Cargando…

Statistical Models for Detecting Differential Chromatin Interactions Mediated by a Protein

Chromatin interactions mediated by a protein of interest are of great scientific interest. Recent studies show that protein-mediated chromatin interactions can have different intensities in different types of cells or in different developmental stages of a cell. Such differences can be associated wi...

Descripción completa

Detalles Bibliográficos
Autores principales: Niu, Liang, Li, Guoliang, Lin, Shili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023970/
https://www.ncbi.nlm.nih.gov/pubmed/24835279
http://dx.doi.org/10.1371/journal.pone.0097560
_version_ 1782316597444083712
author Niu, Liang
Li, Guoliang
Lin, Shili
author_facet Niu, Liang
Li, Guoliang
Lin, Shili
author_sort Niu, Liang
collection PubMed
description Chromatin interactions mediated by a protein of interest are of great scientific interest. Recent studies show that protein-mediated chromatin interactions can have different intensities in different types of cells or in different developmental stages of a cell. Such differences can be associated with a disease or with the development of a cell. Thus, it is of great importance to detect protein-mediated chromatin interactions with different intensities in different cells. A recent molecular technique, Chromatin Interaction Analysis by Paired-End Tag Sequencing (ChIA-PET), which uses formaldehyde cross-linking and paired-end sequencing, is able to detect genome-wide chromatin interactions mediated by a protein of interest. Here we proposed two models (One-Step Model and Two-Step Model) for two sample ChIA-PET count data (one biological replicate in each sample) to identify differential chromatin interactions mediated by a protein of interest. Both models incorporate the data dependency and the extent to which a fragment pair is related to a pair of DNA loci of interest to make accurate identifications. The One-Step Model makes use of the data more efficiently but is more computationally intensive. An extensive simulation study showed that the models can detect those differentially interacted chromatins and there is a good agreement between each classification result and the truth. Application of the method to a two-sample ChIA-PET data set illustrates its utility. The two models are implemented as an R package MDM (available at http://www.stat.osu.edu/~statgen/SOFTWARE/MDM).
format Online
Article
Text
id pubmed-4023970
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-40239702014-05-21 Statistical Models for Detecting Differential Chromatin Interactions Mediated by a Protein Niu, Liang Li, Guoliang Lin, Shili PLoS One Research Article Chromatin interactions mediated by a protein of interest are of great scientific interest. Recent studies show that protein-mediated chromatin interactions can have different intensities in different types of cells or in different developmental stages of a cell. Such differences can be associated with a disease or with the development of a cell. Thus, it is of great importance to detect protein-mediated chromatin interactions with different intensities in different cells. A recent molecular technique, Chromatin Interaction Analysis by Paired-End Tag Sequencing (ChIA-PET), which uses formaldehyde cross-linking and paired-end sequencing, is able to detect genome-wide chromatin interactions mediated by a protein of interest. Here we proposed two models (One-Step Model and Two-Step Model) for two sample ChIA-PET count data (one biological replicate in each sample) to identify differential chromatin interactions mediated by a protein of interest. Both models incorporate the data dependency and the extent to which a fragment pair is related to a pair of DNA loci of interest to make accurate identifications. The One-Step Model makes use of the data more efficiently but is more computationally intensive. An extensive simulation study showed that the models can detect those differentially interacted chromatins and there is a good agreement between each classification result and the truth. Application of the method to a two-sample ChIA-PET data set illustrates its utility. The two models are implemented as an R package MDM (available at http://www.stat.osu.edu/~statgen/SOFTWARE/MDM). Public Library of Science 2014-05-16 /pmc/articles/PMC4023970/ /pubmed/24835279 http://dx.doi.org/10.1371/journal.pone.0097560 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Niu, Liang
Li, Guoliang
Lin, Shili
Statistical Models for Detecting Differential Chromatin Interactions Mediated by a Protein
title Statistical Models for Detecting Differential Chromatin Interactions Mediated by a Protein
title_full Statistical Models for Detecting Differential Chromatin Interactions Mediated by a Protein
title_fullStr Statistical Models for Detecting Differential Chromatin Interactions Mediated by a Protein
title_full_unstemmed Statistical Models for Detecting Differential Chromatin Interactions Mediated by a Protein
title_short Statistical Models for Detecting Differential Chromatin Interactions Mediated by a Protein
title_sort statistical models for detecting differential chromatin interactions mediated by a protein
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023970/
https://www.ncbi.nlm.nih.gov/pubmed/24835279
http://dx.doi.org/10.1371/journal.pone.0097560
work_keys_str_mv AT niuliang statisticalmodelsfordetectingdifferentialchromatininteractionsmediatedbyaprotein
AT liguoliang statisticalmodelsfordetectingdifferentialchromatininteractionsmediatedbyaprotein
AT linshili statisticalmodelsfordetectingdifferentialchromatininteractionsmediatedbyaprotein