The only enterprise analytics platform for low-pass sequencing data
1. Assay development: Our sequencing library preparation method is optimized for output and cost-efficiency, with additional expertise in the design & use of custom probes for targeted sequencing. Approaches are automated, scalable, and battle-tested.
2. Sequencing: We are laser-focused on maximizing the value and power of your samples and are here to help you choose the right genotyping method and instrument for the job. We have several options for sequencing your samples: in our lab, our network of service providers, we can help set up an in-house lab, or you can directly upload a FastQ file to the Gencove platform.
3. Genomics cloud: The Gencove genomics cloud unlocks value in genetic datasets and reduces time to answer, with scalable & repeatable bioinformatics pipelines and advanced data analytics and management tools. By abstracting away process and infrastructure complexity, we are supercharging data science teams.
Pioneering low-pass whole genome sequencing
The Gencove team has led the charge on the utilization and adoption of low-pass whole genome sequencing, showing time and time again its utility across a range of use cases.The Gencove platform delivers more data than arrays, is less expensive, and has higher throughput than whole genome sequencing.
- Do you have FASTQ files? Simply choose the type of analysis and upload sequencing data to the platform.
- Do you need sequencing? We connect you to a partner lab or provide support to set up your lab. With low-pass whole genome sequencing, the genome is shotgun sequenced at low coverage (typically <1x) with or without target capture. Then the resulting FASTQ data is uploaded into the Gencove platform to obtain an imputed VCF file and the analysis you need.
What you get
- >10x more data than microarrays
- >10x lower cost than WGS
- >99% accurate whole genome variant calls