Evidence map›Paper›PMID 28196481›Full record

ArticleBMC genomics2017

NucTools: analysis of chromatin feature occupancy profiles from high-throughput sequencing data.

Yevhen Vainshtein, Karsten Rippe, Vladimir B Teif

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Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

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31citing papers in PubMed
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3 · Its place in the literature

Who cites it

31 citing papers in PubMed.

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  20. Analytical Approaches for ATAC-seq Data Analysis.Current protocols in human genetics · 2020
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5 · Who and what money

Authors and funding

3 authors.

Yevhen VainshteinFunctional Genomics Group, Fraunhofer Institute for Interfacial Engineering and Biotechnology IGB, Nobelstraße 12, 70569, Stuttgart, Germany. yevhen.vainshtein@igb.fraunhofer.de.
Karsten RippeResearch Group Genome Organization & Function, German Cancer Research Center (DKFZ) and Bioquant, Im Neuenheimer Feld 280, 69120, Heidelberg, Germany.
Vladimir B TeifSchool of Biological Sciences, University of Essex, Wivenhoe Park, CO4 3SQ, Colchester, UK. vteif@essex.ac.uk.

Funding

Wellcome Trust 200733/Z/16/Z
6 · The paper itself

Abstract

backgroundBiomedical applications of high-throughput sequencing methods generate a vast amount of data in which numerous chromatin features are mapped along the genome. The results are frequently analysed by creating binary data sets that link the presence/absence of a given feature to specific genomic loci. However, the nucleosome occupancy or chromatin accessibility landscape is essentially continuous. It is currently a challenge in the field to cope with continuous distributions of deep sequencing chromatin readouts and to integrate the different types of discrete chromatin features to reveal linkages between them.

resultsHere we introduce the NucTools suite of Perl scripts as well as MATLAB- and R-based visualization programs for a nucleosome-centred downstream analysis of deep sequencing data. NucTools accounts for the continuous distribution of nucleosome occupancy. It allows calculations of nucleosome occupancy profiles averaged over several replicates, comparisons of nucleosome occupancy landscapes between different experimental conditions, and the estimation of the changes of integral chromatin properties such as the nucleosome repeat length. Furthermore, NucTools facilitates the annotation of nucleosome occupancy with other chromatin features like binding of transcription factors or architectural proteins, and epigenetic marks like histone modifications or DNA methylation. The applications of NucTools are demonstrated for the comparison of several datasets for nucleosome occupancy in mouse embryonic stem cells (ESCs) and mouse embryonic fibroblasts (MEFs).

conclusionsThe typical workflows of data processing and integrative analysis with NucTools reveal information on the interplay of nucleosome positioning with other features such as for example binding of a transcription factor CTCF, regions with stable and unstable nucleosomes, and domains of large organized chromatin K9me2 modifications (LOCKs). As potential limitations and problems we discuss how inter-replicate variability of MNase-seq experiments can be addressed.

Indexed as

High-Throughput Nucleotide SequencingSoftwareChromatinChromatin Assembly and DisassemblyCluster AnalysisComputational BiologySequence Analysis, DNAChromatinChIP-seqChromatinMNase-seqNext-generation sequencing (NGS)Nucleosome positioning

Identifiers

PMID28196481
PMCPMC5309995

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LicenceCC BY
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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.