@StevenJMorg @abacbs Here is the manuscript if you'd like more details. https://t.co/EuwQsG5BQl
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Recurrent miscalling of missense variation from short-read genome sequence data https://t.co/JgGuYvD6fn "In human exome sequences, we identify 2–300 recurrent false positive variants per individual, almost all of which are present in public databases of hu
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RT @GaetanBurgio: This started from a corridor conversation with my colleague Dan Andrews on false positive detection of #CRISPR Off-target…
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"..read length is a strong determinant of whether given false variants will be called for any given genome – which has profound significance for cohort studies that pool datasets collected and sequenced at different points in time.." https://t.co/DkCBEdfWh