NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1846691 Query DataSets for GSM1846691
Status Public on Jan 15, 2016
Title D_T1T1
Sample type RNA
 
Source name Digestive_Gland_Sampling_Time1_Control
Organism Magallana gigas
Characteristics tissue: Digestive_Gland
gender: Female
developmental stage: 1y
Treatment protocol Polystyrene microplastic exposure at 32 µg.L-1
Gonadal maturation
Growth protocol Standard hatchery conditions to induce gametogenesis (2 months at 17°C fed at libitum)
Standard hatchery conditions to induce gametogenesis
Extracted molecule total RNA
Extraction protocol Total RNA extracted using Extract-all Reagent (Eurobio), 1,5 mL per 50 mg of tissue or 20000 oocytes
Total RNA extracted using Extract-all Reagent (Eurobio), 1,5 mL per 50 mg of tissue
Label Cy3
Label protocol 200 ng of total RNA were indirectly labeled with Cy3 using the Low Input Quick Amp Labeling kit One-Color
200 ng of total RNA were indirectly labeled with Cy3 using the Low Input Quick Amp Labeling kit One-Color
 
Hybridization protocol Hybridization was performed using the Agilent Gene expression hybridization kit (5188-5242), with 1.65 μg of labeled RNA for 16 h at 65 °C
Hybridization was performed using the Agilent Gene expression hybridization kit (5188-5242), with 1.65 μg of labeled RNA, randomly onto 48 different slides for 16 h at 65 °C
Scan protocol Slides were scanned on an Agilent Technologies G2565AA Microarray Scanner system at 5 μm resolution, using default parameters
Slides were scanned on an Agilent Technologies G2565AA Microarray Scanner system at 5 μm resolution, using default parameters
Description Microarray_Gene_Expression
Data processing Quantile normalization was performed on background-corrected features with the limma package. Filtering step was performed according to Agilent Feature Extraction software results on spot quality and spot intensity reliability. Missing values were imputed with Impute package.
Quantile normalization was performed on background-corrected features with the limma package. Filtering step was performed according to Agilent Feature Extraction software results on spot quality and spot intensity reliability. Missing values were imputed with Impute package.
 
Submission date Aug 07, 2015
Last update date Jan 16, 2016
Contact name Rossana Sussarellu
E-mail(s) rossana.sussarellu@ifremer.fr
Organization name Ifremer
Department Ressources Biologiques et Environnement
Lab Laboratoire d'Ecotoxicologie
Street address Rue de l'Ile d'Yeu
City Nantes
ZIP/Postal code 44300
Country France
 
Platform ID GPL11353
Series (1)
GSE71845 Oyster reproduction is affected by exposure to polystyrene microplastics

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
13 6.6524313365369
14 6.31706468296832
15 8.1925773416467
17 10.2656037774984
18 5.70310496006092
19 5.61074094191226
20 18.0399722785722
21 6.80636371965455
22 5.30167205833876
23 9.05596023445229
24 5.64219058053732
25 5.44421852469079
26 7.75193023666202
28 6.95955617428889
29 5.99522357864693
30 9.29247649605922
33 5.28540221886225
34 6.63299519714296
36 5.56282948223157
37 5.95106050251165

Total number of rows: 31918

Table truncated, full table size 705 Kbytes.




Supplementary file Size Download File type/resource
GSM1846691_D_T1T1.txt.gz 4.7 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap