Bioinformatics

Auralis Biotech helps labs, diagnostics companies and research teams turn complex biological data into actionable results. From raw sequencing reads to publication-ready outputs, we provide tailored, robust, scalable and reproducible bioinformatics solutions.

We are your partner in building smarter workflows, clearer visualisations and stronger scientific reporting. Scientists focus on discovery, we handle the rest.

The Hidden BottleneckWhy great science gets stuck.

  • Quality Control

    Hidden sequencing errors, biases or mislabelled samples compromise results and waste resources.

  • Biological Interpretation

    Gene lists, variants or clusters remain disconnected from pathways or disease relevance.

  • Data Storytelling

    Findings buried in dense tables or static plots, hard for teams or investors to see significance.

  • Decision-Making

    Unclear, fragmented analysis delays go/no-go decisions and promising results are left unused.

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Core Bioinformatics Services

  • Genomics and NGS Analysis

    RNA-seq, WES, WGS, single-cell RNAseq, long-reads (PacBio and Nanopore). Automated reporting with R, Quarto, R Shiny and Jupyter Notebook.

  • Functional Genomics and CRISPR Screen Analysis

    CRISPR KO, CRISPRa/i, combinatorial, dual gRNA CRISPR, scCRISPR and in-vivo CRISPR.

  • Workflow Optimisation, QC and Experimental Design

    Pipeline and experiment design, multi-layered QC, automated pipelines, Docker, AWS and Nextflow.

  • Data Visualisation and Reporting

    Interactive data exploration via R Shiny apps and custom visualizations. Automated clinical report generation with R Markdown. Publication-ready figures for teams, papers and investors.

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Ready to unlock your data?

Tell us your goal. We design a custom plan, deliver tailored analyses and stay your partner as your project evolves.

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