Output number of SNPs are chaging from run to run
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4.4 years ago
Bioin ▴ 10

Hi Biostars,

I am calling variations from GBS data using TASSEL-5.2. I ran the complete pipeline four times inputting the same data and key file for my surprise total number of variations from each run is slightly different. Is it quite normal or am I doing any mistake? any explanation would be greatly appreciated.

Thanks in advance.

alignment genome SNP next-gen • 536 views
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