Start with a VCF. End with a draft.
Your sequencer already writes a variant file. Send us that. apt Solution sends back a full draft report, fitted to your laboratory's format and ready for your team to review.
What goes in and what comes back
What you send
- VCF
- Fusion calls
- Blood counts
- Clinical history
- Patient and specimen details
- Panel design
- Your report template
What you get back: a draft report
- Executive summary
- Actionable biomarkers
- Disease classification
- Tiered variant and fusion tables
- Gene-by-gene interpretation
- Integrated molecular summary
- Clinical interpretation
Ready for your team to review
Four steps, one case at a time
Step 1: Upload
Add the variant file and clinical details.
Step 2: Sort
Variants are annotated, filtered and tiered against your validated criteria.
Step 3: Write
The full report is drafted in your format, with classification, interpretation and references.
Step 4: Issue
Your team reviews and edits the draft, then issues the final report in your laboratory's name.
What your laboratory gets
- Your house style
- Template, layout and wording all follow your laboratory's own report.
- Guideline-led
- Classification and risk are set against current international guidelines.
- Sourced
- Trace any clinical statement back to its published source.
- Yours to change
- Edit any line of the draft before your laboratory issues it.
- Repeatable
- One set of criteria, whichever the case and whoever reviews it.
- Up to date
- We apply guideline revisions for you, and each report carries the date.
A draft report for your laboratory to review and issue.
Made for
- Molecular pathology laboratories
- Hospitals and cancer centres
- Diagnostic networks