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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Detalhes bibliográficos
Publicado no:Hum Mutat
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha: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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