Evidence map›Paper›PMID 25086505›Full record

ArticleNature methods2014

Epiviz: interactive visual analytics for functional genomics data.

Florin Chelaru, Llewellyn Smith, Naomi Goldstein, Héctor Corrada Bravo

Abstract read
In one paragraph

Article in Nature methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Gosling: A Grammar-based Toolkit for Scalable and Interactive Genomics Data Visualization.IEEE transactions on visualization and computer graphics · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Tasks, Techniques, and Tools for Genomic Data Visualization.Computer graphics forum : journal of the European Association for Computer Graphics · 2019
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. ChAsE: chromatin analysis and exploration tool.Bioinformatics (Oxford, England) · 2016
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Florin Chelaru1] Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland, USA. [2] Department of Computer Science, University of Maryland, College Park, Maryland, USA.
Llewellyn Smith1] Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland, USA. [2] Department of Mathematics, Williams College, Williamstown, Massachusetts, USA. [3] Department of Computer Science, Williams College, Williamstown, Massachusetts, USA.
Naomi Goldstein1] Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland, USA. [2] Department of Mechanical Engineering and Materials Science, Washington University in St. Louis, St. Louis, Missouri, USA.
Héctor Corrada Bravo1] Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland, USA. [2] Department of Computer Science, University of Maryland, College Park, Maryland, USA.

Funding

Overcoming bias and unwanted variability in next generation sequencingR01HG005220 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI IRIZARRY, RAFAEL ANGEL · 2010 to 2018
$3.6M
Alignment Software for Second-Generation SequencingR01HG006102 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI SALZBERG, STEVEN L. · 2011 to 2014
$2.2M
NHGRI NIH HHS R01 HG005220NHGRI NIH HHS R01 HG006102
6 · The paper itself

Abstract

Visualization is an integral aspect of genomics data analysis. Algorithmic-statistical analysis and interactive visualization are most effective when used iteratively. Epiviz (http://epiviz.cbcb.umd.edu/), a web-based genome browser, and the Epivizr Bioconductor package allow interactive, extensible and reproducible visualization within a state-of-the-art data-analysis platform.

Indexed as

Databases, GeneticInternetSoftwareUser-Computer InterfaceAlgorithmsChromosome MappingDatabase Management SystemsData MiningGenomics

Identifiers

PMID25086505
PMCPMC4149593

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.