“Short-read sequencing struggles with certain kinds of sequence variants, so to better capture these, we also used long-read sequencing that reads between 5,000 and 30,000 base pairs at a time ...
News Medical on MSN10d
Long reads can revolutionize genetic diagnosis of rare diseasesThe cause of rare diseases is increasingly being detected through genome sequencing, which involves reading the entire human DNA by first breaking it into small pieces-short reads.
The cause of rare diseases is increasingly being detected through genome sequencing, which involves reading the entire human DNA by first breaking it into small pieces—short reads. Christian Gilissen, ...
PacBio (PACB) announced a significant publication from Radboud University Medical Center and its research partners in the American Journal of ...
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