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Sample GSM4818877 Query DataSets for GSM4818877
Status Public on Oct 07, 2020
Title Mut1_Muscle_E15
Sample type RNA
 
Source name whole back muscle
Organism Mus musculus
Characteristics tissue: whole back muscle
genotype/variation: SIX1/4 mutant
Treatment protocol no treatment
Growth protocol No growth protocol, the tissue is extracted directly from E15 or E18 embryos
Extracted molecule total RNA
Extraction protocol RNA extraction from Pax7-nGFP+ FACS-sorted cells was performed using the Qiagen RNeasy microkit directly after isolation. Whole back muscles required a tissue lyser lyse step in Trizol solution.
Label biotin
Label protocol 50 ng (E18.5 whole back muscles), 2 ng (E15.5 FACS-sorted cells and whole back muscles) or 0.21 ng (E18.5 FACS-sorted cells) of total RNA were reverse-transcribed following the Ovation PicoSL or PicoV2 WTA System (Nugen). Briefly, the resulting double-strand cDNA was used for amplification based on SPIA technology. After purification according to Nugen protocol, 5 μg of single strand DNA was used for generation of Sens Target DNA using Ovation Exon Module kit (Nugen). 2.5 μg of Sens Target DNA were fragmented and labelled with biotin using Encore Biotin Module kit (Nugen).
 
Hybridization protocol The cDNA was then hybridized to GeneChip® Mouse Gene 1.0 or 2.0 ST (Affymetrix) at 45 °C for 17 h. After overnight hybridization, the ChIPs were washed using the fluidic station FS450 following specific protocols (Affymetrix).
Scan protocol the ChIPs were scanned using the GCS3000 7G. The scanned images were then analyzed with Expression Console software (Affymetrix) to obtain raw data (cel files) and metrics for quality controls
Data processing Normalisation with R, by project Project 1 : WT1_Muscle_E15,WT2_Muscle_E15,WT3_Muscle_E15,Mut1_Muscle_E15,Mut2_Muscle_E15,Mut3_Muscle_E15 → mogene20st_Mm_ENTREZG from Brainarray, version 20, Matrix 3 WT1_Muscle_E18,WT2_Muscle_E18,Mut1_Muscle_E18,Mut2_Muscle_E18 → mogene10st_Mm_ENTREZG from Brainarray, version 20, Matrix 2 Then we conserved only common genes between the two lists. Project 2 : WT1_PAX7_E15, WT2_PAX7_E15, WT3_PAX7_E15, Mut1_PAX7_E15, Mut2_PAX7_E15, Mut3_PAX7_E15, WT6_PAX7_E18, WT7_PAX7_E18, WT8_PAX7_E18, Mut6_PAX7_E18,Mut7_PAX7_E18,Mut8_PAX7_E18 mogene20st_Mm_ENTREZG from Brainarray, version 19, Matrix 1 We strictly follow the Brainrray recomandations for the normalisation by using the affy package they provide for each version of their custom CDF files.
 
Submission date Oct 06, 2020
Last update date Oct 07, 2020
Contact name Pascal Maire
E-mail(s) pascal.maire@inserm.fr
Organization name Institut Cochin. INSERM U1016, CNRS UMR 8104, U.Paris
Department Développement Reproduction et Cancer
Street address 24 Rue du Fg St Jacques
City PARIS
ZIP/Postal code 75014
Country France
 
Platform ID GPL22598
Series (1)
GSE159079 SIX1 and SIX4 homeoproteins regulate PAX7+ progenitor cell properties during fetal epaxial myogenesis

Data table header descriptions
ID_REF
VALUE log2 GC-RMA signal

Data table
ID_REF VALUE
100009600_at 4.372720569
100009609_at 2.770672584
100009614_at 4.080256688
100009664_at 3.167284348
100012_at 3.423159003
100017_at 7.243240278
100019_at 7.768234689
100033459_at 2.689616195
100034251_at 4.526574958
100034729_at 2.892665691
100034739_at 4.305124803
100036518_at 2.998433217
100036520_at 4.461812322
100036521_at 5.08690111
100036523_at 5.910387183
100036537_at 5.699812081
100036768_at 3.899691186
100037258_at 8.669828183
100037260_at 3.947212393
100037262_at 6.053365468

Total number of rows: 23748

Table truncated, full table size 498 Kbytes.




Supplementary file Size Download File type/resource
GSM4818877_4_Mut_D_15-1_MoGene-2_0-st.CEL.gz 8.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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