Search results for the GEO ID: GSE41635 |
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GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM1020604 | GPL570 |
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MCF-7 breast cancer cell line, Control clones, 3D
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Human MCF-7 breast cancer cell line, control clones in three dimension
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cell line: MCF-7
genotype: control
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Gene expression data from MCF-7 breast cancer cell line, control clones in three dimension
|
Sample_geo_accession | GSM1020604
| Sample_status | Public on Oct 17 2012
| Sample_submission_date | Oct 16 2012
| Sample_last_update_date | Oct 17 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_growth_protocol_ch1 | MCF-7-Ctrl1, MCF-7-Ctrl2, MCF-7-ALK1 and MCF-7-ALK2 cells are plated into ultra-low adherence culture plates (Corning Co-Star, Tewksbury, MA) in serum-free mammary epithelial growth medium (MEBM, Lonza/Clonetics) supplemented with B27 (Invitrogen/Life Technologies Grand Island, NY), 20 ng/ml epidermal growth factor (EGF), 40 ng/ml bFGF (BD Biosciences, San Jose, CA), 4 mg/ml heparin (Sigma-Aldrich, St. Louis, MO) L-glutamine, and 100 U/ml penicillin and streptomycin. These culture conditions support self-renewal as well as formation and propagation of cells as 3 dimensional tumor spheroids.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA from 3 dimensional tumor spheroids of MCF-7-Ctrl1, MCF-Ctrl2, MCF-7-ALK1 and MCF-7-ALK2 cells was isolated using TRIzol® reagent (Invitrogen/Life Technologies Grand Island, NY), and the quality of the RNA was determined using a Nanodrop 2000 instrument (Thermo Fisher Scientific, Hanover Park, IL).
| Sample_label_ch1 | N/A
| Sample_label_protocol_ch1 | Using GeneChip® One-Cycle cDNA Synthesis Kit (Affymetrix, Santa Clara, CA), total RNA was reverse transcripted to cDNA and synthesized to cRNA using the GeneChip® IVT Labeling kit (Affymetrix) and biotin labeled.
| Sample_hyb_protocol | The cRNA was then purified using a GeneChip® Sample Cleanup Module Kit (Affymetrix) and fragmented before hybridization. Then, hybridization cocktail containing the fragmented target cRNAs and probe array controls using the GeneChip® Hybridization Control Kit (Affymetrix) was hybridized to probe array.
| Sample_scan_protocol | The arrays were washed and stained according to protocol and scanned using the GeneChip® Scanner 3000 (Affymetrix).
| Sample_data_processing | The data were analyzed with using DNA-Chip Analyzer software (dChip; Harvard School of Public Health, Boston, MA) using Affymetrix default analysis settings and global scaling as normalization method. dChipVersion=dChip (DNA-Chip Analyzer), Build date: Dec 17 2010.
| Sample_platform_id | GPL570
| Sample_contact_name | Annie,Z,Luo
| Sample_contact_email | azluo@mdanderson.org
| Sample_contact_phone | 713-745-5516
| Sample_contact_fax | 713-745-9231
| Sample_contact_laboratory | Dr. Robertson
| Sample_contact_department | Experimental Therapeutics
| Sample_contact_institute | M D Anderson Cancer Center
| Sample_contact_address | 1901 East Road 4SCR3.1004
| Sample_contact_city | Houston
| Sample_contact_state | Texas
| Sample_contact_zip/postal_code | 77230-1429
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1020nnn/GSM1020604/suppl/GSM1020604_MCF-7-Ctr_3D.dcp.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1020nnn/GSM1020604/suppl/GSM1020604_MCF_7_Ctr_3D.CEL.gz
| Sample_series_id | GSE41635
| Sample_data_row_count | 54675
| |
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GSM1020605 | GPL570 |
|
MCF-7 breast cancer cell line, Control clones, 3D, 2nd sample
|
Human MCF-7 breast cancer cell line, control clones in three dimension
|
cell line: MCF-7
genotype: control
|
Gene expression data from MCF-7 breast cancer cell line, control clones in three dimension
|
Sample_geo_accession | GSM1020605
| Sample_status | Public on Oct 17 2012
| Sample_submission_date | Oct 16 2012
| Sample_last_update_date | Oct 17 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_growth_protocol_ch1 | MCF-7-Ctrl1, MCF-7-Ctrl2, MCF-7-ALK1 and MCF-7-ALK2 cells are plated into ultra-low adherence culture plates (Corning Co-Star, Tewksbury, MA) in serum-free mammary epithelial growth medium (MEBM, Lonza/Clonetics) supplemented with B27 (Invitrogen/Life Technologies Grand Island, NY), 20 ng/ml epidermal growth factor (EGF), 40 ng/ml bFGF (BD Biosciences, San Jose, CA), 4 mg/ml heparin (Sigma-Aldrich, St. Louis, MO) L-glutamine, and 100 U/ml penicillin and streptomycin. These culture conditions support self-renewal as well as formation and propagation of cells as 3 dimensional tumor spheroids.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA from 3 dimensional tumor spheroids of MCF-7-Ctrl1, MCF-Ctrl2, MCF-7-ALK1 and MCF-7-ALK2 cells was isolated using TRIzol® reagent (Invitrogen/Life Technologies Grand Island, NY), and the quality of the RNA was determined using a Nanodrop 2000 instrument (Thermo Fisher Scientific, Hanover Park, IL).
| Sample_label_ch1 | N/A
| Sample_label_protocol_ch1 | Using GeneChip® One-Cycle cDNA Synthesis Kit (Affymetrix, Santa Clara, CA), total RNA was reverse transcripted to cDNA and synthesized to cRNA using the GeneChip® IVT Labeling kit (Affymetrix) and biotin labeled.
| Sample_hyb_protocol | The cRNA was then purified using a GeneChip® Sample Cleanup Module Kit (Affymetrix) and fragmented before hybridization. Then, hybridization cocktail containing the fragmented target cRNAs and probe array controls using the GeneChip® Hybridization Control Kit (Affymetrix) was hybridized to probe array.
| Sample_scan_protocol | The arrays were washed and stained according to protocol and scanned using the GeneChip® Scanner 3000 (Affymetrix).
| Sample_data_processing | The data were analyzed with using DNA-Chip Analyzer software (dChip; Harvard School of Public Health, Boston, MA) using Affymetrix default analysis settings and global scaling as normalization method. dChipVersion=dChip (DNA-Chip Analyzer), Build date: Dec 17 2010.
| Sample_platform_id | GPL570
| Sample_contact_name | Annie,Z,Luo
| Sample_contact_email | azluo@mdanderson.org
| Sample_contact_phone | 713-745-5516
| Sample_contact_fax | 713-745-9231
| Sample_contact_laboratory | Dr. Robertson
| Sample_contact_department | Experimental Therapeutics
| Sample_contact_institute | M D Anderson Cancer Center
| Sample_contact_address | 1901 East Road 4SCR3.1004
| Sample_contact_city | Houston
| Sample_contact_state | Texas
| Sample_contact_zip/postal_code | 77230-1429
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1020nnn/GSM1020605/suppl/GSM1020605_MCF-7-Ctr_3D_2_.dcp.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1020nnn/GSM1020605/suppl/GSM1020605_MCF_7_Ctr_3D_2_.CEL.gz
| Sample_series_id | GSE41635
| Sample_data_row_count | 54675
| |
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GSM1020606 | GPL570 |
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MCF-7 breast cancer cell line, ALK over-expressed clones, 3D
|
Human MCF-7 breast cancer cell line, ALK over-expressed clones in three dimension
|
cell line: MCF-7
genotype: ALK over-expressed clone
|
Gene expression data from MCF-7 breast cancer cell line, ALK over-expressed clones in three dimension
|
Sample_geo_accession | GSM1020606
| Sample_status | Public on Oct 17 2012
| Sample_submission_date | Oct 16 2012
| Sample_last_update_date | Oct 17 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_growth_protocol_ch1 | MCF-7-Ctrl1, MCF-7-Ctrl2, MCF-7-ALK1 and MCF-7-ALK2 cells are plated into ultra-low adherence culture plates (Corning Co-Star, Tewksbury, MA) in serum-free mammary epithelial growth medium (MEBM, Lonza/Clonetics) supplemented with B27 (Invitrogen/Life Technologies Grand Island, NY), 20 ng/ml epidermal growth factor (EGF), 40 ng/ml bFGF (BD Biosciences, San Jose, CA), 4 mg/ml heparin (Sigma-Aldrich, St. Louis, MO) L-glutamine, and 100 U/ml penicillin and streptomycin. These culture conditions support self-renewal as well as formation and propagation of cells as 3 dimensional tumor spheroids.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA from 3 dimensional tumor spheroids of MCF-7-Ctrl1, MCF-Ctrl2, MCF-7-ALK1 and MCF-7-ALK2 cells was isolated using TRIzol® reagent (Invitrogen/Life Technologies Grand Island, NY), and the quality of the RNA was determined using a Nanodrop 2000 instrument (Thermo Fisher Scientific, Hanover Park, IL).
| Sample_label_ch1 | N/A
| Sample_label_protocol_ch1 | Using GeneChip® One-Cycle cDNA Synthesis Kit (Affymetrix, Santa Clara, CA), total RNA was reverse transcripted to cDNA and synthesized to cRNA using the GeneChip® IVT Labeling kit (Affymetrix) and biotin labeled.
| Sample_hyb_protocol | The cRNA was then purified using a GeneChip® Sample Cleanup Module Kit (Affymetrix) and fragmented before hybridization. Then, hybridization cocktail containing the fragmented target cRNAs and probe array controls using the GeneChip® Hybridization Control Kit (Affymetrix) was hybridized to probe array.
| Sample_scan_protocol | The arrays were washed and stained according to protocol and scanned using the GeneChip® Scanner 3000 (Affymetrix).
| Sample_data_processing | The data were analyzed with using DNA-Chip Analyzer software (dChip; Harvard School of Public Health, Boston, MA) using Affymetrix default analysis settings and global scaling as normalization method. dChipVersion=dChip (DNA-Chip Analyzer), Build date: Dec 17 2010.
| Sample_platform_id | GPL570
| Sample_contact_name | Annie,Z,Luo
| Sample_contact_email | azluo@mdanderson.org
| Sample_contact_phone | 713-745-5516
| Sample_contact_fax | 713-745-9231
| Sample_contact_laboratory | Dr. Robertson
| Sample_contact_department | Experimental Therapeutics
| Sample_contact_institute | M D Anderson Cancer Center
| Sample_contact_address | 1901 East Road 4SCR3.1004
| Sample_contact_city | Houston
| Sample_contact_state | Texas
| Sample_contact_zip/postal_code | 77230-1429
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1020nnn/GSM1020606/suppl/GSM1020606_MCF-7-ALK_3D.dcp.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1020nnn/GSM1020606/suppl/GSM1020606_MCF_7_ALK_3D.CEL.gz
| Sample_series_id | GSE41635
| Sample_data_row_count | 54675
| |
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GSM1020607 | GPL570 |
|
MCF-7 breast cancer cell line, ALK over-expressed clones, 3D, 2nd sample
|
Human MCF-7 breast cancer cell line, ALK over-expressed clones in three dimension
|
cell line: MCF-7
genotype: ALK over-expressed clone
|
Gene expression data from MCF-7 breast cancer cell line, ALK over-expressed clones in three dimension
|
Sample_geo_accession | GSM1020607
| Sample_status | Public on Oct 17 2012
| Sample_submission_date | Oct 16 2012
| Sample_last_update_date | Oct 17 2012
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Homo sapiens
| Sample_taxid_ch1 | 9606
| Sample_growth_protocol_ch1 | MCF-7-Ctrl1, MCF-7-Ctrl2, MCF-7-ALK1 and MCF-7-ALK2 cells are plated into ultra-low adherence culture plates (Corning Co-Star, Tewksbury, MA) in serum-free mammary epithelial growth medium (MEBM, Lonza/Clonetics) supplemented with B27 (Invitrogen/Life Technologies Grand Island, NY), 20 ng/ml epidermal growth factor (EGF), 40 ng/ml bFGF (BD Biosciences, San Jose, CA), 4 mg/ml heparin (Sigma-Aldrich, St. Louis, MO) L-glutamine, and 100 U/ml penicillin and streptomycin. These culture conditions support self-renewal as well as formation and propagation of cells as 3 dimensional tumor spheroids.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Total RNA from 3 dimensional tumor spheroids of MCF-7-Ctrl1, MCF-Ctrl2, MCF-7-ALK1 and MCF-7-ALK2 cells was isolated using TRIzol® reagent (Invitrogen/Life Technologies Grand Island, NY), and the quality of the RNA was determined using a Nanodrop 2000 instrument (Thermo Fisher Scientific, Hanover Park, IL).
| Sample_label_ch1 | N/A
| Sample_label_protocol_ch1 | Using GeneChip® One-Cycle cDNA Synthesis Kit (Affymetrix, Santa Clara, CA), total RNA was reverse transcripted to cDNA and synthesized to cRNA using the GeneChip® IVT Labeling kit (Affymetrix) and biotin labeled.
| Sample_hyb_protocol | The cRNA was then purified using a GeneChip® Sample Cleanup Module Kit (Affymetrix) and fragmented before hybridization. Then, hybridization cocktail containing the fragmented target cRNAs and probe array controls using the GeneChip® Hybridization Control Kit (Affymetrix) was hybridized to probe array.
| Sample_scan_protocol | The arrays were washed and stained according to protocol and scanned using the GeneChip® Scanner 3000 (Affymetrix).
| Sample_data_processing | The data were analyzed with using DNA-Chip Analyzer software (dChip; Harvard School of Public Health, Boston, MA) using Affymetrix default analysis settings and global scaling as normalization method. dChipVersion=dChip (DNA-Chip Analyzer), Build date: Dec 17 2010.
| Sample_platform_id | GPL570
| Sample_contact_name | Annie,Z,Luo
| Sample_contact_email | azluo@mdanderson.org
| Sample_contact_phone | 713-745-5516
| Sample_contact_fax | 713-745-9231
| Sample_contact_laboratory | Dr. Robertson
| Sample_contact_department | Experimental Therapeutics
| Sample_contact_institute | M D Anderson Cancer Center
| Sample_contact_address | 1901 East Road 4SCR3.1004
| Sample_contact_city | Houston
| Sample_contact_state | Texas
| Sample_contact_zip/postal_code | 77230-1429
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1020nnn/GSM1020607/suppl/GSM1020607_MCF-7-ALK_3D_2_.dcp.gz
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM1020nnn/GSM1020607/suppl/GSM1020607_MCF_7_ALK_3D_2_.CEL.gz
| Sample_series_id | GSE41635
| Sample_data_row_count | 54675
| |
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