diff annotate.py @ 0:b001b50f2009 draft default tip

Imported from capsule None

--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/annotate.py	Mon Jan 27 09:28:06 2014 -0500
@@ -0,0 +1,163 @@
+#!/usr/bin/python
+
+import os.path
+import sys
+import optparse
+
+import vcfClass
+from vcfClass import *
+
+import tools
+from tools import *
+
+if __name__ == "__main__":
+  main()
+
+# Check that the reference and alternate in the dbsnp vcf file match those
+# from the input vcf file.
+def checkRefAlt(vcfRef, vcfAlt, dbsnpRef, dbsnpAlt, ref, position, annotation):
+  text = "WARNING: ref and alt alleles differ between vcf and " + annotation + " " + ref + ":" + str(position) + " vcf: " + \
+         vcfRef + "/" + vcfAlt + ", dbsnp: " + dbsnpRef + "/" + dbsnpAlt
+
+  allelesAgree = True
+  if vcfRef.lower() != dbsnpRef.lower():
+    if vcfRef.lower() != dbsnpAlt.lower():
+      #print >> sys.stderr, text
+      allelesAgree = False
+  else:
+    if vcfAlt.lower() != dbsnpAlt.lower():
+      #print >> sys.stderr, text
+      allelesAgree = False
+
+  return allelesAgree
+
+# Intersect two vcf files.  It is assumed that the two files are
+# sorted by genomic coordinates and the reference sequences are
+# in the same order.
+def annotateVcf(v, d, outputFile, annotation):
+  success1 = v.getRecord()
+  success2 = d.getRecord()
+  currentReferenceSequence = v.referenceSequence
+
+# Finish when the end of the first file has been reached.
+  while success1:
+
+# If the end of the dbsnp vcf file is reached, write out the
+# remaining records from the vcf file.
+    if not success2:
+      outputFile.write(v.record)
+      success1 = v.getRecord()
+
+    if v.referenceSequence == d.referenceSequence and v.referenceSequence == currentReferenceSequence:
+      if v.position == d.position:
+        allelesAgree = checkRefAlt(v.ref, v.alt, d.ref, d.alt, v.referenceSequence, v.position, annotation)
+        if annotation == "dbsnp": v.rsid = d.getDbsnpInfo()
+        elif annotation == "hapmap":
+          if allelesAgree: v.info += ";HM3"
+          else: v.info += ";HM3A"
+        record = v.buildRecord(False)
+        outputFile.write(record)
+
+        success1 = v.getRecord()
+        success2 = d.getRecord()
+      elif d.position > v.position: success1 = v.parseVcf(d.referenceSequence, d.position, True, outputFile)
+      elif v.position > d.position: success2 = d.parseVcf(v.referenceSequence, v.position, False, None)
+    else:
+      if v.referenceSequence == currentReferenceSequence: success1 = v.parseVcf(d.referenceSequence, d.position, True, outputFile)
+      elif d.referenceSequence == currentReferenceSequence: success2 = d.parseVcf(v.referenceSequence, v.position, False, None)
+
+# If the last record for a reference sequence is the same for both vcf
+# files, they will both have referenceSequences different from the
+# current reference sequence.  Change the reference sequence to reflect
+# this and proceed.
+      else:
+        if v.referenceSequence != d.referenceSequence:
+          print >> sys.stderr, "ERROR: Reference sequences for both files are unexpectedly different."
+          print >> sys.stderr, "Check that both files contain records for the following reference sequences:"
+          print >> sys.stderr, "\t", v.referenceSequence, " and ", d.referenceSequence
+          exit(1)
+      currentReferenceSequence = v.referenceSequence
+
+def main():
+
+# Parse the command line options
+  usage = "Usage: vcfPytools.py annotate [options]"
+  parser = optparse.OptionParser(usage = usage)
+  parser.add_option("-i", "--in",
+                    action="store", type="string",
+                    dest="vcfFile", help="input vcf files")
+  parser.add_option("-d", "--dbsnp",
+                    action="store", type="string",
+                    dest="dbsnpFile", help="input dbsnp vcf file")
+  parser.add_option("-m", "--hapmap",
+                    action="store", type="string",
+                    dest="hapmapFile", help="input hapmap vcf file")
+  parser.add_option("-o", "--out",
+                    action="store", type="string",
+                    dest="output", help="output vcf file")
+
+  (options, args) = parser.parse_args()
+
+# Check that a single  vcf file is given.
+  if options.vcfFile == None:
+    parser.print_help()
+    print >> sys.stderr, "\nInput vcf file (--in, -i) is required for dbsnp annotation."
+    exit(1)
+
+# Check that either a hapmap or a dbsnp vcf file is included.
+  if options.dbsnpFile == None and options.hapmapFile == None:
+    parser.print_help()
+    print >> sys.stderr, "\ndbSNP or hapmap vcf file is required (--dbsnp, -d, --hapmap, -h)."
+    exit(1)
+  elif options.dbsnpFile != None and options.hapmapFile != None:
+    parser.print_help()
+    print >> sys.stderr, "\ndbSNP or hapmap vcf file is required, not both (--dbsnp, -d, --hapmap, -h)."
+    exit(1)
+
+# Set the output file to stdout if no output file was specified.
+  outputFile, writeOut = setOutput(options.output) # tools.py
+
+  v = vcf() # Define vcf object.
+  d = vcf() # Define dbsnp/hapmap vcf object.
+  if options.dbsnpFile:
+    d.dbsnpVcf = True
+    annotationFile = options.dbsnpFile
+    annotation = "dbsnp"
+  elif options.hapmapFile:
+    d.hapmapVcf = True
+    annotationFile = options.hapmapFile
+    annotation = "hapmap"
+
+# Open the vcf files.
+  v.openVcf(options.vcfFile)
+  d.openVcf(annotationFile)
+
+# Read in the header information.
+  v.parseHeader(options.vcfFile, writeOut)
+  d.parseHeader(annotationFile, writeOut)
+
+# Add an extra line to the vcf header to indicate the file used for
+# performing dbsnp annotation.
+  taskDescriptor = "##vcfPytools=annotated vcf file with "
+  if options.dbsnpFile: taskDescriptor += "dbSNP file " + options.dbsnpFile
+  elif options.hapmapFile:
+    taskDescriptor += "hapmap file " + options.hapmapFile
+    v.infoHeaderString["HM3"] = "##INFO=<ID=HM3,Number=0,Type=Flag,Description=\"Hapmap3.2 membership determined from file " + \
+                                options.hapmapFile + "\">"
+    v.infoHeaderString["HM3A"] = "##INFO=<ID=HM3A,Number=0,Type=Flag,Description=\"Hapmap3.2 membership (with different alleles)" + \
+                                 ", determined from file " + options.hapmapFile + "\">"
+  writeHeader(outputFile, v, False, taskDescriptor) # tools.py
+
+# Annotate the vcf file.
+  annotateVcf(v, d, outputFile, annotation)
+
+# Check that the input files had the same list of reference sequences.
+# If not, it is possible that there were some problems.
+  checkReferenceSequenceLists(v.referenceSequenceList, d.referenceSequenceList) # tools.py
+
+# Close the vcf files.
+  v.closeVcf(options.vcfFile)
+  d.closeVcf(annotationFile)
+
+# End the program.
+  return 0