Thanks a lot
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heureuse •
Single nucleotide variant
Hello, I would like to know if there is a method/pipeline that help to retrieve all single nucleotide variant in human genome that lead to a loss of function . Thanks.
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heureuse •
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https://sites.google.com/site/jpopgen/dbNSFP
dbNSFP is a database developed for functional prediction and annotation of all potential non-synonymous single-nucleotide variants (nsSNVs) in the human genome. I
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Pierre Lindenbaum
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