Literature DB >> 28459977

GSuite HyperBrowser: integrative analysis of dataset collections across the genome and epigenome.

Boris Simovski1, Daniel Vodák2, Sveinung Gundersen1, Diana Domanska1, Abdulrahman Azab1,3, Lars Holden4, Marit Holden4, Ivar Grytten1, Knut Rand5, Finn Drabløs6, Morten Johansen7, Antonio Mora1,8, Christin Lund-Andersen2, Bastian Fromm2, Ragnhild Eskeland8,9, Odd Stokke Gabrielsen8, Egil Ferkingstad10, Sigve Nakken2, Mads Bengtsen8, Alexander Johan Nederbragt1,11, Hildur Sif Thorarensen1, Johannes Andreas Akse1, Ingrid Glad5, Eivind Hovig1,2,4,7, Geir Kjetil Sandve1.   

Abstract

Background: Recent large-scale undertakings such as ENCODE and Roadmap Epigenomics have generated experimental data mapped to the human reference genome (as genomic tracks) representing a variety of functional elements across a large number of cell types. Despite the high potential value of these publicly available data for a broad variety of investigations, little attention has been given to the analytical methodology necessary for their widespread utilisation. Findings: We here present a first principled treatment of the analysis of collections of genomic tracks. We have developed novel computational and statistical methodology to permit comparative and confirmatory analyses across multiple and disparate data sources. We delineate a set of generic questions that are useful across a broad range of investigations and discuss the implications of choosing different statistical measures and null models. Examples include contrasting analyses across different tissues or diseases. The methodology has been implemented in a comprehensive open-source software system, the GSuite HyperBrowser. To make the functionality accessible to biologists, and to facilitate reproducible analysis, we have also developed a web-based interface providing an expertly guided and customizable way of utilizing the methodology. With this system, many novel biological questions can flexibly be posed and rapidly answered. Conclusions: Through a combination of streamlined data acquisition, interoperable representation of dataset collections, and customizable statistical analysis with guided setup and interpretation, the GSuite HyperBrowser represents a first comprehensive solution for integrative analysis of track collections across the genome and epigenome. The software is available at: https://hyperbrowser.uio.no.
© The Author 2017. Published by Oxford University Press.

Entities:  

Keywords:  Galaxy; data integration; epigenomics; genome analysis; genomic track; genomics; statistical genomics

Mesh:

Year:  2017        PMID: 28459977      PMCID: PMC5493745          DOI: 10.1093/gigascience/gix032

Source DB:  PubMed          Journal:  Gigascience        ISSN: 2047-217X            Impact factor:   6.524


  28 in total

1.  A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.

Authors:  Pablo Cingolani; Adrian Platts; Le Lily Wang; Melissa Coon; Tung Nguyen; Luan Wang; Susan J Land; Xiangyi Lu; Douglas M Ruden
Journal:  Fly (Austin)       Date:  2012 Apr-Jun       Impact factor: 2.160

Review 2.  Orchestrating high-throughput genomic analysis with Bioconductor.

Authors:  Wolfgang Huber; Vincent J Carey; Robert Gentleman; Simon Anders; Marc Carlson; Benilton S Carvalho; Hector Corrada Bravo; Sean Davis; Laurent Gatto; Thomas Girke; Raphael Gottardo; Florian Hahne; Kasper D Hansen; Rafael A Irizarry; Michael Lawrence; Michael I Love; James MacDonald; Valerie Obenchain; Andrzej K Oleś; Hervé Pagès; Alejandro Reyes; Paul Shannon; Gordon K Smyth; Dan Tenenbaum; Levi Waldron; Martin Morgan
Journal:  Nat Methods       Date:  2015-02       Impact factor: 28.547

3.  MULTOVL: fast multiple overlaps of genomic regions.

Authors:  András Aszódi
Journal:  Bioinformatics       Date:  2012-10-15       Impact factor: 6.937

4.  The Genomic HyperBrowser: an analysis web server for genome-scale data.

Authors:  Geir K Sandve; Sveinung Gundersen; Morten Johansen; Ingrid K Glad; Krishanthi Gunathasan; Lars Holden; Marit Holden; Knut Liestøl; Ståle Nygård; Vegard Nygaard; Jonas Paulsen; Halfdan Rydbeck; Kai Trengereid; Trevor Clancy; Finn Drabløs; Egil Ferkingstad; Matús Kalas; Tonje Lien; Morten B Rye; Arnoldo Frigessi; Eivind Hovig
Journal:  Nucleic Acids Res       Date:  2013-04-30       Impact factor: 16.971

5.  Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor.

Authors:  William McLaren; Bethan Pritchard; Daniel Rios; Yuan Chen; Paul Flicek; Fiona Cunningham
Journal:  Bioinformatics       Date:  2010-06-18       Impact factor: 6.937

6.  International Cancer Genome Consortium Data Portal--a one-stop shop for cancer genomics data.

Authors:  Junjun Zhang; Joachim Baran; A Cros; Jonathan M Guberman; Syed Haider; Jack Hsu; Yong Liang; Elena Rivkin; Jianxin Wang; Brett Whitty; Marie Wong-Erasmus; Long Yao; Arek Kasprzyk
Journal:  Database (Oxford)       Date:  2011-09-19       Impact factor: 3.451

7.  An integrated encyclopedia of DNA elements in the human genome.

Authors: 
Journal:  Nature       Date:  2012-09-06       Impact factor: 49.962

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.  UCSC Data Integrator and Variant Annotation Integrator.

Authors:  Angie S Hinrichs; Brian J Raney; Matthew L Speir; Brooke Rhead; Jonathan Casper; Donna Karolchik; Robert M Kuhn; Kate R Rosenbloom; Ann S Zweig; David Haussler; W James Kent
Journal:  Bioinformatics       Date:  2016-01-06       Impact factor: 6.937

10.  deepTools2: a next generation web server for deep-sequencing data analysis.

Authors:  Fidel Ramírez; Devon P Ryan; Björn Grüning; Vivek Bhardwaj; Fabian Kilpert; Andreas S Richter; Steffen Heyne; Friederike Dündar; Thomas Manke
Journal:  Nucleic Acids Res       Date:  2016-04-13       Impact factor: 16.971

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  11 in total

1.  ATRX In-Frame Fusion Neuroblastoma Is Sensitive to EZH2 Inhibition via Modulation of Neuronal Gene Signatures.

Authors:  Zulekha A Qadeer; David Valle-Garcia; Dan Hasson; Zhen Sun; April Cook; Christie Nguyen; Aroa Soriano; Anqi Ma; Lyra M Griffiths; Maged Zeineldin; Dan Filipescu; Luz Jubierre; Asif Chowdhury; Orla Deevy; Xiang Chen; David B Finkelstein; Armita Bahrami; Elizabeth Stewart; Sara Federico; Soledad Gallego; Fumiko Dekio; Mary Fowkes; David Meni; John M Maris; William A Weiss; Stephen S Roberts; Nai-Kong V Cheung; Jian Jin; Miguel F Segura; Michael A Dyer; Emily Bernstein
Journal:  Cancer Cell       Date:  2019-10-17       Impact factor: 38.585

2.  Comparing miRNA structure of mirtrons and non-mirtrons.

Authors:  Igor I Titov; Pavel S Vorozheykin
Journal:  BMC Genomics       Date:  2018-02-09       Impact factor: 3.969

3.  Epigenetic dysregulation of naive CD4+ T-cell activation genes in childhood food allergy.

Authors:  David Martino; Melanie Neeland; Thanh Dang; Joanna Cobb; Justine Ellis; Alice Barnett; Mimi Tang; Peter Vuillermin; Katrina Allen; Richard Saffery
Journal:  Nat Commun       Date:  2018-08-17       Impact factor: 14.919

4.  Artificial intelligence predicts the immunogenic landscape of SARS-CoV-2 leading to universal blueprints for vaccine designs.

Authors:  Brandon Malone; Boris Simovski; Clément Moliné; Jun Cheng; Marius Gheorghe; Hugues Fontenelle; Ioannis Vardaxis; Simen Tennøe; Jenny-Ann Malmberg; Richard Stratford; Trevor Clancy
Journal:  Sci Rep       Date:  2020-12-23       Impact factor: 4.379

5.  The uracil-DNA glycosylase UNG protects the fitness of normal and cancer B cells expressing AID.

Authors:  Shiva Safavi; Ariane Larouche; Astrid Zahn; Anne-Marie Patenaude; Diana Domanska; Kiersten Dionne; Torbjørn Rognes; Felix Dingler; Seong-Kwi Kang; Yan Liu; Nathalie Johnson; Josée Hébert; Ramiro E Verdun; Cristina A Rada; Francisco Vega; Hilde Nilsen; Javier M Di Noia
Journal:  NAR Cancer       Date:  2020-08-27

6.  Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB.

Authors:  Roza B Lemma; Marit Ledsaak; Bettina M Fuglerud; Geir Kjetil Sandve; Ragnhild Eskeland; Odd S Gabrielsen
Journal:  Sci Rep       Date:  2021-04-26       Impact factor: 4.379

7.  Recommendations for the FAIRification of genomic track metadata.

Authors:  Sveinung Gundersen; Sanjay Boddu; Salvador Capella-Gutierrez; Finn Drabløs; José M Fernández; Radmila Kompova; Kieron Taylor; Dmytro Titov; Daniel Zerbino; Eivind Hovig
Journal:  F1000Res       Date:  2021-04-01

8.  Coloc-stats: a unified web interface to perform colocalization analysis of genomic features.

Authors:  Boris Simovski; Chakravarthi Kanduri; Sveinung Gundersen; Dmytro Titov; Diana Domanska; Christoph Bock; Lara Bossini-Castillo; Maria Chikina; Alexander Favorov; Ryan M Layer; Andrey A Mironov; Aaron R Quinlan; Nathan C Sheffield; Gosia Trynka; Geir K Sandve
Journal:  Nucleic Acids Res       Date:  2018-07-02       Impact factor: 16.971

Review 9.  Norwegian e-Infrastructure for Life Sciences (NeLS).

Authors:  Kidane M Tekle; Sveinung Gundersen; Kjetil Klepper; Lars Ailo Bongo; Inge Alexander Raknes; Xiaxi Li; Wei Zhang; Christian Andreetta; Teshome Dagne Mulugeta; Matúš Kalaš; Morten B Rye; Erik Hjerde; Jeevan Karloss Antony Samy; Ghislain Fornous; Abdulrahman Azab; Dag Inge Våge; Eivind Hovig; Nils Peder Willassen; Finn Drabløs; Ståle Nygård; Kjell Petersen; Inge Jonassen
Journal:  F1000Res       Date:  2018-06-29

10.  Colocalization analyses of genomic elements: approaches, recommendations and challenges.

Authors:  Chakravarthi Kanduri; Christoph Bock; Sveinung Gundersen; Eivind Hovig; Geir Kjetil Sandve
Journal:  Bioinformatics       Date:  2019-05-01       Impact factor: 6.937

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