For reference https://github.com/epi2me-labs/wf-human-variation
Somatic Variant Calling from Nanopore Data
Hi,
I have some cancer samples and normal control samples, sequenced by Nanopore (Amplicon sequencing). I read about ClairS from one source. I am just curious to know if there are any more tools for doing similar work.
Please suggest.
Thanks
1 answer
Hi, I am not an expert but have you looked at the software EPI2ME from Nanopore for variant calling?
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giulia.trauzzi •
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