Evidence map›Paper›PMID 37202401›Full record

ArticleScientific reports2023

Developing OCHROdb, a comprehensive quality checked database of open chromatin regions from sequencing data.

Parisa Shooshtari, Samantha Feng, Viswateja Nelakuditi, Reza Asakereh, Nader Hosseini Naghavi, Justin Foong, Michael Brudno, Chris Cotsapas

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 76% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. 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

8 authors at 6 institutions in 2 countries.

Parisa ShooshtariDepartment of Pathology and Lab Medicine, University of Western Ontario, London, ON, N6A 5C1, Canada. pshoosh@uwo.ca.
Samantha FengMicrosoft Canada, Toronto, ON, M5K 1E7, Canada.
Viswateja NelakuditiCenter for Computational Medicine, Hospital for Sick Children (SickKids), Toronto, ON, M5G 0A4, Canada.
Reza AsakerehDepartment of Pathology and Lab Medicine, University of Western Ontario, London, ON, N6A 5C1, Canada.
Nader Hosseini NaghaviDepartment of Computer Science, University of Western Ontario, London, ON, N6A 5C1, Canada.
Justin FoongUniversity Health Network, Toronto, ON, M5G 1L7, Canada.
Michael BrudnoUniversity Health Network, Toronto, ON, M5G 1L7, Canada. brudno@cs.toronto.edu.
Chris CotsapasDepartment of Neurology, Yale University, New Haven, CT, 06510, USA. cotsapas@broadinstitute.org.
University Health Network · CAWestern University · CALawson Health Research Institute · CASickKids Foundation · CAUniversity of Waterloo · CAYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

International consortia, including ENCODE, Roadmap Epigenomics, Genomics of Gene Regulation and Blueprint Epigenome have made large-scale datasets of open chromatin regions publicly available. While these datasets are extremely useful for studying mechanisms of gene regulation in disease and cell development, they only identify open chromatin regions in individual samples. A uniform comparison of accessibility of the same regulatory sites across multiple samples is necessary to correlate open chromatin accessibility and expression of target genes across matched cell types. Additionally, although replicate samples are available for majority of cell types, a comprehensive replication-based quality checking of individual regulatory sites is still lacking. We have integrated 828 DNase-I hypersensitive sequencing samples, which we have uniformly processed and then clustered their regulatory regions across all samples. We checked the quality of open-chromatin regions using our replication test. This has resulted in a comprehensive, quality-checked database of Open CHROmatin (OCHROdb) regions for 194 unique human cell types and cell lines which can serve as a reference for gene regulatory studies involving open chromatin. We have made this resource publicly available: users can download the whole database, or query it for their genomic regions of interest and visualize the results in an interactive genome browser.

Indexed as

ChromatinGene Expression RegulationEpigenomicsGenomicsHumansRegulatory Sequences, Nucleic AcidChromatin

Identifiers

PMID37202401
PMCPMC10195780
OpenAlexW4377012855

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.