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Sample GSM663555 Query DataSets for GSM663555
Status Public on Apr 06, 2011
Title breast tumor 2
Sample type SRA
 
Source name Primary breast tumor
Organism Homo sapiens
Characteristics tumor type: basal-like subgroup based on micro array expression data
tissue: mammary gland; breast
Growth protocol standard growth conditions for cell lines
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was hydrosheared, EcoP15I recognition sites were methylated and EcoP15I CAP adaptors were ligated to the ends of DNA fragments. The methylated DNA constructs were separated on agarose gel and 10 Kb sized fragments were selected for ligation resulting in circularized products where 5’ and 3’ ends of 10 Kb fragments were connected by an internal biotinylated adaptor with two flanking non-methylated EcoP15I CAP adaptors. Constructs were digested by methylation sensitive EcoP15I to release 5’ and 3’ paired-end tag (PET) constructs. Sequencing adaptors were ligated to the PET constructs, which were then amplified by PCR and sequenced by the Applied Biosystems SOLiD system.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model AB SOLiD System 2.0
 
Description genomic DNA hydrosheared in 9.4 kb fragments (std dev: 2,403 bp below median; 1,332 above median), 2x25bp paired-end (mate pair) sequences
Data processing For the project, sequence tags were mapped to the human reference sequence (NCBI Build 36) allowing 2 color code mismatches and paired using SOLiD System Analysis Pipeline Tool, Corona Lite (Applied Biosystems). If sequence tags had multiple mapping locations and one of them was located in the expected distance and orientation to its mate, this location was chosen by a process termed ‘rescue’. Discordant paired-end tags (PETs) were defined and clustered to call structural variations as described by Hillmer et al.: Comprehensive Long Span Paired-End-Tag Mapping Reveals Characteristic Patterns of Structural Variations in Epithelial Cancer Genomes. The Readme file includes additional information about the supplementary cluster and gff files.
 
Submission date Jan 29, 2011
Last update date May 15, 2019
Contact name Axel HILLMER
E-mail(s) ahillmer@uni-koeln.de
Organization name University of Cologne
Department Institute of Pathology
Street address Kerpener Str. 62
City Cologne
ZIP/Postal code 50937
Country Germany
 
Platform ID GPL9138
Series (1)
GSE26954 Comprehensive Long Span Paired-End-Tag Mapping Reveals Characteristic Patterns of Structural Variations in Epithelial Cancer Genomes
Relations
SRA SRX039761
BioSample SAMN00199325

Supplementary file Size Download File type/resource
GSM663555_IHB002.clusters.txt.gz 26.6 Kb (ftp)(http) TXT
GSM663555_IHB002_7742_12163.dist.covsmooth.gff.gz 44.2 Mb (ftp)(http) GFF
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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