Description
Customized NGS panels offer flexible and targeted sequencing of multiple genes selected for a specific clinical phenotype, disease category, or research focus. These panels can be tailored to include anywhere from a few genes to several hundred, capturing relevant exonic regions, promoter sequences, and intron–exon junctions associated with the condition of interest. Panels are typically designed using clinical-grade bioinformatics pipelines to detect SNVs, InDels, and CNVs,
Testing is performed in laboratories accredited by CAP, CLIA, and ISO standards.
DNA extraction available from Dried Blood Spots (DBS), Buccal swabs, EDTA blood, Tissue samples
Indications
Sample Type, Quantity & Conditions
Refer to MedLabs genomics department
Special Precautions
Normal Range
As per Report