NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4224233 Query DataSets for GSM4224233
Status Public on Aug 31, 2021
Title wildtype line for PfNot1.1 knockout, TP5, replicate 2
Sample type RNA
 
Channel 1
Source name P. falciparum T996 RNA, wildtype line for PfNot1.1 knockout
Organism Plasmodium falciparum
Characteristics culture, stage, strain, harvest timepoint, estimated developmental age: In vitro culture, asexual blood stage, laboratory strain T996, TP5, 36 hpi
Treatment protocol Selective drugs were removed from medium two intraerythrocytic life cycles before harvesting parasites for RNA extraction.
Growth protocol P. falciparum parasites were cultured in RPMI-HEPES medium , supplemented with 0.25% Albumax , 0.2% sodium bicarbonate, 100 µM hypoxanthine and 10 µg/ml Gentamycin with 2% hematocrit.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol following manufacturer's instructions and as described in Bozdech, Z., S. Mok & A. P. Gupta, (2013) DNA microarray-based genome-wide analyses of Plasmodium parasites. Methods in molecular biology 923: 189-211.
Label Cy5
Label protocol Synthesis of aminoallyl-coupled cDNA by reverse transcription and labeling of samples with cy fluorophore were carried out as described in Bozdech, Z., S. Mok & A. P. Gupta, (2013) DNA microarray-based genome-wide analyses of Plasmodium parasites. Methods in molecular biology 923: 189-211.
 
Channel 2
Source name P. falciparum 3D7 RNA reference pool
Organism Plasmodium falciparum
Characteristics culture, stage, strain, composition: In vitro culture, asexual blood stage, laboratory strain T996, mixture of equal amounts of RNA harvested every 8 hours over the 48-hour parasite's intraerythrocytic life cycle
Treatment protocol Selective drugs were removed from medium two intraerythrocytic life cycles before harvesting parasites for RNA extraction.
Growth protocol P. falciparum parasites were cultured in RPMI-HEPES medium , supplemented with 0.25% Albumax , 0.2% sodium bicarbonate, 100 µM hypoxanthine and 10 µg/ml Gentamycin with 2% hematocrit.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol following manufacturer's instructions and as described in Bozdech, Z., S. Mok & A. P. Gupta, (2013) DNA microarray-based genome-wide analyses of Plasmodium parasites. Methods in molecular biology 923: 189-211.
Label Cy3
Label protocol Synthesis of aminoallyl-coupled cDNA by reverse transcription and labeling of samples with cy fluorophore were carried out as described in Bozdech, Z., S. Mok & A. P. Gupta, (2013) DNA microarray-based genome-wide analyses of Plasmodium parasites. Methods in molecular biology 923: 189-211.
 
 
Hybridization protocol Equal amounts of labelled sample and reference cDNA were hybridized on the microarray chip using the Agilent hybridization system. Hybridizations were performed for 20 hours at 65°C in a rotating hybridization oven at 10rpm.
Scan protocol Microarray scanning was done using PowerScanner (Tecan, Austria) at 10uM resolution and with autogain PMT adjustments for both channels. Data was acquired using GenePix Pro v6.0 software (Axon Instruments, USA) as described in Mok, S., M. Imwong et al (2011) Artemisinin resistance in Plasmodium falciparum is associated with an altered temporal pattern of transcription. BMC Genomics 12: 391.
Description 101047_Cycle1_2017-11-08_WT_TP5_rep2
Transcriptional profiling of the wildtype line for the PfNot1.1 knockout line at Timepoint 5 at around 36 hpi, replicate 2
Data processing Features with flag>0 and with median foreground intensity greater than 1.5 fold median background intensity for either channel passed quality control and were accepted. Local background correction using normexp, followed by lowess normalization across all features were carried out to generate the normalized Log2 gene expression ratios.
 
Submission date Dec 18, 2019
Last update date Aug 31, 2021
Contact name Ying Liu
E-mail(s) yliu037@e.ntu.edu.sg
Phone 84030462
Organization name Nanyang Technological University
Department School of Biological Sciences
Lab Prof. Zbynek Bozdech's lab
Street address 60 Nanyang Drive
City Singapore
ZIP/Postal code 637551
Country Singapore
 
Platform ID GPL11248
Series (1)
GSE142275 Transcriptional profilling of Plasmodium falciparum parasites with disrupted PfNot1.1 (PF3D7_1103800) or PfNot1.2 (PF3D7_1417200)

Data table header descriptions
ID_REF
VALUE Background corrected and lowess normalized log2 transformed ratios (Cy5/Cy3) of the RNA sample/3D7 RNA reference pool.

Data table
ID_REF VALUE
ac11rRNA18s_0 -0.050997153
ac11rRNA18s_1 -0.167583406
ac11rRNA28s_0 -0.018118252
ac11rRNA28s_1 -0.746988296
ac11rRNA28s_2 -0.075896202
ac11rRNA5.8s_0 -0.621798623
ac11rRNAITS1_0 -0.019831806
ac11rRNAITS2_0 0.658528497
ac13rRNA18s_0 -0.392438189
ac13rRNA18s_1 -0.508847095
ac13rRNA18s_2 -0.037582295
ac13rRNA28s_0 -0.456333157
ac13rRNA28s_1 -0.167901044
ac13rRNA5.8s_0 -0.520500461
ac13rRNAITS1_0 0.671256201
ac13rRNAITS2_0 0.860349686
ac14rRNA.1-5s_0 -0.071687994
ac14rRNA.2-5s_0 -0.033819009
ac14rRNA.3-5s_0 -0.015696742
ac1rRNA18s_0 -0.674192389

Total number of rows: 11005

Table truncated, full table size 268 Kbytes.




Supplementary file Size Download File type/resource
GSM4224233_101047_Cycle1_2017-11-08_WT_TP5_rep2.gpr.gz 1.2 Mb (ftp)(http) GPR
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap