Bioinformatics & NGS Data Analysis Services
Send us your data. Get back results you can publish and defend.
A professional analysis service led by Dr Manne Munikumar, PhD (Bioinformatics) — for scholars, faculty, institutions and companies who have sequencing data but not the pipeline, the compute or the time to analyse it properly.
This is a service, not a course. Delivered remotely, anywhere in India.
What we analyse
Complete pipelines, documented end to end.
Genome assembly & annotation
De novo and reference-guided assembly from Nanopore or Illumina reads, with structural and functional annotation and quality metrics.
16S metagenomics & microbiome
Full amplicon pipeline — quality control, ASV/OTU calling, taxonomic assignment, alpha/beta diversity and differential abundance.
RNA-seq & differential expression
Alignment, quantification, differential expression, pathway and GO enrichment, with heatmaps and volcano plots.
Molecular docking & MD simulation
Target preparation, docking, binding-affinity analysis and molecular dynamics with trajectory analysis.
Variant calling & analysis
Alignment, variant calling, filtering and annotation, with interpretation of variants of interest.
Figures & methods write-up
Publication-quality figures plus a written methods section you can adapt directly for your thesis or manuscript.
Who this is for
You have the data. We have the pipeline.
PhD scholars & researchers
You have generated data but need it analysed rigorously — and defended in your viva. We explain the analysis so you can present it as your own work.
Faculty & institutions
Departments without a bioinformatics facility can outsource analysis for funded projects, publications and student dissertations.
Biotech & pharma companies
Project-based analysis for internal R&D programmes, delivered under confidentiality.
Labs that sequence elsewhere
Already have FASTQ files from another provider? Send them across — we analyse data regardless of where it was generated.
How it works
Four steps, no travel required.
Share the scope
Tell us the data type, how it was generated, and the biological question you need answered.
Quote & timeline
We confirm the pipeline, deliverables and turnaround before any work begins.
Transfer your data
Send FASTQ or raw files by cloud link — from our sequencing or from any other provider.
Results & walkthrough
You receive results, publication-quality figures and a methods write-up — plus a call to walk you through it.
Why Manna Biotech
Analysis you can stand behind in a viva.
Led by a PhD bioinformatician
Dr Manne Munikumar, PhD Bioinformatics, Director — Academics, oversees the pipelines and the interpretation.
We run the wet lab too
Because we also do the sequencing, we understand how your data was generated — not just how to process it.
You get the method, not a black box
Every deliverable includes the methodology, so you can explain and defend the work as your own.
Confidential by default
Your data and results remain yours. NDA available on request before any transfer.
Start a project
Tell us about your data.
Include the data type (RNA-seq, 16S, whole genome, docking), roughly how many samples, and the question you are trying to answer. We will come back with the right pipeline, a timeline and a quote.
Questions
Frequently asked questions
Can you analyse data that was sequenced somewhere else?
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Yes. We analyse data regardless of where it was generated — send your FASTQ or raw files by cloud link and we will work from those. Many of our analysis clients sequenced at another facility and only need the bioinformatics.
Is this a course or a service?
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This is a service. You send data and receive analysed results. If you want to learn to do the analysis yourself, that is our separate bioinformatics training programme — the two are different offerings with different outcomes.
Will I be able to explain and defend the analysis in my viva?
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That is the point of how we deliver it. Every project includes a written methods section and a walkthrough call, so you understand what was done and why. We support your work and never ghost-write it — the research and the authorship remain entirely yours.
What kinds of analysis do you cover?
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Genome assembly and annotation, 16S metagenomics and microbiome analysis, RNA-seq and differential expression with pathway and GO enrichment, variant calling and annotation, and molecular docking with MD simulation. Deliverables include publication-quality figures.
Do I need to travel to Hyderabad?
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No. The service is delivered remotely anywhere in India. Data is transferred by cloud link and results are returned the same way, followed by a call to walk you through them.
Is my data kept confidential?
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Yes. Your data and results remain yours, and an NDA is available on request before any transfer. Company projects are routinely run under confidentiality.
Can you guarantee my paper will be published?
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No, and no honest provider can. Journal acceptance depends on your study design, novelty and the reviewers. We make sure the analysis is rigorous, properly documented and defensible, which is what we can genuinely control.