Literature DB >> 32159382

Kinship Solutions for Partially Observed Multiphenotype Data.

Lloyd T Elliott1.   

Abstract

Current work for multivariate analysis of phenotypes in genome-wide association studies often requires that genetic similarity matrices be inverted or decomposed. This can be a computational bottleneck when many phenotypes are presented, each with a different missingness pattern. A usual method in this case is to perform decompositions on subsets of the kinship matrix for each phenotype, with each subset corresponding to the set of observed samples for that phenotype. We provide a new method for decomposing these kinship matrices that can reduce the computational complexity by an order of magnitude by propagating low-rank modifications along a tree spanning the phenotypes. We demonstrate that our method provides speed improvements of around 40% under reasonable conditions.

Entities:  

Keywords:  Cholesky decomposition; genome-wide association study; kinship matrix; linear mixed models; multiphenotype analysis

Year:  2020        PMID: 32159382      PMCID: PMC7482112          DOI: 10.1089/cmb.2019.0440

Source DB:  PubMed          Journal:  J Comput Biol        ISSN: 1066-5277            Impact factor:   1.479


  11 in total

1.  Improved linear mixed models for genome-wide association studies.

Authors:  Jennifer Listgarten; Christoph Lippert; Carl M Kadie; Robert I Davidson; Eleazar Eskin; David Heckerman
Journal:  Nat Methods       Date:  2012-05-30       Impact factor: 28.547

2.  FaST linear mixed models for genome-wide association studies.

Authors:  Christoph Lippert; Jennifer Listgarten; Ying Liu; Carl M Kadie; Robert I Davidson; David Heckerman
Journal:  Nat Methods       Date:  2011-09-04       Impact factor: 28.547

3.  FaST-LMM-Select for addressing confounding from spatial structure and rare variants.

Authors:  Jennifer Listgarten; Christoph Lippert; David Heckerman
Journal:  Nat Genet       Date:  2013-05       Impact factor: 38.330

4.  From 'omics' to complex disease: a systems biology approach to gene-environment interactions in cancer.

Authors:  Sarah S Knox
Journal:  Cancer Cell Int       Date:  2010-04-26       Impact factor: 5.722

5.  Population structure and eigenanalysis.

Authors:  Nick Patterson; Alkes L Price; David Reich
Journal:  PLoS Genet       Date:  2006-12       Impact factor: 5.917

6.  A multiple-phenotype imputation method for genetic studies.

Authors:  Andrew Dahl; Valentina Iotchkova; Amelie Baud; Åsa Johansson; Ulf Gyllensten; Nicole Soranzo; Richard Mott; Andreas Kranis; Jonathan Marchini
Journal:  Nat Genet       Date:  2016-02-22       Impact factor: 38.330

7.  Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Authors: 
Journal:  Nature       Date:  2007-06-07       Impact factor: 49.962

8.  Big data: Some statistical issues.

Authors:  D R Cox; Christiana Kartsonaki; Ruth H Keogh
Journal:  Stat Probab Lett       Date:  2018-05       Impact factor: 0.870

9.  Genome-wide association studies of brain imaging phenotypes in UK Biobank.

Authors:  Lloyd T Elliott; Kevin Sharp; Fidel Alfaro-Almagro; Sinan Shi; Karla L Miller; Gwenaëlle Douaud; Jonathan Marchini; Stephen M Smith
Journal:  Nature       Date:  2018-10-10       Impact factor: 49.962

10.  The UK Biobank resource with deep phenotyping and genomic data.

Authors:  Clare Bycroft; Colin Freeman; Desislava Petkova; Gavin Band; Lloyd T Elliott; Kevin Sharp; Allan Motyer; Damjan Vukcevic; Olivier Delaneau; Jared O'Connell; Adrian Cortes; Samantha Welsh; Alan Young; Mark Effingham; Gil McVean; Stephen Leslie; Naomi Allen; Peter Donnelly; Jonathan Marchini
Journal:  Nature       Date:  2018-10-10       Impact factor: 49.962

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.