| 1 |
GPL10125 |
Nimblegen Rhipicephalus microplus 385K microarray |
385,770 |
DEEDI |
2010-03-03 |
NimbleGen Systems Inc. |
Rhipicephalus microplus
 |
Oligo Array |
in situ oligonucleotide, Nimblegen Rhipicephalus microplus 385K microarray, |
| 2 |
GPL5711 |
Sentrix BeadChip Array HumanHap300 Genotyping BeadChip 317K, TagSNP Phase I, v1.1 |
317,503 |
QIMR |
2007-08-06 |
Illumina,Inc. |
Homo sapiens
 |
Oligo Array |
spotted oligonucleotide, Sentrix BeadChip Array HumanHap300 Genotyping BeadChip 317K, TagSNP Phase I, v1.1, |
| 3 |
GPL14873 |
Agilent-027516 VPC Human 180K v2 |
180,880 |
Queensland University of Technology; University of British Columbia |
2011-11-10 |
Agilent |
Homo sapiens
 |
Oligo Array |
in situ oligonucleotide, Agilent-027516 VPC Human 180K v2, annotation from RefSeq and EntrezGene Database (downloaded: December, 2011) |
| 4 |
GPL14984 |
Agilent-033023 Hzea_Virus_2directions [Feature Number Version] |
180,880 |
The University of Queensland |
2011-12-08 |
Agilent Technologies |
Helicoverpa zea
 |
Oligo Array |
in situ oligonucleotide, Agilent-033023 Hzea_Virus_2directions [Feature Number Version], 29,586 H.zea transcript sequences obtained from denovo assembly were reverse transcribed and then combined with the original sequences to form a final target sequence file that contains 59,172 sequences. Based on these 59,172 sequences, eArray was used to design 3 probes per target, with the options for best distribution method and no 3' bias. Then, all probes with potential cross hybridization were removed, resulting in 153,492 probes. This probe set was divided into 3 probe groups (eArray probe format: complete, Ms-excel), each contains 60,000, 60,000 and 33,000 probes. Another probe set for 135 virus genes and 16 selected insect genes (3 probes/target), which were replicated 10 times. These four probe groups were then used to design the 4x180,000 Agilent arrays. |
| 5 |
GPL16604 |
Agilent-032034 VPC Human 180K v3 (Probe Name version) |
175,337 |
Queensland University of Technology; University of British Columbia |
2013-02-07 |
Agilent |
Homo sapiens
 |
Oligo Array |
in situ oligonucleotide, Agilent-032034 VPC Human 180K v3 (Probe Name version), annotation from RefSeq and EntrezGene Database (downloaded: April, 2012) |
| 6 |
GPL8742 |
AWRI_Oenoccocus_oeni_105kv1.0_016965 |
71,210 |
The Australian Wine Research Institute |
2009-06-18 |
Agilent |
Oenococcus oeni
 |
Oligo Array |
in situ oligonucleotide, AWRI_Oenoccocus_oeni_105kv1.0_016965, |
| 7 |
GPL17190 |
Nimblegen custom 12x135K chicken high-density multiplex microarray |
47,918 |
CSIRO |
2013-05-23 |
Nimblegen Systems Inc. |
Gallus gallus
 |
Oligo Array |
in situ oligonucleotide, Nimblegen custom 12x135K chicken high-density multiplex microarray, A custom designed NimbleGen 12x135K chicken high-density multiplex microarray was used in this experiment. The microarray contained a set of 65,849 long oligonucleotides (60-75nt) based upon chicken UniGene sequence families. Each gene was represented by at least two independently designed probes and each probe was present in duplicate on the array. Each fabricated glass slide contained 12 identical arrays that could were independently hybridized. |
| 8 |
GPL10875 |
Agilent-024207 Schistosoma mansoni 45K array (Feature Number version) |
45,220 |
QIMR |
2010-09-02 |
Agilent Technologies |
Schistosoma mansoni
 |
Oligo Array |
in situ oligonucleotide, Agilent-024207 Schistosoma mansoni 45K array (Feature Number version), schisto-v1_1164838824901_1244575027696 Arrays of this design have barcodes that begin with 16024207 or 2524207. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. The ID column represents the Agilent Feature Extraction feature number. Rows and columns are numbered as scanned by an Axon Scanner (barcode on the bottom, DNA on the front surface). To match data scanned on an Axon scanner, use the RefNumber column contained in the Agilent-provided GAL file as the ID_REF column in sample submissions. |
| 9 |
GPL13794 |
USC_F.merg_44K_v1 |
45,220 |
University of the Sunshine Coast |
2011-06-30 |
Agilent |
Fenneropenaeus merguiensis
 |
Oligo Array |
in situ oligonucleotide, USC_F.merg_44K_v1, Accession strings in the GEO submission refer only to the EST names given to transcriptome sequences by the sequencing company. No annotation/sequence ID from a public database has been included, as sequence information for prawns is very limited and a large proportion of the sequencs were unable to be annotated. |
| 10 |
GPL7160 |
Agilent-016061 QIMR Schistosoma 44k v 1.0 |
45,220 |
QIMR |
2008-08-13 |
Agilent |
Schistosoma japonicum,Schistosoma mansoni
 |
Oligo Array |
in situ oligonucleotide, Agilent-016061 QIMR Schistosoma 44k v 1.0, |
| 11 |
GPL9759 |
QIMR/Agilent-023536 Schistosoma japonicum 44k array_New 2009 Sj |
45,220 |
QIMR |
2009-12-07 |
Agilent Technologies |
Schistosoma japonicum
 |
Oligo Array |
in situ oligonucleotide, QIMR/Agilent-023536 Schistosoma japonicum 44k array_New 2009 Sj, Arrays of this design have barcodes that begin with 16023536 or 2523536. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. The ID column represents the Agilent Feature Extraction feature number. Rows and columns are numbered as scanned by an Axon Scanner (barcode on the bottom, DNA on the front surface). To match data scanned on an Axon scanner, use the RefNumber column contained in the Agilent-provided GAL file as the ID_REF column in sample submissions. |
| 12 |
GPL6076 |
Agilent- Whole Human Genome Oligo Microarray G4112A condensed |
41,059 |
University of Queensland |
2007-11-01 |
Agilent Technologies |
Homo sapiens
 |
Oligo Array |
in situ oligonucleotide, Agilent- Whole Human Genome Oligo Microarray G4112A condensed, This single 44K formatted microarray represents a compiled view of the human genome as it is understood today. The sequence information used to design this product was derived from a broad survey of well known sources such as RefSeq, Goldenpath, Ensembl, Unigene and others. The resulting view of the human genome covers 41K unique genes and transcripts which have been verified and optimized by alignment to the human genome assembly and by Agilent's Empirical Validation process. Arrays of this design have barcodes that begin with 16012391 or 2512391. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. The ID column represents the Agilent Feature Extraction feature number. Rows and columns are numbered as scanned by an Axon Scanner (barcode on the bottom, DNA on the front surface). To match data scanned on an Axon scanner, use the RefNumber column contained in the Agilent-provided GAL file as the ID_REF column in sample submissions. |
| 13 |
GPL16487 |
Agilent-037288 Timecourse_Insect_Virus |
34,489 |
The University of Queensland |
2013-01-10 |
Agilent Technologies |
Helicoverpa zea,Helicoverpa armigera
 |
Oligo Array |
in situ oligonucleotide, Agilent-037288 Timecourse_Insect_Virus, A custom 8x60,000 SurePrint Agilent expression slide (Agilent, Santa Clara, CA) with probes including probes for 27,400 H. zea sequences that were validated previously (Nguyen et al., 2012. PLOS ONE, 7(5), e36324) and all 134 H. armigera single-capsid nucleopolyhedrovirus (HearNPV) genes (Accession: NC_002654). Arrays of this design have barcodes that begin with 16037288 or 2537288. |
| 14 |
GPL4899 |
Compugen mouse 22K array (UQ) |
30,000 |
University of Melbourne |
2007-02-28 |
SRC Microarray Facility, University of Queensland, Australia |
Mus musculus
 |
Oligo Array |
spotted oligonucleotide, Compugen mouse 22K array (UQ), |
| 15 |
GPL7621 |
JCVI Pseudomonas fluorescens Pf-5 28k v2.0 |
27,648 |
Macquarie University |
2008-11-10 |
J. Craig Venter Institute |
unidentified
 |
Oligo Array |
mixed spotted oligonucleotide/cDNA, JCVI Pseudomonas fluorescens Pf-5 28k v2.0, |
| 16 |
GPL13885 |
Agilent-021158 Mouse CNV Microarray (Probe Name version) |
27,274 |
The University of Queensland |
2011-07-11 |
Agilent |
Mus musculus
 |
Oligo Array |
in situ oligonucleotide, Agilent-021158 Mouse CNV Microarray (Probe Name version), Platform is based on mouse genome build NCBI37/mm9. |
| 17 |
GPL15294 |
TIGR PFGRC Aspergillus nidulans version 1 array designed primarily based on strain FGSC A4 |
25,392 |
University of New England |
2012-03-02 |
TIGR PFGRC (The Pathogen Functional Genomics Resource Center) |
Emericella nidulans
 |
Oligo Array |
spotted oligonucleotide, TIGR PFGRC Aspergillus nidulans version 1 array designed primarily based on strain FGSC A4, This set includes 11481 oligonucleotides (ss oligo 70 mer), has 23962 spots (2x oligo replicates) distributed in 48 blocks. |
| 18 |
GPL7620 |
JCVI Pseudomonas fluorescens Pf-5 23k v1.0 |
23,232 |
Macquarie University |
2008-11-10 |
J. Craig Venter Institute |
unidentified
 |
Oligo Array |
mixed spotted oligonucleotide/cDNA, JCVI Pseudomonas fluorescens Pf-5 23k v1.0, |
| 19 |
GPL8926 |
PC Human Operon 21k v2 |
23,232 |
Queensland Institute of Medical Research |
2009-07-24 |
Microarray Facility - the Prostate Centre at Vancouver General Hospital |
Homo sapiens
 |
Oligo Array |
spotted oligonucleotide, PC Human Operon 21k v2, |
| 20 |
GPL1747 |
Ramaciotti Centre 10k combined Rat Oligo |
23,040 |
St Vincents Institute |
2004-12-13 |
|
Rattus norvegicus
 |
Oligo Array |
spotted oligonucleotide, Ramaciotti Centre 10k combined Rat Oligo, Compugen and Operon oligo sets |