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Roadmap

Available now,and in development.

Phases 1, 2 and 4 are available. Phase 3 remains in development and is not part of the current shared demo.

  • Available included in the current product
  • In development not available in the current demo
  1. 01

    Sanger genotyping

    Available
  2. 02

    Molecular workbench

    Available
  3. 03

    NGS core

    In development
  4. 04

    PCR and parentage

    Available

Available · Phase 1

Sanger genotyping.

From sample sheet and original trace to reviewed, signed result, with every action on the record.

Plates and calls

  • Whole-plate AB1 import with every original retained byte for byte
  • Read and plate quality with required controls checked first
  • Calls at each configured target, including heterozygous indels named in HGVS

Review and release

  • Review by exception and one sweep for clear calls
  • Blind second review where the test requires it
  • Locked releases, versioned amendments, reports and checkable certificates
  • Repeat decisions exported into the next plate's sample sheet

Available · Phase 2

The molecular biology workbench.

Designing, building and confirming an assay in the same recorded place as its results.

Assay design

  • Primer design with known variants masked and candidate pairs checked against the genome
  • Primer library with modifications, orders and lots
  • Confirmed constructs pinned into versioned tests as positive controls

Projects and tools

  • Restriction, Gateway, homology and Golden Gate cloning with recorded junction checks
  • Construct confirmation, alignments, trees and Sanger edit analysis
  • Versioned projects, workflows and open-format import and export
  • BLAST, public database, structure, RNA, motif and protein tools

Available · Phase 4

PCR, arrays and parentage.

Controls-first calculations, exact methods and inspectable evidence through review and release. Automatic qPCR calling still requires the laboratory's own validation and concordance pass.

PCR

  • Real-time PCR plate import, raw-curve analysis and explicit quality flags
  • Detection, copy number, gene expression, GMO content and allelic discrimination
  • Digital PCR concentration with uncertainty, LOD and LOQ state
  • RDML export with independent read-back verification

Arrays and parentage

  • SNP-array and supported genotype-table import
  • Parentage verification and discovery kept as distinct workflows
  • Blind review, explicit marker conflicts, locked release and certificates

In development · Phase 3

NGS core.

Phase 3 is being developed and validated. The shared demo does not deploy the separate NGS compute worker or demonstrate unfinished NGS workflows.

Work remaining

  • Sequencing-run intake, demultiplexing and read-quality checks
  • Short-read mapping and lossless alignment and variant artifacts
  • Germline, joint and low-frequency calling with public benchmark evidence
  • Panel results in the same evidence-first review used for Sanger
  • Operational qualification of the separate compute worker

Invite-only demonstration

See the available workflows.

The shared demo uses public and synthetic data. Client and human samples do not go on the shared server.

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