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RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence data
Motivation: Next-generation sequencing technologies have enabled the large-scale assessment of the impact of rare and low-frequency genetic variants for complex human diseases. Gene-level association tests are often performed to analyze rare variants, where multiple rare variants in a gene region ar...
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| Publicado no: | Bioinformatics |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4848408/ https://ncbi.nlm.nih.gov/pubmed/27153000 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btw079 |
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