Manna Biotech

Announcement

Oxford Nanopore Sequencing: Advanced Long-Read NGS, Now at Manna Biotech

By Dr Chathyushya K B·Founder, MD & CEO — PhD Microbiology, ICMR-NIN· 6 min read·Updated 30 May 2026

In short

Manna Biotech now runs Oxford Nanopore long-read sequencing in-house in Hyderabad — the advanced NGS platform used worldwide for real-time genomics and pathogen surveillance. Whole genomes, metagenomics, full-length transcripts and modification detection, scientist-guided from DNA to analysis. You access research-grade long-read sequencing without owning the instrument, and every project begins with a feasibility review.

Why Oxford Nanopore — and why long reads matter

Oxford Nanopore is one of the world's leading long-read sequencing platforms, used internationally for real-time genome analysis and pathogen surveillance. It reads single DNA and RNA molecules to produce reads thousands of bases long.

Long reads resolve what standard short-read NGS cannot: complete genome assemblies, structural variants and repetitive regions, full-length transcripts, and direct detection of base modifications without amplification bias. This is research-grade sequencing, now available locally.

What you can run

The platform supports a broad range of genomics and microbiology work:

  • Whole-genome sequencing of bacteria, viruses, fungi and plants
  • Full-length amplicon sequencing, including 16S and ITS
  • Metagenomics and microbiome community profiling
  • Full-length cDNA transcriptome sequencing
  • Direct RNA and DNA sequencing for epigenetic modification detection
  • Pathogen identification and outbreak surveillance

DNA to analysis, in-house in Hyderabad

Manna Biotech runs the complete workflow under our founding scientist team: sample QC and extraction support, library preparation, sequencing, basecalling, and bioinformatics through to an interpreted report.

For research groups and companies we also provide CRO-style support — assembly, annotation, variant or community analysis, and publication- or grant-ready figures. Every project starts with a feasibility review, so you know what is achievable with your sample before any commitment.

Who it is for

BSc, BTech and MSc students building dissertation and final-year projects on real long-read data; PhD scholars who need experiments their own lab cannot run; faculty and institutional labs who want world-class sequencing without buying an instrument; and biotech, pharma and nutraceutical companies for R&D, strain characterisation and pathogen identification.

How engagements work

Access research-grade long-read sequencing without the capital cost of owning a platform:

  • Pay-per-sample — you provide DNA or RNA meeting input requirements; we quote per sample
  • Collaborative project — scoped jointly, ideal for novel research
  • Institutional MoU — preferred rates for regular or bulk programs

Honest expectations

Sequencing output depends on sample quality and quantity, which is why we run a feasibility review first. We do not guarantee specific results, assemblies, or publication. Where a collaborator makes a genuine intellectual contribution, authorship follows accepted criteria; otherwise contributions are recognised in acknowledgements. Your data and IP remain yours.

How to start

Email admin@mannabiotech.com, or use the contact form at www.mannabiotech.com, with your sample type, organism and goal. You will receive a feasibility assessment and quote — typically within 48 hours — followed by a scientist-guided workflow from extraction to analysis report.

Frequently asked questions

What is Oxford Nanopore long-read sequencing?+

Oxford Nanopore is an advanced sequencing platform that reads single DNA or RNA molecules to produce long reads — valuable for complete genome assembly, metagenomics, full-length transcripts and direct modification detection. It is used worldwide for real-time genomics and pathogen surveillance.

What sample or DNA do I need to provide?+

It depends on the application; generally you need sufficient, good-quality DNA or RNA. Share your sample type and organism and we confirm exact input requirements during the feasibility review.

Do I need my own bioinformatics skills?+

No. Basic analysis and an interpreted report are included. Advanced or custom bioinformatics is available as an add-on, and we offer training for students and scholars.

Can students use it for projects?+

Yes. BSc, MSc and BTech students can base dissertation and final-year projects on real long-read data, with scientist-guided design and an optional hands-on workshop.

How is pricing structured?+

Pay-per-sample, a collaborative project basis, or an institutional MoU with preferred rates for regular or bulk work. You receive a transparent quote after the feasibility review.

Will I get authorship on resulting publications?+

Authorship requires genuine intellectual contribution and follows accepted criteria. Where that threshold is not met, contributions are recognised in the acknowledgements. We never sell or guarantee authorship.

How do I begin?+

Email admin@mannabiotech.com or use the form at www.mannabiotech.com with your sample details. We respond with a feasibility assessment and quote, usually within 48 hours.

Related service

Lab Services & NGS

Whole-genome Nanopore sequencing, 16S metagenomics, PCR/qPCR and bioinformatics — scientist-guided, in Hyderabad.

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