Mercurial > repos > davidvanzessen > imgt_loader_igg
diff imgtconvert.py @ 7:04e72fc8b2c4 draft default tip
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author | davidvanzessen |
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date | Fri, 05 Sep 2014 04:21:48 -0400 |
parents | 5b030e48b308 |
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--- a/imgtconvert.py Mon Jul 07 09:54:42 2014 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,194 +0,0 @@ -import pandas as pd -try: - pd.options.mode.chained_assignment = None # default='warn' -except: - pass -import re -import argparse -import os - -def stop_err( msg, ret=1 ): - sys.stderr.write( msg ) - sys.exit( ret ) - -#docs.python.org/dev/library/argparse.html -parser = argparse.ArgumentParser() -parser.add_argument("--input", help="Input folder with files") -parser.add_argument("--output", help="Output file") - -args = parser.parse_args() - -old_summary_columns = [u'Sequence ID', u'JUNCTION frame', u'V-GENE and allele', u'D-GENE and allele', u'J-GENE and allele', u'CDR1-IMGT length', u'CDR2-IMGT length', u'CDR3-IMGT length', u'Orientation'] -old_sequence_columns = [u'CDR1-IMGT', u'CDR2-IMGT', u'CDR3-IMGT'] -old_junction_columns = [u'JUNCTION'] - -added_summary_columns = [u'Functionality', u'V-REGION identity %', u'V-REGION identity nt', u'D-REGION reading frame', u'AA JUNCTION', u'Functionality comment', u'Sequence'] -added_sequence_columns = [u'FR1-IMGT', u'FR2-IMGT', u'FR3-IMGT', u'CDR3-IMGT', u'JUNCTION', u'J-REGION', u'FR4-IMGT'] -added_junction_columns = [u"P3'V-nt nb", u'N1-REGION-nt nb', u"P5'D-nt nb", u"P3'D-nt nb", u'N2-REGION-nt nb', u"P5'J-nt nb", u"3'V-REGION trimmed-nt nb", u"5'D-REGION trimmed-nt nb", u"3'D-REGION trimmed-nt nb", u"5'J-REGION trimmed-nt nb"] - -inputFolder = args.input - -dirContents = os.listdir(inputFolder) -if len(dirContents) == 1: - inputFolder = os.path.join(inputFolder, dirContents[0]) - if os.path.isdir(inputFolder): - dirContents = os.listdir(inputFolder) -files = sorted([os.path.join(inputFolder, f) for f in dirContents if os.path.isfile(os.path.join(inputFolder, f))]) - -if len(files) % 3 is not 0: - stop_err("Files in zip not a multiple of 3, it should contain the all the 1_, 5_ and 6_ files for a sample") - import sys - sys.exit() - -triplets = [] -step = len(files) / 3 -for i in range(0, step): - triplets.append((files[i], files[i + step], files[i + step + step])) - -outFile = args.output - -#fSummary = pd.read_csv(triplets[0][0], sep="\t", low_memory=False) -fSummary = pd.read_csv(triplets[0][0], sep="\t") -#fSequence = pd.read_csv(triplets[0][1], sep="\t", low_memory=False) -fSequence = pd.read_csv(triplets[0][1], sep="\t") -#fJunction = pd.read_csv(triplets[0][2], sep="\t", low_memory=False) -fJunction = pd.read_csv(triplets[0][2], sep="\t") -tmp = fSummary[["Sequence ID", "JUNCTION frame", "V-GENE and allele", "D-GENE and allele", "J-GENE and allele"]] - -tmp["CDR1 Seq"] = fSequence["CDR1-IMGT"] -tmp["CDR1 Length"] = fSummary["CDR1-IMGT length"] - -tmp["CDR2 Seq"] = fSequence["CDR2-IMGT"] -tmp["CDR2 Length"] = fSummary["CDR2-IMGT length"] - -tmp["CDR3 Seq"] = fSequence["CDR3-IMGT"] -tmp["CDR3 Length"] = fSummary["CDR3-IMGT length"] - -tmp["CDR3 Seq DNA"] = fJunction["JUNCTION"] -tmp["CDR3 Length DNA"] = '1' -tmp["Strand"] = fSummary["Orientation"] -tmp["CDR3 Found How"] = 'a' - -for col in added_summary_columns: - tmp[col] = fSummary[col] - -for col in added_sequence_columns: - tmp[col] = fSequence[col] - -for col in added_junction_columns: - tmp[col] = fJunction[col] - -outFrame = tmp - - - -for triple in triplets[1:]: - fSummary = pd.read_csv(triple[0], sep="\t") - fSequence = pd.read_csv(triple[1], sep="\t") - fJunction = pd.read_csv(triple[2], sep="\t") - - tmp = fSummary[["Sequence ID", "JUNCTION frame", "V-GENE and allele", "D-GENE and allele", "J-GENE and allele"]] - - tmp["CDR1 Seq"] = fSequence["CDR1-IMGT"] - tmp["CDR1 Length"] = fSummary["CDR1-IMGT length"] - - tmp["CDR2 Seq"] = fSequence["CDR2-IMGT"] - tmp["CDR2 Length"] = fSummary["CDR2-IMGT length"] - - tmp["CDR3 Seq"] = fSequence["CDR3-IMGT"] - tmp["CDR3 Length"] = fSummary["CDR3-IMGT length"] - - tmp["CDR3 Seq DNA"] = fJunction["JUNCTION"] - tmp["CDR3 Length DNA"] = '1' - tmp["Strand"] = fSummary["Orientation"] - tmp["CDR3 Found How"] = 'a' - - for col in added_summary_columns: - tmp[col] = fSummary[col] - - for col in added_sequence_columns: - tmp[col] = fSequence[col] - - for col in added_junction_columns: - tmp[col] = fJunction[col] - - outFrame = outFrame.append(tmp) - - -outFrame.columns = [u'ID', u'VDJ Frame', u'Top V Gene', u'Top D Gene', u'Top J Gene', u'CDR1 Seq', u'CDR1 Length', u'CDR2 Seq', u'CDR2 Length', u'CDR3 Seq', u'CDR3 Length', u'CDR3 Seq DNA', u'CDR3 Length DNA', u'Strand', u'CDR3 Found How', u'Functionality', 'V-REGION identity %', 'V-REGION identity nt', 'D-REGION reading frame', 'AA JUNCTION', 'Functionality comment', 'Sequence', 'FR1-IMGT', 'FR2-IMGT', 'FR3-IMGT', 'CDR3-IMGT', 'JUNCTION', 'J-REGION', 'FR4-IMGT', 'P3V-nt nb', 'N1-REGION-nt nb', 'P5D-nt nb', 'P3D-nt nb', 'N2-REGION-nt nb', 'P5J-nt nb', '3V-REGION trimmed-nt nb', '5D-REGION trimmed-nt nb', '3D-REGION trimmed-nt nb', '5J-REGION trimmed-nt nb'] - -""" -IGHV[0-9]-[0-9ab]+-?[0-9]?D? -TRBV[0-9]{1,2}-?[0-9]?-?[123]? -IGKV[0-3]D?-[0-9]{1,2} -IGLV[0-9]-[0-9]{1,2} -TRAV[0-9]{1,2}(-[1-46])?(/DV[45678])? -TRGV[234589] -TRDV[1-3] - -IGHD[0-9]-[0-9ab]+ -TRBD[12] -TRDD[1-3] - -IGHJ[1-6] -TRBJ[12]-[1-7] -IGKJ[1-5] -IGLJ[12367] -TRAJ[0-9]{1,2} -TRGJP?[12] -TRDJ[1-4] -""" - -vPattern = [r"(IGHV[0-9]-[0-9ab]+-?[0-9]?D?)", - r"(TRBV[0-9]{1,2}-?[0-9]?-?[123]?)", - r"(IGKV[0-3]D?-[0-9]{1,2})", - r"(IGLV[0-9]-[0-9]{1,2})", - r"(TRAV[0-9]{1,2}(-[1-46])?(/DV[45678])?)", - r"(TRGV[234589])", - r"(TRDV[1-3])"] - -dPattern = [r"(IGHD[0-9]-[0-9ab]+)", - r"(TRBD[12])", - r"(TRDD[1-3])"] - -jPattern = [r"(IGHJ[1-6])", - r"(TRBJ[12]-[1-7])", - r"(IGKJ[1-5])", - r"(IGLJ[12367])", - r"(TRAJ[0-9]{1,2})", - r"(TRGJP?[12])", - r"(TRDJ[1-4])"] - -vPattern = re.compile(r"|".join(vPattern)) - -dPattern = re.compile(r"|".join(dPattern)) - -jPattern = re.compile(r"|".join(jPattern)) - - -def filterGenes(s, pattern): - if type(s) is not str: - return "NA" - res = pattern.search(s) - if res: - return res.group(0) - return "NA" - - - -outFrame["Top V Gene"] = outFrame["Top V Gene"].apply(lambda x: filterGenes(x, vPattern)) -outFrame["Top D Gene"] = outFrame["Top D Gene"].apply(lambda x: filterGenes(x, dPattern)) -outFrame["Top J Gene"] = outFrame["Top J Gene"].apply(lambda x: filterGenes(x, jPattern)) - -print outFrame - -tmp = outFrame["VDJ Frame"] -tmp = tmp.replace("in-frame", "In-frame") -tmp = tmp.replace("null", "Out-of-frame") -tmp = tmp.replace("out-of-frame", "Out-of-frame") -outFrame["VDJ Frame"] = tmp -outFrame["CDR3 Length DNA"] = outFrame["CDR3 Seq DNA"].map(str).map(len) -safeLength = lambda x: len(x) if type(x) == str else 0 -outFrame = outFrame[(outFrame["CDR3 Seq DNA"].map(safeLength) > 0) & (outFrame["Top V Gene"] != "NA") & (outFrame["Top J Gene"] != "NA")] #filter out weird rows? -#outFrame = outFrame[(outFrame["CDR3 Seq DNA"].map(safeLength) > 0) & (outFrame["Top V Gene"] != "NA") & (outFrame["Top D Gene"] != "NA") & (outFrame["Top J Gene"] != "NA")] #filter out weird rows? -outFrame.to_csv(outFile, sep="\t", index=False, index_label="index")