Source Name	Comment [Sample_description]	Comment [Sample_source_name]	Comment [Sample_title]	Characteristics [organism]	Term Source REF	Term Accession Number	Extract Name	Material Type	Labeled Extract Name	Label	Assay Name	Array Design REF	Term Source REF	Technology Type	Array Data File	Comment [ArrayExpress FTP file]	Protocol REF	Term Source REF	Normalization Name	Derived Array Data File	Comment [Derived ArrayExpress FTP file]
GSM96285 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T4_R3, Monolayer Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96285 extract 1	total RNA	GSM96285 LE 1	1	GSM96285	A-AFFY-44	ArrayExpress	array assay	GSM96285.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96285_sample_table.txt norm	GSM96285_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96284 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T4_R2, Monolayer Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96284 extract 1	total RNA	GSM96284 LE 1	1	GSM96284	A-AFFY-44	ArrayExpress	array assay	GSM96284.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96284_sample_table.txt norm	GSM96284_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96283 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T4_R1, Monolayer Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96283 extract 1	total RNA	GSM96283 LE 1	1	GSM96283	A-AFFY-44	ArrayExpress	array assay	GSM96283.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96283_sample_table.txt norm	GSM96283_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96282 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T3_R3, Spheroid Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96282 extract 1	total RNA	GSM96282 LE 1	1	GSM96282	A-AFFY-44	ArrayExpress	array assay	GSM96282.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96282_sample_table.txt norm	GSM96282_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96281 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T3_R2, Spheroid Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96281 extract 1	total RNA	GSM96281 LE 1	1	GSM96281	A-AFFY-44	ArrayExpress	array assay	GSM96281.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96281_sample_table.txt norm	GSM96281_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96280 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T3_R1, Spheroid Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96280 extract 1	total RNA	GSM96280 LE 1	1	GSM96280	A-AFFY-44	ArrayExpress	array assay	GSM96280.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96280_sample_table.txt norm	GSM96280_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96279 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T2_R3, Spheroid	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96279 extract 1	total RNA	GSM96279 LE 1	1	GSM96279	A-AFFY-44	ArrayExpress	array assay	GSM96279.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96279_sample_table.txt norm	GSM96279_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96278 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T2_R2, Spheroid	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96278 extract 1	total RNA	GSM96278 LE 1	1	GSM96278	A-AFFY-44	ArrayExpress	array assay	GSM96278.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96278_sample_table.txt norm	GSM96278_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96277 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T2_R1, Spheroid	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96277 extract 1	total RNA	GSM96277 LE 1	1	GSM96277	A-AFFY-44	ArrayExpress	array assay	GSM96277.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96277_sample_table.txt norm	GSM96277_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96276 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T1_R3, Monolayer	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96276 extract 1	total RNA	GSM96276 LE 1	1	GSM96276	A-AFFY-44	ArrayExpress	array assay	GSM96276.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96276_sample_table.txt norm	GSM96276_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96275 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T1_R2, Monolayer	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96275 extract 1	total RNA	GSM96275 LE 1	1	GSM96275	A-AFFY-44	ArrayExpress	array assay	GSM96275.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96275_sample_table.txt norm	GSM96275_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96274 1	60% confluent human T98G glioma cancer cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 10% FBS and 5% non essential amino acids supplemented EMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence)samples. All samples were conducted intriplicate. Samples from the two week arrest were removed from storage and supplemented with EMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human T98G Glioma Cancer Cells	T98G_T1_R1, Monolayer	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96274 extract 1	total RNA	GSM96274 LE 1	1	GSM96274	A-AFFY-44	ArrayExpress	array assay	GSM96274.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96274_sample_table.txt norm	GSM96274_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96273 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T4_R3, Monolayer Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96273 extract 1	total RNA	GSM96273 LE 1	1	GSM96273	A-AFFY-44	ArrayExpress	array assay	GSM96273.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96273_sample_table.txt norm	GSM96273_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96272 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T4_R2, Monolayer Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96272 extract 1	total RNA	GSM96272 LE 1	1	GSM96272	A-AFFY-44	ArrayExpress	array assay	GSM96272.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96272_sample_table.txt norm	GSM96272_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96271 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T4_R1, Monolayer Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96271 extract 1	total RNA	GSM96271 LE 1	1	GSM96271	A-AFFY-44	ArrayExpress	array assay	GSM96271.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96271_sample_table.txt norm	GSM96271_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96270 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T3_R3, Spheroid Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96270 extract 1	total RNA	GSM96270 LE 1	1	GSM96270	A-AFFY-44	ArrayExpress	array assay	GSM96270.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.1.zip	P-GSE4219-1	ArrayExpress	GSM96270_sample_table.txt norm	GSM96270_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96269 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T3_R2, Spheroid Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96269 extract 1	total RNA	GSM96269 LE 1	1	GSM96269	A-AFFY-44	ArrayExpress	array assay	GSM96269.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.2.zip	P-GSE4219-1	ArrayExpress	GSM96269_sample_table.txt norm	GSM96269_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96268 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T3_R1, Spheroid Recovery	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96268 extract 1	total RNA	GSM96268 LE 1	1	GSM96268	A-AFFY-44	ArrayExpress	array assay	GSM96268.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.2.zip	P-GSE4219-1	ArrayExpress	GSM96268_sample_table.txt norm	GSM96268_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96267 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T2_R3, Spheroid	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96267 extract 1	total RNA	GSM96267 LE 1	1	GSM96267	A-AFFY-44	ArrayExpress	array assay	GSM96267.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.2.zip	P-GSE4219-1	ArrayExpress	GSM96267_sample_table.txt norm	GSM96267_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96266 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T2_R2, Spheroid	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96266 extract 1	total RNA	GSM96266 LE 1	1	GSM96266	A-AFFY-44	ArrayExpress	array assay	GSM96266.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.2.zip	P-GSE4219-1	ArrayExpress	GSM96266_sample_table.txt norm	GSM96266_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96265 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T2_R1, Spheroid	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96265 extract 1	total RNA	GSM96265 LE 1	1	GSM96265	A-AFFY-44	ArrayExpress	array assay	GSM96265.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.2.zip	P-GSE4219-1	ArrayExpress	GSM96265_sample_table.txt norm	GSM96265_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96264 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T1_R3, Monolayer	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96264 extract 1	total RNA	GSM96264 LE 1	1	GSM96264	A-AFFY-44	ArrayExpress	array assay	GSM96264.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.2.zip	P-GSE4219-1	ArrayExpress	GSM96264_sample_table.txt norm	GSM96264_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96263 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T1_R2, Monolayer	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96263 extract 1	total RNA	GSM96263 LE 1	1	GSM96263	A-AFFY-44	ArrayExpress	array assay	GSM96263.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.2.zip	P-GSE4219-1	ArrayExpress	GSM96263_sample_table.txt norm	GSM96263_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip
GSM96262 1	60% confluent human foreskin fibroblast (HFF2) primary cells were split into suspension over agarose to form spheroids and grown for an additional 4 days in suspension over agarose prepared with 15% FBS supplemented DMEM. Following growth, media was removed and the spheroids were stored on the surface of the agarose in vacuum sealed flasks for a 2 week interval at room temperature in the dark. The samples were compared against monolayer (at 60% confluence). All samples were conducted in triplicate. Samples from the two week arrest were removed from storage and supplemented with DMEM (Invitrogen) containing 15% FBS (spheroid recovery sample).  These cells were then allowed to grow out as adherent monolayers for 7 days (monolayer recovery sample).	Human Foreskin Fibroblast (HFF2) Primary Cells	HFF2_T1_R1, Monolayer	Homo sapiens	EFO	http://purl.obolibrary.org/obo/NCBITaxon_9606	GSM96262 extract 1	total RNA	GSM96262 LE 1	1	GSM96262	A-AFFY-44	ArrayExpress	array assay	GSM96262.CEL	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.raw.2.zip	P-GSE4219-1	ArrayExpress	GSM96262_sample_table.txt norm	GSM96262_sample_table.txt	ftp://ftp.ebi.ac.uk/pub/databases/microarray/data/experiment/GEOD/E-GEOD-4219/E-GEOD-4219.processed.1.zip