Evidence map›Paper›PMID 39391743›Full record

ArticleWiley interdisciplinary reviews. Computational statistics

Genome-wide Prediction of Chromatin Accessibility Based on Gene Expression.

Weiqiang Zhou, Ji Hongkai

Abstract read
In one paragraph

Article in Wiley interdisciplinary reviews. Computational statistics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. GECSI: Large-scale chromatin state imputation from gene expression.bioRxiv : the preprint server for biology · 2025
    Article
  2. Review
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

2 authors.

Weiqiang ZhouDepartment of Biostatistics, Johns Hopkins University Bloomberg School of Public Health, 615 North Wolfe Street, Baltimore, MD 21205, USA.
Ji HongkaiDepartment of Biostatistics, Johns Hopkins University Bloomberg School of Public Health, 615 North Wolfe Street, Baltimore, MD 21205, USA.

Funding

Big Data Methods for Decoding Gene RegulationR01HG009518 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI JI, HONGKAI · 2018 to 2021
$1.7M
Computational tools for regulome mapping using single-cell genomic dataR01HG010889 · NHGRI · JOHNS HOPKINS UNIVERSITY · PI JI, HONGKAI · 2019 to 2022
$1.6M
NHGRI NIH HHS R01 HG009518NHGRI NIH HHS R01 HG010889
6 · The paper itself

Abstract

Decoding gene regulation in a biological system requires information from both transcriptome and regulome. While multiple high-throughput transcriptome and regulome mapping technologies are available, transcriptome profiling is more widely used. Today, over a million bulk and single-cell gene expression samples are stored in public databases. This number is orders of magnitude larger than the number of available regulome samples. Most of the gene expression samples do not have corresponding regulome data. However, it is possible to obtain regulome information via prediction. Open chromatin is a hallmark of active regulatory elements. This mini-review discusses recent advances in predicting chromatin accessibility using gene expression data, including both the development of prediction methods and their applications in expanding the regulome catalog, improving regulome analysis, integrating transcriptome and regulome data, and facilitating single-cell analysis of gene regulation.

Identifiers

PMID39391743
PMCPMC11466374

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Registered trials

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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.