BC|SEQUENCE

BC|SEQUENCE is our module for management and analysis of Next-Generation Sequencing data. BC|SEQUENCE is ideal for projects involving:

• 2nd generation fine-mapping
• Re-sequencing of select areas of the genome
• Variation (SNP) discovery from select regions
• SNP genotyping from study subjects
• Standard association analysis with discovered SNPs

Next-generation sequencing data management and analysis with BC|SEQUENCE

The disk space -efficient database technology used by BC|SEQUENCE makes it possible to effectively query and share sequence data. BC|SEQUENCE supports the most popular academic tools developed for sequence assembly against a reference genome, SNP detection, calling and structural variation detection.

Further statistical analysis using BC|SNPmax

Discovered SNPs can be further analyzed using the BC|SNPmax data management solution. It provides a user-friendly web browser interface for working with the analysis programs of your choice. Additionally, the system offers flexible methods for generating workflows for high-performance, parallel data analysis.

Through the web browser interface, you can combine data from multiple sources, filter individuals or SNPs based on various criteria, such as quality, location, and previous analysis results. Data analysis is further enhanced by automated procedures for data format conversions and speed optimized analysis workflows.

BC|SEQUENCE can be integrated with other BC applications, providing a unique set of tools for combining phenotypes and genotypes and managing the data flows from laboratories and clinics to the research results. To learn more about the general data management features of our platforms, please take a look of our solutions for genotype data management.

For more details about sequence data management, please contact us and request a live demo!