End-to-end NGS, from accessioning to insight.
Sequencing cores and clinical genomics labs run on data lineage. Labitron tracks every sample from the door to the report — and the sequence stays in the same place as the analysis.
What slows your lab down today
The familiar pains.
Massive sequence files
BAMs, FASTQs, and VCFs are too big for the LIMS to handle, so they live on a NAS somewhere with no audit trail tying them to the originating sample.
Sample-to-sequence-to-report gaps
The sequence run knows about the library prep but not the original tissue. The report knows the variant call but not who validated it. The trail breaks at every handoff.
Switching to IGV / desktop tools
Every variant review means leaving the LIMS, opening a desktop app, taking a screenshot, and pasting it back. Annotations end up on personal laptops.
QC bottlenecks
Spreadsheet-based QC means errors only surface at sign-out. By then the sample has moved through three more stages.
How Labitron helps
One trail, one workspace, one truth.
High-throughput sample workflows
96/384-well plate designers, batch accessioning, barcode-driven plating, and library-prep tracking — built for the throughput a sequencing core sees daily.
Sequence viewer in the workspace
Variant review happens on the page where the sample lives. Annotations and comments tie to the sequence, not to a personal app on someone's laptop.
Gigabyte-scale analytics
Drop a 2 GB count matrix or VCF; rows visible in seconds. Run statistics and chart distributions without leaving the dataset.
Full data lineage
Sample → library → run → variants → report. Every transition is a time-stamped event. The trail holds up under any audit.
Get started
See Labitron for genomics.
Bring a typical run worth of samples; we'll walk it from accessioning to report on the demo.