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A Novel Support Vector Machine-Based Approach for Rare Variant Detection
Advances in next-generation sequencing technologies have enabled the identification of multiple rare single nucleotide polymorphisms involved in diseases or traits. Several strategies for identifying rare variants that contribute to disease susceptibility have recently been proposed. An important fe...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Public Library of Science
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3737136/ https://ncbi.nlm.nih.gov/pubmed/23940698 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0071114 |
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