Welcome to the Genome Analysis project focused on uncovering the genetic mechanisms underlying oxytetracycline production in Streptomyces rimosus. The objective of the project is to conduct a comprehensive analysis of the S. rimosus genome to gain insights into the pathways and regulatory elements involved in antibiotic hyperproduction.
-
Genome Assembly:
- Perform de novo assembly of long Nanopore sequencing reads.
- Refine the assembly using short Illumina reads to improve accuracy and completeness.
-
Transcriptomics and Differential Expression Analysis:
- Conduct transcriptomic analysis to compare gene expression profiles between the hyperproducer S. rimosus strain and the wild-type strain.
- Perform differential expression analysis to identify genes and pathways associated with antibiotic hyperproduction.
-
Genome Annotation and Synteny Evaluation:
- Annotate the assembled genome to identify protein-coding genes, non-coding RNAs, and other functional elements.
- Evaluate synteny with the wild-type genome to assess structural conservation and identify genomic variations.
-
Candidate Gene Identification:
- Identify candidate genes and pathways potentially involved in oxytetracycline biosynthesis and regulation.
-
Documentation:
- Document findings, methodologies, and analysis workflows for future reference and reproducibility.