Slice – Single Gene (1 gene)
Use
The Slice – Single Gene (1 gene) test allows selective examination of one gene of interest using next-generation sequencing on custom-selected gene lists, enabling confirmation of clinical diagnoses, genetic counseling, and recurrence‑risk assessment. Reported variants include pathogenic, likely pathogenic, and variants of uncertain significance (VUS); heterozygous VUS in autosomal recessive genes may be reported separately; benign or likely benign variants are excluded.
Special Instructions
Not provided.
Limitations
Only the gene selected and included in the approved gene list will be analyzed. Genes with poor coverage, homologous regions, technical sequencing issues, mitochondrial genes, non‑coding, regulatory or deep intronic regions are not suitable for this method. Coverage data is average; actual coverage for requested genes may vary. Only CNVs involving ≥3 exons may be detected.
Methodology
NGS (Targeted)
Biomarkers
Result Turnaround Time
0 days
Related Documents
For more information, please review the documents below
Specimen
Extracted DNA
Volume
Not provided
Minimum Volume
Not provided
