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Sample GSM4418102 Query DataSets for GSM4418102
Status Public on Mar 27, 2020
Title WHEL ID 9351
Sample type RNA
 
Source name primary breast cancer
Organism Homo sapiens
Characteristics tissue: primary breast cancer
Treatment protocol Refer to https://library.ucsd.edu/dc/object/bb2493244b
Extracted molecule total RNA
Extraction protocol Unstained slides from archival specimens with ≥ 40% tumor cellularity were incubated at 65 °C for 30 minutes and deparaffinized using Citrisolv (Fisher Scientific, Pittsburgh, PA) followed by ethanol wash. Tumor tissues were macrodissected into RNAse-free microfuge tubes, and nucleic acids isolated using the Qiagen AllPrep FFPE kit (#80234). Manufacturer’s instructions were followed with the exception that the proteinase K digestion step was extended to an overnight incubation for the DNA isolation.
Label n/a
Label protocol See manufacturer's website http://www.nanostring.com for procedures
 
Hybridization protocol Transcript expression was quantified with 250 ng of total RNA using the NanoString nCounter analysis system with a custom miRGE CodeSet. Assay reactions were assembled per manufacturer’s specifications (NanoString Technologies, INC Seattle, WA).
Scan protocol See manufacturer's website http://www.nanostring.com for procedures. Digital Analyzer was set to scan at 1155 FOV (fields of view).
Description NanoString reporter probe
X2895383273_5
Data processing R-NanoStringNorm package was used to normalize data. Code count normalization used 6 positive controls and background subtraction used 8 negative controls. All expression values were first log2 transformed. For mRNAs, five (ACTB, PSMC4, MRPL19, RPLPO, SF3A1) genes were used as housekeepers; the data matrix elements are relative gene expression values (log2 transformed) compared to log2 value of the geometric mean of the five house-keepers within each sample. For miRNAs, log2 expression values are presented. For miRNAs, quantile normalization was performed. Normalized datasets for both mRNA and miRNA are available on the series record. Sample data tables include data only for mRNAs.
 
Submission date Mar 17, 2020
Last update date Mar 27, 2020
Contact name Loki Natarajan
E-mail(s) loki@math.ucsd.edu
Organization name University of California, San Diego
Street address 3855 Health Sciences DR
City La Jolla
ZIP/Postal code 92093-0901
Country USA
 
Platform ID GPL28286
Series (1)
GSE147126 mRNAs and miRNAs for Women's Healthy Eating and Living (WHEL) Study

Data table header descriptions
ID_REF
VALUE normalized nCounter signal intensity

Data table
ID_REF VALUE
KRT17 2.192
CD68 -9.048
SPINT2 1.002
ESRP1 1.512
KRT8 1.122
NUF2 -9.048
MYBL2 -9.048
FGFR4 -2.043
ALDOA 1.452
MELK -0.956
FOXC1 -2.043
ACTR3B -2.236
RRAGD -9.048
GUS -9.048
MRPS17 -9.048
GRB7 -0.956
UCHL1 -9.048
TPI1 -0.089
MLPH 3.802
PNP -9.048

Total number of rows: 123

Table truncated, full table size 1 Kbytes.




Supplementary file Size Download File type/resource
GSM4418102_20150821_70004K_2895383273_05.RCC.gz 2.1 Kb (ftp)(http) RCC
Processed data included within Sample table
Processed data are available on Series record

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