Hello, I am a newbie to freebayes and I came across a problem when detecting alternative alleles on SNPs variants. What I am trying to achieve is a .vcf file that would show all ALT alleles found in .bam file on a specific position. I checked a small .bam file by eye and counted how many C,G,T,A should freebayes report on a specific position.
For instance on file.bam on a position chr2:200 there should be base C according to the reference genome. File.bam reports on 2 reads C, 131 reads base G, 2 reads T and no A - I checked this manually, excluding reads with lower mapping quality than 20.
Now, freebayes gave me a .vcf file that reports only 2-C reads and 2-G reads. Where are the reads that reported T? Should I change default options? Is there a parameter that I overlooked? Thank you so much for any help.
My call:
freebayes --min-mapping-quality 20 -f /hg19/hg19.fa DHCR7-p_R352Q.bam >varQ.vcf
Note: I tried to use -r chr2...
in my call, but since the results are not satisfying I tried to make it as simple as possible.