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Series GSE54332 Query DataSets for GSE54332
Status Public on Apr 25, 2014
Title EDD: a program for detection of wide genomic enrichment domains robust against local variations [ChIP-Seq]
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Nuclear lamins contact the genome at the nuclear periphery through large domains and are involved in chromatin organization. Among broad peak calling algorithms available to date, none are suited for mapping lamin-genome interactions genome-wide. We disclose a novel algorithm, Enriched Domain Detector (EDD), for analysis of broad enrichment domains from ChIP-seq data. EDD enables discovery of genomic domains interacting with broadly distributed chromatin-associated proteins such as lamins. The main advantage of EDD over existing broad peak callers is sensitivity to domain width rather than enrichment strength at a particular site, and robustness against local variations. EDD is downloadable from http://github.com/eivindgl/edd.
 
Overall design LMNA ChIP-seq experiments in human normal dermal fibroblasts (Lonza CC-2511; LDFs) and human normal primary dermal fibroblasts (Norwegian Stem Cell Center AD04DFs).
 
Contributor(s) Collas P, Lund E, Oldenburg A
Citation(s) 24782521, 25524705, 25602132
Submission date Jan 23, 2014
Last update date May 15, 2019
Contact name Philippe Collas
Organization name University of Oslo
Department Institute of Basic Medical Sciences
Street address PO Box 1112 Blindern
City Oslo
ZIP/Postal code 0317
Country Norway
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (5)
GSM1313397 LDF_LMNA
GSM1313398 LDF_Input
GSM1313399 ADF04DF_LMNA_rep1
This SubSeries is part of SuperSeries:
GSE54334 EDD: a program for detection of wide genomic enrichment domains robust against local variations
Relations
BioProject PRJNA236221
SRA SRP035616

Download family Format
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Supplementary file Size Download File type/resource
GSE54332_RAW.tar 20.0 Kb (http)(custom) TAR (of BED)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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