Search results for the GEO ID: GSE14274 |
(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 |
GSM357123 | GPL339 |
|
FE65WT_1
|
FE65WT
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357123
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357123/suppl/GSM357123.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
GSM357124 | GPL339 |
|
p97FE65NULL_1
|
p97FE65NULL
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357124
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357124/suppl/GSM357124.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
GSM357125 | GPL339 |
|
p97FE65NULL_2
|
p97FE65NULL
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357125
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357125/suppl/GSM357125.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
GSM357126 | GPL339 |
|
FE65WT_2
|
FE65WT
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357126
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357126/suppl/GSM357126.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
GSM357127 | GPL339 |
|
FE65WT_3
|
FE65WT
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357127
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357127/suppl/GSM357127.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
GSM357128 | GPL339 |
|
p97FE65NULL_3
|
p97FE65NULL
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357128
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357128/suppl/GSM357128.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
GSM357129 | GPL339 |
|
FE65WT_4
|
FE65WT
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357129
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357129/suppl/GSM357129.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
GSM357130 | GPL339 |
|
p97FE65NULL_4
|
p97FE65NULL
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357130
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357130/suppl/GSM357130.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
GSM357131 | GPL339 |
|
p97FE65NULL_5
|
p97FE65NULL
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357131
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357131/suppl/GSM357131.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
GSM357132 | GPL339 |
|
FE65WT_5
|
FE65WT
|
Cerebral cortex tissues were dissected from five FE65 wild-type and p97FE65 null littermate pairs (6 months of age) for RNA purification and array analysis.
|
Cerebral cortex tissue.
|
Sample_geo_accession | GSM357132
| Sample_status | Public on Dec 12 2010
| Sample_submission_date | Jan 04 2009
| Sample_last_update_date | Dec 12 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_biomaterial_provider_ch1 | The University of Washington (Seattle, WA).
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | RNA was converted into double strand cDNA with the SuperScript II double stranded cDNA synthesis kit (Invitrogen, Carlsbad, CA) according to the GeneChipTM Expression Analysis Technical Manual (Chapter 1 section 2.1.15) (Affymetrix, Santa Clara, CA).
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Conversion of double strand cDNA into cRNA was accomplished by in vitro transcription using the BioArray High Yield RNA Transcription Labeling kit (Enzo Diagnostics, Farmingdale, NY) according to the manufacturer’s instructions.
| Sample_hyb_protocol | The standard hybridization protocol was used as recommended by Affymterix.
| Sample_scan_protocol | GeneChips were scanned using the Affymetrix GeneArray Scanner 3000 through the University of Washington Center for Expression Arrays (http://ra.microslu.washington.edu/).
| Sample_data_processing | Bioconductor GCRMA normalization log2
| Sample_platform_id | GPL339
| Sample_contact_name | Richard,,Beyer
| Sample_contact_email | dbeyer@u.washington.edu
| Sample_contact_phone | 206-616-7378
| Sample_contact_laboratory | Center for Ecogenetics and Environmental Health
| Sample_contact_institute | University of Washington
| Sample_contact_address | 4225 Roosevelt Way, NE, Suite 100
| Sample_contact_city | Seattle
| Sample_contact_state | WA
| Sample_contact_zip/postal_code | 98105
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM357nnn/GSM357132/suppl/GSM357132.cel.gz
| Sample_series_id | GSE14274
| Sample_data_row_count | 22690
| |
|
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