Search results for the GEO ID: GSE19210  |
(Click on the check boxes provided under "Select for analysis", to initiate grouping) |
(Once the selection is made, click on "Add groups" in "Make groups for comparison", to make a group. Scroll down) |
|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM476048 | GPL1355 |
|
Failing (rep 1)
|
Failing (rep 1)
|
tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476048
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476048/suppl/GSM476048.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476049 | GPL1355 |
|
Failing (rep 2)
|
Failing (rep 2)
|
tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476049
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476049/suppl/GSM476049.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476050 | GPL1355 |
|
Failing (rep 3)
|
Failing (rep 3)
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tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476050
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476050/suppl/GSM476050.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476051 | GPL1355 |
|
Failing (rep 4)
|
Failing (rep 4)
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tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476051
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476051/suppl/GSM476051.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476052 | GPL1355 |
|
Failing (rep 5)
|
Failing (rep 5)
|
tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476052
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476052/suppl/GSM476052.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476053 | GPL1355 |
|
Failing (rep 6)
|
Failing (rep 6)
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tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476053
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476053/suppl/GSM476053.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476054 | GPL1355 |
|
Control (rep 1)
|
Control (rep 1)
|
tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476054
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476054/suppl/GSM476054.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476055 | GPL1355 |
|
Control (rep 2)
|
Control (rep 2)
|
tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476055
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476055/suppl/GSM476055.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476056 | GPL1355 |
|
Control (rep 3)
|
Control (rep 3)
|
tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476056
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476056/suppl/GSM476056.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476057 | GPL1355 |
|
Control (rep 4)
|
Control (rep 4)
|
tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476057
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476057/suppl/GSM476057.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476058 | GPL1355 |
|
Control (rep 5)
|
Control (rep 5)
|
tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476058
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476058/suppl/GSM476058.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
| | |
|
GSM476059 | GPL1355 |
|
Control (rep 6)
|
Control (rep 6)
|
tissue type: heart
|
Gene expression data from cell line
|
| Sample_geo_accession | GSM476059
| | Sample_status | Public on Feb 01 2010
| | Sample_submission_date | Nov 26 2009
| | Sample_last_update_date | Dec 08 2009
| | Sample_type | RNA
| | Sample_channel_count | 1
| | Sample_organism_ch1 | Rattus norvegicus
| | Sample_taxid_ch1 | 10116
| | Sample_molecule_ch1 | total RNA
| | Sample_extract_protocol_ch1 | Total RNA was isolated from six biological replicates corresponding to Failing, Control, Failing+Captopril and Failing+Captopril+butyrate heart tissue using Trizol (Invitrogen) according to the manufacturer’s protocol, and the RNeasy mini-kit (Qiagen) was used to clean-up the RNA
| | Sample_label_ch1 | biotin
| | Sample_label_protocol_ch1 | Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
| | Sample_hyb_protocol | Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Drosophila Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
| | Sample_scan_protocol | GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
| | Sample_data_processing | data were processed with RMA method
| | Sample_platform_id | GPL1355
| | Sample_contact_name | steve,,shen
| | Sample_contact_department | Biochemistry
| | Sample_contact_institute | New York University
| | Sample_contact_address | 545 First Ave
| | Sample_contact_city | New York
| | Sample_contact_state | NY
| | Sample_contact_zip/postal_code | 10016
| | Sample_contact_country | USA
| | Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM476nnn/GSM476059/suppl/GSM476059.CEL.gz
| | Sample_series_id | GSE19210
| | Sample_data_row_count | 31099
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