Evidence map›Paper›PMID 26016777›Full record

ArticlePLoS computational biology2015

SeqGL Identifies Context-Dependent Binding Signals in Genome-Wide Regulatory Element Maps.

Manu Setty, Christina S Leslie

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.5field-weighted citation impact, top 3% of its field
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

41 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
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  10. A machine learning-based framework for modeling transcription elongation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Review
  12. Article
  13. Article
  14. Enhancer Predictions and Genome-Wide Regulatory Circuits.Annual review of genomics and human genetics · 2020
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Epigenomic analysis reveals DNA motifs regulating histone modifications in human and mouse.Proceedings of the National Academy of Sciences of the United States of America · 2019
    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

2 authors at 1 institution in 1 country.

Manu SettyComputational Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York, United States of America.
Christina S LeslieComputational Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York, United States of America.
Memorial Sloan Kettering Cancer Center · US

Funding

Integrative analysis tools to dissect cell-type specific transcriptional programsR01HG006798 · NHGRI · SLOAN-KETTERING INST CAN RESEARCH · PI LESLIE, CHRISTINA S · 2012 to 2014
$1.6M
NHGRI NIH HHS R01 HG006798NHGRI NIH HHS R01-HG006798
6 · The paper itself

Abstract

Genome-wide maps of transcription factor (TF) occupancy and regions of open chromatin implicitly contain DNA sequence signals for multiple factors. We present SeqGL, a novel de novo motif discovery algorithm to identify multiple TF sequence signals from ChIP-, DNase-, and ATAC-seq profiles. SeqGL trains a discriminative model using a k-mer feature representation together with group lasso regularization to extract a collection of sequence signals that distinguish peak sequences from flanking regions. Benchmarked on over 100 ChIP-seq experiments, SeqGL outperformed traditional motif discovery tools in discriminative accuracy. Furthermore, SeqGL can be naturally used with multitask learning to identify genomic and cell-type context determinants of TF binding. SeqGL successfully scales to the large multiplicity of sequence signals in DNase- or ATAC-seq maps. In particular, SeqGL was able to identify a number of ChIP-seq validated sequence signals that were not found by traditional motif discovery algorithms. Thus compared to widely used motif discovery algorithms, SeqGL demonstrates both greater discriminative accuracy and higher sensitivity for detecting the DNA sequence signals underlying regulatory element maps. SeqGL is available at http://cbio.mskcc.org/public/Leslie/SeqGL/.

Indexed as

GenomeAlgorithmsAmino Acid MotifsBinding SitesCell Line, TumorChromatinChromatin ImmunoprecipitationChromosome MappingCluster AnalysisComputational BiologyDeoxyribonucleasesHigh-Throughput Nucleotide SequencingHumansModels, StatisticalProtein BindingRegulatory Sequences, Nucleic AcidChromatinDeoxyribonucleasesTranscription Factors

Identifiers

PMID26016777
PMCPMC4446265
OpenAlexW370702354

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.