In this class session we will continue with analyzing the tumor gene expression dataset from the NIH human bladder cancer cohort (M=414 tumors), building on what we learned in Class Session 19 (Correlation Network). In order to keep the analysis simple&ast, in this notebook will restrict our analysis to a set of N=164 genes that are very highly expressed in bladder cancer. Using the 164 x 414 matrix of transcript abundance measurements, we will construct a network based on gene-gene partial correlation coefficients. We will also compare the distribution of partial correlation coefficients to the distribution of Pearson correlation coefficients. Do you think they will be different? In what way would you expect them to be different?
&ast Here, "simple" means that the covariance matrix will be nonsingular, so that we can obtain the partial correlation matrix by inversion.
We'll import all of the python modules that we will need for this exercise
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import pandas ## data file loading
import numpy
import sklearn.covariance ## for covariance matrix calculation
import matplotlib.pyplot
import matplotlib
import pylab
import scipy.stats ## for calculating the CDF of normal distribution
import igraph ## for network visualization and finding components
import math
Read the tab-deliminted text file of gene expression measurements (rows correspond to genes, columns correspond to bladder tumor samples). (use Pandas, pandas.read.csv, and as_matrix). As always, sanity check that the file that you loaded has the expected dimensions (4,473 x 414) using shape.
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gene_matrix_for_network_df = pandas.read_csv("shared/bladder_cancer_genes_tcga.txt", sep="\t")
Convert your data frame to a numpy matrix, using the pandas.DataFrame.as_matrix method.
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gene_matrix_for_network = ## add code here ##
As always, sanity check that the file that you loaded has the expected dimensions (4,473 x 414) using shape.
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print(gene_matrix_for_network.shape)
Compute the median expression level for each row of your matrix; use axis=1
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genes_median_expression = ## add code here ##
Filter the matrix to include only rows for which the gene's median expression is > 12; matrix should now be 164 x 414; this will enable us to easily compute the partial correlation matrix using the inverse of the covariance matrix. Print the size of the filtered matrix, as a sanity check.
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gene_matrix_np = numpy.array(gene_matrix_for_network)
genes_keep = ## add code here ##
matrix_filt = gene_matrix_np[genes_keep, ][0]
matrix_filt.shape
N = matrix_filt.shape[0]
Print the shape of your filtered matrix, as a sanity check. It should be 164x414.
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matrix_filt.shape
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Compute the 164 x 164 matrix of gene-gene Pearson correlation coefficients, using numpy.corrcoef (this function treats each row as a random variable, so you don't have to do any transposing of the matrix, unlike the situation in R).
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matrix_cor = ## add code here ##
Compute the covariance matrix using sklearn.covariance.empirical_covariance (from the sklearn.covariance package, . Make sure you take the transpose of the matrix_filt matrix before passing it to the empirical_covariance function!
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matrix_cov = ## add code here ##
Use numpy.linalg.inv to get the inverse matrix.
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matrix_cov_inv = ## add code here ##
Use a double for loop to "scale" the negative of the precision matrix, which will give you the partial correlation. Print the dimensions of the matrix you get back, as a sanity check.
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matrix_pcor = ## add code here ##
for i in range(N):
for j in range(N):
matrix_pcor[i,j] /= numpy.sqrt(matrix_cov_inv[i,i]*matrix_cov_inv[j,j])
print(matrix_pcor.shape)
Get the correlation coefficients and the partial correlation coefficients of the lower triangle of the matrix (not including the diagonal), as two vectors cor_values and pcor_values; your resulting vectors should each have length 13,366. You will want to use numpy.tri and numpy.where (see class session 19 exercise)
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cor_values = matrix_cor[numpy.where(numpy.tri(*matrix_cor.shape, k=-1))]
pcor_values = matrix_pcor[numpy.where(numpy.tri(*matrix_pcor.shape, k=-1))]
print(len(cor_values))
print(len(pcor_values))
plot the histograms of the correlation coefficients (upper triangle only) and the partial correlation coefficients, on the same plot using alpha blending (refer to class session 17 exercise)
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matplotlib.pyplot.hist(cor_values, normed=1, alpha=0.5, label="cor")
matplotlib.pyplot.hist(pcor_values, normed=1, alpha=0.5, label="pcor")
matplotlib.pyplot.legend(loc="upper left")
matplotlib.pyplot.xlabel("R")
matplotlib.pyplot.ylabel("frequency")
matplotlib.pyplot.show()
Fisher transform the partial correlation values, using numpy.log:
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z_scores = 0.5*numpy.log((1+pcor_values)/
(1-pcor_values))
Compute a p-value for each gene pair (upper triangle only), using the fact that sqrt(M-N-5) times the fisher Z sore should be approximately univariate normal (with zero mean) under the null hypothesis that a given gene pair's measurements (conditioned on the measurements for all the other 162 genes) are independent. You will want to use scipy.stats.norm.cdf, numpy.abs, and math.sqrt function (see class session 19 exercise).
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M = gene_matrix_for_network_df.shape[1]
P_values = ## add code here ##
How many gene pairs have a P value less than 0.01? (use which and length)
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len(numpy.where(P_values < 0.01)[0])
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What are the sizes of the components in the undirected graph whose edges have P < 0.05 in the statistical test that you did? You will need to use zip, tolist, list, and igraph.Graph.TupleList (see class session 19 exercise)
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inds_tri = numpy.where(numpy.tri(*matrix_pcor.shape, k=-1))
inds_sig = numpy.where(P_values < 0.01)
graph_edge_list = list(zip(inds_tri[1][inds_sig].tolist(),
inds_tri[0][inds_sig].tolist()))
final_network = igraph.Graph.TupleList(graph_edge_list, directed=False)
final_network.summary()
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Plot the graph degree distribution on log-log scale
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degree_dist = final_network.degree_distribution()
xs, ys = zip(*[(left, count) for left, _, count in degree_dist.bins()])
matplotlib.pyplot.loglog(xs, ys, marker="o")
pylab.xlabel("k")
pylab.ylabel("N(k)")
pylab.show()
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