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Sample GSM4103878 Query DataSets for GSM4103878
Status Public on Jan 19, 2022
Title Brain_control_sample13
Sample type RNA
 
Source name brain tissue
Organism Homo sapiens
Characteristics disease state: Control
age: 55
gender: w
tissue: brain
Extracted molecule total RNA
Extraction protocol RNA was isolated by Trizol™ method (Invitrogen, Karlsruhe, Germany). 100mg deeply frozen human brain tissue (temporal cortex) was homogenized in the presence of 1ml Trizol in a glass-Teflon™ homogenizer. The homogenate was transferred to a microtube and after adding chloroform, samples were centrifuged at 15 000 g (4 °C) for 15min and the supernatant transferred to a fresh tube. Samples were mixed with equal amounts of isopropanol and centrifuged at 12 000 g (4 °C) for 15min to precipitate the RNA. After washing, the pellet was air-dried and dissolved in water. RNA quality was assessed by denaturing formaldehyde agarose gel electrophoresis, by spectrophotometry (scanning at 220−320 nm) and by analysis using Agilent 2100 bioanalyzer. Only samples with RIN > 5 were further processed. The RNA concentration was estimated spectrophotometrically by absorbance at 260 nm, concentration was adjusted to 1mg/ml and RNA was stored at −80 °C until use.
Label Cy3
Label protocol 1 μg of total RNA was labeled using the Quick Amp Labeling Kit (Agilent, Waldbronn, Germany), according to the manufacturer’s instructions with the adaptation of using 120 pmol of a random N6 − T7 primer (Metabion, Planegg, Germany) instead of a polyT-T7 primer. cRNA quantity was checked using a NanoDrop ND-1000 UV-VIS Spectrophotometer, as enlisted in the manufacturer’s instructions.
 
Hybridization protocol 1.65 μg of labeled cRNA was used for hybridization following manufacturer’s instructions.
Scan protocol After hybridization the arrays were washed according to the manual and scanned using the Agilent G2565CA Microarray Scanner System with Agilent Scan Control Software (Version A851) following settings for scanning: Profile: AgilentG3 GX 1Color; Channels Green; Scan Region: Agilent HD (61 × 21.6mm); Resolution 3 μm double pass; Tiff: 20 bit; Green PMT Gain: 100%. Result tables were extracted after grid placement using Agilent Feature Extraction Software (Version 11.5.1.1)
Data processing Differential expression analysis was performed using R and the Bioconductor package Limma. Quality control of arrays was performed by checking distribution of “bright corner”, “dark corner” probes, and relative spike-in concentration versus normalized signal. The controls confirmed high quality of the results and consequently all microarray data were included in the downstream analysis. Initially, independent filtering was performed, removing probes (i) with signal intensity above the background in less than one third of all arrays and (ii) exhibiting an interquartile range of log2 signal intensity across all samples of less than 1. Background expression was defined by the mean intensity plus three times the standard deviation of negative control spots (Agilent’s 3xSLv spots). 113 047 out of 931 898 probes were retained after filtering. Signal intensities were quantile normalized but not background corrected, due to the low background intensities of Agilent arrays. Differential expression between AD and control samples was determined using a linear model that includes age because on average, individuals from the AD group were older than controls. The linear model was fitted using the R package limma and reliable variance estimates were obtained by Empirical Bayes moderated t-statistics. False discovery rate was controlled by a modified Benjamini-Hochberg procedure that incorporates an estimated proportion of the null p-values 23 to compute q-values using the fdrtool R package.
 
Submission date Oct 01, 2019
Last update date Jan 19, 2022
Contact name Kristin Reiche
E-mail(s) kristin.reiche@izi.fraunhofer.de
Organization name Fraunhofer Institute for Cell Therapy and Immunology
Department Diagnostics
Street address Perlickstr. 1
City Leipzig
ZIP/Postal code 04103
Country Germany
 
Platform ID GPL27556
Series (2)
GSE138260 Differential expression analysis of human brain samples with Alzheimer disease versus healthy control samples
GSE138261 Alzheimer-related genes show accelerated evolution

Data table header descriptions
ID_REF
VALUE quantile-normalized signal

Data table
ID_REF VALUE
3xSLv1 1.85385636486533
A_19_P00315452 4.53117005903421
A_19_P00315459 8.93536599215988
A_19_P00315469 4.63106125212569
A_19_P00315473 1.78037630116277
A_19_P00315482 4.68449550741451
A_19_P00315490 1.86205705129831
A_19_P00315492 3.12598635101497
A_19_P00315493 4.98302951951786
A_19_P00315496 1.80094530495855
A_19_P00315499 6.8905580628343
A_19_P00315502 4.17480249672341
A_19_P00315504 5.05065455345259
A_19_P00315506 5.17909094757087
A_19_P00315508 1.85877514896096
A_19_P00315518 2.97215195187949
A_19_P00315519 1.94436083588145
A_19_P00315523 3.65350600526796
A_19_P00315524 10.5092200672064
A_19_P00315526 7.16835322638933

Total number of rows: 947672

Table truncated, full table size 37169 Kbytes.




Supplementary file Size Download File type/resource
GSM4103878_253487910016_201110201056_K13_S01_GE1_107_Sep09.txt.gz 47.0 Mb (ftp)(http) TXT
Processed data included within Sample table

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