Search results for the GEO ID: GSE27494 |
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(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 |
GSM679415 | GPL1352 |
|
Disc Cells in 3D Control (95)
|
Disc Cells in 3D Control
|
cell type: annulus disc cells
tissue grade: IV
feed media: MEM20
|
|
Sample_geo_accession | GSM679415
| Sample_status | Public on Jun 27 2012
| Sample_submission_date | Feb 24 2011
| Sample_last_update_date | Oct 28 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_growth_protocol_ch1 | Human annulus disc cells (100,000) were seeded into each piece (~0.5 cm3) of a collagen construct (Gelfoam; Pharmacia & Upjohn Co., Kalamazoo, MI). They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each piece of Gelfoam was homongenized and RNA isolated using TRIzol reagent
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labeled cRNA were prepard according to the Affymetrix protocol for IVT labeling.
| Sample_hyb_protocol | Fragmented cRNA was hybridized to the X3P chip in the Affymetrix hybridiztion buffer for 16 hrs at 45oC. X3P chips were washed and labeled in the Affymetrix Fluidics Station.
| Sample_scan_protocol | GeneChips were scanned once via the Affymetrix 3000G scanner.
| Sample_data_processing | The data were analyzed with the GCOS Affymetrix GeneChip Operating System (version 1.2) and Microarray Suite version 5.0 (MAS 5.0). Affymetrix default analysis settings and global scaling as normalization were used. Further normalization was acheived using GC-RMA (robust multiarray average) via GeneSifter analysis software (Viz Labs LLC, Seattle , WA; http://www.genesifter.net).
| Sample_platform_id | GPL1352
| Sample_contact_name | Helen,,Gruber
| Sample_contact_email | Helen.Gruber@carolinashealthcare.org
| Sample_contact_laboratory | Orthopaedic Research
| Sample_contact_department | Orthopaedic Surgery
| Sample_contact_institute | Carolinas HealthCare System
| Sample_contact_address | 1542 Graden Terrace
| Sample_contact_city | Charlotte
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 28203
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM679nnn/GSM679415/suppl/GSM679415.CEL.gz
| Sample_relation | Reanalyzed by: GSM1026926
| Sample_series_id | GSE27494
| Sample_data_row_count | 61359
| |
|
GSM679416 | GPL1352 |
|
Disc Cells in 3D IL-1 (95)
|
Disc Cells in 3D IL-1
|
cell type: annulus disc cells
tissue grade: IV
feed media: MEM20 + 10 2 pM
|
|
Sample_geo_accession | GSM679416
| Sample_status | Public on Jun 27 2012
| Sample_submission_date | Feb 24 2011
| Sample_last_update_date | Jun 28 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_growth_protocol_ch1 | Human annulus disc cells (100,000) were seeded into each piece (~0.5 cm3) of a collagen construct (Gelfoam; Pharmacia & Upjohn Co., Kalamazoo, MI). They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each piece of Gelfoam was homongenized and RNA isolated using TRIzol reagent
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labeled cRNA were prepard according to the Affymetrix protocol for IVT labeling.
| Sample_hyb_protocol | Fragmented cRNA was hybridized to the X3P chip in the Affymetrix hybridiztion buffer for 16 hrs at 45oC. X3P chips were washed and labeled in the Affymetrix Fluidics Station.
| Sample_scan_protocol | GeneChips were scanned once via the Affymetrix 3000G scanner.
| Sample_data_processing | The data were analyzed with the GCOS Affymetrix GeneChip Operating System (version 1.2) and Microarray Suite version 5.0 (MAS 5.0). Affymetrix default analysis settings and global scaling as normalization were used. Further normalization was acheived using GC-RMA (robust multiarray average) via GeneSifter analysis software (Viz Labs LLC, Seattle , WA; http://www.genesifter.net).
| Sample_platform_id | GPL1352
| Sample_contact_name | Helen,,Gruber
| Sample_contact_email | Helen.Gruber@carolinashealthcare.org
| Sample_contact_laboratory | Orthopaedic Research
| Sample_contact_department | Orthopaedic Surgery
| Sample_contact_institute | Carolinas HealthCare System
| Sample_contact_address | 1542 Graden Terrace
| Sample_contact_city | Charlotte
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 28203
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM679nnn/GSM679416/suppl/GSM679416.CEL.gz
| Sample_series_id | GSE27494
| Sample_data_row_count | 61359
| |
|
GSM679417 | GPL1352 |
|
Disc Cells in 3D Control (107)
|
Disc Cells in 3D Control
|
cell type: annulus disc cells
tissue grade: IV
feed media: MEM20
|
|
Sample_geo_accession | GSM679417
| Sample_status | Public on Jun 27 2012
| Sample_submission_date | Feb 24 2011
| Sample_last_update_date | Jun 28 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_growth_protocol_ch1 | Human annulus disc cells (100,000) were seeded into each piece (~0.5 cm3) of a collagen construct (Gelfoam; Pharmacia & Upjohn Co., Kalamazoo, MI). They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each piece of Gelfoam was homongenized and RNA isolated using TRIzol reagent
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labeled cRNA were prepard according to the Affymetrix protocol for IVT labeling.
| Sample_hyb_protocol | Fragmented cRNA was hybridized to the X3P chip in the Affymetrix hybridiztion buffer for 16 hrs at 45oC. X3P chips were washed and labeled in the Affymetrix Fluidics Station.
| Sample_scan_protocol | GeneChips were scanned once via the Affymetrix 3000G scanner.
| Sample_data_processing | The data were analyzed with the GCOS Affymetrix GeneChip Operating System (version 1.2) and Microarray Suite version 5.0 (MAS 5.0). Affymetrix default analysis settings and global scaling as normalization were used. Further normalization was acheived using GC-RMA (robust multiarray average) via GeneSifter analysis software (Viz Labs LLC, Seattle , WA; http://www.genesifter.net).
| Sample_platform_id | GPL1352
| Sample_contact_name | Helen,,Gruber
| Sample_contact_email | Helen.Gruber@carolinashealthcare.org
| Sample_contact_laboratory | Orthopaedic Research
| Sample_contact_department | Orthopaedic Surgery
| Sample_contact_institute | Carolinas HealthCare System
| Sample_contact_address | 1542 Graden Terrace
| Sample_contact_city | Charlotte
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 28203
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM679nnn/GSM679417/suppl/GSM679417.CEL.gz
| Sample_series_id | GSE27494
| Sample_data_row_count | 61359
| |
|
GSM679418 | GPL1352 |
|
Disc Cells in 3D IL-1 (107)
|
Disc Cells in 3D IL-1
|
cell type: annulus disc cells
tissue grade: IV
feed media: MEM20 + 10 2 pM
|
|
Sample_geo_accession | GSM679418
| Sample_status | Public on Jun 27 2012
| Sample_submission_date | Feb 24 2011
| Sample_last_update_date | Jun 28 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_growth_protocol_ch1 | Human annulus disc cells (100,000) were seeded into each piece (~0.5 cm3) of a collagen construct (Gelfoam; Pharmacia & Upjohn Co., Kalamazoo, MI). They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each piece of Gelfoam was homongenized and RNA isolated using TRIzol reagent
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labeled cRNA were prepard according to the Affymetrix protocol for IVT labeling.
| Sample_hyb_protocol | Fragmented cRNA was hybridized to the X3P chip in the Affymetrix hybridiztion buffer for 16 hrs at 45oC. X3P chips were washed and labeled in the Affymetrix Fluidics Station.
| Sample_scan_protocol | GeneChips were scanned once via the Affymetrix 3000G scanner.
| Sample_data_processing | The data were analyzed with the GCOS Affymetrix GeneChip Operating System (version 1.2) and Microarray Suite version 5.0 (MAS 5.0). Affymetrix default analysis settings and global scaling as normalization were used. Further normalization was acheived using GC-RMA (robust multiarray average) via GeneSifter analysis software (Viz Labs LLC, Seattle , WA; http://www.genesifter.net).
| Sample_platform_id | GPL1352
| Sample_contact_name | Helen,,Gruber
| Sample_contact_email | Helen.Gruber@carolinashealthcare.org
| Sample_contact_laboratory | Orthopaedic Research
| Sample_contact_department | Orthopaedic Surgery
| Sample_contact_institute | Carolinas HealthCare System
| Sample_contact_address | 1542 Graden Terrace
| Sample_contact_city | Charlotte
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 28203
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM679nnn/GSM679418/suppl/GSM679418.CEL.gz
| Sample_series_id | GSE27494
| Sample_data_row_count | 61359
| |
|
GSM679419 | GPL1352 |
|
Disc Cells in 3D Control (126)
|
Disc Cells in 3D Control
|
cell type: annulus disc cells
tissue grade: III
feed media: MEM20
|
|
Sample_geo_accession | GSM679419
| Sample_status | Public on Jun 27 2012
| Sample_submission_date | Feb 24 2011
| Sample_last_update_date | Oct 28 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_growth_protocol_ch1 | Human annulus disc cells (100,000) were seeded into each piece (~0.5 cm3) of a collagen construct (Gelfoam; Pharmacia & Upjohn Co., Kalamazoo, MI). They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each piece of Gelfoam was homongenized and RNA isolated using TRIzol reagent
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labeled cRNA were prepard according to the Affymetrix protocol for IVT labeling.
| Sample_hyb_protocol | Fragmented cRNA was hybridized to the X3P chip in the Affymetrix hybridiztion buffer for 16 hrs at 45oC. X3P chips were washed and labeled in the Affymetrix Fluidics Station.
| Sample_scan_protocol | GeneChips were scanned once via the Affymetrix 3000G scanner.
| Sample_data_processing | The data were analyzed with the GCOS Affymetrix GeneChip Operating System (version 1.2) and Microarray Suite version 5.0 (MAS 5.0). Affymetrix default analysis settings and global scaling as normalization were used. Further normalization was acheived using GC-RMA (robust multiarray average) via GeneSifter analysis software (Viz Labs LLC, Seattle , WA; http://www.genesifter.net).
| Sample_platform_id | GPL1352
| Sample_contact_name | Helen,,Gruber
| Sample_contact_email | Helen.Gruber@carolinashealthcare.org
| Sample_contact_laboratory | Orthopaedic Research
| Sample_contact_department | Orthopaedic Surgery
| Sample_contact_institute | Carolinas HealthCare System
| Sample_contact_address | 1542 Graden Terrace
| Sample_contact_city | Charlotte
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 28203
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM679nnn/GSM679419/suppl/GSM679419.CEL.gz
| Sample_relation | Reanalyzed by: GSM1026928
| Sample_series_id | GSE27494
| Sample_data_row_count | 61359
| |
|
GSM679420 | GPL1352 |
|
Disc Cells in 3D IL-1 (126)
|
Disc Cells in 3D IL-1
|
cell type: annulus disc cells
tissue grade: III
feed media: MEM20 + 10 2 pM
|
|
Sample_geo_accession | GSM679420
| Sample_status | Public on Jun 27 2012
| Sample_submission_date | Feb 24 2011
| Sample_last_update_date | Jun 28 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_growth_protocol_ch1 | Human annulus disc cells (100,000) were seeded into each piece (~0.5 cm3) of a collagen construct (Gelfoam; Pharmacia & Upjohn Co., Kalamazoo, MI). They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each piece of Gelfoam was homongenized and RNA isolated using TRIzol reagent
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labeled cRNA were prepard according to the Affymetrix protocol for IVT labeling.
| Sample_hyb_protocol | Fragmented cRNA was hybridized to the X3P chip in the Affymetrix hybridiztion buffer for 16 hrs at 45oC. X3P chips were washed and labeled in the Affymetrix Fluidics Station.
| Sample_scan_protocol | GeneChips were scanned once via the Affymetrix 3000G scanner.
| Sample_data_processing | The data were analyzed with the GCOS Affymetrix GeneChip Operating System (version 1.2) and Microarray Suite version 5.0 (MAS 5.0). Affymetrix default analysis settings and global scaling as normalization were used. Further normalization was acheived using GC-RMA (robust multiarray average) via GeneSifter analysis software (Viz Labs LLC, Seattle , WA; http://www.genesifter.net).
| Sample_platform_id | GPL1352
| Sample_contact_name | Helen,,Gruber
| Sample_contact_email | Helen.Gruber@carolinashealthcare.org
| Sample_contact_laboratory | Orthopaedic Research
| Sample_contact_department | Orthopaedic Surgery
| Sample_contact_institute | Carolinas HealthCare System
| Sample_contact_address | 1542 Graden Terrace
| Sample_contact_city | Charlotte
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 28203
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM679nnn/GSM679420/suppl/GSM679420.CEL.gz
| Sample_series_id | GSE27494
| Sample_data_row_count | 61359
| |
|
GSM679421 | GPL1352 |
|
Disc Cells in 3D Control (154)
|
Disc Cells in 3D Control
|
cell type: annulus disc cells
tissue grade: IV
feed media: MEM20
|
|
Sample_geo_accession | GSM679421
| Sample_status | Public on Jun 27 2012
| Sample_submission_date | Feb 24 2011
| Sample_last_update_date | Oct 28 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_growth_protocol_ch1 | Human annulus disc cells (100,000) were seeded into each piece (~0.5 cm3) of a collagen construct (Gelfoam; Pharmacia & Upjohn Co., Kalamazoo, MI). They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each piece of Gelfoam was homongenized and RNA isolated using TRIzol reagent
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labeled cRNA were prepard according to the Affymetrix protocol for IVT labeling.
| Sample_hyb_protocol | Fragmented cRNA was hybridized to the X3P chip in the Affymetrix hybridiztion buffer for 16 hrs at 45oC. X3P chips were washed and labeled in the Affymetrix Fluidics Station.
| Sample_scan_protocol | GeneChips were scanned once via the Affymetrix 3000G scanner.
| Sample_data_processing | The data were analyzed with the GCOS Affymetrix GeneChip Operating System (version 1.2) and Microarray Suite version 5.0 (MAS 5.0). Affymetrix default analysis settings and global scaling as normalization were used. Further normalization was acheived using GC-RMA (robust multiarray average) via GeneSifter analysis software (Viz Labs LLC, Seattle , WA; http://www.genesifter.net).
| Sample_platform_id | GPL1352
| Sample_contact_name | Helen,,Gruber
| Sample_contact_email | Helen.Gruber@carolinashealthcare.org
| Sample_contact_laboratory | Orthopaedic Research
| Sample_contact_department | Orthopaedic Surgery
| Sample_contact_institute | Carolinas HealthCare System
| Sample_contact_address | 1542 Graden Terrace
| Sample_contact_city | Charlotte
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 28203
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM679nnn/GSM679421/suppl/GSM679421.CEL.gz
| Sample_relation | Reanalyzed by: GSM1026930
| Sample_series_id | GSE27494
| Sample_data_row_count | 61359
| |
|
GSM679422 | GPL1352 |
|
Disc Cells in 3D IL-1 (154)
|
Disc Cells in 3D IL-1
|
cell type: annulus disc cells
tissue grade: IV
feed media: MEM20 + 10 2 pM
|
|
Sample_geo_accession | GSM679422
| Sample_status | Public on Jun 27 2012
| Sample_submission_date | Feb 24 2011
| Sample_last_update_date | Jun 28 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_treatment_protocol_ch1 | They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_growth_protocol_ch1 | Human annulus disc cells (100,000) were seeded into each piece (~0.5 cm3) of a collagen construct (Gelfoam; Pharmacia & Upjohn Co., Kalamazoo, MI). They were fed 3 times per week for 9 days with minimal essential medium with 20% fetal bovine serum (MEM20) +/- 102 pM IL-1beta. Cells were allowed to grow an additional 5 days without changing the media.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Each piece of Gelfoam was homongenized and RNA isolated using TRIzol reagent
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Biotin-labeled cRNA were prepard according to the Affymetrix protocol for IVT labeling.
| Sample_hyb_protocol | Fragmented cRNA was hybridized to the X3P chip in the Affymetrix hybridiztion buffer for 16 hrs at 45oC. X3P chips were washed and labeled in the Affymetrix Fluidics Station.
| Sample_scan_protocol | GeneChips were scanned once via the Affymetrix 3000G scanner.
| Sample_data_processing | The data were analyzed with the GCOS Affymetrix GeneChip Operating System (version 1.2) and Microarray Suite version 5.0 (MAS 5.0). Affymetrix default analysis settings and global scaling as normalization were used. Further normalization was acheived using GC-RMA (robust multiarray average) via GeneSifter analysis software (Viz Labs LLC, Seattle , WA; http://www.genesifter.net).
| Sample_platform_id | GPL1352
| Sample_contact_name | Helen,,Gruber
| Sample_contact_email | Helen.Gruber@carolinashealthcare.org
| Sample_contact_laboratory | Orthopaedic Research
| Sample_contact_department | Orthopaedic Surgery
| Sample_contact_institute | Carolinas HealthCare System
| Sample_contact_address | 1542 Graden Terrace
| Sample_contact_city | Charlotte
| Sample_contact_state | NC
| Sample_contact_zip/postal_code | 28203
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM679nnn/GSM679422/suppl/GSM679422.CEL.gz
| Sample_series_id | GSE27494
| Sample_data_row_count | 61359
| |
|
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