ArticleAmerican journal of human genetics2014
A statistical framework to guide sequencing choices in pedigrees.
Article in American journal of human genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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Who cites it
16 citing papers in PubMed.
- Variant Prioritization by Pedigree-Based Haplotyping.Genetic epidemiology · 2026Article
- Revisit Population-based and Family-based Genotype Imputation.Scientific reports · 2019Article
- Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees.Genome research · 2019Article
- Hybrid peeling for fast and accurate calling, phasing, and imputation with sequence data of any coverage in pedigrees.Genetics, selection, evolution : GSE · 2018Article
- Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies.American journal of human genetics · 2018Article
- Robust Rare-Variant Association Tests For Quantitative Traits in General Pedigrees.Statistics in biosciences · 2018Article
- Application of genome analysis strategies in the clinical testing for pediatric diseases.Pediatric investigation · 2018Article
- G-STRATEGY: Optimal Selection of Individuals for Sequencing in Genetic Association Studies.Genetic epidemiology · 2016Article
- Whole-genome characterization in pedigreed non-human primates using genotyping-by-sequencing (GBS) and imputation.BMC genomics · 2016Article
- Lessons learned from gene identification studies in Mendelian epilepsy disorders.European journal of human genetics : EJHG · 2016Review
- Family-based approaches: design, imputation, analysis, and beyond.BMC genetics · 2016Article
- Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data.BMC proceedings · 2016Article
- Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.Human genetics · 2015Article
- Genetic linkage analysis in the age of whole-genome sequencing.Nature reviews. Genetics · 2015Review
- Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm.PloS one · 2015Article
- PedBLIMP: extending linear predictors to impute genotypes in pedigrees.Genetic epidemiology · 2014Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
The use of large pedigrees is an effective design for identifying rare functional variants affecting heritable traits. Cost-effective studies using sequence data can be achieved via pedigree-based genotype imputation in which some subjects are sequenced and missing genotypes are inferred on the remaining subjects. Because of high cost, it is important to carefully prioritize subjects for sequencing. Here, we introduce a statistical framework that enables systematic comparison among subject-selection choices for sequencing. We introduce a metric "local coverage," which allows the use of inferred inheritance vectors to measure genotype-imputation ability specifically in a region of interest, such as one with prior evidence of linkage. In the absence of linkage information, we can instead use a "genome-wide coverage" metric computed with the pedigree structure. These metrics enable the development of a method that identifies efficient selection choices for sequencing. As implemented in GIGI-Pick, this method also flexibly allows initial manual selection of subjects and optimizes selections within the constraint that only some subjects might be available for sequencing. In the present study, we used simulations to compare GIGI-Pick with PRIMUS, ExomePicks, and common ad hoc methods of selecting subjects. In genotype imputation of both common and rare alleles, GIGI-Pick substantially outperformed all other methods considered and had the added advantage of incorporating prior linkage information. We also used a real pedigree to demonstrate the utility of our approach in identifying causal mutations. Our work enables prioritization of subjects for sequencing to facilitate dissection of the genetic basis of heritable traits.
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Registered trials
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