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bcftools not calling variants that appear high quality

Hello,

I am trying to run a variant call using bcftools on a yeast (haploid) DNAseq .bam file. Using the following command I am able to generate a list of variants, but scanning through the .bam file on IGV, I can see variants that appear to be of high quality (100+ read coverage, good cigar scores on individual reads in the read track, etc.) that are not being called using this command.

bcftools mpileup -Ou -f sacCer3.fa -q 10 -d 250 myfile.bam |   bcftools call -Ou -mv --ploidy 1 |   bcftools filter -i 'DP>=50' |   bcftools norm -f sacCer3.fa -Oz -o myfile.vcf.gz

Reading other posts, I have loosened the quality criteria (-q 10) and these variants are still not being called.

Is there a way to interrogate the .bam file to ensure that it is meeting calling criteria at a particular position for bcftools? Any other suggestions?

bcftools 1.19

Thanks, Ben

bcftools dnaseq snps
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updated by Pierre Lindenbaum Pierre Lindenbaum • written by bertb • bertb

1 answer

remove `bcftools filter -i 'DP>=50' , remove the '-v' option of "bcftools cal"l , run bcftools mpileup in a small region known to contain a variant and show us the line of the resulting VCF.

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written by Pierre Lindenbaum Pierre Lindenbaum

Thank you for your response. Here is the adjusted code I ran:

$bcftools mpileup -Ou -f sacCer3.fa -q 10 -d 250 A7_sorted.bam |   bcftools call -Ou -m --ploidy 1 |   bcftools norm -f sacCer3.fa -Oz -o A7pl.vcf.gz
$bcftools view -H C2pl.vcf.gz chrI:26973
chrI    26973   .       A       G       18.4764 .       DP=32;VDB=1.56112e-05;SGB=-0.69312;MQ0F=0;AC=1;AN=1;DP4=0,0,32,0;MQ=11  GT:PL   1:48,0

It appears the variant is now being called with the revised code - thank you! However, the issue I am having is that I am trying to compare two bam files to identify unique variants. When I run the following command to compare variants:

$bcftools isec -n-1 -c none C2n.vcf.gz A7n.vcf.gz -Oz -p var/

many of the sites on this list appear to be calling differences where there don't appear to be any (as viewed in IGV). It seems this is because one of the vcf files will generate two calls. As an example, for position chrI:1469, calling file 1:

$bcftools view -H A7pl.vcf.gz chrI:1469
chrI    1469    .       C       .       284.59  .       DP=202;MQ0F=0;AN=1;DP4=107,91,0,0;MQ=26 GT      0

whereas calling file 2:

$bcftools view -H C2pl.vcf.gz chrI:1469
chrI    1469    .       C       .       284.59  .       DP=185;MQ0F=0;AN=1;DP4=101,81,0,0;MQ=25 GT      0
chrI    1469    .       C       .       29.597  .       INDEL;IDV=12;IMF=0.0648649;DP=185;SGB=-0.379885;RPBZ=2.5594;MQBZ=-5.13732;MQSBZ=-2.0529;BQBZ=-3.44995;SCBZ=1.04845;MQ0F=0;AN=1;DP4=99,71,0,1;MQ=26    GT      0

Given many more reads support the reference (DP4=99,71,0,1), why does bcftools generate this potential variant? Is there a way to screen these lower quality calls out before running my comparison?

Thank you

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written by bertb • bertb

However, the issue I am having is that I am trying to compare two bam files to identify unique variants. When I run the following command to compare variants:

this is another question.

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written by Pierre Lindenbaum Pierre Lindenbaum

DP4=0,0,32,0

you have a bias with the forward/reverse strand

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written by Pierre Lindenbaum Pierre Lindenbaum

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