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Sample GSM474845 Query DataSets for GSM474845
Status Public on Jun 01, 2010
Title BYU_Adams_H_bacteriophora_L5M2
Sample type RNA
 
Source name Heterorhabditis bacteriophora LM5
Organism Heterorhabditis bacteriophora
Characteristics genotype: In-bred laboratory strain L5M
phenotype: entamopathogenic traits deteriorated
Growth protocol An isolate of Heterorhabditis bacteriophora was created by sub-culturing different experimental lines of nematode-bacterium complex over 20 passages in Galleria mellonella . The original parental strain (OHB) was maintained in ringer's solution without sub-culturing while the inbred line (L5M) was continuously cultured in G. mellonella.
Both OHB and L5M were cultured in G. mellonella larvae and emerging infective juveniles (IJs) were collected using white traps. The IJs were stored in ringer's solution at 16ÂșC until used for experiments.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from four biological replicates of IJs of each strain. The IJs (~8-10,000) were transferred to 10 volumes of Trizol Reagent (Molecular Research Center Inc., Cincinnati, OH) and RNA extracted according to manufacturer's protocol.
Label Cy3
Label protocol Labeling was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
 
Hybridization protocol Hybridization was performed by NimbleGen Systems Inc., Madison, WI, USA following their standard operating protocol. See www.nimblegen.com.
Scan protocol Scanning was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
Description Genome not available
This sample is the first of four biological replicates of the L5M in-bred strain of H. bacteriophora.
Data processing The raw data (.pair file) was subjected to RMA (Robust Multi-Array Analysis; Irizarry et al. Biostatistics 4(2):249), quantile normalization (Bolstad et al. Bioinformatics 19(2):185), and background correction as implemented in the NimbleScan software package, version 2.4.27 (Roche NimbleGen, Inc.).
 
Submission date Nov 23, 2009
Last update date Nov 23, 2009
Contact name Chin-Yo Lin
E-mail(s) chinyolin@byu.edu
Phone 801-422-6259
Fax 801-422-0519
Organization name Brigham Young University
Department Microbiology and Molecular Biology
Street address 753 WIDB
City Provo
State/province UT
ZIP/Postal code 84602
Country USA
 
Platform ID GPL9714
Series (1)
GSE19152 Transcriptional profiling of trait deterioration in the insect pathogenic nematode Heterorhabditis bacteriophora

Data table header descriptions
ID_REF
VALUE RMA-normalized, averaged gene-level signal intensity

Data table
ID_REF VALUE
1 1666.9476
2 4420.917
3 4036.6749
4 3522.2249
5 1909.0797
6 4235.2881
7 2234.3496
8 2622.9914
9 4258.3647
10 1361.8689
11 1291.8248
12 3501.459
13 9180.6235
14 4245.885
15 5591.0832
16 1479.6899
17 1340.5601
18 4698.4515
19 2204.5897
20 8067.4414

Total number of rows: 15220

Table truncated, full table size 223 Kbytes.




Supplementary file Size Download File type/resource
GSM474845_17207502_532_RMA_calls.txt.gz 165.4 Kb (ftp)(http) TXT
GSM474845_17207502_532_pair.txt.gz 1.1 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data provided as supplementary file

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