Data for chromosome contacts and matched transcription profiles at three cell cycle phases in the fission yeast

The data described in this article pertains to Grand et al. (2014), “Chromosome conformation maps in fission yeast reveal cell cycle dependent sub nuclear structure” [1]. Temperature sensitive Schizosaccharomyces pombe cell division cycle (cdc) mutants, which are induced by a shift in temperature to...

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Main Authors: Ralph S. Grand, Justin M. O'Sullivan
Format: Article
Language:English
Published: Elsevier 2015-06-01
Series:Genomics Data
Online Access:http://www.sciencedirect.com/science/article/pii/S2213596015000070
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spelling doaj-eda3a8c19f5d48349a424450cf7b62d62020-11-25T02:52:10ZengElsevierGenomics Data2213-59602015-06-014C121610.1016/j.gdata.2015.01.005Data for chromosome contacts and matched transcription profiles at three cell cycle phases in the fission yeastRalph S. Grand0Justin M. O'Sullivan1Liggins institute, University of Auckland, Grafton Auckland 1032, New ZealandLiggins institute, University of Auckland, Grafton Auckland 1032, New ZealandThe data described in this article pertains to Grand et al. (2014), “Chromosome conformation maps in fission yeast reveal cell cycle dependent sub nuclear structure” [1]. Temperature sensitive Schizosaccharomyces pombe cell division cycle (cdc) mutants, which are induced by a shift in temperature to 36 °C, were chosen for the analysis of genome structure in the G1 phase, G2 phase and mitotic anaphase of the cell cycle. Chromatin and total RNA were isolated from the same cell culture following synchronization. Two biological replicates were analyzed for each condition. The global, three-dimensional organization of the chromosomes was captured at high resolution using Genome Conformation Capture (GCC). GCC libraries and RNA samples were sequenced using an Illumina Hi-Seq 2000 platform (Beijing Genomics Institute (China)). DNA sequences were processed using the Topography suite v1.19 [2] to obtain chromosome contact frequency matrices. RNA sequences were processed using the Cufflinks pipeline [3] to measure gene transcript levels and how these varied between the conditions. All sequence data, processed GCC and transcriptome files are available under the Gene Expression Omnibus (GEO) accession number GSE52287 (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE52287).http://www.sciencedirect.com/science/article/pii/S2213596015000070
collection DOAJ
language English
format Article
sources DOAJ
author Ralph S. Grand
Justin M. O'Sullivan
spellingShingle Ralph S. Grand
Justin M. O'Sullivan
Data for chromosome contacts and matched transcription profiles at three cell cycle phases in the fission yeast
Genomics Data
author_facet Ralph S. Grand
Justin M. O'Sullivan
author_sort Ralph S. Grand
title Data for chromosome contacts and matched transcription profiles at three cell cycle phases in the fission yeast
title_short Data for chromosome contacts and matched transcription profiles at three cell cycle phases in the fission yeast
title_full Data for chromosome contacts and matched transcription profiles at three cell cycle phases in the fission yeast
title_fullStr Data for chromosome contacts and matched transcription profiles at three cell cycle phases in the fission yeast
title_full_unstemmed Data for chromosome contacts and matched transcription profiles at three cell cycle phases in the fission yeast
title_sort data for chromosome contacts and matched transcription profiles at three cell cycle phases in the fission yeast
publisher Elsevier
series Genomics Data
issn 2213-5960
publishDate 2015-06-01
description The data described in this article pertains to Grand et al. (2014), “Chromosome conformation maps in fission yeast reveal cell cycle dependent sub nuclear structure” [1]. Temperature sensitive Schizosaccharomyces pombe cell division cycle (cdc) mutants, which are induced by a shift in temperature to 36 °C, were chosen for the analysis of genome structure in the G1 phase, G2 phase and mitotic anaphase of the cell cycle. Chromatin and total RNA were isolated from the same cell culture following synchronization. Two biological replicates were analyzed for each condition. The global, three-dimensional organization of the chromosomes was captured at high resolution using Genome Conformation Capture (GCC). GCC libraries and RNA samples were sequenced using an Illumina Hi-Seq 2000 platform (Beijing Genomics Institute (China)). DNA sequences were processed using the Topography suite v1.19 [2] to obtain chromosome contact frequency matrices. RNA sequences were processed using the Cufflinks pipeline [3] to measure gene transcript levels and how these varied between the conditions. All sequence data, processed GCC and transcriptome files are available under the Gene Expression Omnibus (GEO) accession number GSE52287 (http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE52287).
url http://www.sciencedirect.com/science/article/pii/S2213596015000070
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