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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...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Public Library of Science
2013
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| Θέματα: | |
| Διαθέσιμο Online: | 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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