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Penalized Regression for Genome-Wide Association Screening of Sequence Data
Whole exome and whole genome sequencing are likely to be potent tools in the study of common diseases and complex traits. Despite this promise, some very difficult issues in data management and statistical analysis must be squarely faced. The number of rare variants identified by sequencing is apt t...
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| Publicado no: | Pac Symp Biocomput |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5049883/ https://ncbi.nlm.nih.gov/pubmed/21121038 |
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