Nanopore Sequencing · Hands-on
Nanopore Sequencing Training in Hyderabad
Manna Biotech offers students practical exposure to Nanopore sequencing technology — a rare, hands-on advantage. You understand modern NGS workflows from sample-preparation concepts to sequencing, real-time data generation, quality control, genome analysis and bioinformatics interpretation. This gives life sciences, biotechnology, microbiology, genomics, bioinformatics and pharma students a valuable practical edge.
This is a fee-based hands-on training program. It is not a stipend or salaried internship.
Manna Biotech provides hands-on Nanopore sequencing training in Hyderabad with practical machine exposure, covering NGS workflow concepts, library and sequencing-run demonstration, FASTQ data, quality control, genome assembly and bioinformatics interpretation for education and research training.
Manna Biotech is a Hyderabad-based, founder-led life-sciences research, training and services organisation with a working lab. It offers hands-on internships, academic projects, ethical PhD and MBBS/MD research support, bioinformatics, NGS, Nanopore sequencing, genomics training and authorised research data analysis across India.
Hands-on Nanopore sequencing machine exposure available for NGS & genomics training — a practical edge for your research profile.
Nanopore TrainingWhat is Nanopore sequencing?
Nanopore sequencing is a third-generation, long-read sequencing technology that reads DNA or RNA molecules in real time as they pass through a protein nanopore. Its portability and long reads make it valuable for genome assembly, microbial identification and metagenomics in education and research settings.
Hands-on machine exposure at Manna Biotech
Students get practical exposure to the sequencing workflow and machine demonstration — from library-preparation concepts and loading to watching real-time data generation — then move to the computer to interpret the resulting reads.
The NGS workflow, end to end
- Sample and DNA/RNA preparation concepts
- Library preparation overview
- Sequencing run demonstration and real-time data generation
- FASTQ data, read quality and basic statistics
- Quality control and genome-assembly introduction
- Annotation, variant and comparative-genomics concepts
Applications you will explore
- Microbial genome analysis and pathogen genome concepts
- Metagenomics and microbiome data interpretation
- Plant and microbial genomics applications
- Clinical-genomics research concepts (education only)
- Bioinformatics tools and pipelines for long-read data
Who can apply
Built for these students
- BSc Life Sciences, Biotechnology, Microbiology and Genetics students
- 4-year Honours / Honours-with-Research students
- MSc Biotechnology, Microbiology, Biochemistry, Genetics and Genomics students
- BTech / MTech Biotechnology students
- B.Pharm, M.Pharm and Pharm.D students
- PhD scholars, faculty and researchers
What you learn
Skills you will build
- Basics of Nanopore sequencing technology
- How Sanger, Illumina and Nanopore sequencing differ
- End-to-end NGS workflow concepts
- Sample and library-preparation concepts
- Real-time sequencing data generation and FASTQ basics
- Data quality control, genome-assembly and variant-analysis introduction
- Microbial genomics, metagenomics and bioinformatics interpretation
Practical techniques
Hands-on methods covered
- Sequencing workflow and machine demonstration
- Library-preparation concepts
- FASTQ handling and read quality control
- Long-read genome assembly basics
- Variant and comparative-genomics introduction
- Bioinformatics tools for Nanopore data
Project options
Projects you can take on
- Nanopore sequencing workflow review
- Microbial genome analysis using Nanopore data
- Metagenomics data interpretation
- Bacterial genome assembly mini-project
- Antimicrobial-resistance gene analysis using public datasets
- Nanopore vs Illumina sequencing comparison
- FASTQ quality-control project
- Genome-annotation project
Career benefits
Where this takes you
- A standout NGS / genomics skill on your CV
- Practical edge for genomics-focused MS / PhD and jobs
- Research-CV strength for study-abroad applications
- Foundation for bioinformatics and data-analysis roles
Why Manna Biotech
Why choose Manna Biotech
- Founder-led and scientist-guided by Dr Chathyushya K B, PhD (ICMR-NIN), PGDM in Bioinformatics, Advanced Diploma in Patent Law from NALSAR, with 15+ years of scientific experience.
- Hands-on practical training in a working life-sciences lab in Nacharam, Hyderabad — not slides-only theory.
- Hands-on Nanopore sequencing exposure for NGS and genomics learners — a practical advantage that few student programs offer.
- Research-driven projects mapped, where suitable, to publication, patent-documentation and product-development pathways.
- Verifiable internship and training certificates that students can confirm on our official website.
- Career-oriented mentoring with a higher-study and study-abroad pathway through Manna Biotech research-profile mentoring.
This program is designed for education, research training and academic skill development. It is not a substitute for medical diagnosis, genetic counselling, clinical treatment or licensed diagnostic testing.
FAQ
Common questions.
Does Manna Biotech provide Nanopore sequencing training?+
Yes. Manna Biotech provides Nanopore sequencing technology exposure for educational training, academic projects and research skill development.
Is this hands-on training?+
Yes. Students can receive practical exposure to Nanopore sequencing workflow concepts, machine demonstration, data-generation concepts and bioinformatics analysis.
Is Nanopore sequencing useful for biotechnology students?+
Yes. It is useful for biotechnology, microbiology, genomics, bioinformatics, molecular biology, pharma and life-science students.
Is this useful for 4-year Honours research students?+
Yes. Students pursuing 4-year Honours or Honours-with-Research can use this training to understand modern genomics and NGS-based research workflows.
Do you provide NGS data-analysis training?+
Yes. Manna Biotech provides training in sequencing-data interpretation, quality control, genome analysis and bioinformatics workflows.
Is this a medical diagnostic service?+
No. This program is for education, research training and academic skill development. It is not a substitute for medical diagnosis, genetic counselling, clinical treatment or licensed diagnostic testing.
Need a research service instead of training?
Research-use laboratory services
Need sequencing or testing for your own research samples?
For an institution or company outsourcing sample processing, these are separately scoped commercial services. Training enrolment does not include a commissioned research study. Sample acceptance, methods, turnaround and intended-use limits are agreed before work begins.
Whole Genome Sequencing Services
Scope microbial, probiotic, fungal or plant WGS: sample QC, Oxford Nanopore sequencing, assembly and agreed research outputs.
View service scope →Nanopore Sequencing Services
Choose a commercial long-read workflow for genomes, full-length amplicons, plasmids or suitable metagenomic samples.
View service scope →16S Metagenomics Services
Plan bacterial or fungal microbiome profiling for soil, food, water, aquaculture and authorised research samples.
View service scope →Agri Research & Testing
Discuss soil microbiomes, bio-input strain authentication, plant pathogen PCR and research-grade agri-biotech studies.
View service scope →Aqua Disease Diagnostics
Review shrimp or fish pathogen PCR and pond microbiome requirements, with sample instructions confirmed before dispatch.
View service scope →
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