Ducologix partners with life-science organisations to transform complex genomics, proteomics, and clinical datasets into clear, actionable science — from pipeline to publication.
Trusted by leading life-science organisations
From raw sequencing reads to regulatory-ready reports, we cover the full analytical stack.
NGS pipeline development, variant calling, genome assembly, RNA-seq, single-cell analysis, and multi-omics integration.
Clinical trial analytics, biomarker discovery, drug response modelling, real-world evidence, and safety signal detection.
Predictive models for drug target identification, patient stratification, imaging analysis, and lab automation intelligence.
Cloud-native bioinformatics platforms, LIMS integration, scalable Nextflow/Snakemake pipelines, and FAIR data repositories.
Bioinformatics methods documentation, statistical analysis plans, IND/BLA data packages, and peer-reviewed manuscript support.
Technology roadmaps, build-vs-buy analysis, vendor selection, and scientific due diligence for biotech investments.
We have had the privilege of working alongside some of the world's most innovative life-science organisations.
Next-generation genomics diagnostics & research services across South Asia and beyond.
The global leader in DNA sequencing and array-based technologies for genetic analysis.
Pioneering regulatory T-cell therapies to treat autoimmune and inflammatory diseases.
Global healthcare leader in pharmaceuticals and diagnostics driving personalised medicine.
“Ducologix delivered a production-grade scRNA-seq pipeline that cut our analysis turnaround from weeks to days. Exceptional scientific depth combined with engineering rigour.”
“Their team understood our regulatory constraints from day one and built a fully validated bioinformatics workflow that sailed through our IND submission review.”
Ducologix was founded to bridge the gap between cutting-edge biological research and the robust software infrastructure modern life-science organisations need to move fast.
Our consultants bring PhD-level expertise in genomics, immunology, and computational biology together with production-grade data engineering — so you never have to choose between scientific accuracy and operational scale.
We start with the science, not the tooling. Every project begins with a deep-dive into the underlying biology to ensure the right questions are being asked.
Reproducible, validated, cloud-native. We architect solutions that are transparent, version-controlled, and ready to scale.
Insights your team can act on immediately — with documentation, code, and interpretation built in from the start.
RNA sequencing has become the workhorse of transcriptomics. This post walks through the full RNA-seq workflow — from experimental design to statistical interpretation — with practical guidance for researchers new to the technology.
Tell us about your project. Whether it's a one-off analysis or a multi-year partnership, we'll find the right engagement model for you.