Evidence map›Paper›PMID 38646172›Full record

ArticleiScience2024

Predicting A/B compartments from histone modifications using deep learning.

Suchen Zheng, Nitya Thakkar, Hannah L Harris, Susanna Liu, Megan Zhang, Mark Gerstein, Erez Lieberman Aiden, M Jordan Rowley, William Stafford Noble, Gamze Gürsoy and 1 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 8 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

11 authors at 6 institutions in 1 country.

Suchen ZhengDepartment of Computer Science, Brown University, Providence, RI, USA.
Nitya ThakkarDepartment of Computer Science, Brown University, Providence, RI, USA.
Hannah L HarrisDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Susanna LiuData Science and Statistics, Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA.
Megan ZhangData Science and Statistics, Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA.
Mark GersteinComputational Biology and Bioinformatics, Molecular Biophysics & Biochemistry, Data Science and Statistics, Computer Science, Yale University, New Haven, CT, USA.
Erez Lieberman AidenDepartment of Genetics, Baylor College of Medicine, Department of Computer Science, Computational and Applied Mathematics, Rice University, Houston, TX, USA.
M Jordan RowleyDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
William Stafford NobleDepartment of Genome Sciences, Paul G. Allen School of Computer Science and Engineering, University of Washington, Seattle, WA, USA.
Gamze GürsoyDepartment of Biomedical Informatics, Columbia University, New York Genome Center, New York, NY, USA.
Ritambhara SinghDepartment of Computer Science, Center for Computational Molecular Biology, Brown University, Providence, RI, USA.
Brown University · USYale University · USUniversity of Nebraska Medical Center · USBaylor Genetics · USNew York Genome Center · USUniversity of Washington · US

Funding

EDAC: ENCODE Data Analysis CenterU24HG009446 · NHGRI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI GERSTEIN, MARK BENDER, WENG, ZHIPING · 2017 to 2022
$10.4M
Deep learning for understanding gene regulation in diseases via 'omics' integrationR35HG011939 · NHGRI · BROWN UNIVERSITY · PI SINGH, RITAMBHARA · 2021 to 2025
$1.9M
NHGRI NIH HHS R35 HG011939NHGRI NIH HHS U24 HG009446
6 · The paper itself

Abstract

The three-dimensional organization of genomes plays a crucial role in essential biological processes. The segregation of chromatin into A and B compartments highlights regions of activity and inactivity, providing a window into the genomic activities specific to each cell type. Yet, the steep costs associated with acquiring Hi-C data, necessary for studying this compartmentalization across various cell types, pose a significant barrier in studying cell type specific genome organization. To address this, we present a prediction tool called compartment prediction using recurrent neural networks (CoRNN), which predicts compartmentalization of 3D genome using histone modification enrichment. CoRNN demonstrates robust cross-cell-type prediction of A/B compartments with an average AuROC of 90.9%. Cell-type-specific predictions align well with known functional elements, with H3K27ac and H3K36me3 identified as highly predictive histone marks. We further investigate our mispredictions and found that they are located in regions with ambiguous compartmental status. Furthermore, our model's generalizability is validated by predicting compartments in independent tissue samples, which underscores its broad applicability.

Indexed as

Chromosome organizationGenomicsMachine learning

Identifiers

PMID38646172
PMCPMC11031843
OpenAlexW4393238026

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.