Literature DB >> 31228310

Predicting functional variants in enhancer and promoter elements using RegulomeDB.

Shengcheng Dong1, Alan P Boyle1,2.   

Abstract

Here we present a computational model, Score of Unified Regulatory Features (SURF), that predicts functional variants in enhancer and promoter elements. SURF is trained on data from massively parallel reporter assays and predicts the effect of variants on reporter expression levels. It achieved the top performance in the Fifth Critical Assessment of Genome Interpretation "Regulation Saturation" challenge. We also show that features queried through RegulomeDB, which are direct annotations from functional genomics data, help improve prediction accuracy beyond transfer learning features from DNA sequence-based deep learning models. Some of the most important features include DNase footprints, especially when coupled with complementary ChIP-seq data. Furthermore, we found our model achieved good performance in predicting allele-specific transcription factor binding events. As an extension to the current scoring system in RegulomeDB, we expect our computational model to prioritize variants in regulatory regions, thus help the understanding of functional variants in noncoding regions that lead to disease.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  MPRA; functional genomics; gene regulation; machine learning; variation

Year:  2019        PMID: 31228310      PMCID: PMC6744346          DOI: 10.1002/humu.23791

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  27 in total

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Journal:  Genome Res       Date:  2010-11-24       Impact factor: 9.043

2.  Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Authors:  Lucia A Hindorff; Praveen Sethupathy; Heather A Junkins; Erin M Ramos; Jayashri P Mehta; Francis S Collins; Teri A Manolio
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-27       Impact factor: 11.205

3.  Super-enhancers in the control of cell identity and disease.

Authors:  Denes Hnisz; Brian J Abraham; Tong Ihn Lee; Ashley Lau; Violaine Saint-André; Alla A Sigova; Heather A Hoke; Richard A Young
Journal:  Cell       Date:  2013-10-10       Impact factor: 41.582

Review 4.  Decoding enhancers using massively parallel reporter assays.

Authors:  Fumitaka Inoue; Nadav Ahituv
Journal:  Genomics       Date:  2015-06-10       Impact factor: 5.736

Review 5.  Mining the Unknown: Assigning Function to Noncoding Single Nucleotide Polymorphisms.

Authors:  Sierra S Nishizaki; Alan P Boyle
Journal:  Trends Genet       Date:  2016-12-06       Impact factor: 11.639

6.  A uniform survey of allele-specific binding and expression over 1000-Genomes-Project individuals.

Authors:  Jieming Chen; Joel Rozowsky; Timur R Galeev; Arif Harmanci; Robert Kitchen; Jason Bedford; Alexej Abyzov; Yong Kong; Lynne Regan; Mark Gerstein
Journal:  Nat Commun       Date:  2016-04-18       Impact factor: 14.919

7.  DanQ: a hybrid convolutional and recurrent deep neural network for quantifying the function of DNA sequences.

Authors:  Daniel Quang; Xiaohui Xie
Journal:  Nucleic Acids Res       Date:  2016-04-15       Impact factor: 16.971

8.  GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.

Authors:  Mulin Jun Li; Lily Yan Wang; Zhengyuan Xia; Pak Chung Sham; Junwen Wang
Journal:  Nucleic Acids Res       Date:  2013-05-30       Impact factor: 16.971

9.  JASPAR, the open access database of transcription factor-binding profiles: new content and tools in the 2008 update.

Authors:  Jan Christian Bryne; Eivind Valen; Man-Hung Eric Tang; Troels Marstrand; Ole Winther; Isabelle da Piedade; Anders Krogh; Boris Lenhard; Albin Sandelin
Journal:  Nucleic Acids Res       Date:  2007-11-15       Impact factor: 16.971

10.  DeFine: deep convolutional neural networks accurately quantify intensities of transcription factor-DNA binding and facilitate evaluation of functional non-coding variants.

Authors:  Meng Wang; Cheng Tai; Weinan E; Liping Wei
Journal:  Nucleic Acids Res       Date:  2018-06-20       Impact factor: 16.971

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  24 in total

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Authors:  Daniel L Hertz; Julie A Douglas; Robert M Miller; Kelley M Kidwell; Christina L Gersch; Zeruesenay Desta; Anna Maria Storniolo; Vered Stearns; Todd C Skaar; Daniel F Hayes; N Lynn Henry; James M Rae
Journal:  Support Care Cancer       Date:  2022-07-01       Impact factor: 3.359

2.  Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia.

Authors:  Linda Kachuri; Soyoung Jeon; Andrew T DeWan; Catherine Metayer; Xiaomei Ma; John S Witte; Charleston W K Chiang; Joseph L Wiemels; Adam J de Smith
Journal:  Am J Hum Genet       Date:  2021-08-31       Impact factor: 11.043

3.  NRN1 Gene as a Potential Marker of Early-Onset Schizophrenia: Evidence from Genetic and Neuroimaging Approaches.

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Journal:  Int J Mol Sci       Date:  2022-07-05       Impact factor: 6.208

4.  Gut Microbiome Alterations Associated with Diabetes in Mexican Americans in South Texas.

Authors:  Suet-Ying Kwan; Caroline M Sabotta; Aron Joon; Peng Wei; Lauren E Petty; Jennifer E Below; Xiaogang Wu; Jianhua Zhang; Robert R Jenq; Ernest T Hawk; Joseph B McCormick; Susan P Fisher-Hoch; Laura Beretta
Journal:  mSystems       Date:  2022-04-28       Impact factor: 7.324

5.  Gut microbiome features associated with liver fibrosis in Hispanics, a population at high risk for fatty liver disease.

Authors:  Suet-Ying Kwan; Jingjing Jiao; Aron Joon; Peng Wei; Lauren E Petty; Jennifer E Below; Carrie R Daniel; Xiaogang Wu; Jianhua Zhang; Robert R Jenq; P Andrew Futreal; Ernest T Hawk; Joseph B McCormick; Susan P Fisher-Hoch; Laura Beretta
Journal:  Hepatology       Date:  2021-12-13       Impact factor: 17.298

6.  Genome-wide analyses identify SCN5A as a susceptibility locus for premature atrial contraction frequency.

Authors:  Sébastien Thériault; Medea Imboden; Mary L Biggs; Thomas R Austin; Stefanie Aeschbacher; Emmanuel Schaffner; Jennifer A Brody; Traci M Bartz; Martin Risch; Kirsten Grossmann; Henry J Lin; Elsayed Z Soliman; Wendy S Post; Lorenz Risch; Jose E Krieger; Alexandre C Pereira; Susan R Heckbert; Nona Sotoodehnia; Nicole M Probst-Hensch; David Conen
Journal:  iScience       Date:  2022-09-24

7.  OPRD1 SNPs associated with opioid addiction are cis-eQTLs for the phosphatase and actin regulator 4 gene, PHACTR4, a mediator of cytoskeletal dynamics.

Authors:  Orna Levran; Matthew Randesi; Miriam Adelson; Mary Jeanne Kreek
Journal:  Transl Psychiatry       Date:  2021-05-25       Impact factor: 6.222

8.  Investigation of genetic loci shared between bipolar disorder and risk-taking propensity: potential implications for pharmacological interventions.

Authors:  Claudia Pisanu; Donatella Congiu; Giovanni Severino; Raffaella Ardau; Caterina Chillotti; Maria Del Zompo; Bernhard T Baune; Alessio Squassina
Journal:  Neuropsychopharmacology       Date:  2021-05-25       Impact factor: 8.294

9.  Genome-wide association study of letrozole plasma concentrations identifies non-exonic variants that may affect CYP2A6 metabolic activity.

Authors:  Daniel L Hertz; Julie A Douglas; Kelley M Kidwell; Christina L Gersch; Zeruesenay Desta; Ana-Maria Storniolo; Vered Stearns; Todd C Skaar; Daniel F Hayes; N Lynn Henry; James M Rae
Journal:  Pharmacogenet Genomics       Date:  2021-07-01       Impact factor: 2.000

10.  Resolving mechanisms of immune-mediated disease in primary CD4 T cells.

Authors:  Christophe Bourges; Abigail F Groff; Oliver S Burren; Chiara Gerhardinger; Kaia Mattioli; Anna Hutchinson; Theodore Hu; Tanmay Anand; Madeline W Epping; Chris Wallace; Kenneth Gc Smith; John L Rinn; James C Lee
Journal:  EMBO Mol Med       Date:  2020-04-01       Impact factor: 12.137

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