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Sample GSM4498930 Query DataSets for GSM4498930
Status Public on May 17, 2021
Title 3D7-A Control, 8h Replicate 2
Sample type RNA
 
Channel 1
Source name 3D7-A_2
Organism Plasmodium falciparum
Characteristics strain: 3D7-A
status: Control
age (hpi): 8
replicate: Biological replicate 2
Treatment protocol All cultures (control and previously heat shock-adapted lines) were maintained at 37 ºC for the transcriptome characterization.
Growth protocol Parasites were cultured under standard conditions in media containing Albumax II and no human serum, in a 5% CO2, 3% O2, 92% N2 atmosphere. Tight synchronization was achieved by Percoll or magnet purification of schizonts followed by sorbitol lysis 5 h later, to obtain a population of a defined age window of 0–5 h post- invasion. Parasites were cultured undisturbed for different periods of time (8, 16, 24, 32 and 40 h) before collecting in TRIzol for total RNA extraction.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol following manufacturer's instructions. For genomic DNA (gDNA) extraction, parasites were lysed with SDS and gDNA purified by double phenol/chloroform extraction and ethanol precipitation, followed by mild sonication.
Label Cy5
Label protocol Test sample, Cy5; reference pool, Cy3. Labeling was carried out as previously described [Bozdech Z et al Genome biol 2003, 4(2):R9].
 
Channel 2
Source name 3D7-A mixed stage Reference Pool
Organism Plasmodium falciparum
Characteristics strain: 3D7-A
age (hpi): Samples of synchronized cultures covering the whole asexual cycle.
Treatment protocol All cultures (control and previously heat shock-adapted lines) were maintained at 37 ºC for the transcriptome characterization.
Growth protocol Parasites were cultured under standard conditions in media containing Albumax II and no human serum, in a 5% CO2, 3% O2, 92% N2 atmosphere. Tight synchronization was achieved by Percoll or magnet purification of schizonts followed by sorbitol lysis 5 h later, to obtain a population of a defined age window of 0–5 h post- invasion. Parasites were cultured undisturbed for different periods of time (8, 16, 24, 32 and 40 h) before collecting in TRIzol for total RNA extraction.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol following manufacturer's instructions. For genomic DNA (gDNA) extraction, parasites were lysed with SDS and gDNA purified by double phenol/chloroform extraction and ethanol precipitation, followed by mild sonication.
Label Cy3
Label protocol Test sample, Cy5; reference pool, Cy3. Labeling was carried out as previously described [Bozdech Z et al Genome biol 2003, 4(2):R9].
 
 
Hybridization protocol Microarray hybridizations were carried out using a MAUI hybridization system (BioMicro Systems) as previously described [Bozdech Z et al Genome biol 2003, 4(2):R9].
Scan protocol Scanning was performed with a GenePix Pro 6.0 (Axon Instruments) as previously described [Bozdech Z et al Genome biol 2003, 4(2):R9].
Description 3D7-A-CTL_8h_repl2
Data processing Microarray background for each channel (635 nm for Cy5 and 532 nm for Cy3) was calculated as the minimum between the median intensity of the 100 spots with lowest intensity and the median of the local background of all spots in the microarray. Spots with a signal in both channels lower than 1.5 fold times the background were eliminated. When a spot had intensity higher than 1.5 times the background in only one of the two channels, the other channel was assigned a value of 1.5 times the background of this channel, to avoid extreme ratio values. Background was subtracted before normalization. Log2(Cy5/Cy3) was normalized using LOESS.
 
Submission date Apr 27, 2020
Last update date May 18, 2021
Contact name Elisabet Tinto-Font
E-mail(s) elisabet.tinto@gmail.com
Organization name ISGlobal
Department Malaria
Street address c/Rossello 153
City Barcelona
ZIP/Postal code 08036
Country Spain
 
Platform ID GPL11248
Series (2)
GSE149393 Transcriptional alterations of P. falciparum 3D7-A heat shock-adapted vs control parasites.
GSE149394 Transcriptomic analysis of heat shock resistance in Plasmodium falciparum

Data table header descriptions
ID_REF
VALUE Normalized log2 ratio (Cy5/Cy3) representing test/reference.

Data table
ID_REF VALUE
ac11rRNA18s_0 -0.625506031
ac11rRNA18s_1 -0.284881692
ac11rRNA28s_0 -0.582834945
ac11rRNA28s_1 -0.45888522
ac11rRNA28s_2 -0.461298499
ac11rRNA5.8s_0 0.711978802
ac11rRNAITS1_0 -0.21126448
ac11rRNAITS2_0 0.993124005
ac13rRNA18s_0 -0.797533412
ac13rRNA18s_1 -0.184770346
ac13rRNA18s_2 -0.67864427
ac13rRNA28s_0 -0.443802854
ac13rRNA28s_1 -0.340554794
ac13rRNA5.8s_0 0.079129959
ac13rRNAITS1_0 0.19215619
ac13rRNAITS2_0 0.917854858
ac14rRNA.1-5s_0 1.879111489
ac14rRNA.2-5s_0 1.899381606
ac14rRNA.3-5s_0 1.993462534
ac1rRNA18s_0 -0.299441448

Total number of rows: 10429

Table truncated, full table size 254 Kbytes.




Supplementary file Size Download File type/resource
GSM4498930_Acon_2_08.gpr.gz 1.0 Mb (ftp)(http) GPR
Processed data included within Sample table
Processed data are available on Series record

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