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Rare variant association test in family-based sequencing studies
The objective of this article is to introduce valid and robust methods for the analysis of rare variants for family-based exome chips, whole-exome sequencing or whole-genome sequencing data. Family-based designs provide unique opportunities to detect genetic variants that complement studies of unrel...
Shranjeno v:
| izdano v: | Brief Bioinform |
|---|---|
| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5862290/ https://ncbi.nlm.nih.gov/pubmed/27677958 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbw083 |
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