HGCS: an online tool for prioritizing disease-causing gene variants by biological distance

BACKGROUND: Identifying the genotypes underlying human disease phenotypes is a fundamental step in human genetics and medicine. High-throughput genomic technologies provide thousands of genetic variants per individual. The causal genes of a specific phenotype are usually expected to be functionally...

Descripción completa

Detalles Bibliográficos
Autores principales: Itan, Yuval, Mazel, Mark, Mazel, Benjamin, Abhyankar, Avinash, Nitschke, Patrick, Quintana-Murci, Lluis, Boisson-Dupuis, Stephanie, Boisson, Bertrand, Abel, Laurent, Zhang, Shen-Ying, Casanova, Jean-Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051124/
https://www.ncbi.nlm.nih.gov/pubmed/24694260
http://dx.doi.org/10.1186/1471-2164-15-256

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051124/
https://www.ncbi.nlm.nih.gov/pubmed/24694260
http://dx.doi.org/10.1186/1471-2164-15-256

Ejemplares similares