|
Status |
Public on Aug 18, 2010 |
Title |
Mesorhabditis sp. (isolate KS587) |
Sample type |
genomic |
|
|
Source name |
Genomic DNA from Mesorhabditis sp. (isolate KS587)
|
Organism |
Mesorhabditis sp. MAH-2010 |
Characteristics |
isolate: KS587 tissue: whole-body
|
Treatment protocol |
Maintained on NGM growth media at 20 degrees C, seeded with E. coli OP50
|
Growth protocol |
Maintained on NGM growth media at 20 degrees C, seeded with E. coli OP50
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Whole individuals were washed off NGM plates with M9 buffer and genomic DNA was extracted with phenol-chloroform
|
Label |
biotin
|
Label protocol |
GeneChip WT Double-Stranded DNA Terminal Labeling Kit, according to manufacturer's specifications
|
|
|
Hybridization protocol |
GeneChip Hybridization, Wash, and Stain kit, according to manufacturer's specifics, using GeneChip Fluidics station 400
|
Scan protocol |
Arrays were scanned on an Affymetrix Scanner 3000 7G
|
Description |
CEL files contain raw intensity data, without scaling or smoothing
|
Data processing |
Data was extracted with GeneChip Operating Software (GCOS) and processed using Tiling Analysis Software (TAS). Normalized intensity file is tab-delimited and contains probe-level normalized intensity for each species, as described in the manuscript.
|
|
|
Submission date |
Aug 17, 2010 |
Last update date |
Aug 17, 2010 |
Contact name |
Michael A Herman |
E-mail(s) |
[email protected]
|
Organization name |
Kansas State University, Ecological Genomics Institute
|
Department |
Division of Biology
|
Street address |
266 Chalmers Hall
|
City |
Manhattan |
State/province |
KS |
ZIP/Postal code |
66506 |
Country |
USA |
|
|
Platform ID |
GPL5634 |
Series (1) |
GSE23667 |
Array-based cross-species hybridization between genera of Rhabditidae (Nematoda) |
|