Search results for the GEO ID: GSE21833 |
(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 |
GSM543406 | GPL1261 |
|
Stomach_control_rep1
|
Gastric mucosa
|
tissue: gastric mucosa
infection: uninfected
|
n/a
|
Sample_geo_accession | GSM543406
| Sample_status | Public on Nov 13 2010
| Sample_submission_date | May 14 2010
| Sample_last_update_date | May 14 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Gastric mucosa were obtained from uninfected mice or those infected with one of the two isogenic strains of H. pylori (cagA+, cagA-)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After homogenization of tissue, total RNA was extracted and purified using the RNAeasy system according to manufacturer’s instructions (Qiagen Valencia, CA). The QIAGEN RNase-free DNase supplement kit was used to ensure that the RNA was free from DNA contamination.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA was processed and labeled according to the standard target labeling protocols.
| Sample_hyb_protocol | The samples were hybridized and stained per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_scan_protocol | The samples were scanned per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_data_processing | The data were normalized using GC-RMA algorithm in R statistical environment (version 2.9.0). Gene set enrichment analysis was applied using bioconductor packages GSEABase and Category.
| Sample_platform_id | GPL1261
| Sample_contact_name | Saroj,K,Mohapatra
| Sample_contact_email | skmohapatra@yahoo.com
| Sample_contact_department | VBI
| Sample_contact_institute | Virginia Tech
| Sample_contact_address | washington Street
| Sample_contact_city | blacksburg
| Sample_contact_state | VA
| Sample_contact_zip/postal_code | 24060
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM543nnn/GSM543406/suppl/GSM543406_Bassa_1_1_stomach.CEL.gz
| Sample_series_id | GSE21833
| Sample_data_row_count | 45101
| |
|
GSM543407 | GPL1261 |
|
Stomach_control_rep2
|
Gastric mucosa
|
tissue: gastric mucosa
infection: uninfected
|
n/a
|
Sample_geo_accession | GSM543407
| Sample_status | Public on Nov 13 2010
| Sample_submission_date | May 14 2010
| Sample_last_update_date | May 14 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Gastric mucosa were obtained from uninfected mice or those infected with one of the two isogenic strains of H. pylori (cagA+, cagA-)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After homogenization of tissue, total RNA was extracted and purified using the RNAeasy system according to manufacturer’s instructions (Qiagen Valencia, CA). The QIAGEN RNase-free DNase supplement kit was used to ensure that the RNA was free from DNA contamination.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA was processed and labeled according to the standard target labeling protocols.
| Sample_hyb_protocol | The samples were hybridized and stained per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_scan_protocol | The samples were scanned per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_data_processing | The data were normalized using GC-RMA algorithm in R statistical environment (version 2.9.0). Gene set enrichment analysis was applied using bioconductor packages GSEABase and Category.
| Sample_platform_id | GPL1261
| Sample_contact_name | Saroj,K,Mohapatra
| Sample_contact_email | skmohapatra@yahoo.com
| Sample_contact_department | VBI
| Sample_contact_institute | Virginia Tech
| Sample_contact_address | washington Street
| Sample_contact_city | blacksburg
| Sample_contact_state | VA
| Sample_contact_zip/postal_code | 24060
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM543nnn/GSM543407/suppl/GSM543407_Bassa_2_3_stomach.CEL.gz
| Sample_series_id | GSE21833
| Sample_data_row_count | 45101
| |
|
GSM543408 | GPL1261 |
|
Stomach_control_rep3
|
Gastric mucosa
|
tissue: gastric mucosa
infection: uninfected
|
n/a
|
Sample_geo_accession | GSM543408
| Sample_status | Public on Nov 13 2010
| Sample_submission_date | May 14 2010
| Sample_last_update_date | May 14 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Gastric mucosa were obtained from uninfected mice or those infected with one of the two isogenic strains of H. pylori (cagA+, cagA-)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After homogenization of tissue, total RNA was extracted and purified using the RNAeasy system according to manufacturer’s instructions (Qiagen Valencia, CA). The QIAGEN RNase-free DNase supplement kit was used to ensure that the RNA was free from DNA contamination.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA was processed and labeled according to the standard target labeling protocols.
| Sample_hyb_protocol | The samples were hybridized and stained per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_scan_protocol | The samples were scanned per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_data_processing | The data were normalized using GC-RMA algorithm in R statistical environment (version 2.9.0). Gene set enrichment analysis was applied using bioconductor packages GSEABase and Category.
| Sample_platform_id | GPL1261
| Sample_contact_name | Saroj,K,Mohapatra
| Sample_contact_email | skmohapatra@yahoo.com
| Sample_contact_department | VBI
| Sample_contact_institute | Virginia Tech
| Sample_contact_address | washington Street
| Sample_contact_city | blacksburg
| Sample_contact_state | VA
| Sample_contact_zip/postal_code | 24060
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM543nnn/GSM543408/suppl/GSM543408_Bassa_9_14_stomach.CEL.gz
| Sample_series_id | GSE21833
| Sample_data_row_count | 45101
| |
|
GSM543409 | GPL1261 |
|
Stomach_Hpmutant_rep1
|
Gastric mucosa
|
tissue: gastric mucosa
infection: H. pylori strain 99-305 (mutant, HpcagA-)
|
n/a
|
Sample_geo_accession | GSM543409
| Sample_status | Public on Nov 13 2010
| Sample_submission_date | May 14 2010
| Sample_last_update_date | May 14 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Gastric mucosa were obtained from uninfected mice or those infected with one of the two isogenic strains of H. pylori (cagA+, cagA-)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After homogenization of tissue, total RNA was extracted and purified using the RNAeasy system according to manufacturer’s instructions (Qiagen Valencia, CA). The QIAGEN RNase-free DNase supplement kit was used to ensure that the RNA was free from DNA contamination.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA was processed and labeled according to the standard target labeling protocols.
| Sample_hyb_protocol | The samples were hybridized and stained per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_scan_protocol | The samples were scanned per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_data_processing | The data were normalized using GC-RMA algorithm in R statistical environment (version 2.9.0). Gene set enrichment analysis was applied using bioconductor packages GSEABase and Category.
| Sample_platform_id | GPL1261
| Sample_contact_name | Saroj,K,Mohapatra
| Sample_contact_email | skmohapatra@yahoo.com
| Sample_contact_department | VBI
| Sample_contact_institute | Virginia Tech
| Sample_contact_address | washington Street
| Sample_contact_city | blacksburg
| Sample_contact_state | VA
| Sample_contact_zip/postal_code | 24060
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM543nnn/GSM543409/suppl/GSM543409_Bassa_3_7_stomach.CEL.gz
| Sample_series_id | GSE21833
| Sample_data_row_count | 45101
| |
|
GSM543410 | GPL1261 |
|
Stomach_Hpmutant_rep2
|
Gastric mucosa
|
tissue: gastric mucosa
infection: H. pylori strain 99-305 (mutant, HpcagA-)
|
n/a
|
Sample_geo_accession | GSM543410
| Sample_status | Public on Nov 13 2010
| Sample_submission_date | May 14 2010
| Sample_last_update_date | May 14 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Gastric mucosa were obtained from uninfected mice or those infected with one of the two isogenic strains of H. pylori (cagA+, cagA-)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After homogenization of tissue, total RNA was extracted and purified using the RNAeasy system according to manufacturer’s instructions (Qiagen Valencia, CA). The QIAGEN RNase-free DNase supplement kit was used to ensure that the RNA was free from DNA contamination.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA was processed and labeled according to the standard target labeling protocols.
| Sample_hyb_protocol | The samples were hybridized and stained per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_scan_protocol | The samples were scanned per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_data_processing | The data were normalized using GC-RMA algorithm in R statistical environment (version 2.9.0). Gene set enrichment analysis was applied using bioconductor packages GSEABase and Category.
| Sample_platform_id | GPL1261
| Sample_contact_name | Saroj,K,Mohapatra
| Sample_contact_email | skmohapatra@yahoo.com
| Sample_contact_department | VBI
| Sample_contact_institute | Virginia Tech
| Sample_contact_address | washington Street
| Sample_contact_city | blacksburg
| Sample_contact_state | VA
| Sample_contact_zip/postal_code | 24060
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM543nnn/GSM543410/suppl/GSM543410_Bassa_4_8_stomach.CEL.gz
| Sample_series_id | GSE21833
| Sample_data_row_count | 45101
| |
|
GSM543411 | GPL1261 |
|
Stomach_Hpmutant_rep3
|
Gastric mucosa
|
tissue: gastric mucosa
infection: H. pylori strain 99-305 (mutant, HpcagA-)
|
n/a
|
Sample_geo_accession | GSM543411
| Sample_status | Public on Nov 13 2010
| Sample_submission_date | May 14 2010
| Sample_last_update_date | May 14 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Gastric mucosa were obtained from uninfected mice or those infected with one of the two isogenic strains of H. pylori (cagA+, cagA-)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After homogenization of tissue, total RNA was extracted and purified using the RNAeasy system according to manufacturer’s instructions (Qiagen Valencia, CA). The QIAGEN RNase-free DNase supplement kit was used to ensure that the RNA was free from DNA contamination.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA was processed and labeled according to the standard target labeling protocols.
| Sample_hyb_protocol | The samples were hybridized and stained per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_scan_protocol | The samples were scanned per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_data_processing | The data were normalized using GC-RMA algorithm in R statistical environment (version 2.9.0). Gene set enrichment analysis was applied using bioconductor packages GSEABase and Category.
| Sample_platform_id | GPL1261
| Sample_contact_name | Saroj,K,Mohapatra
| Sample_contact_email | skmohapatra@yahoo.com
| Sample_contact_department | VBI
| Sample_contact_institute | Virginia Tech
| Sample_contact_address | washington Street
| Sample_contact_city | blacksburg
| Sample_contact_state | VA
| Sample_contact_zip/postal_code | 24060
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM543nnn/GSM543411/suppl/GSM543411_Bassa_8_9_stomach.CEL.gz
| Sample_series_id | GSE21833
| Sample_data_row_count | 45101
| |
|
GSM543412 | GPL1261 |
|
Stomach_HpWT_rep1
|
Gastric mucosa
|
tissue: gastric mucosa
infection: H. pylori strain 98-325 (wild-type, HpcagA+)
|
n/a
|
Sample_geo_accession | GSM543412
| Sample_status | Public on Nov 13 2010
| Sample_submission_date | May 14 2010
| Sample_last_update_date | May 14 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Gastric mucosa were obtained from uninfected mice or those infected with one of the two isogenic strains of H. pylori (cagA+, cagA-)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After homogenization of tissue, total RNA was extracted and purified using the RNAeasy system according to manufacturer’s instructions (Qiagen Valencia, CA). The QIAGEN RNase-free DNase supplement kit was used to ensure that the RNA was free from DNA contamination.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA was processed and labeled according to the standard target labeling protocols.
| Sample_hyb_protocol | The samples were hybridized and stained per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_scan_protocol | The samples were scanned per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_data_processing | The data were normalized using GC-RMA algorithm in R statistical environment (version 2.9.0). Gene set enrichment analysis was applied using bioconductor packages GSEABase and Category.
| Sample_platform_id | GPL1261
| Sample_contact_name | Saroj,K,Mohapatra
| Sample_contact_email | skmohapatra@yahoo.com
| Sample_contact_department | VBI
| Sample_contact_institute | Virginia Tech
| Sample_contact_address | washington Street
| Sample_contact_city | blacksburg
| Sample_contact_state | VA
| Sample_contact_zip/postal_code | 24060
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM543nnn/GSM543412/suppl/GSM543412_Bassa_7_2_stomach.CEL.gz
| Sample_series_id | GSE21833
| Sample_data_row_count | 45101
| |
|
GSM543413 | GPL1261 |
|
Stomach_HpWT_rep2
|
Gastric mucosa
|
tissue: gastric mucosa
infection: H. pylori strain 98-325 (wild-type, HpcagA+)
|
n/a
|
Sample_geo_accession | GSM543413
| Sample_status | Public on Nov 13 2010
| Sample_submission_date | May 14 2010
| Sample_last_update_date | May 14 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Gastric mucosa were obtained from uninfected mice or those infected with one of the two isogenic strains of H. pylori (cagA+, cagA-)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After homogenization of tissue, total RNA was extracted and purified using the RNAeasy system according to manufacturer’s instructions (Qiagen Valencia, CA). The QIAGEN RNase-free DNase supplement kit was used to ensure that the RNA was free from DNA contamination.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA was processed and labeled according to the standard target labeling protocols.
| Sample_hyb_protocol | The samples were hybridized and stained per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_scan_protocol | The samples were scanned per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_data_processing | The data were normalized using GC-RMA algorithm in R statistical environment (version 2.9.0). Gene set enrichment analysis was applied using bioconductor packages GSEABase and Category.
| Sample_platform_id | GPL1261
| Sample_contact_name | Saroj,K,Mohapatra
| Sample_contact_email | skmohapatra@yahoo.com
| Sample_contact_department | VBI
| Sample_contact_institute | Virginia Tech
| Sample_contact_address | washington Street
| Sample_contact_city | blacksburg
| Sample_contact_state | VA
| Sample_contact_zip/postal_code | 24060
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM543nnn/GSM543413/suppl/GSM543413_Bassa_5_11_stomach.CEL.gz
| Sample_series_id | GSE21833
| Sample_data_row_count | 45101
| |
|
GSM543414 | GPL1261 |
|
Stomach_HpWT_rep3
|
Gastric mucosa
|
tissue: gastric mucosa
infection: H. pylori strain 98-325 (wild-type, HpcagA+)
|
n/a
|
Sample_geo_accession | GSM543414
| Sample_status | Public on Nov 13 2010
| Sample_submission_date | May 14 2010
| Sample_last_update_date | May 14 2010
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Mus musculus
| Sample_taxid_ch1 | 10090
| Sample_growth_protocol_ch1 | Gastric mucosa were obtained from uninfected mice or those infected with one of the two isogenic strains of H. pylori (cagA+, cagA-)
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | After homogenization of tissue, total RNA was extracted and purified using the RNAeasy system according to manufacturer’s instructions (Qiagen Valencia, CA). The QIAGEN RNase-free DNase supplement kit was used to ensure that the RNA was free from DNA contamination.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | RNA was processed and labeled according to the standard target labeling protocols.
| Sample_hyb_protocol | The samples were hybridized and stained per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_scan_protocol | The samples were scanned per standard Affymetrix protocols at VBI core laboratory on Mouse 430 2.0 expression arrays (Affymetrix Inc., Santa Clara, CA).
| Sample_data_processing | The data were normalized using GC-RMA algorithm in R statistical environment (version 2.9.0). Gene set enrichment analysis was applied using bioconductor packages GSEABase and Category.
| Sample_platform_id | GPL1261
| Sample_contact_name | Saroj,K,Mohapatra
| Sample_contact_email | skmohapatra@yahoo.com
| Sample_contact_department | VBI
| Sample_contact_institute | Virginia Tech
| Sample_contact_address | washington Street
| Sample_contact_city | blacksburg
| Sample_contact_state | VA
| Sample_contact_zip/postal_code | 24060
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM543nnn/GSM543414/suppl/GSM543414_Bassa_6_12_stomach.CEL.gz
| Sample_series_id | GSE21833
| Sample_data_row_count | 45101
| |
|
|
|
Make groups for comparisons |
(2 groups will be compared at a time) |
|
Select GSMs and click on "Add groups" |
Enter the group name here: |
|
|
|