Seave: a comprehensive web platform for storing and interrogating human genomic variation

MOTIVATION: Genome sequencing has had a remarkable impact on our ability to study the effects of human genetic variation, however, variant interpretation remains the major bottleneck. Understanding the potential impact of variants, including structural variants, requires extensive annotation from di...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Bioinformatics
Asıl Yazarlar: Gayevskiy, Velimir, Roscioli, Tony, Dinger, Marcel E, Cowley, Mark J
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2019
Konular:
Applications Notes
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6298057/
https://ncbi.nlm.nih.gov/pubmed/30561546
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty540
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