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GEO help: Mouse over screen elements for information. |
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Status |
Public on Oct 17, 2014 |
Title |
Bru-seq nascent RNA sequencing of human and mouse cells: correlation to replication timing and genome instability |
Organisms |
Homo sapiens; Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Bru-seq nascent RNA sequencing (PubMed ID 23973811) was performed on two primary human fibroblast cell lines, mouse embryonic stem cells, and GM12878 human lymphoblastoid cells. Read data, which include both exon and intron signals, were used to identify transcription unit spans genome-wide, where a transcription unit is roughly correspondent to the longest expressed isoform of a gene. However, because algorithms were not constrained by annotated genes, transcription units need not and often do not correspond precisely to gene boundaries and include extragenic transcription. Transcription units were then compared to separate data sets that comprised induced copy number variants, common fragile sites, and Repli-seq replication timing. The objective was to discover the relationships between transcription unit span and size, local genomic instability, and replication timing. This GEO sample series provides the span and intensity of transcription units called genome-wide in the various samples. Correlations to genome stability and replication timing are provided in the associated manuscript. In addition, one human fibroblast line and the mouse embryonic stem cells had paired samples treated and untreated with low dose aphidicolin. Gene RPKM signal intensities are provided for these samples, although comparing these was not the principal objective of the study.
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Overall design |
Bru-seq single-read nascent RNA sequencing on human 090 fibroblasts +/- aphidicolin treatment, human UMHF1 fibroblasts (3 replicates), human GM12878 lymphoblastoid cells, and mouse embryonic stem cells+/- aphidicolin treatment.
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Contributor(s) |
Wilson TE, Arlt MF, Park SH, Rajendran S, Paulsen M, Ljungman M, Glover TW |
Citation(s) |
25373142 |
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Submission date |
Mar 13, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Thomas E. Wilson |
Organization name |
University of Michigan
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Department |
Department of Pathology
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Street address |
2065 BSRB, 109 Zina Pitcher
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City |
Ann Arbor |
State/province |
MI |
ZIP/Postal code |
48109-2200 |
Country |
USA |
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Platforms (2) |
GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (8)
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Relations |
BioProject |
PRJNA241165 |
SRA |
SRP040075 |
Supplementary file |
Size |
Download |
File type/resource |
GSE55862_RAW.tar |
6.5 Mb |
(http)(custom) |
TAR (of BED) |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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