Evidence map›Paper›PMID 31125519›Full record

ArticleCurrent protocols in bioinformatics2019

R Tutorial: Detection of Differentially Interacting Chromatin Regions From Multiple Hi-C Datasets.

John C Stansfield, Duc Tran, Tin Nguyen, Mikhail G Dozmorov

Abstract read
In one paragraph

Article in Current protocols in bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Methods for the Differential Analysis of Hi-C Data.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
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

4 authors.

John C StansfieldDepartment of Biostatistics, Virginia Commonwealth University, Richmond, Virginia.
Duc TranDepartment of Computer Science & Engineering, University of Nevada, Reno, Nevada.
Tin NguyenDepartment of Computer Science & Engineering, University of Nevada, Reno, Nevada.
Mikhail G DozmorovDepartment of Biostatistics, Virginia Commonwealth University, Richmond, Virginia.

Funding

Integration of Mixtures Toxicology, Toxicogenomics, and StatisticsT32ES007334 · NIEHS · VIRGINIA COMMONWEALTH UNIVERSITY · PI WHEELER, DAVID CHARLES · 2002 to 2018
$2.5M
NIEHS NIH HHS T32 ES007334
6 · The paper itself

Abstract

The three-dimensional (3D) interactions of chromatin regulate cell-type-specific gene expression, recombination, X-chromosome inactivation, and many other genomic processes. High-throughput chromatin conformation capture (Hi-C) technologies capture the structure of the chromatin on a global scale by measuring all-vs.-all interactions and can provide new insights into genomic regulation. The workflow presented here describes how to analyze and interpret a comparative Hi-C experiment. We describe the process of obtaining Hi-C data from public repositories and give suggestions for pre-processing pipelines for users who intend to analyze their own raw data. We then describe the data normalization and comparative analysis process. We present three protocols describing the use of the multiHiCcompare, diffHic, and FIND R packages, respectively, to perform a comparative analysis of Hi-C experiments. Finally, visualization of the results and downstream interpretation of the differentially interacting regions are discussed. The bulk of this tutorial uses the R programming environment, and the processes described can be performed with most operating systems and a single computer. © 2019 by John Wiley & Sons, Inc.

Indexed as

Databases, Nucleic AcidSoftwareBinding SitesChromatinGene Expression ProfilingMolecular Dynamics SimulationChromatinchromosome conformation capturecomparisondifferential analysisHi-CHiCcomparemultiHiCcomparenormalization

Identifiers

PMID31125519
PMCPMC6588411

What OpenQuestion holds

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LicenceTDM
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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.