Meet us at Frontiers - TileDB events

Efficiently scale genomics data analysis for newborn sequencing

Handling large volumes of variant data with traditional tools is time-consuming and cumbersome. The work of NICU doctors, genetic counselors and genomic researchers is hindered by underlying data engineering struggles with scale, performance and siloed governance. TileDB offers a comprehensive population genomics solution that stores a wide range of variant and clinical data that can be analyzed at unprecedented scale and at low cost — and it all runs natively in the cloud with governance and security built in.

We were thrilled to sponsor the Frontiers in Pediatric Genomic Medicine event hosted by the Rady Children's Institute Genomic Medicine.

Learn about the breakthrough genomics data management behind BeginNGS

To meet us, please submit the form above.

You heard from TileDB experts about the data management challenges that were overcome in BeginNGS, an innovative newborn screening and treatment system at Rady Children's Institute of Genomic Medicine.

The TileDB data management solution for just-in-time analysis for newly sequenced genomes delivered:

Significant time savings to add samples to datasets and compute variant statistics across an entire population
Ability to easily fuse variant data with other phenotypic data and variant annotations
97% cost reduction in data access vs. file-based approaches
7-hour turnaround to clinical insights

Scaling genomic analysis with TileDB

Frontiers in Pediatric Genomic Medicine

Book a meeting with us

Efficiently scale genomics data analysis for newborn sequencing

Learn about the breakthrough genomics data management behind BeginNGS

Not attending? We’re flexible.

Meet the team of TileDB experts

Chad Krilow

Seth Shelnutt

Jeremy Leipzig