Evidence map›Paper›PMID 37146087›Full record

ArticlePLoS genetics2023

Genetic variation in chromatin state across multiple tissues in Drosophila melanogaster.

Khoi Huynh, Brittny R Smith, Stuart J Macdonald, Anthony D Long

Abstract read
In one paragraph

Article in PLoS genetics, 2023. 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. Article
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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.

Khoi HuynhDepartment of Ecology and Evolutionary Biology, University of California, Irvine, California, United States of America.
Brittny R SmithDepartment of Molecular Biosciences, University of Kansas, Lawrence, Kansas, United States of America.
Stuart J MacdonaldDepartment of Molecular Biosciences, University of Kansas, Lawrence, Kansas, United States of America.
Anthony D LongDepartment of Ecology and Evolutionary Biology, University of California, Irvine, California, United States of America.ORCID 0000-0002-5007-8514

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Douglas E Wright · 2012 to 2026
$63.0M
Understanding the mechanobiology of stem cells in a microengineered 3D cardiac tissue environment with cardiomyopathyP20GM103638 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI LUNTE, SUSAN M · 2012 to 2021
$22.1M
A resource for the genetic analysis of complex traitsR01OD010974 · OD · UNIVERSITY OF KANSAS LAWRENCE · PI LONG, ANTHONY DOUGLAS, MACDONALD, STUART JOHN · 2012 to 2019
$3.1M
Elucidating Mechanisms of Adaptive Change Using Outbred Recombining YeastR01GM115562 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LONG, ANTHONY DOUGLAS · 2015 to 2018
$1.6M
Toxicogenomics of metal response in genetically-variable DrosophilapopulationsR01ES029922 · NIEHS · UNIVERSITY OF KANSAS LAWRENCE · PI MACDONALD, STUART JOHN · 2019 to 2021
$682k
NIEHS NIH HHS R01 ES029922NIGMS NIH HHS P20 GM103418NIGMS NIH HHS P20 GM103638NIGMS NIH HHS R01 GM115562NIH HHS R01 OD010974
6 · The paper itself

Abstract

We use ATAC-seq to examine chromatin accessibility for four different tissues in Drosophila melanogaster: adult female brain, ovaries, and both wing and eye-antennal imaginal discs from males. Each tissue is assayed in eight different inbred strain genetic backgrounds, seven associated with a reference quality genome assembly. We develop a method for the quantile normalization of ATAC-seq fragments and test for differences in coverage among genotypes, tissues, and their interaction at 44099 peaks throughout the euchromatic genome. For the strains with reference quality genome assemblies, we correct ATAC-seq profiles for read mis-mapping due to nearby polymorphic structural variants (SVs). Comparing coverage among genotypes without accounting for SVs results in a highly elevated rate (55%) of identifying false positive differences in chromatin state between genotypes. After SV correction, we identify 1050, 30383, and 4508 regions whose peak heights are polymorphic among genotypes, among tissues, or exhibit genotype-by-tissue interactions, respectively. Finally, we identify 3988 candidate causative variants that explain at least 80% of the variance in chromatin state at nearby ATAC-seq peaks.

Indexed as

ChromatinDrosophila melanogasterAnimalsChromatin Immunoprecipitation SequencingFemaleGenetic VariationGenotypeHigh-Throughput Nucleotide SequencingMaleChromatin

Identifiers

PMID37146087
PMCPMC10191298

What OpenQuestion holds

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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.