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SEQMINER: An R‐Package to Facilitate the Functional Interpretation of Sequence‐Based Associations
Next‐generation sequencing has enabled the study of a comprehensive catalogue of genetic variants for their impact on various complex diseases. Numerous consortia studies of complex traits have publically released their summary association statistics, which have become an invaluable resource for lea...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4794281/ https://www.ncbi.nlm.nih.gov/pubmed/26394715 http://dx.doi.org/10.1002/gepi.21918 |