Genomize
partners.compatible_products_services
- partners.product_title:
- SEQ Platform
- partners.product_description:
SEQ Platform by Genomize is a comprehensive genomic analysis and interpretation platform, supporting the tertiary analysis of data generated by Oxford Nanopore Technologies. The Platform incorporates a proprietary variant prioritization algorithm, advanced filtering options, and integrated access to a wide range of genomic and clinical databases.
SEQ Platform supports the analysis of single nucleotide variants (SNVs), indels, structural variants (SVs), and repeat expansions derived from Oxford Nanopore sequencing data, including filtering of compound heterozygous variants for accurate interpretation of complex genomic regions. In addition to the software, Genomize also provides variant interpretation services for Oxford Nanopore users who require additional clinical genomics expertise.
- partners.compatible_ont_products:
EPI2ME workflows:
- wf-human-variation
- wf-hereditary-cancer
- partners.specific_use_application:
- Rare & Undiagnosed Diseases, Hereditary Cancer
- partners.territory:
- Worldwide
