Nalaganje...

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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:Bioinformatics
Main Authors: Gayevskiy, Velimir, Roscioli, Tony, Dinger, Marcel E, Cowley, Mark J
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2019
Teme:
Online dostop: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
Oznake: Označite
Brez oznak, prvi označite!