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Sample GSM7659766 Query DataSets for GSM7659766
Status Public on Jul 25, 2023
Title PMY2570_C
Sample type SRA
 
Source name segregant of Bt22xFtc555-1
Organism Cryptococcus neoformans
Characteristics cell line: segregant of Bt22xFtc555-1
cell type: yeast
treatment: control
Growth protocol Samples were grown overnight in liquid YPD on a rollerdrum and were added to V8 petri dishes. V8 cultures were grown at 30◦C for 60 hours. Amoeba cultures were collected and suspended at a concentration of 1 × 106 cells/mL. 450 μL of amoeba culture was added to the center of the Cryptococcus lawn with slight agitation to aid in the spread of the culture. Plates were allowed to dry on the benchtop for 30 minutes before being incubated at 25◦C for 48 hours. A consistent area of 30 cm2 was cut from the plates and then scraped to collect cells. Collected cells were resuspended in 1 mL of PBS and were placed in dry ice for 10 minutes. Samples were then lyophilized for 12 - 18 hours.
Extracted molecule polyA RNA
Extraction protocol Whole RNA was extracted using the RNAeasy Plant Mini Kit (Qiagen 74904).
Libraries were prepared and sequenced by the using the Illumina NextSeq 500 High Output Kit producing 150-base pair paired end read.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Description 15
Data processing Reads were aligned using the CNA3 of H99 C. neoformans var. grubii (accession GCA_000149245.3) from the Ensemble Fungi database. Reads were aligned using Kallisto.
Analysis of RNA sequences was performed using Deseq2 in R. Briefly, transcript abundance was normalized using a built in median of ratios method. Samples were normalized based on condition (amobea or control). GO term analysis was performed using the fungidb GeneByLocusTag tool. Correlation of gene expression with BZP4 was performed using the normalized count output from Deseq2.
Assembly: GCA_000149245.3
Supplementary files format and content: tab delimited files containing read counts and TPK values for each gene
 
Submission date Jul 24, 2023
Last update date Jul 25, 2023
Contact name Paul Magwene
E-mail(s) paul.magwene@duke.edu
Organization name Duke University
Department Biology
Lab Magwene
Street address 124 Science dr.
City Durham
State/province North Carolina
ZIP/Postal code 27701
Country USA
 
Platform ID GPL27451
Series (1)
GSE238170 Amoeba Predation of Cryptococcus: A Quantitative and Population Genomic Evaluation of the Accidental Pathogen Hypothesis
Relations
BioSample SAMN36698811
SRA SRX21144779

Supplementary file Size Download File type/resource
GSM7659766_15_abundance_2022_10_25_06_07_42_UTC_.tsv.gz 134.4 Kb (ftp)(http) TSV
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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