End-to-End Analysis for Accurate, Actionable Genomic Insights
The IVDNGS™ & GENHUMANID™ NGS Data Analysis Services provide advanced, customizable, and regulatory-compliant bioinformatics solutions for clinical and forensic genomics. These services are designed to process and interpret large-scale sequencing data generated from various NGS platforms, transforming raw reads into reliable, medically relevant reports.
From inherited diseases and oncology to identity verification and research, these platforms deliver rapid variant detection, clinical interpretation, and forensic STR profiling, with built-in compatibility for ISO 13485-compliant workflows.
Comprehensive pipelines for WES, WGS, Targeted Panels, and STR-based identity testing
Compatible with multiple input formats: FASTQ, BAM, VCF
Detects SNVs, Indels, CNVs, STRs, and structural variants
Includes annotation from ClinVar, HGMD, COSMIC, dbSNP, OMIM
Generates customized clinical reports with phenotype correlation
Rapid turnaround time with cloud or on-premise deployment
Ideal for hospitals, labs, research centers, and law enforcement
| Parameter | Details |
|---|---|
| Service Name | IVDNGS™ & GENHUMANID™ NGS Data Analysis Services |
| Applications | Clinical Diagnostics, Oncology, Inherited Disorders, Forensics, Research |
| Data Inputs Supported | FASTQ, BAM, VCF |
| Variant Types Detected | SNVs, Indels, CNVs, STRs, Structural Variants |
| Compatible Assays | Whole Exome, Whole Genome, Cancer Panels, Forensic STR, Prenatal Testing |
| Annotation Databases | ClinVar, HGMD, COSMIC, dbSNP, OMIM |
| Report Type | Raw Data QC, Variant Summary, Annotated Reports |
| Regulatory Compliance | ISO 13485, IVD-ready |
| Deployment | Cloud-based or Local Server |
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