Gene Expression Omnibus (GEO) Overview Version:2013-04-06Japanese page
An overview of the GEO entries broken down by the measurement platforms and the features of the measured samples.
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Data Unit : [ DataSet / Sample / Platform ] Show explanation>> <<Hide explanation
DataSet : Series(GSE) x Platform(GPL). A set of related gene expression data.
Sample : Biological materials.
platform : Methods or instruments used for the gene expression profilings.
The numbers shown in the tabs are the numbers of the data (series, samples or platforms) belonging to the groups.
  Human
(102)
  Primates
(1)
  Rodents
(48)
  Mammals
(5)
  Vertebrates
(8)
  Invertebrates
(16)
  Plants
(65)
  Bacteria
(39)
  Viruses
(0)
  Phages
(0)
  Unclassified
(5)
  All
(289)
 
  SAGE NlaIII
(0)
  SAGE RsaI
(0)
  SAGE Sau3A
(0)
  MPSS
(0)
  GeneChip
(0)
  Tiling Array
(0)
  cDNA Array
(0)
  Oligo Array
(5)
  Bead Array
(0)
  Protein Array
(0)
  Antibody
(0)
  RT-PCR
(0)
  HT-Seq
(0)
  Other
(0)
  All
(5)
 
Platform ID Title Number of the probes Institute Submission date Manufacturer Species Platform class Reasoning of the classification
Keywords used for the classification are shown with bold font.
1 GPL6253 JCVI PFGRC Plasmodium Sal-1 18K v1 array designed primarily based on strain Sal-1 17,218 J. Craig Venter Institute 2007-12-06 JCVI PFGRC unidentified
unidentified
Oligo Array spotted oligonucleotide, JCVI PFGRC Plasmodium Sal-1 18K v1 array designed primarily based on strain Sal-1, This set includes 16120 oligonucleotides, has 18240 spots distributed in 48 blocks.
2 GPL6123 UCD_Ronald_XOarray_5K_V1.0 10,080 University of California, Davis 2007-11-13 Microarray Core Facility. University of California, Davis unidentified,Xanthomonas oryzae pv. oryzicola BLS256
unidentified,Xanthomonas oryzae pv. oryzicola BLS256
Oligo Array spotted oligonucleotide, UCD_Ronald_XOarray_5K_V1.0,
3 GPL6055 University of Adelaide microarray facility Exiqon LNA miRNA microarray_version8.1 1,487 CSIRO 2007-10-25 University of Adelaide microarray facility Arabidopsis thaliana,Caenorhabditis elegans,Drosophila melanogaster,Gallus gallus,Macaca mulatta,Homo sapiens,Bos taurus,Mus musculus,Rattus norvegicus
Arabidopsis thaliana,Caenorhabditis elegans,Drosophila melanogaster,Gallus gallus,Macaca mulatta,Homo sapiens,Bos taurus,Mus musculus,Rattus norvegicus
Oligo Array spotted oligonucleotide, University of Adelaide microarray facility Exiqon LNA miRNA microarray_version8.1,
4 GPL6298 miMAX microRNA Array 1,231 National Institutes of Health 2007-12-18 Rutgers University Caenorhabditis elegans,Drosophila melanogaster,Homo sapiens,Mus musculus,Rattus norvegicus
Caenorhabditis elegans,Drosophila melanogaster,Homo sapiens,Mus musculus,Rattus norvegicus
Oligo Array spotted oligonucleotide, miMAX microRNA Array, http://cord.rutgers.edu/mirmax/index.html
5 GPL6012 A genome proxy array for profiling marine micobial communities 428 University of Arizona 2007-10-15 DeLong Lab uncultured crenarchaeote 4B7,Prochlorococcus marinus subsp. pastoris str. CCMP1986,uncultured marine alpha proteobacterium,uncultured marine gamma proteobacterium EBAC31A08,uncultured marine group II euryarchaeote 37F11,uncultured proteobacterium,uncultur
uncultured crenarchaeote 4B7,Prochlorococcus marinus subsp. pastoris str. CCMP1986,uncultured marine alpha proteobacterium,uncultured marine gamma proteobacterium EBAC31A08,uncultured marine group II euryarchaeote 37F11,uncultured proteobacterium,uncultur
Oligo Array spotted oligonucleotide, A genome proxy array for profiling marine micobial communities, ***Design Overview*** The prototype microarray targeted thirteen BAC or fosmid genome fragments (20-160kb) from both bacteria and archaea (Table 1), recovered from a variety of marine habitats (Table 2), as well as the cyanobacterium Prochlorococcus MED4. These clones were originally sequenced because of the presence of taxonomic marker or specific functional genes. This array consisted of sets of 70-bp oligonucleotides targeting each genome or genome fragment (Fig. 1), dispersed along the target sequences with no more than one probe per gene, and excluding rRNA genes as targets. The probes were selected solely based on theoretical thermodynamic properties and GC content (~40%); that is, probe selection did not focus on specific genes or regions, but simply produced the “optimal” probes for each genome proxy based on the probes’ predicted hybridization properties. rRNA genes were excluded, because this probe design approach, which avoids sequence alignments and considerations of RNA secondary structure, would be unlikely to result in useful rRNA probes. Furthermore, rRNA probes of traditional design could not be included on the array because their appropriate hybridization conditions would be very different from those of this array’s probes.