Nucleiq unifies sample tracking, QC automation, bioinformatics pipelines, and clinical reporting — powered by AI — across genomics, diagnostics, biorepository, and clinical research.
Nine integrated modules covering every workflow from sample intake to data delivery — with AI running through all of it.
Auto-generated accession numbers, full lifecycle tracking from intake to delivery, aliquot management, consent verification, and QR barcode labels — all in real time.
Configurable pass/fail thresholds per assay type. Import from Qubit, NanoDrop, Bioanalyzer, and TapeStation. AI predicts QC failure risk at intake before you even run the sample.
Powered by AWS Bedrock. Generates plain-language QC reports, detects sequencing run anomalies in real time, forecasts turnaround times, and drafts clinical variant interpretations.
Researchers and clinicians log in to track their samples, view QC results, download data securely via time-limited signed URLs, and pay invoices online — without emailing the lab.
One-click launch of nf-core pipelines (RNA-seq, WGS, scRNA-seq) on AWS Batch. Live run dashboard showing Q30, yield, and cluster density. Interactive results viewer with IGV.js.
Service catalogue with configurable pricing. Invoices auto-generated on data delivery. Stripe integration for online payment. Export to Xero and MYOB for Australian accounting.
One unified patient record and one login across all four verticals — so your data isn't siloed across multiple systems.
Library preparation tracking, Illumina SampleSheet generation, live sequencing run dashboard, pipeline launcher, variant interpretation with live ClinVar and gnomAD lookups.
Electronic test ordering, ACMG/AMP 2015 variant classification, AI-assisted report drafting, MDT sign-off workflow, and HL7 FHIR R4 output for Epic and Cerner integration.
Specimen catalogue with researcher self-service request portal, MTA workflow, AI-driven viability prediction before thaw, consent management, and multi-site biobank support.
Study and protocol management, multi-site trial coordination, REDCap bidirectional sync, biomarker discovery, regulatory submission support, and randomisation management.
Three powerful analysis modules plug directly into the Nucleiq LIMS — sharing your sample data, your storage, and your AI layer. Add only what your lab needs.
End-to-end DNA analysis from FASTQ to clinical report. Genome assembly, alignment, variant calling, SNP analysis, and full annotation against ClinVar, gnomAD, and OncoKB.
Complete transcriptomics analysis — bulk RNA-seq, single-cell, and long-read. Interactive volcano plots, heatmaps, PCA, pathway enrichment, and GO analysis — publication-ready figures built in.
Protein structure prediction, annotation, motif and domain analysis, and quantitative proteomics. AlphaFold2 powered — predict 3D structure of any protein and visualise variant effects interactively.
No hidden fees. No per-sample charges. LIMS core subscriptions below — add NucleiDNA, NucleiRNA, or NucleiPro as optional modules at any time.
Nucleiq Pty Ltd is a leading life science intelligence platform provider based in Launceston, Tasmania, Australia. We accelerate research and clinical workflows across genomics, clinical diagnostics, biorepository management, and clinical research — through intelligent, integrated software built for life science laboratories worldwide.
Nucleiq is committed to the development of user-friendly, AI-powered software solutions for life science laboratories. Our mission is to transform complex laboratory workflows — from sample intake to biological insight — into an intelligent, seamless, and connected experience. Nucleiq is devoted to closing the gap between laboratory operations, bioinformatics analysis, and clinical reporting.
The Nucleiq platform — with its four verticals and three analysis modules — presents a unified, AI-native solution for genomics core facilities, clinical diagnostic laboratories, biorepositories, and clinical research programmes worldwide. Nucleiq is used by life science institutions across the globe, combining LIMS management with end-to-end DNA, RNA, and protein analysis in a single platform. Our AI-assisted clinical reporting, powered by AWS Bedrock, is setting a new standard for genomics intelligence in research and clinical settings internationally.
At Nucleiq we believe that genomic research has extraordinary potential to improve human health, advance food safety, protect environmental quality, and contribute to the welfare of humankind. However, to realise this potential, software solutions that make the analysis and interpretation of genomic and clinical data an easy, intelligent, and effective task must be built and made accessible to every laboratory — regardless of size or bioinformatics expertise.
Nucleiq is committed to the development of user-friendly, AI-powered software solutions for biological and clinical research — and to making them readily accessible to every laboratory around the world. Our mission is to transform complex data analysis, sample management, and clinical reporting into an attractive, interactive, and intelligent experience. Nucleiq is devoted to closing the gap between experimental laboratory work, bioinformatics analysis, and applied clinical research.
With a team combining deep experience in life science research and modern cloud software development, Nucleiq transfers the latest genomics and clinical informatics advances directly into well-designed, production-ready software. We maintain close relationships with research institutions and clinical laboratories worldwide, which allows us to stay at the forefront of genomics innovation and translate this knowledge into software that genuinely improves laboratory efficiency and patient outcomes globally.
Hosted on AWS Sydney by default. Enterprise customers can choose their preferred AWS region — US, EU, UK, or Asia-Pacific. Your data stays where you need it.
HIPAA, ISO 20387, CAP/CLIA, GCP, HL7 FHIR R4, and 21 CFR Part 11 — built into the architecture, not added as an afterthought.
Every interface, every workflow, and every report is designed by people who understand what happens at the bench and at the clinic.
Our AI layer drafts, predicts, and interprets — but every clinical report requires scientist review and approval before delivery.
Built on open bioinformatics standards — Nextflow, nf-core, HL7 FHIR, CDISC SDTM. No proprietary lock-in.
Book a free 30-minute demo and we'll walk you through how Nucleiq works for your specific laboratory type — whether you're running a genomics core facility, a diagnostic lab, a biorepository, or a clinical research programme.