Literature DB >> 23910464

RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference.

Brian K Maples1, Simon Gravel, Eimear E Kenny, Carlos D Bustamante.   

Abstract

Local-ancestry inference is an important step in the genetic analysis of fully sequenced human genomes. Current methods can only detect continental-level ancestry (i.e., European versus African versus Asian) accurately even when using millions of markers. Here, we present RFMix, a powerful discriminative modeling approach that is faster (~30×) and more accurate than existing methods. We accomplish this by using a conditional random field parameterized by random forests trained on reference panels. RFMix is capable of learning from the admixed samples themselves to boost performance and autocorrect phasing errors. RFMix shows high sensitivity and specificity in simulated Hispanics/Latinos and African Americans and admixed Europeans, Africans, and Asians. Finally, we demonstrate that African Americans in HapMap contain modest (but nonzero) levels of Native American ancestry (~0.4%).
Copyright © 2013 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2013        PMID: 23910464      PMCID: PMC3738819          DOI: 10.1016/j.ajhg.2013.06.020

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  29 in total

1.  Reconstructing genetic ancestry blocks in admixed individuals.

Authors:  Hua Tang; Marc Coram; Pei Wang; Xiaofeng Zhu; Neil Risch
Journal:  Am J Hum Genet       Date:  2006-05-17       Impact factor: 11.025

2.  Effect of genetic divergence in identifying ancestral origin using HAPAA.

Authors:  Andreas Sundquist; Eugene Fratkin; Chuong B Do; Serafim Batzoglou
Journal:  Genome Res       Date:  2008-03-18       Impact factor: 9.043

3.  Whole population, genome-wide mapping of hidden relatedness.

Authors:  Alexander Gusev; Jennifer K Lowe; Markus Stoffel; Mark J Daly; David Altshuler; Jan L Breslow; Jeffrey M Friedman; Itsik Pe'er
Journal:  Genome Res       Date:  2008-10-29       Impact factor: 9.043

4.  The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research.

Authors:  Matthew R Nelson; Katarzyna Bryc; Karen S King; Amit Indap; Adam R Boyko; John Novembre; Linda P Briley; Yuka Maruyama; Dawn M Waterworth; Gérard Waeber; Peter Vollenweider; Jorge R Oksenberg; Stephen L Hauser; Heide A Stirnadel; Jaspal S Kooner; John C Chambers; Brendan Jones; Vincent Mooser; Carlos D Bustamante; Allen D Roses; Daniel K Burns; Margaret G Ehm; Eric H Lai
Journal:  Am J Hum Genet       Date:  2008-08-28       Impact factor: 11.025

5.  Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering.

Authors:  Sharon R Browning; Brian L Browning
Journal:  Am J Hum Genet       Date:  2007-09-21       Impact factor: 11.025

6.  Genes mirror geography within Europe.

Authors:  John Novembre; Toby Johnson; Katarzyna Bryc; Zoltán Kutalik; Adam R Boyko; Adam Auton; Amit Indap; Karen S King; Sven Bergmann; Matthew R Nelson; Matthew Stephens; Carlos D Bustamante
Journal:  Nature       Date:  2008-08-31       Impact factor: 49.962

7.  Inferring genome-wide patterns of admixture in Qataris using fifty-five ancestral populations.

Authors:  Larsson Omberg; Jacqueline Salit; Neil Hackett; Jennifer Fuller; Rebecca Matthew; Lotfi Chouchane; Juan L Rodriguez-Flores; Carlos Bustamante; Ronald G Crystal; Jason G Mezey
Journal:  BMC Genet       Date:  2012-06-26       Impact factor: 2.797

8.  The UCSC Genome Browser Database: update 2006.

Authors:  A S Hinrichs; D Karolchik; R Baertsch; G P Barber; G Bejerano; H Clawson; M Diekhans; T S Furey; R A Harte; F Hsu; J Hillman-Jackson; R M Kuhn; J S Pedersen; A Pohl; B J Raney; K R Rosenbloom; A Siepel; K E Smith; C W Sugnet; A Sultan-Qurraie; D J Thomas; H Trumbower; R J Weber; M Weirauch; A S Zweig; D Haussler; W J Kent
Journal:  Nucleic Acids Res       Date:  2006-01-01       Impact factor: 16.971

9.  An integrated map of genetic variation from 1,092 human genomes.

Authors:  Goncalo R Abecasis; Adam Auton; Lisa D Brooks; Mark A DePristo; Richard M Durbin; Robert E Handsaker; Hyun Min Kang; Gabor T Marth; Gil A McVean
Journal:  Nature       Date:  2012-11-01       Impact factor: 49.962

10.  Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.

Authors:  Wenqing Fu; Timothy D O'Connor; Goo Jun; Hyun Min Kang; Goncalo Abecasis; Suzanne M Leal; Stacey Gabriel; Mark J Rieder; David Altshuler; Jay Shendure; Deborah A Nickerson; Michael J Bamshad; Joshua M Akey
Journal:  Nature       Date:  2012-11-28       Impact factor: 49.962

View more
  277 in total

1.  Robust Hi-C Maps of Enhancer-Promoter Interactions Reveal the Function of Non-coding Genome in Neural Development and Diseases.

Authors:  Leina Lu; Xiaoxiao Liu; Wei-Kai Huang; Paola Giusti-Rodríguez; Jian Cui; Shanshan Zhang; Wanying Xu; Zhexing Wen; Shufeng Ma; Jonathan D Rosen; Zheng Xu; Cynthia F Bartels; Riki Kawaguchi; Ming Hu; Peter C Scacheri; Zhili Rong; Yun Li; Patrick F Sullivan; Hongjun Song; Guo-Li Ming; Yan Li; Fulai Jin
Journal:  Mol Cell       Date:  2020-06-26       Impact factor: 17.970

2.  The Italian genome reflects the history of Europe and the Mediterranean basin.

Authors:  Giovanni Fiorito; Cornelia Di Gaetano; Simonetta Guarrera; Fabio Rosa; Marcus W Feldman; Alberto Piazza; Giuseppe Matullo
Journal:  Eur J Hum Genet       Date:  2015-11-11       Impact factor: 4.246

3.  Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.

Authors:  Ursula M Schick; Deepti Jain; Chani J Hodonsky; Jean V Morrison; James P Davis; Lisa Brown; Tamar Sofer; Matthew P Conomos; Claudia Schurmann; Caitlin P McHugh; Sarah C Nelson; Swarooparani Vadlamudi; Adrienne Stilp; Anna Plantinga; Leslie Baier; Stephanie A Bien; Stephanie M Gogarten; Cecelia A Laurie; Kent D Taylor; Yongmei Liu; Paul L Auer; Nora Franceschini; Adam Szpiro; Ken Rice; Kathleen F Kerr; Jerome I Rotter; Robert L Hanson; George Papanicolaou; Stephen S Rich; Ruth J F Loos; Brian L Browning; Sharon R Browning; Bruce S Weir; Cathy C Laurie; Karen L Mohlke; Kari E North; Timothy A Thornton; Alex P Reiner
Journal:  Am J Hum Genet       Date:  2016-01-21       Impact factor: 11.025

4.  Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics.

Authors:  Quinn T Ostrom; Kathleen M Egan; L Burt Nabors; Travis Gerke; Reid C Thompson; Jeffrey J Olson; Renato LaRocca; Sajeel Chowdhary; Jeanette E Eckel-Passow; Georgina Armstrong; John K Wiencke; Jonine L Bernstein; Elizabeth B Claus; Dora Il'yasova; Christoffer Johansen; Daniel H Lachance; Rose K Lai; Ryan T Merrell; Sara H Olson; Siegal Sadetzki; Joellen M Schildkraut; Sanjay Shete; Richard S Houlston; Robert B Jenkins; Margaret R Wrensch; Beatrice Melin; Christopher I Amos; Jason T Huse; Jill S Barnholtz-Sloan; Melissa L Bondy
Journal:  Int J Cancer       Date:  2019-04-22       Impact factor: 7.396

5.  Versatile simulations of admixture and accurate local ancestry inference with mixnmatch and ancestryinfer.

Authors:  Molly Schumer; Daniel L Powell; Russ Corbett-Detig
Journal:  Mol Ecol Resour       Date:  2020-05-25       Impact factor: 7.090

6.  Standardized Biogeographic Grouping System for Annotating Populations in Pharmacogenetic Research.

Authors:  Rachel Huddart; Alison E Fohner; Michelle Whirl-Carrillo; Genevieve L Wojcik; Christopher R Gignoux; Alice B Popejoy; Carlos D Bustamante; Russ B Altman; Teri E Klein
Journal:  Clin Pharmacol Ther       Date:  2019-01-21       Impact factor: 6.875

7.  Modeling Human Population Separation History Using Physically Phased Genomes.

Authors:  Shiya Song; Elzbieta Sliwerska; Sarah Emery; Jeffrey M Kidd
Journal:  Genetics       Date:  2016-11-09       Impact factor: 4.562

8.  A Fast and Simple Method for Detecting Identity-by-Descent Segments in Large-Scale Data.

Authors:  Ying Zhou; Sharon R Browning; Brian L Browning
Journal:  Am J Hum Genet       Date:  2020-03-12       Impact factor: 11.025

9.  Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders.

Authors:  Robert Brown; Hane Lee; Ascia Eskin; Gleb Kichaev; Kirk E Lohmueller; Bruno Reversade; Stanley F Nelson; Bogdan Pasaniuc
Journal:  Eur J Hum Genet       Date:  2015-04-22       Impact factor: 4.246

10.  Local ancestry transitions modify snp-trait associations.

Authors:  Alexandra E Fish; Dana C Crawford; John A Capra; William S Bush
Journal:  Pac Symp Biocomput       Date:  2018
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.