|
From: Thomas W. B. <tb...@um...> - 2016-07-22 21:46:38
|
I'm guessing that these are IUPAC ambiguity codes for cases where the indel overlaps a SNP in other individuals, or the other allele in the same individual. Look in the bcftools documentation for ways to suppress the ambiguity codes. I don't know if there is a way or not. - tom blackwell - On Fri, 22 Jul 2016, Annie Cowell wrote: > Hello, > > I'm calling variants the following way for single or multiple samples using > samtools and bcftools version 1.3.1 > > samtools mpileup -C50 -Bug -t AD -Q10 -f my.fasta sample.bam | bcftools > call -mv -Ov > my.vcf > > However, I am getting unusual bases for a couple of indels in the reference > field, such as W (as below) and R. > > AAKM01000065 8883 . GGW G 228 . > INDEL;IDV=40;IMF=0.888889;DP=45;VDB=0.880501;SGB=-0.692976;MQSB=0.114162;MQ0F=0;AC=2;AN=2;DP4=0,0,8,18;MQ=49 > GT:PL:AD 1/1:255,78,0:0,26 > > What causes this and how do I fix it? > > Thank you, > Annie > |