- Home
- Applications
- usa north carolina
- genomics partnering with genome
Show results for
Refine by
Genomics Partnering With Genome Product Applications In Usa North Carolina
2 applications found
Copy Number Variants (CNV) are a clinically important variant type to identify in both somatic and germline genomes. NGS workflows and analytics are increasingly able to resolve duplications, deletions, and other CNVs, alongside SNVs and Indels in a streamlined workflow. These detection algorithms rely on consistent coverage and reads across the genome to accurately identify copy number changes within the genome. However, GC rich regions, suboptimal capture and sequencing primers can impact resolution of CNVs ...
ByAccuGenomics, Inc. based in Wilmington, NORTH CAROLINA (USA)
Locus has built an automated, generalizable platform that is systematically unlocking the power of bacteriophage and CRISPR-Cas3 across multiple therapeutic ...
ByLocus Biosciences, Inc. based in Morrisville, NORTH CAROLINA (USA)