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#67 variant calling using samtools mpileup

v1.0_(example)
open
None
1
2019-05-14
2019-05-14
No

I am using samtools mpileup and bcf tools to make a variant calling in RNAseq data. In the vcf file I can see genotypes 1/1 1/0 2/0 2/2 ....etc but the homozygous for the reference allele does not appear (0/0).
Someone can help me with this topic?

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