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https://github.com/arjunrajlaboratory/RajLabSeqTools
10 December 2020, 08:13:14 UTC
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  • Snakemake_bulkRNA
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  • count-matrix.py
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Tip revision: c8b8c79b2ec9c1bd9eb7ced427bb2aec25f19506 authored by Benjamin Emert on 26 March 2020, 17:37:11 UTC
Updated reorganizeBasespaceFiles.py to better parse samples with same first index (e.g. sample 1 and sample10)
Tip revision: c8b8c79
count-matrix.py
import pandas as pd

def get_column(strandedness):
    if pd.isnull(strandedness) or strandedness == "none":
        return 1 #non stranded protocol
    elif strandedness == "yes":
        return 2 #3rd column
    elif strandedness == "reverse":
        return 3 #4th column, usually for Illumina truseq
    else:
        raise ValueError(("'strandedness' column should be empty or have the " 
                          "value 'none', 'yes' or 'reverse', instead has the " 
                          "value {}").format(repr(strandedness)))

counts = [pd.read_table(f, index_col=0, usecols=[0, get_column(strandedness)], 
          header=None, skiprows=4) 
          for f, strandedness in zip(snakemake.input, snakemake.params.strand)]

for t, sample in zip(counts, snakemake.params.samples):
    t.columns = [sample]

matrix = pd.concat(counts, axis=1)
matrix.index.name = "gene"
# collapse technical replicates
matrix = matrix.groupby(matrix.columns, axis=1).sum()
matrix.to_csv(snakemake.output[0], sep="\t")

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