Literature DB >> 26708335

Fast and efficient QTL mapper for thousands of molecular phenotypes.

Halit Ongen1, Alfonso Buil1, Andrew Anand Brown2, Emmanouil T Dermitzakis1, Olivier Delaneau1.   

Abstract

MOTIVATION: In order to discover quantitative trait loci, multi-dimensional genomic datasets combining DNA-seq and ChiP-/RNA-seq require methods that rapidly correlate tens of thousands of molecular phenotypes with millions of genetic variants while appropriately controlling for multiple testing.
RESULTS: We have developed FastQTL, a method that implements a popular cis-QTL mapping strategy in a user- and cluster-friendly tool. FastQTL also proposes an efficient permutation procedure to control for multiple testing. The outcome of permutations is modeled using beta distributions trained from a few permutations and from which adjusted P-values can be estimated at any level of significance with little computational cost. The Geuvadis & GTEx pilot datasets can be now easily analyzed an order of magnitude faster than previous approaches.
AVAILABILITY AND IMPLEMENTATION: Source code, binaries and comprehensive documentation of FastQTL are freely available to download at http://fastqtl.sourceforge.net/ CONTACT: emmanouil.dermitzakis@unige.ch or olivier.delaneau@unige.ch SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author 2015. Published by Oxford University Press.

Entities:  

Mesh:

Year:  2015        PMID: 26708335      PMCID: PMC4866519          DOI: 10.1093/bioinformatics/btv722

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  20 in total

1.  Matrix eQTL: ultra fast eQTL analysis via large matrix operations.

Authors:  Andrey A Shabalin
Journal:  Bioinformatics       Date:  2012-04-06       Impact factor: 6.937

2.  Permutation P-values should never be zero: calculating exact P-values when permutations are randomly drawn.

Authors:  Belinda Phipson; Gordon K Smyth
Journal:  Stat Appl Genet Mol Biol       Date:  2010-10-31

3.  Tabix: fast retrieval of sequence features from generic TAB-delimited files.

Authors:  Heng Li
Journal:  Bioinformatics       Date:  2011-01-05       Impact factor: 6.937

4.  GenABEL: an R library for genome-wide association analysis.

Authors:  Yurii S Aulchenko; Stephan Ripke; Aaron Isaacs; Cornelia M van Duijn
Journal:  Bioinformatics       Date:  2007-03-23       Impact factor: 6.937

5.  Using probabilistic estimation of expression residuals (PEER) to obtain increased power and interpretability of gene expression analyses.

Authors:  Oliver Stegle; Leopold Parts; Matias Piipari; John Winn; Richard Durbin
Journal:  Nat Protoc       Date:  2012-02-16       Impact factor: 13.491

6.  Transcriptome genetics using second generation sequencing in a Caucasian population.

Authors:  Stephen B Montgomery; Micha Sammeth; Maria Gutierrez-Arcelus; Radoslaw P Lach; Catherine Ingle; James Nisbett; Roderic Guigo; Emmanouil T Dermitzakis
Journal:  Nature       Date:  2010-03-10       Impact factor: 49.962

7.  Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.

Authors:  Alexandra C Nica; Stephen B Montgomery; Antigone S Dimas; Barbara E Stranger; Claude Beazley; Inês Barroso; Emmanouil T Dermitzakis
Journal:  PLoS Genet       Date:  2010-04-01       Impact factor: 5.917

8.  Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease.

Authors:  Norbert Hubner; Caroline A Wallace; Heike Zimdahl; Enrico Petretto; Herbert Schulz; Fiona Maciver; Michael Mueller; Oliver Hummel; Jan Monti; Vaclav Zidek; Alena Musilova; Vladimir Kren; Helen Causton; Laurence Game; Gabriele Born; Sabine Schmidt; Anita Müller; Stuart A Cook; Theodore W Kurtz; John Whittaker; Michal Pravenec; Timothy J Aitman
Journal:  Nat Genet       Date:  2005-02-13       Impact factor: 38.330

9.  Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles.

Authors:  Benjamin P Fairfax; Seiko Makino; Jayachandran Radhakrishnan; Katharine Plant; Stephen Leslie; Alexander Dilthey; Peter Ellis; Cordelia Langford; Fredrik O Vannberg; Julian C Knight
Journal:  Nat Genet       Date:  2012-03-25       Impact factor: 38.330

10.  Joint modelling of confounding factors and prominent genetic regulators provides increased accuracy in genetical genomics studies.

Authors:  Nicoló Fusi; Oliver Stegle; Neil D Lawrence
Journal:  PLoS Comput Biol       Date:  2012-01-05       Impact factor: 4.475

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  163 in total

1.  An Efficient Multiple-Testing Adjustment for eQTL Studies that Accounts for Linkage Disequilibrium between Variants.

Authors:  Joe R Davis; Laure Fresard; David A Knowles; Mauro Pala; Carlos D Bustamante; Alexis Battle; Stephen B Montgomery
Journal:  Am J Hum Genet       Date:  2015-12-31       Impact factor: 11.025

2.  Dectin-1 genetic deficiency predicts chronic lung allograft dysfunction and death.

Authors:  Daniel R Calabrese; Ping Wang; Tiffany Chong; Jonathan Hoover; Jonathan P Singer; Dara Torgerson; Steven R Hays; Jeffrey A Golden; Jasleen Kukreja; Daniel Dugger; Jason D Christie; John R Greenland
Journal:  JCI Insight       Date:  2019-11-14

3.  Genetic variant rs17185536 regulates SIM1 gene expression in human brain hypothalamus.

Authors:  Guiyou Liu; Yang Hu; Zhifa Han; Shuilin Jin; Qinghua Jiang
Journal:  Proc Natl Acad Sci U S A       Date:  2019-02-12       Impact factor: 11.205

4.  ORE identifies extreme expression effects enriched for rare variants.

Authors:  F Richter; G E Hoffman; K B Manheimer; N Patel; A J Sharp; D McKean; S U Morton; S DePalma; J Gorham; A Kitaygorodksy; G A Porter; A Giardini; Y Shen; W K Chung; J G Seidman; C E Seidman; E E Schadt; B D Gelb
Journal:  Bioinformatics       Date:  2019-10-15       Impact factor: 6.937

5.  Genetic Regulatory Mechanisms of Smooth Muscle Cells Map to Coronary Artery Disease Risk Loci.

Authors:  Boxiang Liu; Milos Pjanic; Ting Wang; Trieu Nguyen; Michael Gloudemans; Abhiram Rao; Victor G Castano; Sylvia Nurnberg; Daniel J Rader; Susannah Elwyn; Erik Ingelsson; Stephen B Montgomery; Clint L Miller; Thomas Quertermous
Journal:  Am J Hum Genet       Date:  2018-08-23       Impact factor: 11.025

6.  Systematic integrated analysis of genetic and epigenetic variation in diabetic kidney disease.

Authors:  Xin Sheng; Chengxiang Qiu; Hongbo Liu; Caroline Gluck; Jesse Y Hsu; Jiang He; Chi-Yuan Hsu; Daohang Sha; Matthew R Weir; Tamara Isakova; Dominic Raj; Hernan Rincon-Choles; Harold I Feldman; Raymond Townsend; Hongzhe Li; Katalin Susztak
Journal:  Proc Natl Acad Sci U S A       Date:  2020-11-03       Impact factor: 11.205

7.  An enhanced machine learning tool for cis-eQTL mapping with regularization and confounder adjustments.

Authors:  Kang K Yan; Hongyu Zhao; Joseph T Wu; Herbert Pang
Journal:  Genet Epidemiol       Date:  2020-07-22       Impact factor: 2.135

8.  Quantifying the regulatory effect size of cis-acting genetic variation using allelic fold change.

Authors:  Pejman Mohammadi; Stephane E Castel; Andrew A Brown; Tuuli Lappalainen
Journal:  Genome Res       Date:  2017-10-11       Impact factor: 9.043

9.  Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits.

Authors:  Chelsea K Raulerson; Arthur Ko; John C Kidd; Kevin W Currin; Sarah M Brotman; Maren E Cannon; Ying Wu; Cassandra N Spracklen; Anne U Jackson; Heather M Stringham; Ryan P Welch; Christian Fuchsberger; Adam E Locke; Narisu Narisu; Aldons J Lusis; Mete Civelek; Terrence S Furey; Johanna Kuusisto; Francis S Collins; Michael Boehnke; Laura J Scott; Dan-Yu Lin; Michael I Love; Markku Laakso; Päivi Pajukanta; Karen L Mohlke
Journal:  Am J Hum Genet       Date:  2019-09-26       Impact factor: 11.025

10.  The GTEx Consortium atlas of genetic regulatory effects across human tissues.

Authors: 
Journal:  Science       Date:  2020-09-11       Impact factor: 47.728

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