Evidence map›Paper›PMID 36807060›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2023

Genome-Wide Mapping of Active Regulatory Elements Using ATAC-seq.

Georgi K Marinov, Zohar Shipony, Anshul Kundaje, William J Greenleaf

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
5.5field-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

9 citing papers in PubMed, 11 citations in OpenAlex.

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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 at 1 institution in 1 country.

Georgi K MarinovDepartment of Genetics, Stanford University, Stanford, CA, USA. marinovg@stanford.edu.
Zohar ShiponyDepartment of Genetics, Stanford University, Stanford, CA, USA.
Anshul KundajeDepartment of Genetics, Stanford University, Stanford, CA, USA.
William J GreenleafDepartment of Genetics, Stanford University, Stanford, CA, USA. wjg@stanford.edu.
Stanford University · US

Funding

Special EquipmentP50HG007735 · NHGRI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2014 to 2018
$15.2M
High-throughput systematic characterization of regulatory element functionUM1HG009436 · NHGRI · STANFORD UNIVERSITY · PI BASSIK, MICHAEL C, GREENLEAF, WILLIAM JAMES · 2017 to 2021
$5.4M
NHGRI NIH HHS P50 HG007735NHGRI NIH HHS UM1 HG009436
6 · The paper itself

Abstract

Active cis-regulatory elements (cREs) in eukaryotes are characterized by nucleosomal depletion and, accordingly, higher accessibility. This property has turned out to be immensely useful for identifying cREs genome-wide and tracking their dynamics across different cellular states and is the basis of numerous methods taking advantage of the preferential enzymatic cleavage/labeling of accessible DNA. ATAC-seq (Assay for Transposase-Accessible Chromatin using sequencing) has emerged as the most versatile and widely adaptable method and has been widely adopted as the standard tool for mapping open chromatin regions. Here, we discuss the current optimal practices and important considerations for carrying out ATAC-seq experiments, primarily in the context of mammalian systems.

Indexed as

Chromatin Immunoprecipitation SequencingHigh-Throughput Nucleotide SequencingAnimalsChromatinMammalsRegulatory Sequences, Nucleic AcidSequence Analysis, DNAChromatinATAC-seqChromatin accessibilityEnhancersHigh-throughput sequencingPromoters

Identifiers

PMID36807060
OpenAlexW4321478241

What OpenQuestion holds

Textmetadata
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.