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Strand Analytics Clinical Exome (All Pathogenic/ Likely pathogenic variants)

SKU: SANGS

$120.00 per sample

Variations are identified using Strand’s integrated proprietary software STRAND®NGS – which provides analysis, management and visualization tools for next-generation sequencing data, and interpreted using Strand’s proprietary interpretation and reporting platform StrandOmics™ –   which combines bioinformatics algorithms, public data from external sources/knowledge databases, visualization interfaces and reporting capabilities.

Variations are identified using Strand’s integrated proprietary software STRAND®NGS – which provides analysis, management and visualization tools for next-generation sequencing data, and interpreted using Strand’s proprietary interpretation and reporting platform StrandOmics™ –   which combines bioinformatics algorithms, public data from external sources/knowledge databases, visualization interfaces and reporting capabilities.

The Fine Print

Strand clinical interpretation service is driven by an expert and clinically trained team of variant scientists and medical geneticists, who aid in the professional review and sign-out of clinical NGS reports. The variant interpretation and reporting will be supported by Strand’s secondary/tertiary analysis tools STRAND®NGS and StrandOmics™. STRAND®NGS enables the secondary analysis of (FASTQ) data generated from next-generation sequencing (NGS) experiments, and supports extensive workflows for the analysis and visualization of a range of NGS data including DNA-Seq data from whole genome, whole exome or targeted resequencing experiments. StrandOmics™, a proprietary and robust platform for tertiary analysis and report generation, is a semi-automated pipeline that starts with VCF files, allows easy and secure data upload through the web interface, and also has a curation on the fly portal, which enables rapid curation on new variants. It is comprehensive and accepts all variant types, including reporting on variants in pseudogenes.

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