Evidence map›Paper›PMID 26926147›Full record

ArticleBMC genomics2016

Overlapping cell population expression profiling and regulatory inference in C. elegans.

Joshua Burdick, Travis Walton, Elicia Preston, Amanda Zacharias, Arjun Raj, John Isaac Murray

Abstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. bioRxiv : the preprint server for biology · 2026
    Article
  2. G3 (Bethesda, Md.) · 2020
    Article
  3. TheGenome research · 2019
    Article
  4. Article
  5. 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

6 authors.

Joshua BurdickDepartment of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania, USA. jburdick@mail.med.upenn.edu.
Travis WaltonDepartment of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania, USA. twalton@fas.harvard.edu.
Elicia PrestonDepartment of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania, USA. eliciap@mail.med.upenn.edu.
Amanda ZachariasDepartment of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania, USA. azach@mail.med.upenn.edu.
Arjun RajDepartment of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania, USA. arjunrajlab@gmail.com.
John Isaac MurrayDepartment of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania, USA. jmurr@mail.med.upenn.edu.

Funding

Training Program in Computational GenomicsT32HG000046 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI JUNHYONG KIM, Mingyao Li · 1999 to 2026
$9.5M
Mechanisms integrating lineage history with fate specification in C. elegansR01GM105676 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI MURRAY, JOHN ISAAC · 2013 to 2017
$1.5M
Dissecting the Regulation of Gene Expression during C. elegans EmbryogenesisR00GM083145 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI MURRAY, JOHN ISAAC · 2010 to 2012
$742k
Dissecting the Regulation of Gene Expression during C. elegans EmbryogenesisK99GM083145 · NIGMS · UNIVERSITY OF WASHINGTON · PI MURRAY, JOHN ISAAC · 2008 to 2009
$175k
Mechanisms governing context-dependent Wnt activity in C. elegans embryogenesisK99GM111825 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI ZACHARIAS, AMANDA LUCILLE · 2014 to 2015
$146k
NHGRI NIH HHS HG000046-13NHGRI NIH HHS T32 HG000046NIGMS NIH HHS GM083145NIGMS NIH HHS GM105676NIGMS NIH HHS K99 GM083145NIGMS NIH HHS K99 GM111825NIGMS NIH HHS R00 GM083145NIGMS NIH HHS R01 GM105676
6 · The paper itself

Abstract

backgroundUnderstanding gene expression across the diverse metazoan cell types during development is critical to understanding their function and regulation. However, most cell types have not been assayed for expression genome-wide.

resultsWe applied a novel approach we term "Profiling of Overlapping Populations of cells (POP-Seq)" to assay differential expression across all embryonic cells in the nematode Caenorhabditis elegans. In this approach, we use RNA-seq to define the transcriptome of diverse partially overlapping FACS-sorted cell populations. This identified thousands of transcripts differentially expressed across embryonic cells. Hierarchical clustering analysis identified over 100 sets of coexpressed genes corresponding to distinct patterns of cell type specific expression. We identified thousands of candidate regulators of these clusters based on enrichment of transcription factor motifs and experimentally determined binding sites.

conclusionsOur analysis provides new insight into embryonic gene regulation, and provides a resource for improving our knowledge of tissue-specific expression and its regulation throughout C. elegans development.

Indexed as

Gene Expression Regulation, DevelopmentalTranscriptomeAnimalsBinding SitesCaenorhabditis elegansCaenorhabditis elegans ProteinsCluster AnalysisGene Expression ProfilingRNA, HelminthSequence Analysis, RNATranscription FactorsCaenorhabditis elegans ProteinsRNA, HelminthTranscription Factors

Identifiers

PMID26926147
PMCPMC4772325

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.