|
Status |
Public on Jul 13, 2022 |
Title |
SCHU S4, rep9 |
Sample type |
SRA |
|
|
Source name |
SCHU S4
|
Organism |
Francisella tularensis subsp. tularensis |
Characteristics |
clade: Francisella tularensis subspecies tularensis subtype A.I strain: SCHU S4
|
Treatment protocol |
To preserve RNA integrity, bacterial cultures were added to RNAprotect Bacteria Reagent (Qiagen), as recommended by the manufacturer.
|
Growth protocol |
Bacterial strains were cultured in BHI broth to mid-log growth phase.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using the FastRNA Pro Blue Kit (MP Biomedicals), and then RNA was treated with DNase I and column purified, as recommended by the respective manufacturer. To produce the the RNA-Seq libraries, ScriptSeq v2 Complete Library Preparation Kit for Bacteria (Epicentre) was utilized according to the manufacturer's instructions and included Ribo-Zero Ribosomal RNA (rRNA) Reagents for Bacteria to remove rRNA.
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|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NextSeq 500 |
|
|
Description |
SCHUS4-9
|
Data processing |
Trimmomatic was utilized to remove low-quality reads obtained by FastQC, and reads with less than 35 bp were removed from the analysis. FastQC was applied again and alignments were obtained by using the TopHat2. Bowtie 2 was utilized for indexing the genes. Cufflink identified expressed genes and calculated transcript levels in the aligned reads within the TopHat2 generated Sequence Alignment/Map (SAM) formatted files. Genes transcribed were measured using fragments per kilobase of exon per million (FPKM) reads. Assembly: Francisella tularensis genome sequences were obtained from NCBI microbial genome database and had the following accession numbers: SCHU S4 (NC_006570.2), MA00-2987 (NZ_CP012372.1), WY96-3418 (NC_009257.1), and LVS (NC_07880.1). Supplementary files format and content: Cufflinks FPKM data
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|
|
Submission date |
May 13, 2022 |
Last update date |
Jul 13, 2022 |
Contact name |
Robert Bristow Moore |
E-mail(s) |
rmoore14@unl.edu
|
Organization name |
University of Nebraska - Lincoln
|
Department |
Biochemistry
|
Lab |
Helikar Lab
|
Street address |
1901 vine street
|
City |
LINCOLN |
State/province |
NE |
ZIP/Postal code |
68504 |
Country |
USA |
|
|
Platform ID |
GPL32256 |
Series (1) |
GSE202948 |
Arginine catabolism and polyamine biosynthesis pathway disparities within Francisella tularensis subpopulations |
|
Relations |
BioSample |
SAMN28233104 |
SRA |
SRX15255169 |