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Sample GSM3484100 Query DataSets for GSM3484100
Status Public on Feb 14, 2019
Title PBMC_BrightLight_DayOrientedSchedule_RelTime_8.2_Subject_T13
Sample type RNA
 
Source name PBMC_DayOrientedSchedule_RelTime_8.2
Organism Homo sapiens
Characteristics subject: T13
experimentalgroup: BrightLight
condition: DayOrientedSchedule
relclocktime: 8.2
Treatment protocol Peripheral blood mononuclear cells (PBMCs) were isolated by centrifugation for 30 minutes at 1600rpm on a density gradient (Histopaque-1077, Sigma Aldrich, Oakville, ON, Canada). PBMCs were washed 3 times in phosphate-buffered saline (PBS), lysed in TRIzol (Life Technologies, Burlington, ON, Canada) and stored at -80°C until further processing.
Growth protocol An indwelling catheter was inserted in a forearm vein at least 4 hours prior to the start of each 24-hour measurement period.
Extracted molecule total RNA
Extraction protocol Extraction of RNA was performed by addition of chloroform in order to separate organic and aqueous components. Isopropanol and subsequent ethanol washes were used to precipitate and purify the RNA. RNA was dissolved in RNase-free H2O (Qiagen, Toronto, ON, Canada). Total RNA was quantified using a NanoDrop Spectrophotometer ND-1000 (NanoDrop Technologies, Inc.) and its integrity was assessed using a 2100 Bioanalyzer (Agilent Technologies).
Label Biotin
Label protocol Sense-strand cDNA was synthesized from 10 ng of total RNA, and fragmentation and labeling were performed to produce ds-cDNA with the GeneChip® Pico Reagent Kit according to manufacturer’s instructions (ThermoFisher Scientific-Affymetrix).
 
Hybridization protocol After fragmentation and labeling, 2.8 µg DNA target was hybridized on Clariom™S HT, Human (ThermoFisher Scientific-Affymetrix).
Scan protocol Arrays were scanned on a Affymetrix GeneTitan instrument (ThermoFisher Scientific-Affymetrix) according to the manufacturer’s protocol.
Description PBMC sample taken at 8.2 h after habitual wake time during day-oriented schedule in Subject T13 in the BrightLight group
Data processing Affymetrix CEL files were normalized by RMA preprocessing methodology using the Oligo package (v1.38.0) in R (v3.4.1).
 
Submission date Nov 19, 2018
Last update date Feb 16, 2019
Contact name Laura Kervezee
E-mail(s) [email protected]
Organization name McGill University
Department Douglas Mental Health University Institute
Street address 6875 LaSalle Boulevard
City Montreal
State/province Quebec
ZIP/Postal code H4H 1R3
Country Canada
 
Platform ID GPL24324
Series (1)
GSE122725 The phase-shifting effect of bright light exposure on circadian rhythmicity in the human transcriptome

Data table header descriptions
ID_REF
VALUE RMA normalized log2 intensity signal

Data table
ID_REF VALUE
TC0100006437.hg.1 4.337346768
TC0100006476.hg.1 4.322972891
TC0100006479.hg.1 6.359682587
TC0100006480.hg.1 5.518681955
TC0100006483.hg.1 7.482128603
TC0100006486.hg.1 4.956879816
TC0100006490.hg.1 4.039402838
TC0100006492.hg.1 5.163465396
TC0100006494.hg.1 5.955574178
TC0100006497.hg.1 5.08381861
TC0100006499.hg.1 4.877431919
TC0100006501.hg.1 5.423304338
TC0100006502.hg.1 4.034077887
TC0100006514.hg.1 5.079395743
TC0100006516.hg.1 5.115146447
TC0100006517.hg.1 3.586121779
TC0100006524.hg.1 6.948554957
TC0100006540.hg.1 3.459100472
TC0100006548.hg.1 3.165087776
TC0100006550.hg.1 5.549149353

Total number of rows: 27189

Table truncated, full table size 730 Kbytes.




Supplementary file Size Download File type/resource
GSM3484100_DBN087.CEL.gz 1.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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