Evidence map›Paper›PMID 30918937›Full record

ArticleBioinformatics (Oxford, England)2019

Kinpute: using identity by descent to improve genotype imputation.

Mark Abney, Aisha ElSherbiny

Abstract read
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Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Mark AbneyDepartment of Human Genetics, University of Chicago, Chicago, IL, USA.
Aisha ElSherbinyDepartment of Human Genetics, University of Chicago, Chicago, IL, USA.

Funding

Methods for Human Genetic MappingR01HG001645 · NHGRI · UNIVERSITY OF CHICAGO · PI MCPEEK, MARY SARA · 2003 to 2023
$6.8M
Methods for Complex Trait Mapping in Large PedigreesR01HG002899 · NHGRI · UNIVERSITY OF CHICAGO · PI ABNEY, MARK A · 2004 to 2015
$3.5M
NHGRI NIH HHS R01 HG001645NHGRI NIH HHS R01 HG002899
6 · The paper itself

Abstract

motivationGenotype imputation, though generally accurate, often results in many genotypes being poorly imputed, particularly in studies where the individuals are not well represented by standard reference panels. When individuals in the study share regions of the genome identical by descent (IBD), it is possible to use this information in combination with a study-specific reference panel (SSRP) to improve the imputation results. Kinpute uses IBD information-due to recent, familial relatedness or distant, unknown ancestors-in conjunction with the output from linkage disequilibrium (LD) based imputation methods to compute more accurate genotype probabilities. Kinpute uses a novel method for IBD imputation, which works even in the absence of a pedigree, and results in substantially improved imputation quality.

resultsGiven initial estimates of average IBD between subjects in the study sample, Kinpute uses a novel algorithm to select an optimal set of individuals to sequence and use as an SSRP. Kinpute is designed to use as input both this SSRP and the genotype probabilities output from other LD-based imputation software, and uses a new method to combine the LD imputed genotype probabilities with IBD configurations to substantially improve imputation. We tested Kinpute on a human population isolate where 98 individuals have been sequenced. In half of this sample, whose sequence data was masked, we used Impute2 to perform LD-based imputation and Kinpute was used to obtain higher accuracy genotype probabilities. Measures of imputation accuracy improved significantly, particularly for those genotypes that Impute2 imputed with low certainty. AVAILABILITY AND IMPLEMENTATION: Kinpute is an open-source and freely available C++ software package that can be downloaded from. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

SoftwareGenotypeHumansLinkage DisequilibriumPedigreePolymorphism, Single Nucleotide

Identifiers

PMID30918937
PMCPMC6821425

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.