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Learning gene networks underlying clinical phenotypes using SNP perturbation
Availability of genome sequence, molecular, and clinical phenotype data for large patient cohorts generated by recent technological advances provides an opportunity to dissect the genetic architecture of complex diseases at system level. However, previous analyses of such data have largely focused o...
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| Publicado no: | PLoS Comput Biol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7584257/ https://ncbi.nlm.nih.gov/pubmed/33095769 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1007940 |
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