Who’s Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy
Author:
Funder
US National Human Genome Research Institute
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference13 articles.
1. PLINK: a tool set for whole-genome association and population-based linkage analyses;Purcell;Am. J. Hum. Genet.,2007
2. bam.iobio: a web-based, real-time, sequence alignment file inspector;Miller;Nat. Methods,2014
3. The Sequence Alignment/Map format and SAMtools;Li;Bioinformatics,2009
4. Robust relationship inference in genome-wide association studies;Manichaikul;Bioinformatics,2010
5. A likelihood ratio-based method to predict exact pedigrees for complex families from next-generation sequencing data;Heinrich;Bioinformatics,2017
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