Genomics & variants
From microbial isolates to complex genomes—QC, mapping, variant discovery, and interpretation-ready outputs.
- Coverage, contamination, and QC summaries
- SNP/indel/SV workflows (as appropriate)
- Comparative genomics and phylogenomics
MR DNA provides analysis across the full range of modern sequencing—genomes, transcriptomes, targeted panels, epigenetics, microbial ecology, and applied R&D. We focus on defensible methods, transparent QC, and outputs that are easy to use in publications, proposals, and product decisions.
A broad toolkit—so your analysis can match your question. We support standard workflows and custom designs.
From microbial isolates to complex genomes—QC, mapping, variant discovery, and interpretation-ready outputs.
De novo assembly and functional annotation with repeatable methods and clear deliverables.
Expression analysis that respects study design—mechanisms, response, and discovery programs.
Focused workflows when you know what you’re looking for—amplicons, capture/enrichment, and custom targets.
Methylation workflows for regulation and discovery (e.g., bisulfite-based approaches).
Community and functional profiling for environmental, agricultural, and host-associated systems.
We work across research and product programs—so you’re not boxed into a niche.
Designed for clarity and decision-making:
A simple process that keeps scope clear and results defensible.
Data type, sample count, study design, and the decision you need to make.
Transparent QC gates and workflow choices aligned to your project.
Clear reports, figures, and tables—plus optional iteration for manuscripts or internal reviews.
Share sample counts and the research goal. We’ll recommend a workflow and provide a quote.