Thank you Zaag for mention. Probably this kind of caller would be best. Is there any other free solution? Did anybody tested bcftools, varscan, freebayes...?
Dear all,
lets assume we have reference genome and its mapped reads:
ref: ACGTCTTCGTCAATG
read1: ACGA
read2: ACGA
read3: ACGC
read4: ACGC
my variant caller should generate something like: het A/C - 50%. Dou you have any experiences with this calling? What caller can handle this problem? I found that some callers just skip this site.
Best,
Paul.
1 answer
GATK's HaplotypeCaller would call this:
| CHROM | POS | REF | ALT | GT |
|-------|----------|-----|-----|------|
| chr | 1 | T | A,C | 1/2 |
So for GT the ref (T) is 0, the first alternate (A) is 1 and the second (C) is 2, so
TT = 0/0 = WT
AA = 1/1 = Homozygous variant first alternate
CC = 2/2 = Homozygous variant and the second alternate
TA = 0/1 = Heterozygote with REF and first alternate allele
TC = 0/2 = Heterozygote with REF and second alternate allele
and what you described above:
A/C = 1/2 = Heterozygote with both alternate alleles
bcftools does not work for this, the other ones I've never used
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