Nalaganje...
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...
Shranjeno v:
| izdano v: | Bioinformatics |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2016
|
| Teme: | |
| Online dostop: | 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 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|