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Sample GSM4498922 Query DataSets for GSM4498922
Status Public on May 17, 2021
Title 3D7-A Control, 24h Replicate 1
Sample type RNA
 
Channel 1
Source name 3D7-A_1
Organism Plasmodium falciparum
Characteristics strain: 3D7-A
status: Control
age (hpi): 24
replicate: Biological replicate 1
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_24h_repl1
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 -0.443127165
ac11rRNA18s_1 -0.118618847
ac11rRNA28s_0 0.182392683
ac11rRNA28s_1 -0.242004022
ac11rRNA28s_2 -0.139281589
ac11rRNA5.8s_0 1.083786624
ac11rRNAITS1_0 0.166179987
ac11rRNAITS2_0 2.050147367
ac13rRNA18s_0 0.200696332
ac13rRNA18s_1 0.015684061
ac13rRNA18s_2 -0.250845407
ac13rRNA28s_0 0.455603448
ac13rRNA28s_1 -0.366595681
ac13rRNA5.8s_0 1.269968213
ac13rRNAITS1_0 1.500254689
ac13rRNAITS2_0 1.127566532
ac14rRNA.1-5s_0 2.63248214
ac14rRNA.2-5s_0 2.828124951
ac14rRNA.3-5s_0 2.67726075
ac1rRNA18s_0 -0.29950121

Total number of rows: 10429

Table truncated, full table size 253 Kbytes.




Supplementary file Size Download File type/resource
GSM4498922_Acon_1_24.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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