Genomic Analysis News

Announcing CBMi-Seq Seamless NGS Data Management and Analysis

CBMi-Seq analysis provides primary analysis and management of researchers' next generation sequencing data-from delivery of raw data to sequence assembly, variant detection, annotation, and discovery.

You provide:
Raw whole exome, whole genome, or targeted DNA-Seq data in a standard format

CBMiSeq provides:

  • Alignment of raw sequence data to a reference genome
  • Delivery of variant call files (.vcf files) on a shared drive
  • Storage of aligned data (for 3 months) and .vcf files (permanently)
  • Genomic annotation of aligned data from a variety of sources
  • An automated, quality controlled process to ensure integrity of results
  • Access to project-specific, CHOP-wide, and externally derived variant frequencies
  • Customer service and training for every step of the process

See how it works here.

How Much Is It?
Currently, we are charging $110 per sample run. This fee helps us cover our personnel costs. Special pricing is available for large orders

Register to Set Up Your Account
Register at get started. (URL accessible from CHOP internal network)