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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...
Gorde:
| Argitaratua izan da: | Bioinformatics |
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| Egile Nagusiak: | , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Oxford University Press
2014
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| Gaiak: | |
| Sarrera elektronikoa: | 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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