Interactive exploration, analysis and visualization of complex phenomegenome datasets with ASPIREdb

Identifying variants causal for complex genetic disorders is challenging. With the advent of whole exome and genome sequencing, computational tools are needed to explore and analyze the list of variants for further validation. Correlating genetic variants with subject phenotype is crucial for the in...

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Bibliografski detalji
Izdano u:Hum Mutat
Glavni autori: Tan, Powell Patrick Cheng, Rogic, Sanja, Zoubarev, Anton, McDonald, Cameron, Lui, Frances, Charathsandran, Gayathiri, Jacobson, Matthew, Belmadani, Manuel, Leong, Justin, Van Rossum, Thea, Portales-Casamar, Elodie, Qiao, Ying, Calli, Kristina, Liu, Xudong, Hudson, Melissa, Rajcan-Separovic, Evica, Lewis, ME Suzanne, Pavlidis, Paul
Format: Artigo
Jezik:Inglês
Izdano: 2016
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4940263/
https://ncbi.nlm.nih.gov/pubmed/27158917
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.23011
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