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Sample GSM1409324 Query DataSets for GSM1409324
Status Public on Mar 16, 2015
Title DNASeq-BCC10-control
Sample type SRA
 
Source name matched adjacent normal skin
Organism Homo sapiens
Characteristics tissue/cell type: normal skin
Extracted molecule genomic DNA
Extraction protocol Fresh tissue samples of resistant BCCs and adjacent normal skin were obtained and stored in RNALater at -20 ̊C (Ambion). DNA was isolated using the DNeasy Blood & Tissue kit according to manufacturer’s protocols (Qiagen).
Capture libraries were constructed from 2 μg of DNA from BCC and normal skin using the Agilent SureSelect XT Human All Exon V4 kit according to manufacturer’s specifications. Enriched exome libraries were multiplexed and sequenced on the Illumina HiSeq 2500 platform.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model Illumina HiSeq 2500
 
Data processing Sequencing reads were aligned to the human reference genome sequence (hg19) using Burrows-Wheeler Aligner (BWA). SAM to BAM conversion and marking of PCR duplicates were performed using Picard tools (version 1.86), followed by local realignment around indels and base quality score recalibration using the Genome Analysis Toolkit (GATK) (v2.3.9). Somatic SNVs and indels were called using GATK.
Genome_build: hg19
 
Submission date Jun 10, 2014
Last update date May 15, 2019
Contact name Jiang Li
E-mail(s) jiangli@stanford.edu
Phone 6507258839
Organization name Stanford University
Department Dermatology
Lab Tony Oro
Street address 269 Campus Drive, Stanford University
City Stanford
State/province CA
ZIP/Postal code 94305
Country USA
 
Platform ID GPL16791
Series (2)
GSE58374 SMO variants explain the majority of drug resistance in basal cell carcinoma [exome-seq]
GSE58377 SMO variants explain the majority of drug resistance in basal cell carcinoma
Relations
BioSample SAMN02849593
SRA SRX588219

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data not provided for this record

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