Evidence map›Paper›PMID 24727652›Full record

ArticleNature methods2014

Multiscale representation of genomic signals.

Theo A Knijnenburg, Stephen A Ramsey, Benjamin P Berman, Kathleen A Kennedy, Arian F A Smit, Lodewyk F A Wessels, Peter W Laird, Alan Aderem, Ilya Shmulevich

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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Computational Methods for Single-cell DNA Methylome Analysis.Genomics, proteomics & bioinformatics · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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  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

9 authors.

Theo A KnijnenburgInstitute for Systems Biology, Seattle, Washington, USA.
Stephen A Ramsey1] Seattle Biomedical Research Institute, Seattle, Washington, USA. [2].
Benjamin P BermanUniversity of Southern California Epigenome Center, University of Southern California, Keck School of Medicine, Los Angeles, California, USA.
Kathleen A KennedySeattle Biomedical Research Institute, Seattle, Washington, USA.
Arian F A SmitInstitute for Systems Biology, Seattle, Washington, USA.
Lodewyk F A Wessels1] Division of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, The Netherlands. [2] Faculty of Electrical Engineering, Mathematics and Computer Science, Delft University of Technology, Delft, The Netherlands.
Peter W LairdUniversity of Southern California Epigenome Center, University of Southern California, Keck School of Medicine, Los Angeles, California, USA.
Alan AderemSeattle Biomedical Research Institute, Seattle, Washington, USA.
Ilya ShmulevichInstitute for Systems Biology, Seattle, Washington, USA.

Funding

Systems Biology CoreU19AI100627 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI ULEVITCH, RICHARD J · 2012 to 2021
$49.1M
LPS Signaling in Macrophages: The Roll of TollR01AI032972 · NIAID · UNIVERSITY OF WASHINGTON · PI ADEREM, ALAN A · 1992 to 2020
$14.6M
The USC-JHU Cancer Epigenome Characterization CenterU24CA143882 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BAYLIN, STEPHEN B., WEISENBERGER, DANIEL JOSEPH · 2009 to 2016
$13.3M
Maintenance and Development of RepeatMasker and RepeatModelerR01HG002939 · NHGRI · INSTITUTE FOR SYSTEMS BIOLOGY · PI Robert MacDonald Hubley, Arian Fredericus Anthonius Smit · 2003 to 2026
$9.1M
LPS REGULATION OF MACROPHAGE FUNCTIONR01AI025032 · NIAID · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI ADEREM, ALAN A · 1987 to 2016
$6.7M
Systems analysis of transcriptional interactions underlying foam cell formationK25HL098807 · NHLBI · SEATTLE BIOMEDICAL RESEARCH INSTITUTE · PI RAMSEY, STEPHEN A. · 2010 to 2013
$584k
NCI NIH HHS U24 CA143882NHGRI NIH HHS R01 HG002939NHGRI NIH HHS R01HG002939NHLBI NIH HHS K25 HL098807NHLBI NIH HHS K25HL098807NIAID NIH HHS HHSN272200700038CNIAID NIH HHS R01 AI025032NIAID NIH HHS R01AI025032NIAID NIH HHS U19 AI100627NIAID NIH HHS U19AI100627NIAID NIH HHS U54-AI54253
6 · The paper itself

Abstract

Genomic information is encoded on a wide range of distance scales, ranging from tens of bases to megabases. We developed a multiscale framework to analyze and visualize the information content of genomic signals. Different types of signals, such as G+C content or DNA methylation, are characterized by distinct patterns of signal enrichment or depletion across scales spanning several orders of magnitude. These patterns are associated with a variety of genomic annotations. By integrating the information across all scales, we demonstrated improved prediction of gene expression from polymerase II chromatin immunoprecipitation sequencing (ChIP-seq) measurements, and we observed that gene expression differences in colorectal cancer are related to methylation patterns that extend beyond the single-gene scale. Our software is available at https://github.com/tknijnen/msr/.

Indexed as

SoftwareTranscriptomeAnimalsDNADNA MethylationGenomicsHumansSequence Analysis, DNADNA

Identifiers

PMID24727652
PMCPMC4040162

What OpenQuestion holds

Textmetadata
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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.