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Nebula: ultra-efficient mapping-free structural variant genotyper

Large scale catalogs of common genetic variants (including indels and structural variants) are being created using data from second and third generation whole-genome sequencing technologies. However, the genotyping of these variants in newly sequenced samples is a nontrivial task that requires exten...

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Bibliografske podrobnosti
izdano v:Nucleic Acids Res
Main Authors: Khorsand, Parsoa, Hormozdiari, Fereydoun
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2021
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8096284/
https://ncbi.nlm.nih.gov/pubmed/33503255
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkab025
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