Evidence map›Paper›PMID 40832233›Full record

ArticlebioRxiv : the preprint server for biology2025

Chrom-Sig: de-noising 1-dimensional genomic profiles by signal processing methods.

Nandita J Gupta, Zachary Apell, Minji Kim

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Nandita J GuptaDepartment of Electrical and Computer Engineering, University of Michigan, Ann Arbor, MI, USA.
Zachary ApellDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.
Minji KimGilbert S. Omenn Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-7282-8224

Funding

Roles of allele-specific chromatin interactions in transcription regulation during developmentR00HG011542 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KIM, MINJI · 2023 to 2025
$731k
NHGRI NIH HHS R00 HG011542
6 · The paper itself

Abstract

Motivation: Modern genomic research is driven by next-generation sequencing experiments such as ChIP-seq, CUT&Tag, and CUT&RUN that generate coverage files for transcription factor binding, as well as ATAC-seq that yield coverage files for chromatin accessibility. Due to the inherent technical noise present in the experimental protocols, researchers need statistically rigorous and computational efficient methods to extract true biological signal from a mixture of signal and noise. However, existing approaches are often computationally demanding or require input or spike-in controls. Results: We developed Chrom-Sig, a Python package to quickly de-noise 1-dimensional genomic coverage tracks by computing the empirical null distribution without prior assumptions or experimental controls. When tested on 19 ChIP-seq, CUT&RUN, ATAC-seq, snATAC-seq datasets, Chrom-Sig can effectively decompose the data into signal and noise. Notably, Chrom-Sig performs de-noising and peak calling in 1-2 hours using around 20 GB of memory. The de-noised signal corroborates with biologically meaningful results: CTCF CUT&RUN data retained a higher percentage of peaks overlapping CTCF binding motifs and ATAC-seq and RNA Polymerase II data resulted in enhancers and promoters. We envision Chrom-Sig to be a highly versatile and general tool for current and future genomic technologies. Availability: Chrom-Sig is publicly available at https://github.com/minjikimlab/chromsig under the MIT license.

Identifiers

PMID40832233
PMCPMC12363972

What OpenQuestion holds

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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.