Literature DB >> 35100400

Haplotype-based inference of the distribution of fitness effects.

Diego Ortega-Del Vecchyo1,2, Kirk E Lohmueller2,3,4, John Novembre5,6.   

Abstract

Recent genome sequencing studies with large sample sizes in humans have discovered a vast quantity of low-frequency variants, providing an important source of information to analyze how selection is acting on human genetic variation. In order to estimate the strength of natural selection acting on low-frequency variants, we have developed a likelihood-based method that uses the lengths of pairwise identity-by-state between haplotypes carrying low-frequency variants. We show that in some nonequilibrium populations (such as those that have had recent population expansions) it is possible to distinguish between positive or negative selection acting on a set of variants. With our new framework, one can infer a fixed selection intensity acting on a set of variants at a particular frequency, or a distribution of selection coefficients for standing variants and new mutations. We show an application of our method to the UK10K phased haplotype dataset of individuals.
© The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America.

Entities:  

Keywords:  DFE; haplotype; inference; selection

Mesh:

Year:  2022        PMID: 35100400      PMCID: PMC8982047          DOI: 10.1093/genetics/iyac002

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  136 in total

1.  Global landscape of recent inferred Darwinian selection for Homo sapiens.

Authors:  Eric T Wang; Greg Kodama; Pierre Baldi; Robert K Moyzis
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-21       Impact factor: 11.205

2.  Controlling type-I error of the McDonald-Kreitman test in genomewide scans for selection on noncoding DNA.

Authors:  Peter Andolfatto
Journal:  Genetics       Date:  2008-09-14       Impact factor: 4.562

3.  Estimating the age of alleles by use of intraallelic variability.

Authors:  M Slatkin; B Rannala
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

4.  A hidden Markov model for investigating recent positive selection through haplotype structure.

Authors:  Hua Chen; Jody Hey; Montgomery Slatkin
Journal:  Theor Popul Biol       Date:  2014-11-13       Impact factor: 1.570

5.  Evolutionary processes acting on candidate cis-regulatory regions in humans inferred from patterns of polymorphism and divergence.

Authors:  Dara G Torgerson; Adam R Boyko; Ryan D Hernandez; Amit Indap; Xiaolan Hu; Thomas J White; John J Sninsky; Michele Cargill; Mark D Adams; Carlos D Bustamante; Andrew G Clark
Journal:  PLoS Genet       Date:  2009-08-07       Impact factor: 5.917

6.  Inferring the distribution of fitness effects of spontaneous mutations in Chlamydomonas reinhardtii.

Authors:  Katharina B Böndel; Susanne A Kraemer; Toby Samuels; Deirdre McClean; Josianne Lachapelle; Rob W Ness; Nick Colegrave; Peter D Keightley
Journal:  PLoS Biol       Date:  2019-06-26       Impact factor: 8.029

7.  A reference panel of 64,976 haplotypes for genotype imputation.

Authors:  Shane McCarthy; Sayantan Das; Warren Kretzschmar; Olivier Delaneau; Andrew R Wood; Alexander Teumer; Hyun Min Kang; Christian Fuchsberger; Petr Danecek; Kevin Sharp; Yang Luo; Carlo Sidore; Alan Kwong; Nicholas Timpson; Seppo Koskinen; Scott Vrieze; Laura J Scott; He Zhang; Anubha Mahajan; Jan Veldink; Ulrike Peters; Carlos Pato; Cornelia M van Duijn; Christopher E Gillies; Ilaria Gandin; Massimo Mezzavilla; Arthur Gilly; Massimiliano Cocca; Michela Traglia; Andrea Angius; Jeffrey C Barrett; Dorrett Boomsma; Kari Branham; Gerome Breen; Chad M Brummett; Fabio Busonero; Harry Campbell; Andrew Chan; Sai Chen; Emily Chew; Francis S Collins; Laura J Corbin; George Davey Smith; George Dedoussis; Marcus Dorr; Aliki-Eleni Farmaki; Luigi Ferrucci; Lukas Forer; Ross M Fraser; Stacey Gabriel; Shawn Levy; Leif Groop; Tabitha Harrison; Andrew Hattersley; Oddgeir L Holmen; Kristian Hveem; Matthias Kretzler; James C Lee; Matt McGue; Thomas Meitinger; David Melzer; Josine L Min; Karen L Mohlke; John B Vincent; Matthias Nauck; Deborah Nickerson; Aarno Palotie; Michele Pato; Nicola Pirastu; Melvin McInnis; J Brent Richards; Cinzia Sala; Veikko Salomaa; David Schlessinger; Sebastian Schoenherr; P Eline Slagboom; Kerrin Small; Timothy Spector; Dwight Stambolian; Marcus Tuke; Jaakko Tuomilehto; Leonard H Van den Berg; Wouter Van Rheenen; Uwe Volker; Cisca Wijmenga; Daniela Toniolo; Eleftheria Zeggini; Paolo Gasparini; Matthew G Sampson; James F Wilson; Timothy Frayling; Paul I W de Bakker; Morris A Swertz; Steven McCarroll; Charles Kooperberg; Annelot Dekker; David Altshuler; Cristen Willer; William Iacono; Samuli Ripatti; Nicole Soranzo; Klaudia Walter; Anand Swaroop; Francesco Cucca; Carl A Anderson; Richard M Myers; Michael Boehnke; Mark I McCarthy; Richard Durbin
Journal:  Nat Genet       Date:  2016-08-22       Impact factor: 38.330

8.  Natural Selection Shapes Codon Usage in the Human Genome.

Authors:  Ryan S Dhindsa; Brett R Copeland; Anthony M Mustoe; David B Goldstein
Journal:  Am J Hum Genet       Date:  2020-06-08       Impact factor: 11.043

9.  Comparison of Single Genome and Allele Frequency Data Reveals Discordant Demographic Histories.

Authors:  Annabel C Beichman; Tanya N Phung; Kirk E Lohmueller
Journal:  G3 (Bethesda)       Date:  2017-11-06       Impact factor: 3.154

10.  Greater strength of selection and higher proportion of beneficial amino acid changing mutations in humans compared with mice and Drosophila melanogaster.

Authors:  Ying Zhen; Christian D Huber; Robert W Davies; Kirk E Lohmueller
Journal:  Genome Res       Date:  2020-11-18       Impact factor: 9.043

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