Did any one tried importing varscan variant caller ( V.2.3.2) VCF output to IGV (V 2.1.2.4)?. I tried indexing VCF file using igvtools-index & Tabix command. It says error Error for input string:"PASS
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A few lines of my VCF format:
##fileformat=VCFv4.0
##source=VarScan2
##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
##FILTER=<ID=str10,Description="Less than 10% or more than 90% of variant supporting reads on one strand">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT Sample1
gi|671553188|gb|JH556661.1| 2200443 . G A PASS DP=21 GT:GQ:DP 0/1:1:21
gi|671553188|gb|JH556661.1| 2594155 . C A PASS DP=24 GT:GQ:DP 0/1:3:24
gi|671553188|gb|JH556661.1| 2594175 . C A PASS DP=26 GT:GQ:DP 0/1:4:26
gi|671553188|gb|JH556661.1| 2594192 . A G PASS DP=25 GT:GQ:DP 0/1:3:25
can you show us the first lines of the VCF...