Evidence map›Paper›PMID 29186324›Full record

ArticleBioinformatics (Oxford, England)2018

Robust inference of population structure from next-generation sequencing data with systematic differences in sequencing.

Peizhou Liao, Glen A Satten, Yi-Juan Hu

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Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Peizhou LiaoDepartment of Biostatistics and Bioinformatics, Emory University, Atlanta, GA 30322, USA.
Glen A SattenDivision of Reproductive Health, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Yi-Juan HuDepartment of Biostatistics and Bioinformatics, Emory University, Atlanta, GA 30322, USA.

Funding

Association Tests of Rare Variants Using Sequence Reads without Calling GenotypesR01GM116065 · NIGMS · EMORY UNIVERSITY · PI HU, YIJUAN · 2015 to 2019
$1.5M
NIGMS NIH HHS R01 GM116065
6 · The paper itself

Abstract

Motivation: Inferring population structure is important for both population genetics and genetic epidemiology. Principal components analysis (PCA) has been effective in ascertaining population structure with array genotype data but can be difficult to use with sequencing data, especially when low depth leads to uncertainty in called genotypes. Because PCA is sensitive to differences in variability, PCA using sequencing data can result in components that correspond to differences in sequencing quality (read depth and error rate), rather than differences in population structure. We demonstrate that even existing methods for PCA specifically designed for sequencing data can still yield biased conclusions when used with data having sequencing properties that are systematically different across different groups of samples (i.e. sequencing groups). This situation can arise in population genetics when combining sequencing data from different studies, or in genetic epidemiology when using historical controls such as samples from the 1000 Genomes Project. Results: To allow inference on population structure using PCA in these situations, we provide an approach that is based on using sequencing reads directly without calling genotypes. Our approach is to adjust the data from different sequencing groups to have the same read depth and error rate so that PCA does not generate spurious components representing sequencing quality. To accomplish this, we have developed a subsampling procedure to match the depth distributions in different sequencing groups, and a read-flipping procedure to match the error rates. We average over subsamples and read flips to minimize loss of information. We demonstrate the utility of our approach using two datasets from 1000 Genomes, and further evaluate it using simulation studies. Availability and implementation: TASER-PC software is publicly available at http://web1.sph.emory.edu/users/yhu30/software.html. Contact: yijuan.hu@emory.edu. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

Genome, HumanPrincipal Component AnalysisSoftwareAlgorithmsGenetics, PopulationHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNA

Identifiers

PMID29186324
PMCPMC6031038

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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.