Genomes, exomes, transcriptomes, single cells and proteomes — analysed stringently, checked by people, and explained so you can trust what the data is telling you.
Based in India. Working with researchers worldwide.
Every dataset has its own quirks. Quality, alignment, thresholds, annotation and biological context all shape what becomes a "result". We look at every one of them.
Every parameter, version and filtering decision is documented, so your analysis is reproducible and ready for your methods section.
We sit with your data, examine its quality and investigate anything unexpected before it reaches a report.
You get clear figures and a walkthrough of what the results mean for your scientific question — not just a folder of files.
Send us your raw or processed data from any platform. Each analysis is tailored to your organism, design and question.
Microbial, human, animal and plant genomes
Our first and most battle-tested pipeline. Every step from read quality to final variant list is checked and justified for your dataset.
Focused on the protein-coding genome
Target-aware analysis that checks capture efficiency and coverage before calling, then narrows thousands of variants to the ones that matter.
Transcriptomes across conditions, timepoints and treatments
From raw reads to differential expression and pathways, with every normalisation and threshold choice made for your experimental design.
10x Genomics and other droplet or plate-based data
Careful filtering of empty droplets, doublets and ambient RNA before anything is clustered, so the cell types you find are real.
DDA, DIA and labelled quantitative LC-MS/MS
Robust handling of missing values and normalisation, which is where most proteomics analyses quietly go wrong.
Have a different kind of omics data? Tell us about it — that's exactly the kind of problem we like.
No software to install and no pipelines to learn. You focus on the science.
Share your data type, organism, design and question through the form or by email.
We set up a secure transfer for your FASTQ, BAM or raw MS files — from anywhere in the world.
Quality checks, tailored workflows, thresholds chosen for your data, and re-runs where needed.
Reports, figures, documented methods and a call to walk you through what it all means.
Data travels faster than samples. Wherever your lab is, we can work on your sequencing and proteomics data.
strand + node stranode
Research taught us that clarity doesn't come from data alone — it comes from how you approach it. Making sense of omics data can feel like searching for a needle in a haystack. Stranode exists to make that search easier.
We're also building a community of analysts, researchers and curious minds who want to go beyond running workflows. Follow us on LinkedIn.
Tell us what you've sequenced or measured. We'll reply with how we'd approach it.
A few details about your data and question are all we need to get started.