Search results for the GEO ID: GSE31678 |
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|
GSM ID | GPL ID |
Select for analysis |
Title |
Source name |
Description |
Characteristics |
GSM786342 | GPL1355 |
|
Control - NV, biological rep 1
|
Rat Lung - dorsal caudal quadrant
|
strain: Sprague-Dawley
condition: Non-ventilated
gender: Male
|
|
Sample_geo_accession | GSM786342
| Sample_status | Public on Aug 27 2011
| Sample_submission_date | Aug 26 2011
| Sample_last_update_date | Aug 27 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Male Harlan Sprague-Dawley rats (340~400 g; Indianapolis, IN) were anesthetized and a tracheotomy and jugular cannulation performed. High Vt ventilation (HVt; 18 ml/Kg, RR 40 breaths/min, PEEP 0 cmH2O), in either the prone or supine position (PPV or SPV, respectively) was administered for up to 3 hours. Non-ventilated rats were used as controls.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Microarray targets were prepared and labeled from 300 ng total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin,TX) following the manufacturer’s instructions.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures, using the Affy GCS3000
| Sample_data_processing | Hybridization intensities were quantified and normalized across all arrays using GC-RMA as implemented by Partek Genomics Suite v6.5 software (St.Louis, MO). Non-expressed transcripts were eliminated if all values for a transcript were below background levels of expression (calculated at 3.5 log2 expression units). The remaining ‘present’ transcripts (20,242 of 31,099) were used for all subsequent statistical and visual analysis.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,,Edwards
| Sample_contact_email | michael.edwards@ucdenver.edu
| Sample_contact_phone | 303-724-6054
| Sample_contact_fax | 303-724-6042
| Sample_contact_department | Pulmonary
| Sample_contact_institute | UC Denver
| Sample_contact_address | 12700 East 19th Avenue, Box C272
| Sample_contact_city | Aurora
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80045
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM786nnn/GSM786342/suppl/GSM786342_Rat_Control_NV_R1.CEL.gz
| Sample_series_id | GSE31678
| Sample_data_row_count | 20242
| |
|
GSM786343 | GPL1355 |
|
Control - NV, biological rep 2
|
Rat Lung - dorsal caudal quadrant
|
strain: Sprague-Dawley
condition: Non-ventilated
gender: Male
|
|
Sample_geo_accession | GSM786343
| Sample_status | Public on Aug 27 2011
| Sample_submission_date | Aug 26 2011
| Sample_last_update_date | Aug 27 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Male Harlan Sprague-Dawley rats (340~400 g; Indianapolis, IN) were anesthetized and a tracheotomy and jugular cannulation performed. High Vt ventilation (HVt; 18 ml/Kg, RR 40 breaths/min, PEEP 0 cmH2O), in either the prone or supine position (PPV or SPV, respectively) was administered for up to 3 hours. Non-ventilated rats were used as controls.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Microarray targets were prepared and labeled from 300 ng total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin,TX) following the manufacturer’s instructions.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures, using the Affy GCS3000
| Sample_data_processing | Hybridization intensities were quantified and normalized across all arrays using GC-RMA as implemented by Partek Genomics Suite v6.5 software (St.Louis, MO). Non-expressed transcripts were eliminated if all values for a transcript were below background levels of expression (calculated at 3.5 log2 expression units). The remaining ‘present’ transcripts (20,242 of 31,099) were used for all subsequent statistical and visual analysis.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,,Edwards
| Sample_contact_email | michael.edwards@ucdenver.edu
| Sample_contact_phone | 303-724-6054
| Sample_contact_fax | 303-724-6042
| Sample_contact_department | Pulmonary
| Sample_contact_institute | UC Denver
| Sample_contact_address | 12700 East 19th Avenue, Box C272
| Sample_contact_city | Aurora
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80045
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM786nnn/GSM786343/suppl/GSM786343_Rat_Control_NV_R2.CEL.gz
| Sample_series_id | GSE31678
| Sample_data_row_count | 20242
| |
|
GSM786344 | GPL1355 |
|
Prone - HVt, biological rep 1
|
Rat Lung - dorsal caudal quadrant
|
strain: Sprague-Dawley
condition: High Vt
body position: Prone
gender: Male
|
|
Sample_geo_accession | GSM786344
| Sample_status | Public on Aug 27 2011
| Sample_submission_date | Aug 26 2011
| Sample_last_update_date | Aug 27 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Male Harlan Sprague-Dawley rats (340~400 g; Indianapolis, IN) were anesthetized and a tracheotomy and jugular cannulation performed. High Vt ventilation (HVt; 18 ml/Kg, RR 40 breaths/min, PEEP 0 cmH2O), in either the prone or supine position (PPV or SPV, respectively) was administered for up to 3 hours. Non-ventilated rats were used as controls.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Microarray targets were prepared and labeled from 300 ng total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin,TX) following the manufacturer’s instructions.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures, using the Affy GCS3000
| Sample_data_processing | Hybridization intensities were quantified and normalized across all arrays using GC-RMA as implemented by Partek Genomics Suite v6.5 software (St.Louis, MO). Non-expressed transcripts were eliminated if all values for a transcript were below background levels of expression (calculated at 3.5 log2 expression units). The remaining ‘present’ transcripts (20,242 of 31,099) were used for all subsequent statistical and visual analysis.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,,Edwards
| Sample_contact_email | michael.edwards@ucdenver.edu
| Sample_contact_phone | 303-724-6054
| Sample_contact_fax | 303-724-6042
| Sample_contact_department | Pulmonary
| Sample_contact_institute | UC Denver
| Sample_contact_address | 12700 East 19th Avenue, Box C272
| Sample_contact_city | Aurora
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80045
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM786nnn/GSM786344/suppl/GSM786344_Rat_Prone_HVt_R1.CEL.gz
| Sample_series_id | GSE31678
| Sample_data_row_count | 20242
| |
|
GSM786345 | GPL1355 |
|
Prone - HVt, biological rep 2
|
Rat Lung - dorsal caudal quadrant
|
strain: Sprague-Dawley
condition: High Vt
body position: Prone
gender: Male
|
|
Sample_geo_accession | GSM786345
| Sample_status | Public on Aug 27 2011
| Sample_submission_date | Aug 26 2011
| Sample_last_update_date | Aug 27 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Male Harlan Sprague-Dawley rats (340~400 g; Indianapolis, IN) were anesthetized and a tracheotomy and jugular cannulation performed. High Vt ventilation (HVt; 18 ml/Kg, RR 40 breaths/min, PEEP 0 cmH2O), in either the prone or supine position (PPV or SPV, respectively) was administered for up to 3 hours. Non-ventilated rats were used as controls.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Microarray targets were prepared and labeled from 300 ng total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin,TX) following the manufacturer’s instructions.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures, using the Affy GCS3000
| Sample_data_processing | Hybridization intensities were quantified and normalized across all arrays using GC-RMA as implemented by Partek Genomics Suite v6.5 software (St.Louis, MO). Non-expressed transcripts were eliminated if all values for a transcript were below background levels of expression (calculated at 3.5 log2 expression units). The remaining ‘present’ transcripts (20,242 of 31,099) were used for all subsequent statistical and visual analysis.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,,Edwards
| Sample_contact_email | michael.edwards@ucdenver.edu
| Sample_contact_phone | 303-724-6054
| Sample_contact_fax | 303-724-6042
| Sample_contact_department | Pulmonary
| Sample_contact_institute | UC Denver
| Sample_contact_address | 12700 East 19th Avenue, Box C272
| Sample_contact_city | Aurora
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80045
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM786nnn/GSM786345/suppl/GSM786345_Rat_Prone_HVt_R2.CEL.gz
| Sample_series_id | GSE31678
| Sample_data_row_count | 20242
| |
|
GSM786346 | GPL1355 |
|
Prone - HVt, biological rep 3
|
Rat Lung - dorsal caudal quadrant
|
strain: Sprague-Dawley
condition: High Vt
body position: Prone
gender: Male
|
|
Sample_geo_accession | GSM786346
| Sample_status | Public on Aug 27 2011
| Sample_submission_date | Aug 26 2011
| Sample_last_update_date | Aug 27 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Male Harlan Sprague-Dawley rats (340~400 g; Indianapolis, IN) were anesthetized and a tracheotomy and jugular cannulation performed. High Vt ventilation (HVt; 18 ml/Kg, RR 40 breaths/min, PEEP 0 cmH2O), in either the prone or supine position (PPV or SPV, respectively) was administered for up to 3 hours. Non-ventilated rats were used as controls.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Microarray targets were prepared and labeled from 300 ng total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin,TX) following the manufacturer’s instructions.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures, using the Affy GCS3000
| Sample_data_processing | Hybridization intensities were quantified and normalized across all arrays using GC-RMA as implemented by Partek Genomics Suite v6.5 software (St.Louis, MO). Non-expressed transcripts were eliminated if all values for a transcript were below background levels of expression (calculated at 3.5 log2 expression units). The remaining ‘present’ transcripts (20,242 of 31,099) were used for all subsequent statistical and visual analysis.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,,Edwards
| Sample_contact_email | michael.edwards@ucdenver.edu
| Sample_contact_phone | 303-724-6054
| Sample_contact_fax | 303-724-6042
| Sample_contact_department | Pulmonary
| Sample_contact_institute | UC Denver
| Sample_contact_address | 12700 East 19th Avenue, Box C272
| Sample_contact_city | Aurora
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80045
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM786nnn/GSM786346/suppl/GSM786346_Rat_Prone_HVt_R3.CEL.gz
| Sample_series_id | GSE31678
| Sample_data_row_count | 20242
| |
|
GSM786347 | GPL1355 |
|
Supine - SVt, biological rep 1
|
Rat Lung - dorsal caudal quadrant
|
strain: Sprague-Dawley
condition: High Vt
body position: Supine
gender: Male
|
|
Sample_geo_accession | GSM786347
| Sample_status | Public on Aug 27 2011
| Sample_submission_date | Aug 26 2011
| Sample_last_update_date | Aug 27 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Male Harlan Sprague-Dawley rats (340~400 g; Indianapolis, IN) were anesthetized and a tracheotomy and jugular cannulation performed. High Vt ventilation (HVt; 18 ml/Kg, RR 40 breaths/min, PEEP 0 cmH2O), in either the prone or supine position (PPV or SPV, respectively) was administered for up to 3 hours. Non-ventilated rats were used as controls.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Microarray targets were prepared and labeled from 300 ng total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin,TX) following the manufacturer’s instructions.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures, using the Affy GCS3000
| Sample_data_processing | Hybridization intensities were quantified and normalized across all arrays using GC-RMA as implemented by Partek Genomics Suite v6.5 software (St.Louis, MO). Non-expressed transcripts were eliminated if all values for a transcript were below background levels of expression (calculated at 3.5 log2 expression units). The remaining ‘present’ transcripts (20,242 of 31,099) were used for all subsequent statistical and visual analysis.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,,Edwards
| Sample_contact_email | michael.edwards@ucdenver.edu
| Sample_contact_phone | 303-724-6054
| Sample_contact_fax | 303-724-6042
| Sample_contact_department | Pulmonary
| Sample_contact_institute | UC Denver
| Sample_contact_address | 12700 East 19th Avenue, Box C272
| Sample_contact_city | Aurora
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80045
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM786nnn/GSM786347/suppl/GSM786347_Rat_Supine_HVt_R1.CEL.gz
| Sample_series_id | GSE31678
| Sample_data_row_count | 20242
| |
|
GSM786348 | GPL1355 |
|
Supine - SVt, biological rep 2
|
Rat Lung - dorsal caudal quadrant
|
strain: Sprague-Dawley
condition: High Vt
body position: Supine
gender: Male
|
|
Sample_geo_accession | GSM786348
| Sample_status | Public on Aug 27 2011
| Sample_submission_date | Aug 26 2011
| Sample_last_update_date | Aug 27 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Male Harlan Sprague-Dawley rats (340~400 g; Indianapolis, IN) were anesthetized and a tracheotomy and jugular cannulation performed. High Vt ventilation (HVt; 18 ml/Kg, RR 40 breaths/min, PEEP 0 cmH2O), in either the prone or supine position (PPV or SPV, respectively) was administered for up to 3 hours. Non-ventilated rats were used as controls.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Microarray targets were prepared and labeled from 300 ng total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin,TX) following the manufacturer’s instructions.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures, using the Affy GCS3000
| Sample_data_processing | Hybridization intensities were quantified and normalized across all arrays using GC-RMA as implemented by Partek Genomics Suite v6.5 software (St.Louis, MO). Non-expressed transcripts were eliminated if all values for a transcript were below background levels of expression (calculated at 3.5 log2 expression units). The remaining ‘present’ transcripts (20,242 of 31,099) were used for all subsequent statistical and visual analysis.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,,Edwards
| Sample_contact_email | michael.edwards@ucdenver.edu
| Sample_contact_phone | 303-724-6054
| Sample_contact_fax | 303-724-6042
| Sample_contact_department | Pulmonary
| Sample_contact_institute | UC Denver
| Sample_contact_address | 12700 East 19th Avenue, Box C272
| Sample_contact_city | Aurora
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80045
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM786nnn/GSM786348/suppl/GSM786348_Rat_Supine_HVt_R2.CEL.gz
| Sample_series_id | GSE31678
| Sample_data_row_count | 20242
| |
|
GSM786349 | GPL1355 |
|
Supine - SVt, biological rep 3
|
Rat Lung - dorsal caudal quadrant
|
strain: Sprague-Dawley
condition: High Vt
body position: Supine
gender: Male
|
|
Sample_geo_accession | GSM786349
| Sample_status | Public on Aug 27 2011
| Sample_submission_date | Aug 26 2011
| Sample_last_update_date | Aug 27 2011
| Sample_type | RNA
| Sample_channel_count | 1
| Sample_organism_ch1 | Rattus norvegicus
| Sample_taxid_ch1 | 10116
| Sample_treatment_protocol_ch1 | Male Harlan Sprague-Dawley rats (340~400 g; Indianapolis, IN) were anesthetized and a tracheotomy and jugular cannulation performed. High Vt ventilation (HVt; 18 ml/Kg, RR 40 breaths/min, PEEP 0 cmH2O), in either the prone or supine position (PPV or SPV, respectively) was administered for up to 3 hours. Non-ventilated rats were used as controls.
| Sample_molecule_ch1 | total RNA
| Sample_extract_protocol_ch1 | Trizol extraction of total RNA was performed according to the manufacturer's instructions.
| Sample_label_ch1 | biotin
| Sample_label_protocol_ch1 | Microarray targets were prepared and labeled from 300 ng total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin,TX) following the manufacturer’s instructions.
| Sample_hyb_protocol | standard Affymetrix procedures
| Sample_scan_protocol | standard Affymetrix procedures, using the Affy GCS3000
| Sample_data_processing | Hybridization intensities were quantified and normalized across all arrays using GC-RMA as implemented by Partek Genomics Suite v6.5 software (St.Louis, MO). Non-expressed transcripts were eliminated if all values for a transcript were below background levels of expression (calculated at 3.5 log2 expression units). The remaining ‘present’ transcripts (20,242 of 31,099) were used for all subsequent statistical and visual analysis.
| Sample_platform_id | GPL1355
| Sample_contact_name | Michael,,Edwards
| Sample_contact_email | michael.edwards@ucdenver.edu
| Sample_contact_phone | 303-724-6054
| Sample_contact_fax | 303-724-6042
| Sample_contact_department | Pulmonary
| Sample_contact_institute | UC Denver
| Sample_contact_address | 12700 East 19th Avenue, Box C272
| Sample_contact_city | Aurora
| Sample_contact_state | CO
| Sample_contact_zip/postal_code | 80045
| Sample_contact_country | USA
| Sample_supplementary_file | ftp://ftp.ncbi.nlm.nih.gov/geo/samples/GSM786nnn/GSM786349/suppl/GSM786349_Rat_Supine_HVt_R3.CEL.gz
| Sample_series_id | GSE31678
| Sample_data_row_count | 20242
| |
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