Evidence map›Paper›PMID 35478247›Full record

ReviewNature protocols2022

Chromatin accessibility profiling by ATAC-seq.

Fiorella C Grandi, Hailey Modi, Lucas Kampman, M Ryan Corces

Abstract readReview
In one paragraph

Review in Nature protocols, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 349 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
349citing papers in PubMed, 1 pooled it
–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

349 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  9. The dark genome in cardiovascular medicine.European heart journal · 2026
    Review
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289 more citing papers are in PubMed but not listed here.

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.

Fiorella C GrandiGladstone Institute of Neurological Disease, San Francisco, CA, USA.
Hailey ModiGladstone Institute of Neurological Disease, San Francisco, CA, USA.ORCID 0000-0001-6177-9087
Lucas KampmanGladstone Institute of Neurological Disease, San Francisco, CA, USA.ORCID 0000-0002-2008-549X
M Ryan CorcesGladstone Institute of Neurological Disease, San Francisco, CA, USA. ryan.corces@gladstone.ucsf.edu.ORCID 0000-0001-7465-7652

Funding

Project 4: Cross-species Dissection of Cellular Response to APOE Genotype and AD Pathology Using Single-cell Multi-omicsP01AG073082 · NIA · J. DAVID GLADSTONE INSTITUTES · PI HUANG, YADONG, MUCKE, LENNART · 2021 to 2025
$23.4M
Single-cell Mapping Center for Human Regulatory Elements and Gene ActivityUM1HG012076 · NHGRI · STANFORD UNIVERSITY · PI Michael Ryan Corces, Ansuman Satpathy · 2021 to 2026
$13.8M
Multi-omic functional assessment of novel AD variants using high-throughput and single-cell technologiesU01AG072573 · NIA · STANFORD UNIVERSITY · PI KUNDAJE, ANSHUL, MONTGOMERY, STEPHEN · 2021 to 2025
$8.3M
Functional characterization of the Alzheimer's disease EpigenomeR00AG059918 · NIA · J. DAVID GLADSTONE INSTITUTES · PI CORCES, MICHAEL RYAN · 2020 to 2022
$944k
NHGRI NIH HHS UM1 HG012076NIA NIH HHS P01 AG073082NIA NIH HHS R00 AG059918NIA NIH HHS U01 AG072573
6 · The paper itself

Abstract

The assay for transposase-accessible chromatin using sequencing (ATAC-seq) provides a simple and scalable way to detect the unique chromatin landscape associated with a cell type and how it may be altered by perturbation or disease. ATAC-seq requires a relatively small number of input cells and does not require a priori knowledge of the epigenetic marks or transcription factors governing the dynamics of the system. Here we describe an updated and optimized protocol for ATAC-seq, called Omni-ATAC, that is applicable across a broad range of cell and tissue types. The ATAC-seq workflow has five main steps: sample preparation, transposition, library preparation, sequencing and data analysis. This protocol details the steps to generate and sequence ATAC-seq libraries, with recommendations for sample preparation and downstream bioinformatic analysis. ATAC-seq libraries for roughly 12 samples can be generated in 10 h by someone familiar with basic molecular biology, and downstream sequencing analysis can be implemented using benchmarked pipelines by someone with basic bioinformatics skills and with access to a high-performance computing environment.

Indexed as

ChromatinChromatin Immunoprecipitation SequencingHigh-Throughput Nucleotide SequencingSequence Analysis, DNATransposasesChromatinTransposases

Identifiers

PMID35478247
PMCPMC9189070

What OpenQuestion holds

Textmetadata
LicenceTDM
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.