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Identification of common genetic variants controlling transcript isoform variation in human whole blood
An understanding of the genetic variation underlying transcript splicing is essential to dissect the molecular mechanisms of common disease. The available evidence from splicing quantitative trait locus (sQTL) studies has been limited to small samples. We performed genome-wide screening to identify...
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| Pubblicato in: | Nat Genet |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8273720/ https://ncbi.nlm.nih.gov/pubmed/25685889 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.3220 |
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