A reference haplotype panel for genome-wide imputation of short tandem repeats.

A reference haplotype panel for genome-wide imputation of short tandem repeats.
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DOI:
10.1038/s41467-018-06694-0
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发表时间:
2018-10-23
影响因子:
16.6
通讯作者:
Gymrek M
Gymrek M
中科院分区:
综合性期刊1区
文献类型:
--
作者:
Saini S;Mitra I;Mousavi N;Fotsing SF;Gymrek M

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Short tandem repeats (STRs) are involved in dozens of Mendelian disorders and have been implicated in complex traits. However, genotyping arrays used in genome-wide association studies focus on single nucleotide polymorphisms (SNPs) and do not readily allow identification of STR associations. We leverage next-generation sequencing (NGS) from 479 families to create a SNP + STR reference haplotype panel. Our panel enables imputing STR genotypes into SNP array data when NGS is not available for directly genotyping STRs. Imputed genotypes achieve mean concordance of 97% with observed genotypes in an external dataset compared to 71% expected under a naive model. Performance varies widely across STRs, with near perfect concordance at bi-allelic STRs vs. 70% at highly polymorphic repeats. Imputation increases power over individual SNPs to detect STR associations with gene expression. Imputing STRs into existing SNP datasets will enable the first large-scale STR association studies across a range of complex traits. Short-tandem repeats (STR), similar to single nucleotide polymorphisms (SNP), contribute to complex traits, but their ascertainment by next-generation sequencing is costly. Here, Saini et al. provide a SNP+STR haplotype reference panel that allows imputation of STRs from SNP array data.
遗传对人体组织基因表达的影响。
DOI: 10.1038/nature24277
发表时间: 2017-10-11
期刊: Nature
影响因子: 64.8
作者:
GTEx Consortium;Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group;Statistical Methods groups—Analysis Working Group;Enhancing GTEx (eGTEx) groups;NIH Common Fund;NIH/NCI;NIH/NHGRI;NIH/NIMH;NIH/NIDA;Biospecimen Collection Source Site—NDRI;Biospecimen Collection Source Site—RPCI;Biospecimen Core Resource—VARI;Brain Bank Repository—University of Miami Brain Endowment Bank;Leidos Biomedical—Project Management;ELSI Study;Genome Browser Data Integration &Visualization—EBI;Genome Browser Data Integration &Visualization—UCSC Genomics Institute, University of California Santa Cruz;Lead analysts:;Laboratory, Data Analysis &Coordinating Center (LDACC):;NIH program management:;Biospecimen collection:;Pathology:;eQTL manuscript working group:;Battle A;Brown CD;Engelhardt BE;Montgomery SB
通讯作者: Montgomery SB
DOI: 10.1186/s13059-016-1110-1
发表时间: 2016-11-28
期刊: Genome biology
影响因子: 12.3
作者:
Acuna-Hidalgo R;Veltman JA;Hoischen A
通讯作者: Hoischen A
DOI: 10.1038/nature18642
发表时间: 2016-08-04
期刊: NATURE
影响因子: 64.8
作者:
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DOI: 10.1038/ng.3510
发表时间: 2016-04-01
期刊: NATURE GENETICS
影响因子: 30.8
作者:
Boettger, Linda M.;Salem, Rany M.;McCarroll, Steven A.
通讯作者: McCarroll, Steven A.
DOI: 10.1002/humu.22115
发表时间: 2012-08-01
期刊: HUMAN MUTATION
影响因子: 3.9
作者:
Borel, Christelle;Migliavacca, Eugenia;Antonarakis, Stylianos E.
通讯作者: Antonarakis, Stylianos E.