Genomics Expertise,
On Demand
From raw sequencing data to publication-ready results - bioinformatics consulting, analysis pipelines, and data infrastructure tailored to your research.
Service Categories
We collaborate with researchers, labs, and organisations who need expert bioinformatics support - whether for a single project or ongoing partnership. Reach out for anything beyond what's listed.
Omics Data Analysis
End-to-end processing of next-generation sequencing and multi-omics data.
- RNA-seq, ChIP-seq, whole-genome resequencing, targeted sequencing
- scRNA-seq and scATAC-seq - cellular heterogeneity, trajectories, expression profiles
- Multi-omics integration (genomics, transcriptomics, proteomics, metabolomics)
- Microarray analysis - gene expression, SNP arrays, methylation, arrayCGH
Omics Data Analysis
End-to-end workflows for RNA-seq, ChIP-seq, whole-genome resequencing, and targeted sequencing - preprocessing, alignment, and variant calling.
scRNA-seq and scATAC-seq analysis to uncover cellular heterogeneity, identify trajectories, and explore gene expression profiles.
Combine genomics, transcriptomics, proteomics, and metabolomics data to create a unified biological model.
Interpret data from gene expression, SNP arrays, DNA methylation, and copy number variation (arrayCGH).
Data Integration & Mining
Unlock insights from complex, multidimensional datasets.
- Biomedical data integration - reveal hidden patterns and associations
- Advanced data mining with customised methods for actionable results
- Causal inference for predictive or diagnostic purposes
Data Integration & Mining
Combine diverse datasets to reveal hidden patterns, causal relationships, or associations across biological systems.
Develop customised methods to extract actionable insights from large, multidimensional datasets.
Identify relationships between measured variables for predictive or diagnostic purposes across clinical and research contexts.
Statistical & AI Modelling
Advanced statistical and AI methods for data-driven research.
- Hypothesis testing, regression, multivariate modelling, survival analysis
- Custom ML models - classification, clustering, genomic predictions
- Deep learning for sequence analysis and feature extraction
Statistical & AI Modelling
Hypothesis testing, regression analysis, multivariate modelling, and survival analysis tailored to biological data.
Custom-built models for classification, clustering, genomic predictions, and high-dimensional data analysis.
Apply neural networks to genomic sequence analysis, feature extraction, and other complex biological challenges.
Evolutionary Biology
Evolutionary studies and microbial ecology expertise.
- Metagenomics - microbial communities and their functional roles
- Phylogenetics - evolutionary histories from molecular data
- Population genetics - diversity, gene flow, evolutionary pressures
Evolutionary Biology
Analyse microbial communities and their functional roles in ecosystems using cutting-edge sequencing approaches.
Reconstruct evolutionary histories and relationships using molecular data across populations and species.
Investigate genetic diversity, gene flow, and evolutionary pressures within and across populations.
Software & IT Solutions
Tailored technical solutions for research and operations.
- Pipeline development - Nextflow, WDL, Docker, Singularity
- Custom bioinformatics tools in Python, R, and more
- Relational and non-relational database solutions
- Cloud-based infrastructure for scalable workflows
Software & IT Solutions
Design and implement scalable pipelines using Nextflow, WDL, Docker, and Singularity for reproducible data processing.
Develop bioinformatics tools and applications using Python, R, and other technologies to meet specific research needs.
Create and manage relational and non-relational databases for large-scale biomedical data storage and retrieval.
Deploy scalable cloud-based solutions for efficient data analysis workflows on AWS, GCP, or Azure.
Training & Education
Hands-on workshops for researchers and professionals.
- Genomics and transcriptomics - RNA-seq, ChIP-seq, pathway analysis
- Single-cell sequencing - clustering, trajectory inference
- Machine learning and AI for genomic data
- Data visualisation with R (ggplot2) and Python
- Pipeline development and automated workflows
- 1-on-1 tutoring - personalised sessions for students and researchers at any level
Training & Education
Learn RNA-seq and ChIP-seq data analysis, including preprocessing and pathway analysis for gene expression studies.
Explore scRNA-seq and scATAC-seq data processing, clustering, and trajectory inference methods.
Build models for genomic data analysis, including feature selection, clustering, and deep learning applications.
Master tools like R (ggplot2) and Python for creating publication-quality, insightful visualisations.
Hands-on sessions for creating automated workflows using scripting and programming languages.
Personalised sessions tailored to your skill level and goals - covering any topic above. View tutoring plans →
General Support
Additional support for research teams across the funding and clinical spectrum.
- Grant writing assistance with a focus on bioinformatics methodologies and computational study design
- Healthcare & precision medicine - patient data analysis for personalised treatment strategies
General Support
Craft effective grant proposals with a focus on bioinformatics research methodologies and computational study design.
Analyse patient data for precision medicine and personalised treatment strategies in clinical and research settings.
A dedicated bioinformatics team on retainer - without the cost of full-time hires.
$2,800 /month
For grant-funded labs, small biotechs, and early-stage R&D.
- Up to 15 support hours/month
- 1 priority project
- Monthly check-in
- Slack/email support
$5,500 /month
For active labs with diverse workflows and scaling biotech teams.
- Up to 30 hours/month
- 2 strategy calls/month
- Multi-project support
- Priority turnaround
$8,500 /month
For diagnostics, scale-ups, consortia, or clinical genomics.
- 45+ hours/month
- Dedicated lead analyst
- Weekly check-ins
- Priority delivery
Interested? Send us a message or view the subscriptions page.
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From Sample to Sequence
Whole genome kits for individuals and sequencing guidance for research teams.
Genome Kits
Explore your own DNA through whole genome sequencing with trusted research-grade lab partners. All data stored securely and under your control.
| Genome Kit (WGS) | $500 |
| Consulting & Analysis | $200/hr |
Sequencing Partners
For academic, clinical, or industry projects, we recommend established sequencing facilities:
Services include whole genome and exome sequencing, RNA-seq, ChIP-seq and epigenomic assays, targeted panels, genotyping, and methylation profiling.
Secure, affordable research data storage fully integrated with the Doppeldata platform - seamlessly move files between archive tiers and analysis environments.
Cloud Storage Vaults
Setup and management of AWS Glacier / Google Cloud Archive Storage for deep archival at a fraction of institutional rates.
Web Dashboard
Simple interface for data uploads, archive tracking, and retrieval - no command-line required.
Platform Integration
Seamlessly retrieve archived data for re-analysis, sharing, or downstream processing within the Doppeldata ecosystem.
Automation
Optional automated upload, verification, and deletion policies to keep your archive compliant and tidy.
Future: Subscription Portal
Portal-based platform with user accounts, upload dashboards, and automated billing - scalable archiving for research groups.
Bioinformatics, statistical genomics & computational biology - practical tools, learning resources, and expert guidance based in South Australia. We are a community that believes in accessible knowledge and learning together.