TAWIL brings end-to-end analysis of genomic, transcriptomic, proteomic and methylomic data together with a report builder that turns findings into polished, fully referenced reports in any organization's own brand.
Start from FASTQ files from any sequencer and get analysed results for genomics, transcriptomics, proteomics and methylomics.
Upload findings and patient details, enrich them with curated public evidence, and publish branded, referenced PDF reports.
Open the report builder →From a raw variant list to a signed, branded PDF without copy-pasting between databases.
Excel, CSV/TSV, MAF, annotated VCF or JSON. Column names are matched automatically, including patient and specimen details.
Gene and variant interpretations, therapy evidence levels and matching clinical trials, drafted from public sources.
Every statement is cited and the reference list is built automatically in Vancouver style, with PMIDs and DOIs.
Logo, colours, fonts, addresses, e-signatures, section headings and boilerplate text, set once per organization.
Every draft is editable: add or remove findings, therapies and trials, then mark the report final after sign-off.
Only gene, variant and cancer-type terms are sent to public databases, never patient identifiers. Each organization sees only its own data.
Drop the lab's findings file. Patient, specimen and variant fields are recognised automatically.
One click looks up every variant and biomarker and drafts cited interpretations.
Edit text, choose therapies and trials, and add, remove or rename sections and sub-sections.
Preview and download a branded PDF with headers, footers and signatures on every page.
Each organization keeps its own branded template, and team members only see the organizations they belong to.
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