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Sample GSM560162 Query DataSets for GSM560162
Status Public on Dec 09, 2011
Title Human - cerebellar cortex - 443 days old
Sample type RNA
 
Source name Dissected Human post-mortem cerebellar cortex
Organism Homo sapiens
Characteristics age: 443 days
gender: m
tissue: cerebellar cortex of the brain
post-mortem interval (hours): 19
rna integrity number (rin): 7.4
batch: 2
Biomaterial provider NICHDBB-Baltimore, MD
Treatment protocol All human postmortem brain tissue samples were obtained from the NICHD Brain and Tissue Bank for Developmental Disorders (NICHDBB)(Baltimore, MD, USA). All subjects were defined as normal controls by forensic pathologists at the NICHDBB. No subjects with prolonged agonal state were used. Chimpanzee samples were obtained from the Yerkes Primate Center (Atlanta, GA, USA), from the Biomedical Primate Research Centre (Rijswijk, Netherlands) and from the Anthropological Institute of the University of Zurich (Switzerland). Rhesus macaque brains were obtained from the SuZhou Experimental Animal Center (SuZhou, China). The dissections were made from the cerebellar cortex.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA from 100 mg of tissue was performed according to the manufacturer's instructions. RNA integrity number (RIN) was measured by the Agilent® 2100 Bioanalyzer.
Label biotin
Label protocol Biotinylated cRNA were prepared from 2 microg. total RNA following standard Affymetrix protocols.
 
Hybridization protocol Hybridization to Affymetrix® Human Gene 1.0 ST arrays was carried out following standard Affymetrix protocols. The RNA extraction and hybridization was carried out in two batches for human and macaque samples. Batches were relatively balanced with respect to age.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneChip Scanner 3000.
Description The dataset contains two prenatal individuals; these were predicted to be ~15 and ~30 days before birth. Detailed postmortem interval (PMI) information is available only for human subjects. Macaque subjects' PMI was less than 20 minutes. Within a species, each subject used in this experiment had a unique age; samples with the same age and species identity are technical replicates.
Gene expression data from post-mortem cerebellar cortex of a 443 days old human individual
Hsa_443days_batch2
Data processing Affymetrix microarray image data were collected with Affymetrix GeneChip Operating Software version 1.1 using default parameters. To identify array probes that contain mismatches among species, we mapped HuGene-1_0-st probe sequences (http://www.affymetrix.com/Auth/analysis/downloads/na23/wtgene/HuGene-1_0-st-v1.probe.tab.zip) to the human (hg18), chimpanzee (panTro2), and rhesus macaque (rheMac2) genomes using BLAT (http://genome.ucsc.edu/FAQ/FAQblat.html). Based on these alignments, we only included probes which matched all three genomes perfectly and at a single location (27% of the original array probes). Intensities of probes that passed this mask were corrected for background using the antigenomic probes with the same GC content; the latter are used as an estimator of the unspecific background hybridization (http://www.affymetrix.com/support/technical/whitepapers/exon_background_correction_whitepaper.pdf). Probe intensities were then log-transformed and quantile normalized. Intensity values per transcript were calculated by median polishing. To determine whether the signal intensity of a given probe was above the expected level of background noise, we compared each probe's signal intensity to a distribution of signal intensities of the antigenomic probes with the same GC content (a GC-bin). For each GC-bin, except the ones with the most extreme GC content, the numbers of antigenomic probes are close to 1,000. We considered a probe signal as detected if its intensity is higher than 95% of the background probes' intensities (see PMID: 17456239). In each array, we considered a transcript as “detected” if more than 50% of probes and at least 8 probes per transcript were detected. We considered a transcript as “expressed” if it was detected in >70% of human, chimpanzee or macaque individuals.
 
Submission date Jun 25, 2010
Last update date Jan 08, 2019
Contact name Mehmet Somel
E-mail(s) [email protected]
Phone +49-(0)341-3550-530
Fax +49-(0)341-3550-555
Organization name Max Planck Institute for Evolutionary Anthropology
Department Evolutionary Genetics
Street address Deutscher Platz 6
City Leipzig
ZIP/Postal code D-04103
Country Germany
 
Platform ID GPL6244
Series (2)
GSE22569 Gene expression in primate postnatal brain through lifespan - cerebellar cortex
GSE22570 Gene expression in primate postnatal brain through lifespan
Relations
Reanalyzed by GSE124814

Data table header descriptions
ID_REF
VALUE Quantile normalized log2-transformed signal intensities

Data table
ID_REF VALUE
7906878 4.02473111474177
8148358 4.55080655799802
7976128 3.76824872918214
8056408 1.27086338459722
8139021 5.5854403062694
7999387 4.10626883899991
8060539 4.26866023970957
8079746 4.32206457585666
7977149 4.19658859249618
8058512 4.76784910392738
7932911 4.4203967418305
8095697 2.20397855580958
8009685 3.97154770667889
8120431 4.23741949189178
8098204 7.05211016213114
8150698 1.38909368857338
8006187 2.90445427284382
8089835 3.41954794995693
7932938 4.2763638808475
8172914 5.60951994384241

Total number of rows: 13657

Table truncated, full table size 332 Kbytes.




Supplementary file Size Download File type/resource
GSM560162.CEL.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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