Haplotype caller for SNP calling from RNA seq data

Hello,
I have a general question. Why is it recommended to use single sample for SNP calling from RNA-seq data when using Haplotype caller? Isn't possible to provide all the samples together for the SNP calling purpose? Is it a rather technical aspect of Haplotype Caller or it helps to reduce errors?
Thanks a lot in advance for your help,
Homa

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