An innovative, scalable cloud computing platform for comprehensive genome analysis.

You’ve sequenced genomes.
Use a platform that finds all the genetic variation they contain.

The Base2 Genomics Platform

Base2 provides a state-of-the-art, highly-scalable, cloud computing platform for characterizing all forms of genetic variation in human genomes. We integrate our own innovative tools and proprietary databases to maximize speed, economy, and accuracy. We can find SNP, INDEL, SV, and STR variation in single genomes to 1000s of genomes in hours to days. Check out this video to learn more.

WHAT WE DO

Base2’s provides a state-of-the-art, highly-scalable, cloud computing platform for characterizing all forms of genetic variation in human genomes. We provide a secure, HIPAA conformant system for uploading your raw genome sequence data into the Base2 platform. Once uploaded, your data will be aligned, variant-called, and analyzed for quality control with the most advanced genome analysis platform available.

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TEAM

Base2 was founded by scientists with deep expertise in computational genomics. We have long history of developing innovative methods for detecting genetic variation, variant interpretation, and scalable algorithms for genome research. Base2 has developed powerful new technologies for quality control, data visualization, and interpreting structural variation.

Meet the team

NEWS

  • Base2 Genomics will be at AWS reInvent and is presenting in session CMP323, “AWS Batch: Easy and Efficient Batch Computing on AWS
  • Base2 recently processed a cohort of 1,049 human genomes from a large study of Ewing sarcoma in 3 days. This included comprehensive discovery of all forms of genetic variation, as well as extensive annotation and quality control.
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