<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Alex Mullins</submitter><organism>Burkholderia gladioli</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-13521</full_dataset_link><description>The experiment was intended to understand the influence of growth media on the expression of biosynthetic gene clusters responsible for natural product production.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Growth Protocol - Growth conditions varied depending on species/strain and experimental variables - see publication for details</sample_protocol><sample_protocol>Library Construction - Illumina library preparation followed the Illumina Stranded Total RNA Library Prep reference guide. Primer dimers were removed from the pooled library by SPRI bead size selection.</sample_protocol><sample_protocol>Sequencing - Novaseq S1 (200 cycle) sequencing run. Two lanes per sample and data combined.</sample_protocol><sample_protocol>Sample Collection - Starting culture OD of 0.05 (600 nm). 1 ml of liquid culture was harvested for each replicate at the desired optical density. Each 1 ml aliquot was centrifuged, supernatant discarded, and Monarch® DNA/RNA Protection Reagent added prior to snap-freezing in liquid nitrogen.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA extracted using Monarch® Total RNA Miniprep Kit (NEB) as described in the NEB Gram-negative bacteria protocol. A final DNase treatment was included using the TURBO DNA-free™ Kit for 1 h.</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>Data Transformation - Count data determined with htseq applying union mode to non-stranded read data, and non-unique reads were assigned to all overlapping features. Log2 fold change and statistical significance determed with DESeq2 v1.32.0 - count data normalised and shrinkage of LFC effect size achieved using apeglm in DESeq2.</data_protocol><data_protocol>Sequence Alignment - Reads were trimmed with Trim Galore v0.6.7, quality assessed with FastQC v0.11.9. Processed reads were mapped to references with Bowtie 2 followed by sorting and indexing with samtools v1.7.</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 6000</instrument_platform><study_type>RNA-seq of total RNA</study_type><species>Burkholderia gladioli</species><pubmed_authors>Alex Mullins</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq of Burkholderia gladioli and Burkholderia ambifaria strains on TSB, BSMG, and PEM growth media</name><description>The experiment was intended to understand the influence of growth media on the expression of biosynthetic gene clusters responsible for natural product production.</description><dates><release>2026-06-30T00:00:00Z</release><modification>2026-06-30T01:00:54.571Z</modification><creation>2023-11-07T15:14:43.108Z</creation></dates><accession>E-MTAB-13521</accession><cross_references><ENA>ERP153256</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0009653</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>