Thank you, snp-sites works for my analyses!
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vivien.wee16 •
Variant calling following multiple sequence alignment
Hi everyone,
Are there any tools/pipelines available that I can use to call for variants/SNPs following multiple sequence alignment? I need something that can call for variants between the sequences, and not from a reference genome.
Thank you in advance!
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great, clicks the green mark on left to accept and close the question please.
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Pierre Lindenbaum
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