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DyogenIBENS / FINSURF

FINSURF is a tool designed to analyse lists of sequences variants in the human genome.
https://www.finsurf.bio.ens.psl.eu/
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No hg38 build ? #3

Open byeongill opened 1 year ago

byeongill commented 1 year ago

Hi Does FINSURF only support hg19 ?

lambosaur commented 1 year ago

Hi,

We are currently applying a liftover of scores and regulatory regions from hg19 to hg38. Once converted, we will update the set of download links to include the hg38 data.