Understanding every genetic variantin seconds.

Because no family should wait months for an answer.

LIA is named after my daughter, diagnosed with SYNGAP1, a rare genetic condition affecting brain development.

The evidence existed. The tools to assemble it quickly did not.

Philipp KangFounder

Runs where your data lives

Your data stays with you, always.

Everything LIA needs travels inside it, so it runs right where your data already lives: on your own computers or servers, even offline. Nothing to upload; nothing leaves the building. A full answer comes back in about a second, right there on your own machine. Parts of it are already headed for open source.

Everything runs inside your own environment. Nothing leaves it.

sub-ms
every lookup
< 1 s
a full answer, backed by the evidence
~30 s
a whole genome, every variant, on one laptop

Speed figures are performance targets and a measured test run; real-world speed varies by machine.

Integrates everywhere

It fits the way you already work.

LIA slots into the systems and tools your lab already uses, instead of making everyone change how they work. Give it a single case or an entire genome. It takes the files you already have and hands back results your other software can use right away.

It slots into the workflow you already run.

Connect it, or just run it

Link LIA to the software you already use, or run it with a single command. Whatever fits your setup.

Works with your files

It reads and writes the file formats your lab already uses, so your data never gets trapped in ours.

Any size, one tool

The same LIA whether you're checking a single result or an entire genome.

Nothing hidden

Nothing about the verdict is hidden.

Every verdict comes with the full reasoning behind it: traceable, reproducible, and yours to challenge.

Fully accountable

Every verdict is traceable end to end: auditable, defensible, ready for validation.

Yours to override

Disagree with any call and record why. Your judgment goes on the record, not buried.

Reproducible by design

Run the same case next year, or in five years, and get exactly the same result.

Never a guess

Every verdict is grounded in real evidence, never invented to fill a gap. Where the science is genuinely uncertain, LIA says so plainly.

Worked exampleSYNGAP1
Variant
NM_006772.3:c.490C>T
SYNGAP1·p.(Arg164*)·GRCh38·NM_006772.3·MANE Select
Pathogenic
Method
Tavtigian 2020
2026-06-18
0 benignpathogenic +15
Net+15evidence points
Applied criteria
PVS1Null variant where loss of function causes diseaseVery Strong
PS2Confirmed de novo in an affected patientStrong
PS4Enriched in affected individuals versus controlsModerate
PM2Absent or ultra-rare in population databasesSupporting

Built by a parent, for every family still waiting.

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