Evidence map›Paper›PMID 42642589›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Chromatin Immunoprecipitation Sequencing in Cancer Cells.

Zachary Bigelow, Sergei Nechaev, Archana Dhasarathy

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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

3 authors.

Zachary BigelowDepartment of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND, 58202-9061, USA.
Sergei Nechaev *Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND, 58202-9061, USA. sergei.nechaev@und.edu.
Archana Dhasarathy *Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND, 58202-9061, USA. archana.dhasarathy@und.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analysis of DNA co-immunoprecipitated with proteins of interest has been foundational to our understanding of chromatin and its regulation. Despite the emergence of crosslink-free techniques such as CUT&RUN and CUT&TAG, Chromatin Immunoprecipitation followed by sequencing (ChIP) remains a method of choice for profiling of protein binding at individual DNA sites and, when combined with sequencing (ChIP-seq), across the genome. ChIP-seq can provide insights into transcription factor binding sites, histone modification patterns and chromatin structure, and has broad applications in the study of cancer and other diseases. Here, we outline the protocols for ChIP-seq, including immunoprecipitation, library preparation for high-throughput sequencing, and bioinformatics analysis of sequencing data that we routinely perform in our lab groups. We also include troubleshooting tips for each step. We hope this guide will be helpful to laboratories that wish to adopt this method for their cancer biology studies.

Indexed as

Chromatin ImmunoprecipitationChromatin Immunoprecipitation SequencingNeoplasmsBinding SitesChromatinComputational BiologyGene LibraryHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNAChromatinCancerChIP-seqChromatinEpigeneticsGenomicsImmunoprecipitation

Identifiers

What OpenQuestion holds

Textmetadata
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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.