Walking the interactome for candidate prioritization in exome sequencing studies of Mendelian diseases

Motivation: Whole-exome sequencing (WES) has opened up previously unheard of possibilities for identifying novel disease genes in Mendelian disorders, only about half of which have been elucidated to date. However, interpretation of WES data remains challenging. Results: Here, we analyze protein–pro...

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Bibliografiske detaljer
Udgivet i:Bioinformatics
Main Authors: Smedley, Damian, Köhler, Sebastian, Czeschik, Johanna Christina, Amberger, Joanna, Bocchini, Carol, Hamosh, Ada, Veldboer, Julian, Zemojtel, Tomasz, Robinson, Peter N.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2014
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Original Papers
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4221119/
https://ncbi.nlm.nih.gov/pubmed/25078397
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu508
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