> 1 experiments_all = s.get(root_url+'experiments')
      2 experiments_all_json = json.loads(experiments_all.text)

C:\Users\cico\Anaconda3\lib\site-packages\requests\sessions.py in get(self, url, **kwargs)
    478 
    479         kwargs.setdefault('allow_redirects', True)
--> 480         return self.request('GET', url, **kwargs)
    481 
    482     def options(self, url, **kwargs):

C:\Users\cico\Anaconda3\lib\site-packages\requests\sessions.py in request(self, method, url, params, data, headers, cookies, files, auth, timeout, allow_redirects, proxies, hooks, stream, verify, cert, json)
    466         }
    467         send_kwargs.update(settings)
--> 468         resp = self.send(prep, **send_kwargs)
    469 
    470         return resp

C:\Users\cico\Anaconda3\lib\site-packages\requests\sessions.py in send(self, request, **kwargs)
    574 
    575         # Send the request
--> 576         r = adapter.send(request, **kwargs)
    577 
    578         # Total elapsed time of the request (approximately)

C:\Users\cico\Anaconda3\lib\site-packages\requests\adapters.py in send(self, request, stream, timeout, verify, cert, proxies)
    374                     decode_content=False,
    375                     retries=self.max_retries,
--> 376                     timeout=timeout
    377                 )
    378 

C:\Users\cico\Anaconda3\lib\site-packages\requests\packages\urllib3\connectionpool.py in urlopen(self, method, url, body, headers, retries, redirect, assert_same_host, timeout, pool_timeout, release_conn, **response_kw)
    557             httplib_response = self._make_request(conn, method, url,
    558                                                   timeout=timeout_obj,
--> 559                                                   body=body, headers=headers)
    560 
    561             # If we're going to release the connection in ``finally:``, then

C:\Users\cico\Anaconda3\lib\site-packages\requests\packages\urllib3\connectionpool.py in _make_request(self, conn, method, url, timeout, **httplib_request_kw)
    376                 httplib_response = conn.getresponse(buffering=True)
    377             except TypeError:  # Python 2.6 and older
--> 378                 httplib_response = conn.getresponse()
    379         except (SocketTimeout, BaseSSLError, SocketError) as e:
    380             self._raise_timeout(err=e, url=url, timeout_value=read_timeout)

C:\Users\cico\Anaconda3\lib\http\client.py in getresponse(self)
   1172         try:
   1173             try:
-> 1174                 response.begin()
   1175             except ConnectionError:
   1176                 self.close()

C:\Users\cico\Anaconda3\lib\http\client.py in begin(self)
    280         # read until we get a non-100 response
    281         while True:
--> 282             version, status, reason = self._read_status()
    283             if status != CONTINUE:
    284                 break

C:\Users\cico\Anaconda3\lib\http\client.py in _read_status(self)
    241 
    242     def _read_status(self):
--> 243         line = str(self.fp.readline(_MAXLINE + 1), "iso-8859-1")
    244         if len(line) > _MAXLINE:
    245             raise LineTooLong("status line")

C:\Users\cico\Anaconda3\lib\socket.py in readinto(self, b)
    573         while True:
    574             try:
--> 575                 return self._sock.recv_into(b)
    576             except timeout:
    577                 self._timeout_occurred = True

C:\Users\cico\Anaconda3\lib\ssl.py in recv_into(self, buffer, nbytes, flags)
    922                   "non-zero flags not allowed in calls to recv_into() on %s" %
    923                   self.__class__)
--> 924             return self.read(nbytes, buffer)
    925         else:
    926             return socket.recv_into(self, buffer, nbytes, flags)

C:\Users\cico\Anaconda3\lib\ssl.py in read(self, len, buffer)
    784             raise ValueError("Read on closed or unwrapped SSL socket.")
    785         try:
--> 786             return self._sslobj.read(len, buffer)
    787         except SSLError as x:
    788             if x.args[0] == SSL_ERROR_EOF and self.suppress_ragged_eofs:

C:\Users\cico\Anaconda3\lib\ssl.py in read(self, len, buffer)
    568         """
    569         if buffer is not None:
--> 570             v = self._sslobj.read(len, buffer)
    571         else:
    572             v = self._sslobj.read(len or 1024)

KeyboardInterrupt: 

In [5]:
# List experiments ids
[item['egaAccessionId'] for item in experiments_all_json['response']['result']]


---------------------------------------------------------------------------
NameError                                 Traceback (most recent call last)
<ipython-input-5-9e64753ab996> in <module>()
      1 # List experiments ids
----> 2 [item['egaAccessionId'] for item in experiments_all_json['response']['result']]

NameError: name 'experiments_all_json' is not defined

In [6]:
experiments_single = s.get(root_url+'experiments/EGAX00001000001')
json.loads(experiments_single.text)


Out[6]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'SC_EXP_4115_6',
    'centerName': 'SC',
    'creationTime': 1290441165000,
    'designDescription': 'Illumina sequencing of sample "PD2126b"; library "Exp2_PD2126b 1" for the "Renal Cancer Exome Sequencing" study.',
    'ebiId': 'ERX009001',
    'ebiSubmissionDetailsIds': None,
    'editionTime': 1377184334000,
    'egaAccessionId': 'EGAX00001000001',
    'egaAccessionIds': None,
    'eraSubmissionId': 'ERA015321',
    'firstPublic': 1462898381821,
    'generatedExperimentIds': None,
    'globalExperimentId': None,
    'id': 'ERX009001',
    'instrumentModel': 'Illumina Genome Analyzer II',
    'instrumentModelId': None,
    'instrumentPlatform': 'ILLUMINA',
    'json': '""',
    'libraryConstructionProtocol': 'qPCR only',
    'libraryLayout': 'PAIRED',
    'libraryLayoutId': '0',
    'libraryName': 'Exp2_PD2126b 1',
    'librarySelection': 'RANDOM',
    'librarySelectionId': None,
    'librarySource': 'GENOMIC',
    'librarySourceId': None,
    'libraryStrategy': 'WGS',
    'libraryStrategyId': None,
    'pairedNominalLength': 250,
    'pairedNominalSdev': 0.0,
    'sampleAlias': None,
    'sampleId': 'ERS014986',
    'status': 'SUBMITTED',
    'studyAlias': None,
    'studyId': 'ERP000376',
    'submissionCommandIds': None,
    'submissionErrorMessages': None,
    'submissionId': 'ERA015321',
    'submissionInfoMessages': None,
    'submitterId': 'ega-box-03',
    'title': None,
    'userId': None,
    'validationErrorMessages': None,
    'validationResult': False,
    'version': 5,
    'xml': "<EXPERIMENT_SET>  <EXPERIMENT alias='SC_EXP_4115_6' center_name='SC' accession='ERX009001' broker_name='EGA'>    <IDENTIFIERS>      <PRIMARY_ID>ERX009001</PRIMARY_ID>      <SUBMITTER_ID namespace='SC'>SC_EXP_4115_6</SUBMITTER_ID>    </IDENTIFIERS>    <STUDY_REF accession='ERP000376' refname='Renal_Cancer_Exome_Sequencing-sc-2010-10-28' refcenter='SC'>      <IDENTIFIERS>        <PRIMARY_ID>ERP000376</PRIMARY_ID>        <SUBMITTER_ID namespace='SC'>Renal_Cancer_Exome_Sequencing-sc-2010-10-28</SUBMITTER_ID>      </IDENTIFIERS>    </STUDY_REF>    <DESIGN>      <DESIGN_DESCRIPTION>Illumina sequencing of sample &quot;PD2126b&quot;; library &quot;Exp2_PD2126b 1&quot; for the &quot;Renal Cancer Exome Sequencing&quot; study.</DESIGN_DESCRIPTION>      <SAMPLE_DESCRIPTOR accession='ERS014986' refname='PD2126b-sc-2010-09-13-9187' refcenter='SC'>        <IDENTIFIERS>          <PRIMARY_ID>ERS014986</PRIMARY_ID>          <SUBMITTER_ID namespace='SC'>PD2126b-sc-2010-09-13-9187</SUBMITTER_ID>        </IDENTIFIERS>      </SAMPLE_DESCRIPTOR>      <LIBRARY_DESCRIPTOR>        <LIBRARY_NAME>Exp2_PD2126b 1</LIBRARY_NAME>        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>        <LIBRARY_LAYOUT>          <PAIRED NOMINAL_LENGTH='250'/>        </LIBRARY_LAYOUT>        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>      </LIBRARY_DESCRIPTOR>      <SPOT_DESCRIPTOR>        <SPOT_DECODE_SPEC>          <SPOT_LENGTH>152</SPOT_LENGTH>          <READ_SPEC>            <READ_INDEX>0</READ_INDEX>            <READ_CLASS>Application Read</READ_CLASS>            <READ_TYPE>Forward</READ_TYPE>            <BASE_COORD>1</BASE_COORD>          </READ_SPEC>          <READ_SPEC>            <READ_INDEX>1</READ_INDEX>            <READ_CLASS>Application Read</READ_CLASS>            <READ_TYPE>Reverse</READ_TYPE>            <BASE_COORD>77</BASE_COORD>          </READ_SPEC>        </SPOT_DECODE_SPEC>      </SPOT_DESCRIPTOR>    </DESIGN>    <PLATFORM>      <ILLUMINA>        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>      </ILLUMINA>    </PLATFORM>    <PROCESSING/>  </EXPERIMENT></EXPERIMENT_SET>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.ExperimentData'}}

Policies


In [7]:
policies_all = s.get(root_url+'policies')
policies_all_json = json.loads(policies_all.text)

In [8]:
# List policies ids
[item['egaAccessionId'] for item in policies_all_json['response']['result']]


Out[8]:
['EGAP00001000398',
 'EGAP00001000159',
 'EGAP00001000285',
 'EGAP00001000386',
 'EGAP00001000366',
 'EGAP00001000261',
 'EGAP00001000301',
 'EGAP00001000434',
 'EGAP00001000418',
 'EGAP00001000227']

In [9]:
policies_single = s.get(root_url+'policies/EGAP00001000227')
json.loads(policies_single.text)


Out[9]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'ena-POLICY-BGI-11-08-2014-10:30:54:643-153',
    'centerName': 'BGI',
    'creationTime': 1407746417000,
    'dacId': None,
    'ebiId': 'EGAP00001000227',
    'ebiSubmissionDetailsIds': None,
    'editionTime': 1407746417000,
    'egaAccessionId': 'EGAP00001000227',
    'eraSubmissionId': 'ERA345974',
    'firstPublic': 1462898442449,
    'id': 'EGAP00001000227',
    'json': '""',
    'policyText': 'BGI is willing to share the data to related researcher, we invested a lot of resources in acquiring these data, and we request that you follow these guidelines when using data provided by us.1.conducting appropriate research2.protecting the confidentiality of managed access data sets3.carefully communicating research results4.respecting rights to first publication and to acknowledgementIf you have any questions regarding the data or their use in publications, please contact lilin@genomics.cnDisclaimerBGI provides these data in good faith, but makes no warranty, express or implied, nor assumes any legal liability or responsibility for any purpose for which the data are used.',
    'status': 'SUBMITTED',
    'submissionCommandIds': None,
    'submissionErrorMessages': None,
    'submissionId': 'ERA345974',
    'submissionInfoMessages': None,
    'submitterId': 'ega-box-02',
    'title': 'BGI data share policy',
    'url': '',
    'userId': None,
    'validationErrorMessages': None,
    'validationResult': False,
    'version': 1,
    'xml': "<POLICY_SET>  <POLICY alias='ena-POLICY-BGI-11-08-2014-10:30:54:643-153' center_name='BGI' accession='EGAP00001000227' broker_name='EGA'>    <IDENTIFIERS>      <PRIMARY_ID>EGAP00001000227</PRIMARY_ID>      <SUBMITTER_ID namespace='BGI'>ena-POLICY-BGI-11-08-2014-10:30:54:643-153</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>BGI data share policy</TITLE>    <DAC_REF accession='EGAC00001000227' refname='ena-DAC-BGI-11-08-2014-10:25:03:569-151' refcenter='BGI'>      <IDENTIFIERS>        <PRIMARY_ID>EGAC00001000227</PRIMARY_ID>        <SUBMITTER_ID namespace='BGI'>ena-DAC-BGI-11-08-2014-10:25:03:569-151</SUBMITTER_ID>      </IDENTIFIERS>    </DAC_REF>    <POLICY_TEXT>BGI is willing to share the data to related researcher, we invested a lot of resources in acquiring these data, and we request that you follow these guidelines when using data provided by us.1.conducting appropriate research2.protecting the confidentiality of managed access data sets3.carefully communicating research results4.respecting rights to first publication and to acknowledgementIf you have any questions regarding the data or their use in publications, please contact lilin@genomics.cnDisclaimerBGI provides these data in good faith, but makes no warranty, express or implied, nor assumes any legal liability or responsibility for any purpose for which the data are used.</POLICY_TEXT>  </POLICY></POLICY_SET>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.PolicyData'}}

In [10]:
policies_single = s.get(root_url+'policies/EGAP00001000228')
json.loads(policies_single.text)


Out[10]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'ena-POLICY-LundGoth-Stroke-11-08-2014-12:32:29:800-212',
    'centerName': 'LundGoth-Stroke',
    'creationTime': 1407753165000,
    'dacId': None,
    'ebiId': 'EGAP00001000228',
    'ebiSubmissionDetailsIds': None,
    'editionTime': 1407753165000,
    'egaAccessionId': 'EGAP00001000228',
    'eraSubmissionId': 'ERA346369',
    'firstPublic': 1462898455376,
    'id': 'EGAP00001000228',
    'json': '""',
    'policyText': '•Use the data only for the approved research; •Protect data confidentiality; •Follow appropriate data security protections; •Follow all applicable laws, regulations and local institutional policies and procedures for handling genetic data; •Not attempt to identify individual participants from whom data within a dataset were obtained; •Not sell any of the data elements from datasets obtained from the EBI EGA data repository;•Not share with individuals other than those listed in the request any of the data elements from datasets obtained from the EBI EGA data repository; •Agree to the listing of a summary of approved research uses within the NIH GWAS data repository along with his or her name and organizational affiliation; •Agree to report, in real time, violations of the EBI EGA policy to the appropriate DAC;•Acknowledge the EBI EGA policy with regard to publication and intellectual property.',
    'status': 'SUBMITTED',
    'submissionCommandIds': None,
    'submissionErrorMessages': None,
    'submissionId': 'ERA346369',
    'submissionInfoMessages': None,
    'submitterId': 'ega-box-181',
    'title': 'Data access policy for the MDC-LSR-SAHLSIS ischemic stroke study',
    'url': '',
    'userId': None,
    'validationErrorMessages': None,
    'validationResult': False,
    'version': 1,
    'xml': "<POLICY_SET>  <POLICY alias='ena-POLICY-LundGoth-Stroke-11-08-2014-12:32:29:800-212' center_name='LundGoth-Stroke' accession='EGAP00001000228' broker_name='EGA'>    <IDENTIFIERS>      <PRIMARY_ID>EGAP00001000228</PRIMARY_ID>      <SUBMITTER_ID namespace='LundGoth-Stroke'>ena-POLICY-LundGoth-Stroke-11-08-2014-12:32:29:800-212</SUBMITTER_ID>    </IDENTIFIERS>    <TITLE>Data access policy for the MDC-LSR-SAHLSIS ischemic stroke study</TITLE>    <DAC_REF accession='EGAC00001000226' refname='ena-DAC-LundGoth-Stroke-10-08-2014-06:57:51:828-78' refcenter='LundGoth-Stroke'>      <IDENTIFIERS>        <PRIMARY_ID>EGAC00001000226</PRIMARY_ID>        <SUBMITTER_ID namespace='LundGoth-Stroke'>ena-DAC-LundGoth-Stroke-10-08-2014-06:57:51:828-78</SUBMITTER_ID>      </IDENTIFIERS>    </DAC_REF>    <POLICY_TEXT>•Use the data only for the approved research; •Protect data confidentiality; •Follow appropriate data security protections; •Follow all applicable laws, regulations and local institutional policies and procedures for handling genetic data; •Not attempt to identify individual participants from whom data within a dataset were obtained; •Not sell any of the data elements from datasets obtained from the EBI EGA data repository;•Not share with individuals other than those listed in the request any of the data elements from datasets obtained from the EBI EGA data repository; •Agree to the listing of a summary of approved research uses within the NIH GWAS data repository along with his or her name and organizational affiliation; •Agree to report, in real time, violations of the EBI EGA policy to the appropriate DAC;•Acknowledge the EBI EGA policy with regard to publication and intellectual property.</POLICY_TEXT>  </POLICY></POLICY_SET>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.PolicyData'}}

Runs


In [11]:
runs_all = s.get(root_url+'runs')
runs_all_json = json.loads(runs_all.text)

In [12]:
# List runs ids
[item['egaAccessionId'] for item in runs_all_json['response']['result']]


Out[12]:
['EGAR00001133823',
 'EGAR00001305188',
 'EGAR00001129538',
 'EGAR00001347438',
 'EGAR00001340990',
 'EGAR00001205664',
 'EGAR00001242797',
 'EGAR00001291988',
 'EGAR00001067703',
 'EGAR00001024702']

In [13]:
runs_single = s.get(root_url+'runs/EGAR00001133823')
json.loads(runs_single.text)


Out[13]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'SC_RUN_9916_6#53',
    'centerName': 'SC',
    'creationTime': 1378192116000,
    'ebiId': 'ERR337184',
    'ebiSubmissionDetailsIds': None,
    'editionTime': 1378192116000,
    'egaAccessionId': 'EGAR00001133823',
    'eraSubmissionId': 'ERA248725',
    'experimentId': 'ERX310089',
    'files': [{'checksum': None,
      'checksumMethod': None,
      'fileId': None,
      'fileName': '9916_6#53.bam.gpg',
      'source': None,
      'unencryptedChecksum': None}],
    'firstPublic': 1462898912762,
    'generatedExperimentId': None,
    'id': 'ERR337184',
    'json': '""',
    'runFileType': 'bam',
    'runFileTypeId': None,
    'sampleAlias': None,
    'sampleId': None,
    'status': 'SUBMITTED',
    'submissionCommandIds': None,
    'submissionErrorMessages': None,
    'submissionId': 'ERA248725',
    'submissionInfoMessages': None,
    'submitterId': 'ega-box-03',
    'userId': None,
    'validationErrorMessages': None,
    'validationResult': False,
    'version': 1,
    'xml': "<RUN_SET>  <RUN alias='SC_RUN_9916_6#53' center_name='SC' accession='ERR337184' broker_name='EGA' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance'>    <IDENTIFIERS>      <PRIMARY_ID>ERR337184</PRIMARY_ID>      <SUBMITTER_ID namespace='SC'>SC_RUN_9916_6#53</SUBMITTER_ID>    </IDENTIFIERS>    <EXPERIMENT_REF refname='SC_EXP_9916_6#53' refcenter='SC' accession='ERX310089'>      <IDENTIFIERS>        <PRIMARY_ID>ERX310089</PRIMARY_ID>        <SUBMITTER_ID namespace='SC'>SC_EXP_9916_6#53</SUBMITTER_ID>      </IDENTIFIERS>    </EXPERIMENT_REF>    <DATA_BLOCK>      <FILES>        <FILE filename='9916_6#53.bam.gpg' filetype='bam' checksum_method='MD5' checksum='191ca9c3797e6f2d47c1f5fa06a3fd3b' unencrypted_checksum='7a757a1f9190b2eef51054fb4cc9d9af'/>      </FILES>    </DATA_BLOCK>  </RUN></RUN_SET>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.RunData'}}

In [ ]:
runs_single = s.get(root_url+'runs/EGAR00001133824')
json.loads(runs_single.text)

Samples


In [14]:
samples_all = s.get(root_url+'samples')
samples_all_json = json.loads(samples_all.text)

In [15]:
# List samples ids
[item['egaAccessionId'] for item in samples_all_json['response']['result']]


Out[15]:
['EGAN00001150966',
 'EGAN00001126446',
 'EGAN00001138199',
 'EGAN00001133869',
 'EGAN00001154692',
 'EGAN00001111905',
 'EGAN00001158099',
 'EGAN00001158436',
 'EGAN00001150517',
 'EGAN00001159764']

In [16]:
samples_single = s.get(root_url+'samples/EGAN00001138199')
json.loads(samples_single.text)


Out[16]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'sample20645',
    'anonymizedName': None,
    'attributes': None,
    'bioSampleId': 'SAMEA2119535',
    'caseOrControl': None,
    'caseOrControlId': None,
    'cellLine': None,
    'centerName': 'SMD',
    'creationTime': 1371500468000,
    'description': None,
    'ebiId': 'ERS287903',
    'ebiSubmissionDetailsIds': None,
    'editionTime': 1371500468000,
    'egaAccessionId': 'EGAN00001138199',
    'eraSubmissionId': 'ERA227653',
    'firstPublic': 1462899126703,
    'gender': None,
    'genderId': None,
    'id': 'ERS287903',
    'json': '""',
    'organismPart': None,
    'phenotype': None,
    'region': None,
    'sampleAge': None,
    'sampleDetail': None,
    'status': 'SUBMITTED',
    'subjectId': None,
    'submissionCommandIds': None,
    'submissionErrorMessages': None,
    'submissionId': 'ERA227653',
    'submissionInfoMessages': None,
    'submitterId': 'ega-box-29',
    'title': None,
    'userId': None,
    'validationErrorMessages': None,
    'validationResult': False,
    'version': 1,
    'xml': "<SAMPLE_SET>  <SAMPLE alias='sample20645' center_name='SMD' broker_name='EGA' accession='ERS287903'>    <IDENTIFIERS>      <PRIMARY_ID>ERS287903</PRIMARY_ID>      <SUBMITTER_ID namespace='SMD'>sample20645</SUBMITTER_ID>    </IDENTIFIERS>    <SAMPLE_NAME>      <TAXON_ID>9606</TAXON_ID>      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>      <COMMON_NAME>human</COMMON_NAME>    </SAMPLE_NAME>  </SAMPLE></SAMPLE_SET>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.SampleData'}}

Studies


In [17]:
studies_all = s.get(root_url+'studies')
studies_all_json = json.loads(studies_all.text)

In [18]:
# List samples ids
[item['egaAccessionId'] for item in studies_all_json['response']['result']]


Out[18]:
['EGAS00001001225',
 'EGAS00001001472',
 'EGAS00001001177',
 'EGAS00001000762',
 'EGAS00001000544',
 'EGAS00001000421',
 'EGAS00001000835',
 'EGAS00001000345',
 'EGAS00001000012',
 'EGAS00001001052']

In [19]:
studies_single = s.get(root_url+'studies/EGAS00001000421')
json.loads(studies_single.text)


Out[19]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'Paroxysmal_Neurological_Disorders___rare_epilepsies-sc-2013-01-30T13:52:40Z-2514',
    'centerName': 'SC',
    'creationTime': 1359550361000,
    'customTags': None,
    'ebiId': 'ERP002182',
    'ebiSubmissionDetailsIds': None,
    'editionTime': 1359550361000,
    'egaAccessionId': 'EGAS00001000421',
    'eraSubmissionId': 'ERA192047',
    'firstPublic': 1462899422293,
    'id': 'ERP002182',
    'json': '""',
    'ownTerm': 'Exome Sequencing',
    'pubMedIds': None,
    'shortName': '',
    'status': 'SUBMITTED',
    'studyAbstract': 'We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of  EuroEPINOMICS. Most cases have a strong family history. The study sample will include both cases and controls.',
    'studyType': 'Other',
    'studyTypeId': None,
    'submissionCommandIds': None,
    'submissionErrorMessages': None,
    'submissionId': 'ERA192047',
    'submissionInfoMessages': None,
    'submitterId': 'ega-box-03',
    'title': 'Paroxysmal_Neurological_Disorders___rare_epilepsies',
    'userId': None,
    'validationErrorMessages': None,
    'validationResult': False,
    'version': 1,
    'xml': "<STUDY_SET>  <STUDY alias='Paroxysmal_Neurological_Disorders___rare_epilepsies-sc-2013-01-30T13:52:40Z-2514' accession='ERP002182' center_name='SC' broker_name='EGA' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance'>    <IDENTIFIERS>      <PRIMARY_ID>ERP002182</PRIMARY_ID>      <SUBMITTER_ID namespace='SC'>Paroxysmal_Neurological_Disorders___rare_epilepsies-sc-2013-01-30T13:52:40Z-2514</SUBMITTER_ID>    </IDENTIFIERS>    <DESCRIPTOR>      <STUDY_TITLE>Paroxysmal_Neurological_Disorders___rare_epilepsies</STUDY_TITLE>      <STUDY_DESCRIPTION>We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of  EuroEPINOMICS. Most cases have a strong family history. The study sample will include both cases and controls.</STUDY_DESCRIPTION>      <CENTER_PROJECT_NAME>Paroxysmal_Neurological_Disorders___rare_epilepsies</CENTER_PROJECT_NAME>      <STUDY_ABSTRACT>We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of  EuroEPINOMICS. Most cases have a strong family history. The study sample will include both cases and controls.</STUDY_ABSTRACT>      <STUDY_TYPE existing_study_type='Other' new_study_type='Exome Sequencing'/>      <RELATED_STUDIES>        <RELATED_STUDY>          <RELATED_LINK>            <DB>PROJECT</DB>            <ID>2514</ID>          </RELATED_LINK>          <IS_PRIMARY>false</IS_PRIMARY>        </RELATED_STUDY>      </RELATED_STUDIES>    </DESCRIPTOR>  </STUDY></STUDY_SET>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.StudyData'}}

In [20]:
studies_single = s.get(root_url+'studies/EGAS00001000422')
json.loads(studies_single.text)


Out[20]:
{'header': {'apiVersion': 'v1',
  'code': '200',
  'developerMessage': '',
  'docLink': 'https://ega.crg.eu',
  'errorCode': '1',
  'errorStack': '',
  'service': 'catalogservice',
  'userMessage': 'OK'},
 'response': {'numTotalResults': 1,
  'result': [{'alias': 'ChIP_Seq_of_different_histone_modifications_in_human_primary_megakaryocytes_and_erythroblasts_and_in_a_human_megakaryocytic_cell_line__CHRF__-sc-2013-01-31T10:15:55Z-1694',
    'centerName': 'SC',
    'creationTime': 1359623756000,
    'customTags': None,
    'ebiId': 'ERP002186',
    'ebiSubmissionDetailsIds': None,
    'editionTime': 1359623756000,
    'egaAccessionId': 'EGAS00001000422',
    'eraSubmissionId': 'ERA192170',
    'firstPublic': 1462899482219,
    'id': 'ERP002186',
    'json': '""',
    'ownTerm': '',
    'pubMedIds': None,
    'shortName': '',
    'status': 'SUBMITTED',
    'studyAbstract': 'Study of the transcription factor NF-E2 important for hematopoiesis in human megakaryocytes and erythroblasts as well as study of histone marks in human megakaryocytic and erythroblastic cells and cell lines.',
    'studyType': 'Epigenetics',
    'studyTypeId': None,
    'submissionCommandIds': None,
    'submissionErrorMessages': None,
    'submissionId': 'ERA192170',
    'submissionInfoMessages': None,
    'submitterId': 'ega-box-03',
    'title': 'ChIP_Seq_of_different_histone_modifications_in_human_primary_megakaryocytes_and_erythroblasts_and_in_a_human_megakaryocytic_cell_line__CHRF__',
    'userId': None,
    'validationErrorMessages': None,
    'validationResult': False,
    'version': 1,
    'xml': "<STUDY_SET>  <STUDY alias='ChIP_Seq_of_different_histone_modifications_in_human_primary_megakaryocytes_and_erythroblasts_and_in_a_human_megakaryocytic_cell_line__CHRF__-sc-2013-01-31T10:15:55Z-1694' accession='ERP002186' center_name='SC' broker_name='EGA' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance'>    <IDENTIFIERS>      <PRIMARY_ID>ERP002186</PRIMARY_ID>      <SUBMITTER_ID namespace='SC'>ChIP_Seq_of_different_histone_modifications_in_human_primary_megakaryocytes_and_erythroblasts_and_in_a_human_megakaryocytic_cell_line__CHRF__-sc-2013-01-31T10:15:55Z-1694</SUBMITTER_ID>    </IDENTIFIERS>    <DESCRIPTOR>      <STUDY_TITLE>ChIP_Seq_of_different_histone_modifications_in_human_primary_megakaryocytes_and_erythroblasts_and_in_a_human_megakaryocytic_cell_line__CHRF__</STUDY_TITLE>      <STUDY_DESCRIPTION>Study of the transcription factor NF-E2 important for hematopoiesis in human megakaryocytes and erythroblasts as well as study of histone marks in human megakaryocytic and erythroblastic cells and cell lines.</STUDY_DESCRIPTION>      <CENTER_PROJECT_NAME>ChIP_Seq_of_different_histone_modifications_in_human_primary_megakaryocytes_and_erythroblasts_and_in_a_human_megakaryocytic_cell_line__CHRF__</CENTER_PROJECT_NAME>      <STUDY_ABSTRACT>Study of the transcription factor NF-E2 important for hematopoiesis in human megakaryocytes and erythroblasts as well as study of histone marks in human megakaryocytic and erythroblastic cells and cell lines.</STUDY_ABSTRACT>      <STUDY_TYPE existing_study_type='Epigenetics'/>      <RELATED_STUDIES>        <RELATED_STUDY>          <RELATED_LINK>            <DB>PROJECT</DB>            <ID>1694</ID>          </RELATED_LINK>          <IS_PRIMARY>false</IS_PRIMARY>        </RELATED_STUDY>      </RELATED_STUDIES>    </DESCRIPTOR>  </STUDY></STUDY_SET>",
    'xmlRootElement': None}],
  'resultType': 'eu.crg.ega.microservice.dto.submitter.StudyData'}}