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Status |
Public on Mar 01, 2024 |
Title |
Scer, heatshock, RNA, rep3 |
Sample type |
SRA |
|
|
Source name |
BJ5464 (delta-URA3)
|
Organism |
Saccharomyces cerevisiae |
Characteristics |
strain: BJ5464 (delta-URA3) treatment: Heatshocked
|
Treatment protocol |
Splitting the culture into equal volumes, one underwent 37°C heat stress for 20 minutes.
|
Growth protocol |
We grew Saccharomyces cerevisiae strain BJ5464 auxotroph ΔURA3 in 500 mL Yeast Extract-Peptone-Dextrose (YPD) medium to OD600 = 0.75 at 28°C.
|
Extracted molecule |
polyA RNA |
Extraction protocol |
We resuspended three 2 mL aliquots per culture in 450 mL RLT Buffer and followed the manufacturer’s instructions for the Qiagen RNeasy plant mini kit, eluting in 30 mL nuclease-free water. Illumina stranded mRNA library prep
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|
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
|
|
Data processing |
Genome preparation : We performed repeat masking with RepeatMasker v.4.1.0 (http://www.repeatmasker.org) through two rounds of masking, first with default settings and with standard Illumina adapters using -e rmblast enabled. Alignment: We aligned RNA-Seq reads with kalign (ngskit4b tool suite version 200218) with options -c25 -l25 -d50 -U4. We removed PCR and optical duplicates using MarkDuplicates (PICARD) enabling REMOVE_DUPLICATES=TRUE. FPKM: We calculated FPKM using the Tuxedo pipeline. We then z-transformed the FPKM values using the R package zFPKM. edgeR: For the differential expression analyses, we used the Trinity edgeR pipeline to calculate log2FC between treatments. Assembly: S288C R64/sacCer3 Supplementary files format and content: tab-delimited text file including FPKM for all samples Supplementary files format and content: tab-delimited text file output from edgeR including logFC between treatments for each gene
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Submission date |
Feb 20, 2024 |
Last update date |
Mar 01, 2024 |
Contact name |
Erin Elizabeth Hahn |
E-mail(s) |
erin.hahn@csiro.au
|
Organization name |
CSIRO
|
Department |
National Research Collections Australia
|
Street address |
Clunies Ross
|
City |
Canberra |
State/province |
ACT |
ZIP/Postal code |
2611 |
Country |
Australia |
|
|
Platform ID |
GPL27812 |
Series (1) |
GSE256160 |
Effects of formalin-fixation on FAIRE-Seq and MNase-Seq signatures in yeast (RNA-Seq) |
|
Relations |
BioSample |
SAMN40008069 |
SRA |
SRX23677962 |