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Unified tests for fine-scale mapping and identifying sparse high-dimensional sequence associations
Motivation: In searching for genetic variants for complex diseases with deep sequencing data, genomic marker sets of high-dimensional genotypic data and sparse functional variants are quite common. Existing sequence association tests are incapable of identifying such marker sets or individual causal...
में बचाया:
| में प्रकाशित: | Bioinformatics |
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| मुख्य लेखकों: | , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Oxford University Press
2016
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5006306/ https://ncbi.nlm.nih.gov/pubmed/26458888 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv586 |
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