Molecular Testing · Contract Testing · Analytical Research
Research-use laboratory testing — scope review in Hyderabad.
Discuss a research-use DNA, PCR, microbiology or sequencing requirement with Manna Biotech. The method, sample matrix, executing facility, quality checks and reporting responsibilities must be confirmed before sample acceptance. Listed topics are scope-discussion options; an enquiry does not establish current availability or accredited reporting.
Plan your project
Choose a test around the decision and the sample
The same material can raise very different questions: identity, a defined molecular target, a community profile or a comparison between batches. For research and internal product-development work, state what the result must help you decide before selecting a method or requesting a price per sample.
Decision 1
Identify what a result can establish
A targeted assay asks about a defined target; a broader sequencing study asks a different question. For pharma, food, nutraceutical or agricultural R&D, separate identity or composition questions from efficacy, safety and release decisions. Tell us the required report purpose so unsuitable research-use routes can be identified before samples move.
Decision 2
Treat the sample matrix as part of the scope
Describe whether the material is a culture, tissue, extract, formulated product, soil or another matrix. Include available quality information, handling history and the number of distinct batches or groups. Sample count alone is not enough to determine extraction, controls or suitability. Obtain confirmed preparation and transfer instructions first.
Decision 3
Agree how uncertain results will be reported
Ask which controls and quality checks are included, how failed or inconclusive results are flagged and when repeat testing would be proposed. A report should distinguish an observed signal, a quality limitation and the interpretation for the stated question. Agree the raw outputs and report detail needed for your own review.
Ask for a written sample-to-report scope
Confirm the accepted material, method, controls, output files, report interpretation and handling of unsuitable samples in the quotation. If a regulatory or accredited report is essential, that requirement must be resolved through a separately verified qualified facility before a research-use test is commissioned.
Confirm the testing scope
Sequencing, molecular biology and microbiology — scope the required evidence.
The named method, sample matrix, executing facility, instruments, quality controls and reporting responsibilities must be confirmed for each project. The topics below are scope-discussion options and do not establish in-house equipment ownership or availability.
Sequencing & genomics
Whole Genome Sequencing (WGS)
Long-read sequencing with assembly and annotation — strain-level characterisation, genome confirmation and comparative analysis.
Sanger sequencing
Targeted sequencing for gene confirmation, clone verification, species identification and phylogenetic work.
16S metagenomics — bacterial
Bacterial community profiling of soil, water, gut, fermented and clinical-research samples, with diversity and composition analysis.
18S metagenomics — fungal & eukaryotic
Eukaryotic and fungal community profiling — far less commonly offered than 16S, and often the missing half of a microbiome study.
Transcriptomics analysis
RNA-level analysis of what a genome is actually expressing — differential expression, pathway and functional interpretation.
AMR genomics
Genome-level detection of antimicrobial-resistance determinants — resistance gene profiling and interpretation alongside phenotypic susceptibility.
Molecular biology & PCR
Gene-expression assay planning
Define whether the research needs endpoint amplification or quantitative expression analysis. The scientist must confirm the reverse-transcription step, assay method, controls and validation before acceptance.
Primer design & validation
Primer design, specificity review and laboratory-validation requirements must be scoped and confirmed for the proposed target.
Aquaculture pathogen PCR
Proposed shrimp or fish pathogen targets, sample matrices, intended use and validation requirements must be reviewed separately. No named panel or accepted matrix is confirmed here.
Species ID, adulteration & GMO screening
DNA barcoding to confirm what a sample really is — meat and fish substitution, spice and herbal authentication — plus PCR screening for GM elements.
Microbiology & bioactivity
Microbial identification
Identification of bacterial and fungal isolates by culture, biochemical profile and rRNA sequencing — with a defensible taxonomic call.
Biochemical characterisation
Full biochemical profiling of isolates — the classical characterisation that supports and confirms a molecular identification.
Antibiotic susceptibility testing
Phenotypic susceptibility profiling of isolates — the practical counterpart to AMR genomics.
Antibacterial activity
Evaluation of extracts, formulations, actives and finished products against bacterial test organisms.
Antifungal activity
Evaluation of extracts, formulations and products against fungal test organisms.
Why genotype and phenotype together matters
Molecular and classical microbiology findings can address different parts of a research question: AMR genomics tells you which resistance genes an organism carries, while antibiotic susceptibility testing tells you how it actually behaves — and the two do not always agree. The same applies to a molecular identification confirmed by biochemical characterisation. That is a materially stronger answer than either half alone.
Straight answer on scope and accreditation.
Any accepted molecular testing scope on this page is limited to research, product development and internal quality monitoring. They are not currently offered as accredited regulatory tests, and we will never tell you otherwise.
Tell us if you require an accredited or statutory report — for example, for FSSAI compliance, export certification, pesticide residues, heavy metals or proximate analysis. Before any such work is accepted, the executing laboratory, applicable accreditation and test scope, current validity, and responsibility for delivery and report issue must be verified. An enquiry does not confirm availability or approval.
Who we work with
Built around real sector problems.
Food & nutraceutical
Ingredient authenticity, species verification, microbial identity and contamination tracing.
Aquaculture & hatcheries
Research questions about shrimp or fish pathogen detection; target, sample, method and reporting suitability require review before any decision-making use.
Probiotics & fermentation
Strain identity and purity confirmation at genome level — the evidence your dossier needs.
Herbal, AYUSH & botanicals
Botanical authentication and adulteration detection on raw material and finished powders.
Agri-input & biofertiliser
Soil and formulation microbiome profiling, strain confirmation and shelf-life monitoring.
Pharma, biotech & research teams
Sequencing, molecular assays, microbiology and bioinformatics for defined R&D and outsourced research modules.
How you receive the result
Choose how much interpretation you need.
Standard report
The analytical result, delivered to a clear, documented format with methodology stated.
Best for: Routine screening and repeat samples
Expert report
The result plus a written scientific interpretation — what it means, the likely cause, and the corrective action we would recommend.
Best for: Investigations, dossiers and decisions
Scientist consultation
A direct discussion with our founder-scientist to design the study, review findings or plan a corrective programme.
Best for: Recurring problems and study design
Charges depend on the test, matrix and sample volume — a counsellor confirms the exact scope and cost for your requirement.
Why the interpretation matters
Define the report and scientific review before testing.
A result on its own rarely solves the problem. Knowing whether contamination came from raw material or from handling, whether a species mismatch is substitution or mislabelling, or whether a result needs repeat testing or independent confirmation — that is a judgement call, and it is where a working scientist earns their place.
At Manna Biotech that judgement comes from the people who lead our research, not from an automated template.
Dr Chathyushya K B, PhD
Founder, MD & CEO — Microbiology
Project-specific scientific review, methods, interpretation and reporting responsibilities must be confirmed before acceptance.
Bioinformatics & NGS Analysis Team
Sequence Analysis & Bioinformatics
For a proposed sequencing analysis, confirm the responsible reviewer, pipeline, versions, quality checks and reporting scope.
How it works
From sample to decision, in one window.
Tell us the problem
Share the sample type, what you need to know, and whether the result is for internal use or a statutory submission.
Scope & quote
We confirm the right test, the sample quantity required, turnaround time and cost before anything moves.
Send the sample
Indian samples can be couriered or dropped at our Nacharam laboratory after instructions are issued. International samples move only after biosafety, courier, customs and import feasibility are confirmed.
Result & interpretation
You receive the analytical report, and — on the Expert tier — a scientist’s written interpretation and recommended next step.
Testing every batch, every month?
For recurring testing requirements, request a scope review covering the proposed panel, sample cadence, reporting format, scientific contact and scheduling constraints. Any turnaround, price or volume discount must be confirmed in an approved agreement; no saving or priority availability is promised here.
Discuss a testing agreement →Request a test or quote
Tell us what you need tested.
Include the sample type, the tests you think you need, and whether the report is for internal use or a regulatory submission — that last point decides how we route it. If you are not sure which test applies, describe the problem and we will advise.
Related services
Find the testing route that matches your sample and decision.
Whole genome sequencing
Oxford Nanopore long-read sequencing, assembly, annotation and raw-data delivery for research-led genome questions.
16S metagenomics
Microbial-community profiling, OTU or ASV analysis, diversity interpretation and research-ready community outputs.
PCR & qPCR testing
Targeted molecular-assay support for gene expression, pathogen detection, primer design and research use.
Food testing & authenticity
DNA-based food authentication, probiotic strain identity and contamination investigations for food, nutraceutical and herbal products.
Aquaculture disease diagnostics
Focused PCR screening for shrimp and fish disease-management decisions, from pre-stocking checks to hatchery monitoring.
Bioinformatics & NGS analysis
Send existing sequence data for genome, 16S, RNA-seq, variant and publication-ready analysis support.
Agri-biotech research & testing
Scope suitable plant, soil, microbial and biofertilizer research-use questions.
CRO & contract research services
Move from a defined test to a multi-stage research programme with NDA, milestones, documented deliverables and client-owned IP.
Questions
Frequently asked questions
Which tests does Manna Biotech run in its own laboratory?
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The executing facility and equipment must be confirmed for each requested test. Provide the target, sample matrix, intended use and required report; no listed method or named pathogen panel should be treated as verified in-house availability from this page alone.
Are you NABL accredited or ISO 17025 accredited?
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No accreditation is claimed on this page. The scope discussed here is research, product development or internal quality monitoring, not accredited or statutory testing. Any accredited-report requirement must be identified and verified separately before acceptance.
Can you still arrange accredited or statutory testing?
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Tell us whether an accredited or statutory report is required, including the intended use and tests. Before any such work is accepted, the executing laboratory, applicable accreditation and test scope, current validity, and responsibility for delivery and report issue must be verified. An enquiry does not confirm availability or approval.
What is the difference between a Standard report and an Expert report?
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A Standard report gives you the analytical result in a clear, documented format. An Expert report adds a written scientific interpretation — what the result means, the likely cause, and the corrective action we would recommend. Most laboratories give you a number; the interpretation is where the decision actually gets made.
Do you offer ongoing testing arrangements?
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A recurring requirement can be submitted for scope review. Panels, cadence, reporting, availability, turnaround and price require an approved agreement. No volume discount or priority scheduling is guaranteed.
How do I send samples and how much do tests cost?
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Samples can be couriered to our Nacharam, Hyderabad laboratory or dropped in person, and we provide packing instructions first. Charges depend on the test, the matrix and the sample volume, so tell us what you need established and we will send a scoped quote.
Can international clients send samples to Manna Biotech?
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Eligible international projects can begin with remote scope review, data analysis or reporting. Physical samples are accepted only after the exact matrix, biosafety classification, packaging, courier route, customs and Indian import requirements are confirmed. Do not ship a sample before receiving written instructions.
What should I prepare before requesting a testing quote?
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Describe what you need to establish, the sample matrix and approximate count, any relevant reference material or control information, the intended use and format of the report, your preferred timeline, and any method or acceptance questions. Tell us at the outset if an accredited, statutory or clinical report is required; the website does not establish that the requested scope is approved. Use a non-confidential sample description initially and request confirmed submission guidance before preparing or dispatching material.