Evidence map›Paper›PMID 27812282›Full record

ArticleBioinformatics and biology insights2016

Iterative Fragmentation Improves the Detection of ChIP-seq Peaks for Inactive Histone Marks.

Miklós Laczik, Jan Hendrickx, Anne-Clémence Veillard, Mustafa Tammoh, Sarah Marzi, Dominique Poncelet

Abstract read
In one paragraph

Article in Bioinformatics and biology insights, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

6 authors.

Miklós LaczikDoctorate Student, Doctoral College of Agronomy and Bioengineering, Gembloux Agro-Biotech, University of Liège, Liège, Belgium.; Researcher, R&D Epigenetics Department of Diagenode SA, Liège, Belgium.
Jan HendrickxResearcher, R&D Epigenetics Department of Diagenode SA, Liège, Belgium.
Anne-Clémence VeillardResearcher, R&D Epigenetics Department of Diagenode SA, Liège, Belgium.
Mustafa TammohResearcher, R&D Epigenetics Department of Diagenode SA, Liège, Belgium.
Sarah MarziDoctorate Student, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Dominique PonceletResearcher, R&D Epigenetics Department of Diagenode SA, Liège, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As chromatin immunoprecipitation (ChIP) sequencing is becoming the dominant technique for studying chromatin modifications, new protocols surface to improve the method. Bioinformatics is also essential to analyze and understand the results, and precise analysis helps us to identify the effects of protocol optimizations. We applied iterative sonication - sending the fragmented DNA after ChIP through additional round(s) of shearing - to a number of samples, testing the effects on different histone marks, aiming to uncover potential benefits of inactive histone marks specifically. We developed an analysis pipeline that utilizes our unique, enrichment-type specific approach to peak calling. With the help of this pipeline, we managed to accurately describe the advantages and disadvantages of the iterative refragmentation technique, and we successfully identified possible fields for its applications, where it enhances the results greatly. In addition to the resonication protocol description, we provide guidelines for peak calling optimization and a freely implementable pipeline for data analysis.

Indexed as

bioinformaticsChIPChIP-seqchromatinheterochromatinhistone markspeak callingsonication

Identifiers

PMID27812282
PMCPMC5081244

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.