<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Frances Marks</submitter><organism>Mycobacterium tuberculosis</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16127</full_dataset_link><description>This experiment was done to look at the transcriptional profile of bacteria upon whiB2 transcriptional depletion. RNA-seq of an inducible whiB2 CRISPRi strain grown with 0 or 500 ng/mL anhydrotetracycline, which turns on the CRISPRi machinery. Samples were collected after 2 days of treatment.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Libraries were constructed using NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (New England Biolabs) using 150 ng of input RNA. Libraries were amplified using 8 cycles on the thermocycler. Post amplification libraries were size selected ay 250-450 bp in length using SparQ beads. Libraries were validated using Bioanalyzer high sensitivity DNA analysis.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA extraction was performed using Zymo RNA miniprep kit</sample_protocol><sample_protocol>Sequencing - Sequencing was done using a Illumina NovaSeq X Plus</sample_protocol><sample_protocol>Sample Collection - Bacteria were mixed with 5M GTC, pelleted, and resuspended in Trizol.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Sequence Alignment - Trimmed a filtered sequencing reads were mapped to the H37Rv reference genome (GenBank AL123456.3; RefSeq NC_000962.3; GCF_000195955.2; Genome assembly ASM19595v2)</data_protocol><data_protocol>Data Transformation - Raw read counts were done using featureCounts and normalized read counts were done using DESeq2</data_protocol><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Illumina NovaSeq X</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Mycobacterium tuberculosis</species><pubmed_authors>Frances Marks</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq of an inducible whiB2 CRISPRi strain grown with 0 or 500 ng/mL anhydrotetracycline, which turns on the CRISPRi machinery</name><description>This experiment was done to look at the transcriptional profile of bacteria upon whiB2 transcriptional depletion. RNA-seq of an inducible whiB2 CRISPRi strain grown with 0 or 500 ng/mL anhydrotetracycline, which turns on the CRISPRi machinery. Samples were collected after 2 days of treatment.</description><dates><release>2026-08-06T00:00:00Z</release><modification>2026-08-06T21:35:42.924Z</modification><creation>2025-11-14T13:19:52.251Z</creation></dates><accession>E-MTAB-16127</accession><cross_references><ENA>ERP184448</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>