| 1 |
GPL980 |
15 K cDNA |
17,280 |
U.T. Southwestern Medical Center |
2004-02-10 |
|
Homo sapiens,Mus musculus
 |
cDNA Array |
spotted DNA/cDNA, 15 K cDNA, Mouse and human 15,000 gene cDNA array |
| 2 |
GPL3032 |
16S and 23S rRNA CodeLink Microarray |
202 |
Catholic University of Louvain |
2005-10-28 |
University of Washington, Seattle, Civil and Environmental Engineering |
unidentified
 |
Oligo Array |
spotted oligonucleotide, 16S and 23S rRNA CodeLink Microarray, Probes targeting the 16S and 23S rRNA of various microorganisms (mainly Bacteria). |
| 3 |
GPL2993 |
16S and 23S rRNA Gel Pad Microarray |
270 |
Catholic University of Louvain |
2005-10-20 |
Argonne National Laboratory |
unidentified
 |
Oligo Array |
spotted oligonucleotide, 16S and 23S rRNA Gel Pad Microarray, Probes targeting the 16S and 23S rRNA of various organisms (mainly Bacteria) |
| 4 |
GPL6461 |
2D-LC MS/MS Analyses of HLA Class I Peptides Isolated from B-cells Infected with Vaccinia Virus |
23,797 |
Mayo Clinic |
2008-02-05 |
|
Homo sapiens,Bos taurus,Vaccinia virus
 |
Other |
MS, 2D-LC MS/MS Analyses of HLA Class I Peptides Isolated from B-cells Infected with Vaccinia Virus, B-cell cultures were infected with live vaccinia virus (NYBOH strain). Cells were lysed, HLA/peptide complexes were enriched by immunoaffinity (W6/32 mAb), peptides were released with acid and separated from HLA proteins by 10 kDa ultrafilitration. HLA class I peptides were separated and identified by 2-dimensional liquid chromatography and tandem mass spectrometry to identify class I peptides derived from vaccinia proteins, that were being presented to the immune system. |
| 5 |
GPL11099 |
454 GS (Caenorhabditis elegans; Escherichia coli) |
0 |
|
2010-10-22 |
|
Escherichia coli,Caenorhabditis elegans
 |
HT Sequencing |
high-throughput sequencing, 454 GS (Caenorhabditis elegans; Escherichia coli), |
| 6 |
GPL15026 |
454 GS (Cymbidium ringspot virus; Nicotiana benthamiana) |
0 |
|
2011-12-19 |
|
Nicotiana benthamiana,Cymbidium ringspot virus
 |
HT Sequencing |
high-throughput sequencing, 454 GS (Cymbidium ringspot virus; Nicotiana benthamiana), |
| 7 |
GPL15201 |
454 GS FLX (Aliivibrio fischeri; environmental samples) |
0 |
|
2012-02-08 |
|
Aliivibrio fischeri,
 |
HT Sequencing |
high-throughput sequencing, 454 GS FLX (Aliivibrio fischeri; environmental samples), |
| 8 |
GPL15200 |
454 GS FLX (environmental samples) |
0 |
|
2012-02-08 |
|
 |
HT Sequencing |
high-throughput sequencing, 454 GS FLX (environmental samples), |
| 9 |
GPL11212 |
454 GS FLX (unidentified) |
0 |
|
2010-11-15 |
|
unidentified
 |
HT Sequencing |
high-throughput sequencing, 454 GS FLX (unidentified), |
| 10 |
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
 |
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. |
| 11 |
GPL16418 |
AB 5500xl Genetic Analyzer (Pseudomonas chlororaphis subsp. aureofaciens 30-84) |
0 |
|
2012-12-20 |
|
unidentified
 |
HT Sequencing |
high-throughput sequencing, AB 5500xl Genetic Analyzer (Pseudomonas chlororaphis subsp. aureofaciens 30-84), |
| 12 |
GPL15993 |
AB SOLiD 4 System (Trichophytom rubrum) |
0 |
|
2012-08-28 |
|
unidentified
 |
HT Sequencing |
high-throughput sequencing, AB SOLiD 4 System (Trichophytom rubrum), |
| 13 |
GPL11652 |
AbC_ELTE_human_432_v1 |
432 |
Eötvös Loránd University |
2011-01-26 |
Eotvos Lorand University, Budapest, Hungary |
Homo sapiens,Sus scrofa,Bos taurus,Capra hircus,Oryctolagus cuniculus
 |
Other |
spotted peptide or protein, AbC_ELTE_human_432_v1, |
| 14 |
GPL7563 |
ACGT Pearl Millet SSH library 4K v1.0 |
4,224 |
CSIR Biosciences |
2008-11-05 |
ACGT Microarray Facility, University of Pretoria, Pretoria, South Africa (http://www.microarray.up.ac.za ) |
unidentified
 |
cDNA Array |
spotted DNA/cDNA, ACGT Pearl Millet SSH library 4K v1.0, |
| 15 |
GPL2889 |
Acyrthosiphon pisum + Buchnera aphidicola dual genome array |
1,904 |
University of Arizona |
2005-09-26 |
GATC - University of Arizona |
Buchnera aphidicola,Acyrthosiphon pisum
 |
cDNA Array |
spotted DNA/cDNA, Acyrthosiphon pisum + Buchnera aphidicola dual genome array, Dual-genome microarray for the pea aphid, Acyrthosiphon pisum, and its obligate bacterial symbiont, Buchnera aphidicola The platform table is condensed to show each GENE on the array. The full array table, showing all spots, is linked as a supplementary file (see download link below). |
| 16 |
GPL9472 |
Adelaide microarray facility Exiqon LNA miRNA microarray_version8.1 |
3,072 |
SA Pathology |
2009-10-21 |
Adelaide Microarray Facility |
Arabidopsis thaliana,Saccharomyces cerevisiae,Caenorhabditis elegans,Drosophila melanogaster,Gallus gallus,Macaca mulatta,Homo sapiens,Bos taurus,Mus musculus,Rattus norvegicus
 |
Oligo Array |
spotted oligonucleotide, Adelaide microarray facility Exiqon LNA miRNA microarray_version8.1, The actual (physical) array contains duplicate spots, 1487 x 2 + empty -> 3072 spots |
| 17 |
GPL4335 |
Affymetrix custom made array SFORV2_2 |
10,098 |
University of Chicago |
2006-09-15 |
Affymetrix |
Pan troglodytes,Homo sapiens,Canis lupus familiaris,Rattus norvegicus
 |
GeneChip |
in situ oligonucleotide, Affymetrix custom made array SFORV2_2, |
| 18 |
GPL10501 |
Agilent Custom Gene Expression Array for Saccharomyces castellii |
5,688 |
MIT |
2010-06-08 |
Agilent |
unidentified
 |
Oligo Array |
in situ oligonucleotide, Agilent Custom Gene Expression Array for Saccharomyces castellii, Agilent Custom Oligo Microarray 8x15K G4427A |
| 19 |
GPL11330 |
Agilent custom Leishmania microarray v2 |
9,709 |
Université Laval |
2010-12-17 |
Agilent |
 |
Oligo Array |
in situ oligonucleotide, Agilent custom Leishmania microarray v2, Multispecies Leishmania microarray |
| 20 |
GPL15030 |
Agilent Human, KSHV, and EBV 44K AMADID #027774 |
14,601 |
University of Pittsburgh |
2011-12-19 |
Agilent Technologies |
Homo sapiens,Human herpesvirus 4,Human herpesvirus 8
 |
Oligo Array |
in situ oligonucleotide, Agilent Human, KSHV, and EBV 44K AMADID #027774, |