Literature DB >> 31601707

Genetic regulatory variation in populations informs transcriptome analysis in rare disease.

Pejman Mohammadi1,2,3,4, Stephane E Castel5,2, Beryl B Cummings6,7, Jonah Einson5,2, Christina Sousa3,4, Paul Hoffman5,2, Sandra Donkervoort8, Zhuoxun Jiang9, Payam Mohassel8, A Reghan Foley8, Heather E Wheeler10,11, Hae Kyung Im9, Carsten G Bonnemann8, Daniel G MacArthur6,7, Tuuli Lappalainen1,2.   

Abstract

Transcriptome data can facilitate the interpretation of the effects of rare genetic variants. Here, we introduce ANEVA (analysis of expression variation) to quantify genetic variation in gene dosage from allelic expression (AE) data in a population. Application of ANEVA to the Genotype-Tissues Expression (GTEx) data showed that this variance estimate is robust and correlated with selective constraint in a gene. Using these variance estimates in a dosage outlier test (ANEVA-DOT) applied to AE data from 70 Mendelian muscular disease patients showed accuracy in detecting genes with pathogenic variants in previously resolved cases and led to one confirmed and several potential new diagnoses. Using our reference estimates from GTEx data, ANEVA-DOT can be incorporated in rare disease diagnostic pipelines to use RNA-sequencing data more effectively.
Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

Entities:  

Mesh:

Year:  2019        PMID: 31601707      PMCID: PMC6814274          DOI: 10.1126/science.aay0256

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  39 in total

Review 1.  A copy number variation map of the human genome.

Authors:  Mehdi Zarrei; Jeffrey R MacDonald; Daniele Merico; Stephen W Scherer
Journal:  Nat Rev Genet       Date:  2015-02-03       Impact factor: 53.242

2.  The 2016 version of the gene table of monogenic neuromuscular disorders (nuclear genome).

Authors:  Jean-Claude Kaplan; Dalil Hamroun
Journal:  Neuromuscul Disord       Date:  2015-12-02       Impact factor: 4.296

3.  Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins.

Authors:  Alfonso Buil; Andrew Anand Brown; Tuuli Lappalainen; Ana Viñuela; Matthew N Davies; Hou-Feng Zheng; J Brent Richards; Daniel Glass; Kerrin S Small; Richard Durbin; Timothy D Spector; Emmanouil T Dermitzakis
Journal:  Nat Genet       Date:  2014-12-01       Impact factor: 38.330

4.  Integrative approaches for large-scale transcriptome-wide association studies.

Authors:  Alexander Gusev; Arthur Ko; Huwenbo Shi; Gaurav Bhatia; Wonil Chung; Brenda W J H Penninx; Rick Jansen; Eco J C de Geus; Dorret I Boomsma; Fred A Wright; Patrick F Sullivan; Elina Nikkola; Marcus Alvarez; Mete Civelek; Aldons J Lusis; Terho Lehtimäki; Emma Raitoharju; Mika Kähönen; Ilkka Seppälä; Olli T Raitakari; Johanna Kuusisto; Markku Laakso; Alkes L Price; Päivi Pajukanta; Bogdan Pasaniuc
Journal:  Nat Genet       Date:  2016-02-08       Impact factor: 38.330

5.  Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts.

Authors:  Laure Frésard; Craig Smail; Nicole M Ferraro; Nicole A Teran; Xin Li; Kevin S Smith; Devon Bonner; Kristin D Kernohan; Shruti Marwaha; Zachary Zappala; Brunilda Balliu; Joe R Davis; Boxiang Liu; Cameron J Prybol; Jennefer N Kohler; Diane B Zastrow; Chloe M Reuter; Dianna G Fisk; Megan E Grove; Jean M Davidson; Taila Hartley; Ruchi Joshi; Benjamin J Strober; Sowmithri Utiramerur; Lars Lind; Erik Ingelsson; Alexis Battle; Gill Bejerano; Jonathan A Bernstein; Euan A Ashley; Kym M Boycott; Jason D Merker; Matthew T Wheeler; Stephen B Montgomery
Journal:  Nat Med       Date:  2019-06-03       Impact factor: 53.440

6.  Genic intolerance to functional variation and the interpretation of personal genomes.

Authors:  Slavé Petrovski; Quanli Wang; Erin L Heinzen; Andrew S Allen; David B Goldstein
Journal:  PLoS Genet       Date:  2013-08-22       Impact factor: 5.917

7.  A phenotype centric benchmark of variant prioritisation tools.

Authors:  Denise Anderson; Timo Lassmann
Journal:  NPJ Genom Med       Date:  2018-02-05       Impact factor: 8.617

8.  GeneHancer: genome-wide integration of enhancers and target genes in GeneCards.

Authors:  Simon Fishilevich; Ron Nudel; Noa Rappaport; Rotem Hadar; Inbar Plaschkes; Tsippi Iny Stein; Naomi Rosen; Asher Kohn; Michal Twik; Marilyn Safran; Doron Lancet; Dana Cohen
Journal:  Database (Oxford)       Date:  2017-01-01       Impact factor: 3.451

9.  The Ensembl Variant Effect Predictor.

Authors:  William McLaren; Laurent Gil; Sarah E Hunt; Harpreet Singh Riat; Graham R S Ritchie; Anja Thormann; Paul Flicek; Fiona Cunningham
Journal:  Genome Biol       Date:  2016-06-06       Impact factor: 13.583

10.  WASP: allele-specific software for robust molecular quantitative trait locus discovery.

Authors:  Bryce van de Geijn; Graham McVicker; Yoav Gilad; Jonathan K Pritchard
Journal:  Nat Methods       Date:  2015-09-14       Impact factor: 28.547

View more
  36 in total

Review 1.  Regulatory genome variants in human susceptibility to infection.

Authors:  Amalio Telenti; Julia di Iulio
Journal:  Hum Genet       Date:  2019-12-05       Impact factor: 4.132

Review 2.  Genetic testing for kidney disease of unknown etiology.

Authors:  Thomas Hays; Emily E Groopman; Ali G Gharavi
Journal:  Kidney Int       Date:  2020-04-24       Impact factor: 10.612

3.  Co-localization between Sequence Constraint and Epigenomic Information Improves Interpretation of Whole-Genome Sequencing Data.

Authors:  Danqing Xu; Chen Wang; Krzysztof Kiryluk; Joseph D Buxbaum; Iuliana Ionita-Laza
Journal:  Am J Hum Genet       Date:  2020-04-02       Impact factor: 11.025

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

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

5.  A Transcriptome-Based Drug Discovery Paradigm for Neurodevelopmental Disorders.

Authors:  Ryan S Dhindsa; Anthony W Zoghbi; Daniel K Krizay; Chirag Vasavda; David B Goldstein
Journal:  Ann Neurol       Date:  2020-11-18       Impact factor: 10.422

Review 6.  [Application of RNA sequencing in clinical diagnosis of Mendelian disease].

Authors:  Hui Xiao; Wen-Hao Zhou
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2020-10

Review 7.  Rare genetic causes of complex kidney and urological diseases.

Authors:  Emily E Groopman; Gundula Povysil; David B Goldstein; Ali G Gharavi
Journal:  Nat Rev Nephrol       Date:  2020-08-17       Impact factor: 28.314

Review 8.  Review of multi-omics data resources and integrative analysis for human brain disorders.

Authors:  Xianjun Dong; Chunyu Liu; Mikhail Dozmorov
Journal:  Brief Funct Genomics       Date:  2021-07-17       Impact factor: 4.241

Review 9.  Systems biology in cardiovascular disease: a multiomics approach.

Authors:  Abhishek Joshi; Marieke Rienks; Konstantinos Theofilatos; Manuel Mayr
Journal:  Nat Rev Cardiol       Date:  2020-12-18       Impact factor: 32.419

10.  Detection of aberrant gene expression events in RNA sequencing data.

Authors:  Vicente A Yépez; Christian Mertes; Michaela F Müller; Daniela Klaproth-Andrade; Leonhard Wachutka; Laure Frésard; Mirjana Gusic; Ines F Scheller; Patricia F Goldberg; Holger Prokisch; Julien Gagneur
Journal:  Nat Protoc       Date:  2021-01-18       Impact factor: 13.491

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.