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Rare Variant Association Testing Under Low-Coverage Sequencing
Deep sequencing technologies enable the study of the effects of rare variants in disease risk. While methods have been developed to increase statistical power for detection of such effects, detecting subtle associations requires studies with hundreds or thousands of individuals, which is prohibitive...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Genetics Society of America
2013
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3697979/ https://ncbi.nlm.nih.gov/pubmed/23636738 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.113.150169 |
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