Evidence map›Paper›PMID 41068566›Full record

ArticleBMC bioinformatics2025

H

Hyeon Ho Heo, Soo-Jong Um

Abstract read
In one paragraph

Article in BMC bioinformatics, 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

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.

Hyeon Ho HeoDepartment of Integrative Bioscience and Biotechnology, Sejong University, 209 Neungdong-Ro, Gwangjin-Gu, Seoul, 05006, South Korea.
Soo-Jong UmDepartment of Integrative Bioscience and Biotechnology, Sejong University, 209 Neungdong-Ro, Gwangjin-Gu, Seoul, 05006, South Korea. umsj@sejong.ac.kr.

Funding

Korea Basic Science Institute RS-2023-NF001356National Research Foundation of Korea RS-2025-00562288
6 · The paper itself

Abstract

backgroundChromatin immunoprecipitation followed by sequencing (ChIP-seq) is a widely used technique for mapping protein-DNA interactions and histone modifications across the genome. Despite its utility, current analysis tools often require manual file processing, rigid input formats, and a significant level of bioinformatics expertise, posing a challenge for many experimental researchers.

resultsWe present H3NGST (Hybrid, High-throughput, and High-resolution NGS Toolkit), a fully automated and user-friendly web-based platform for ChIP-seq analysis. H3NGST streamlines the entire analysis workflow, including raw data retrieval via BioProject ID, quality control, adapter trimming, reference genome alignment, peak calling, and genomic annotation. The system also categorizes peaks by genomic region, such as promoters. With minimal user input, H3NGST provides high resolution and reproducible results for both transcription factor binding and histone modification studies.

conclusionsH3NGST significantly reduces the technical barriers to ChIP-seq analysis by eliminating the need for local installations, programming skills, or large file uploads. Its intuitive web interface and mobile accessibility extend its usability to researchers with different computational backgrounds. The platform is scalable for high-throughput studies and is freely available at https://ngschiphhh.duckdns.org .

Indexed as

Chromatin ImmunoprecipitationChromatin Immunoprecipitation SequencingInternetSoftwareComputational BiologyHigh-Throughput Nucleotide SequencingHistonesSequence Analysis, DNAHistonesAutomated analysisChIP-seqEpigenomicsNext-generation sequencingWeb-based pipeline

Identifiers

PMID41068566
PMCPMC12512806

What OpenQuestion 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 OpenQuestion graph.