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Sample GSM4418179 Query DataSets for GSM4418179
Status Public on Mar 27, 2020
Title WHEL ID 1075
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
X2895390308_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 -0.9844
CD68 -2.6004
SPINT2 0.6146
ESRP1 0.2846
KRT8 0.4346
NUF2 -9.6154
MYBL2 -9.6154
FGFR4 -3.1814
ALDOA 1.7746
MELK -5.2454
FOXC1 -3.6724
ACTR3B -2.8554
RRAGD -4.8784
GUS -3.4754
MRPS17 -3.6264
GRB7 -2.0444
UCHL1 -6.8654
TPI1 -0.2074
MLPH 0.4546
PNP -3.1324

Total number of rows: 123

Table truncated, full table size 1 Kbytes.




Supplementary file Size Download File type/resource
GSM4418179_20150722_70003O_2895390308_05.RCC.gz 2.2 Kb (ftp)(http) RCC
Processed data included within Sample table
Processed data are available on Series record

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