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Sample GSM5628290 Query DataSets for GSM5628290
Status Public on Oct 16, 2021
Title HT29_ORF_KIF3B_107
Sample type RNA
Source name HT-29 KIF3B transduction, UniqueID 107
Organism Homo sapiens
Characteristics cell_line: HT-29
orf: KIF3B
uniqueid: 107
arraybatch: E1
transductiondate: 2015-02-26
Treatment protocol ORFs for IBD gene candidates were cloned into a GATEWAY® compatible polycistronic lentiviral expression vector, pLVX-EF1a-IRES-PURO/eGFP expressing an enhanced green fluorescent protein (eGFP) and puromycin N-acetyl-transferase fusion protein.
Proliferative HT-29 cells at 50% confluency in 12 well plate (Corning) were transduced in triplicate with the different ORFs (multiplicity of infection) MOI of 40-100 with 8µg/ml of polybrene (Sigma, Cat: H-9268).
Twenty-four hours post-transduction, media was changed and 3ug/ml puromycin (Millipore Sigma) was added.
The appearance and confluence of the cultures were recorded daily, and cells were grown for an average of 8 days (with a range of 5-27 days) to select successfully transduced cells and reach confluence before RNA extraction.
Transduction of the whole set of IBD gene candidate ORFs was performed in batches of about 15 ORFs, each done in triplicate, and including an empty vector control.
Growth protocol The colorectal adenocarcinoma cell line HT-29 (ATCC HTB-38) was maintained at confluence between 20% and 80% at all times in McCoy’s 5A (Wisent, 317-010CL) 10% FBS. All experiments described herein were performed in cell at passages below 25.
Extracted molecule total RNA
Extraction protocol The RNeasy Plus Mini kit (#74036, Qiagen Inc Canada) according to manufacturer’s protocol.
The RNA samples were quantified, and quality controlled using an Agilent RNA 6000 Nano kit (Agilent, Cat No./ID 5067-1511) on 2100 Bioanalyzer system.
Number (RIN) below 8 were discarded; RIN values were routinely in the range of 9.2-10
Label Cy3
Label protocol Agilent One-Color Microarray-Based Exon Analysis Low Input Quick Amp WT Labeling kit using Cyanine 3-CTP label.
Hybridization protocol Samples were blocked with Agilent blocking reagent and incubated for 17h at 65C in the Agilent Microarray Hybridization oven
Scan protocol Agilent SureScan Microarray scanner
Data processing We used Limma v3.26.9 and sva v3.18.0 packages (Bioconductor v3.1-3.2) to load the fluorescence intensity files and handle the data into R V3.2.0. Arrays failing Agilent quality control according to the Agilent Feature Extraction software were flagged. Manual quality control of each array was also performed.
Quality control was performed within each batch of arrays. Fluorescence signal was processed to remove local background (bakgroundCorrect, method “normexp”) and then normalized using cyclic loess algorithm.
Batch effects were then corrected using ComBat for known batches and sva for unknown systematic artefacts (both from sva library v3.18.0). Given the experiment was performed in three parts (E1-E4 & P7, E5-E11, E14-E15), the batches from each part were combined first and then combined together.
To reduce impact of residual background, noise and batch effects on very low expression values, the fluorescence intensity values were truncated at 8, and translated down by the same amount.
Duplicated probes were combined, and repeated samples removed. The truncating threshold was determined based on the distribution of negative control probes and detected vs non-detected signals. Data provided includes only samples included in the final dataset.
Submission date Oct 15, 2021
Last update date Oct 16, 2021
Contact name John D Rioux
Organization name Montreal Heart Institute
Department Research Center
Lab Genetics and genomic medecine of Inflammation
Street address 5000 Bélanger St.
City Montréal
State/province QC
ZIP/Postal code H1T 1C8
Country Canada
Platform ID GPL30867
Series (1)
GSE186001 Functional screen of Inflammatory bowel disease genes reveals key epithelial functions: Agilent Targeted Dataset

Data table header descriptions
VALUE background corrected,cyclic loess normalized batch effect removed (using ComBat) log2-transformed data

Data table
A_37_P136616 13.0785673133522
A_37_P136110 4.52325219940396
A_24_P904903 9.86811802402723
A_37_P136602 6.63631430803899
A_37_P458316 10.7908939065253
A_37_P136604 9.65178918669683
A_37_P136607 11.5616122879667
A_37_P360319 11.4752291488032
A_37_P136600 2.2028605253988
A_37_P136605 11.0872698825178
A_37_P136601 4.22080941899642
A_37_P136611 12.3136504150469
A_37_P136603 8.16916945544904
A_37_P136610 11.591691432893
A_37_P136599 4.17898178332078
A_37_P136608 11.238597846176
A_23_P71624 2.76136753328218
A_37_P096846 4.79509964027891
A_37_P096849 5.82683683708501
A_37_P096841 2.69100274496022

Total number of rows: 27439

Table truncated, full table size 756 Kbytes.

Supplementary file Size Download File type/resource
GSM5628290_SG12024163_255950510081_S001_GE1_107_Sep09_2_3.txt.gz 3.0 Mb (ftp)(http) TXT
Raw data provided as supplementary file
Processed data included within Sample table

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