Medical software NₓClinical

analysisinterpretationNGS

Comprehensive and up-to-date decision support solution for cytogenomics and molecular genetics to assist with the analysis and interpretation of genomic variants from microarray and NGS data. Achieve accurate, efficient variant interpretation from a single-screen view. With the NₓClinical software, you get: Complete visibility into a comprehensive set of public repositories for germline and somatic pipelines Event-level details Pre-classification according to published society guidelines (i.e. ACMG, NCCN, and WHO guidelines) or SAP scoring Historical contextualization to previous calls Custom Knowledgebase Audit log Similarity to previous cases Visualize multiple tracks of genomic data for the at-a-glance context of variant calls. NₓClinical offers multi-platform integration by: Combining current and historical molecular data from array and sequencing for sample continuity Comparing and contrasting outputs from multiple technologies to understand the underlying biology Allowing custom loading of .BED files to highlight areas of specific interest Uncovering compound heterozygous aberrations et continuous, community-driven updates that match the pace of innovation in genomics. Bionano is committed to providing: Current reference genomes Updated pipelines Curation excellence Regular introduction of new features for emerging applications