|
Status |
Public on Oct 05, 2020 |
Title |
LXHWT2 |
Sample type |
SRA |
|
|
Source name |
strain
|
Organism |
Mycobacterium tuberculosis H37Ra |
Characteristics |
genotype/variation: H37Ra/WT
|
Extracted molecule |
total RNA |
Extraction protocol |
Retinas were removed, flash frozen on dry ice, and RNA was harvested using Trizol reagent. RNeasy Mini Kit (Cat#74106, Qiagen) was used with 1 ug of total RNA for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Data processing |
Illumina Casava1.7 software used for basecalling. Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to Mycobacterium tuberculosis H37Ra whole genome using bowtie2 v2-2.0.5 Fragments per kilobase of exon per million fragments mapped(FPKM). In short, exons from all isoforms of a gene were merged to create one meta-transcript. The number of fragments falling in the exons of this meta-transcript were counted and normalized by the size of the meta-transcript and by the size of the library. Genome_build: Mycobacterium tuberculosis H37Ra Supplementary_files_format_and_content: gene_expression.xls file includes FPKM values for each Sample ...
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|
|
Submission date |
Nov 07, 2019 |
Last update date |
Oct 05, 2020 |
Contact name |
Li xiao hui |
E-mail(s) |
chenliu@mail.hzau.edu.cn
|
Organization name |
Huazhong Agricultural University
|
Street address |
Shizishan Street No. 1, Hongshan District
|
City |
Wuhan |
State/province |
Hubei |
ZIP/Postal code |
430070 |
Country |
China |
|
|
Platform ID |
GPL27144 |
Series (1) |
GSE140113 |
Next Generation Sequencing Facilitates Quantitative Analysis of cmtR-deleted mutant and wild-type strains Transcriptomes in Mycobacterium tuberculosis H37Ra |
|
Relations |
BioSample |
SAMN13241021 |
SRA |
SRX7115494 |