Literature DB >> 34993494

Detection of quantitative trait loci from RNA-seq data with or without genotypes using BaseQTL.

Elena Vigorito1, Wei-Yu Lin1, Colin Starr1, Paul D W Kirk1,2, Simon R White1,3, Chris Wallace1,2.   

Abstract

Detecting genetic variants associated with traits (quantitative trait loci, QTL) requires genotyped study individuals. Here we describe BaseQTL, a Bayesian method that exploits allele-specific expression to map molecular QTL from sequencing reads (eQTL for gene expression) even when no genotypes are available. When used with genotypes to map eQTL, BaseQTL has lower error rates and increased power compared with existing QTL mapping methods. Running without genotypes limits how many tests can be performed, but due to the proximity of QTL variants to gene bodies, the 2.8% of variants within a 100 kB window that could be tested contained 26% of eQTL detectable with genotypes. eQTL effect estimates were invariably consistent between analyses performed with and without genotypes. Often, sequencing data may be generated in the absence of genotypes on patients and controls in differential expression studies, and we identified an apparent psoriasis-specific eQTL for GSTP1 in one such dataset, providing new insights into disease-dependent gene regulation.

Entities:  

Year:  2021        PMID: 34993494      PMCID: PMC7612174          DOI: 10.1038/s43588-021-00087-y

Source DB:  PubMed          Journal:  Nat Comput Sci        ISSN: 2662-8457


  37 in total

1.  A statistical framework for eQTL mapping using RNA-seq data.

Authors:  Wei Sun
Journal:  Biometrics       Date:  2011-08-12       Impact factor: 2.571

2.  Assessment of the psoriatic transcriptome in a large sample: additional regulated genes and comparisons with in vitro models.

Authors:  Johann E Gudjonsson; Jun Ding; Andrew Johnston; Trilokraj Tejasvi; Andrew M Guzman; Rajan P Nair; John J Voorhees; Goncalo R Abecasis; James T Elder
Journal:  J Invest Dermatol       Date:  2010-03-11       Impact factor: 8.551

3.  Systematic localization of common disease-associated variation in regulatory DNA.

Authors:  Matthew T Maurano; Richard Humbert; Eric Rynes; Robert E Thurman; Eric Haugen; Hao Wang; Alex P Reynolds; Richard Sandstrom; Hongzhu Qu; Jennifer Brody; Anthony Shafer; Fidencio Neri; Kristen Lee; Tanya Kutyavin; Sandra Stehling-Sun; Audra K Johnson; Theresa K Canfield; Erika Giste; Morgan Diegel; Daniel Bates; R Scott Hansen; Shane Neph; Peter J Sabo; Shelly Heimfeld; Antony Raubitschek; Steven Ziegler; Chris Cotsapas; Nona Sotoodehnia; Ian Glass; Shamil R Sunyaev; Rajinder Kaul; John A Stamatoyannopoulos
Journal:  Science       Date:  2012-09-05       Impact factor: 47.728

4.  Gene expression in skin and lymphoblastoid cells: Refined statistical method reveals extensive overlap in cis-eQTL signals.

Authors:  Jun Ding; Johann E Gudjonsson; Liming Liang; Philip E Stuart; Yun Li; Wei Chen; Michael Weichenthal; Eva Ellinghaus; Andre Franke; William Cookson; Rajan P Nair; James T Elder; Gonçalo R Abecasis
Journal:  Am J Hum Genet       Date:  2010-12-10       Impact factor: 11.025

5.  Population genomics of human gene expression.

Authors:  Barbara E Stranger; Alexandra C Nica; Matthew S Forrest; Antigone Dimas; Christine P Bird; Claude Beazley; Catherine E Ingle; Mark Dunning; Paul Flicek; Daphne Koller; Stephen Montgomery; Simon Tavaré; Panos Deloukas; Emmanouil T Dermitzakis
Journal:  Nat Genet       Date:  2007-09-16       Impact factor: 38.330

6.  Predicting causal variants affecting expression by using whole-genome sequencing and RNA-seq from multiple human tissues.

Authors:  Andrew Anand Brown; Ana Viñuela; Olivier Delaneau; Tim D Spector; Kerrin S Small; Emmanouil T Dermitzakis
Journal:  Nat Genet       Date:  2017-10-23       Impact factor: 38.330

7.  Quality control and preprocessing of metagenomic datasets.

Authors:  Robert Schmieder; Robert Edwards
Journal:  Bioinformatics       Date:  2011-01-28       Impact factor: 6.937

8.  Genotype imputation with thousands of genomes.

Authors:  Bryan Howie; Jonathan Marchini; Matthew Stephens
Journal:  G3 (Bethesda)       Date:  2011-11-01       Impact factor: 3.154

9.  Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.

Authors:  Roby Joehanes; Xiaoling Zhang; Tianxiao Huan; Chen Yao; Sai-Xia Ying; Quang Tri Nguyen; Cumhur Yusuf Demirkale; Michael L Feolo; Nataliya R Sharopova; Anne Sturcke; Alejandro A Schäffer; Nancy Heard-Costa; Han Chen; Po-Ching Liu; Richard Wang; Kimberly A Woodhouse; Kahraman Tanriverdi; Jane E Freedman; Nalini Raghavachari; Josée Dupuis; Andrew D Johnson; Christopher J O'Donnell; Daniel Levy; Peter J Munson
Journal:  Genome Biol       Date:  2017-01-25       Impact factor: 13.583

10.  Transcriptome and genome sequencing uncovers functional variation in humans.

Authors:  Tuuli Lappalainen; Michael Sammeth; Marc R Friedländer; Peter A C 't Hoen; Jean Monlong; Manuel A Rivas; Mar Gonzàlez-Porta; Natalja Kurbatova; Thasso Griebel; Pedro G Ferreira; Matthias Barann; Thomas Wieland; Liliana Greger; Maarten van Iterson; Jonas Almlöf; Paolo Ribeca; Irina Pulyakhina; Daniela Esser; Thomas Giger; Andrew Tikhonov; Marc Sultan; Gabrielle Bertier; Daniel G MacArthur; Monkol Lek; Esther Lizano; Henk P J Buermans; Ismael Padioleau; Thomas Schwarzmayr; Olof Karlberg; Halit Ongen; Helena Kilpinen; Sergi Beltran; Marta Gut; Katja Kahlem; Vyacheslav Amstislavskiy; Oliver Stegle; Matti Pirinen; Stephen B Montgomery; Peter Donnelly; Mark I McCarthy; Paul Flicek; Tim M Strom; Hans Lehrach; Stefan Schreiber; Ralf Sudbrak; Angel Carracedo; Stylianos E Antonarakis; Robert Häsler; Ann-Christine Syvänen; Gert-Jan van Ommen; Alvis Brazma; Thomas Meitinger; Philip Rosenstiel; Roderic Guigó; Ivo G Gut; Xavier Estivill; Emmanouil T Dermitzakis
Journal:  Nature       Date:  2013-09-15       Impact factor: 49.962

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  1 in total

1.  DeCAF: a novel method to identify cell-type specific regulatory variants and their role in cancer risk.

Authors:  Cynthia A Kalita; Alexander Gusev
Journal:  Genome Biol       Date:  2022-07-08       Impact factor: 17.906

  1 in total

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