Reporting that fits.
apt Draft
Give apt Draft your variant calls and it returns a full, referenced draft report, made to measure for your laboratory. Your team reviews it, finalises it and issues it.
Your VCF goes in. A draft in your format comes out. Your laboratory issues it.
Why it matters
The sequencer finishes in days. Reading the results can still take a specialist hours per case: classifying every variant, working through current guidelines and typing up the report. apt Draft prepares the whole draft, leaving your experts free for review and clinical judgement.
Drafted to fit.
- 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.
From variant file to issued report
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 it covers
More panels
Further haematological and solid tumour panels and sequencing platforms.
apt means exactly suited. Your draft should be too.
How to begin
Step 1: Share your panel
Your gene list, filtering criteria and current report format.
Step 2: Validate
We set up your template and check drafts with your team before go-live.
Step 3: Go live
Send cases as they arrive.