|
| Status |
Public on Sep 03, 2021 |
| Title |
RNA-Seq Healthy control sample 2, Alveolar macrophage, Mycobacterium tuberculosis non-challenged library |
| Sample type |
SRA |
| |
|
| Source name |
bronchoalveolar lavage
|
| Organism |
Homo sapiens |
| Characteristics |
ethnicity: Caucasian
Sex: M
age: 59
medical.history: None
sexually transmitted infections: no
quantiferon tb reagent: no
cd4 count: 495
viral load: not tested
prescription drugs: none
active ingredient: none
art start year: none
recreational drugs: cannabis
cigarette smoker: yes
bal sampling date: 2017/02/01
mtb challenged: no
rin: 9.6
average library size: 261
sequencing run: centre1_batch1
lane: L7
|
| Treatment protocol |
Bronchoalveolar lavage samples were filtered to remove macro contaminants and alveolar macrophages (AM) cells enrich via tube adhesion method. 1 x 106 AM cells were cultured with media (not challenged) or media + Mtb (challenged) for 20h.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Cells were lysed with Trizol and kept at -80°C until extraction. RNA isolation was performed with miRNeasy kit and RNA integrity (RIN) was assessed with the Agilent 2100 Bioanalyzer.
RNA libraries were prepared for sequencing using standard unstrand Illumina protocols (TruSeq RNA Library Preparation Kit v2, Set A ).
|
| |
|
| Library strategy |
RNA-Seq |
| Library source |
transcriptomic |
| Library selection |
cDNA |
| Instrument model |
Illumina HiSeq 4000 |
| |
|
| Description |
Healthy control sample 2, Alveolar macrophage, Mycobacterium tuberculosis non-challenged library
mRNA, poly-A selected
HC.AMC2.MTB.0_RNA_R1_quant.sf
|
| Data processing |
Basecalling was done with Illumina Casava 1.8.2 and fastq files generated via bcl2fastq v2.18.
Fastq files were trimmed to remove leftover adaptor sequences and < phred 20 bases using cutadapt v2.6.
Read alignment was performed with STAR v2.7.3a and resulting alignments in transcriptomic coordinates was input to Salmon v1.1.0 for gene expression estimation.
Gene level estimated counts matrix was created in R v3.6.1, using tximport v1.12.3 with the option “lengthScaledTPM”.
Libray depth and compositional bias scaling factors were calculated via the function calcNormFactors from edgeR v3.26.8 and used by limma’s voom function (v3.40.6) to generate the normalized log2(CPM) expression matrix.
Genome_build: GRCh38.p13 (ENSEMBL v99)
Supplementary_files_format_and_content: tab-delimited text files including transcript estimated counts and TPM values for each sample.
Supplementary_files_format_and_content: tab-delimited matrix table with raw estimated gene counts for every gene and sample (lengthScaledTPM).
Supplementary_files_format_and_content: tab-delimited matrix table with normalized gene expression in log2 scale for tested genes (created with limma's voom function). Covariates not regressed out.
|
| |
|
| Submission date |
Jan 28, 2021 |
| Last update date |
Sep 03, 2021 |
| Contact name |
Erwin Schurr |
| E-mail(s) |
erwin.schurr@mcgill.ca
|
| Organization name |
McGill University Health Centre
|
| Street address |
1001 boulevard Decarie
|
| City |
Montreal |
| ZIP/Postal code |
H4A 3J1 |
| Country |
Canada |
| |
|
| Platform ID |
GPL20301 |
| Series (2) |
| GSE165708 |
Epigenetic impairment and blunted transcriptional response to Mycobacterium tuberculosis of alveolar macrophages from persons living with HIV (RNA-Seq) |
| GSE165709 |
Epigenetic impairment and blunted transcriptional response to Mycobacterium tuberculosis of alveolar macrophages from persons living with HIV |
|
| Relations |
| BioSample |
SAMN17615603 |
| SRA |
SRX9969404 |
