The Accel-Amplicon™ Sample_ID Panel includes 95 primer pairs targeting exonic single nucleotide polymorphisms (SNPs) with high minor allele frequency (MAF) and 9 amplicons to determine gender. With the advent of liquid biopsy assays to monitor circulating nucleic acids in oncology studies, proper tracking of samples has become more and more critical. The power of discrimination of this panel is over 1 in 85,000, making this product suitable for longitudinal studies and scenarios in which genetic fingerprinting is relevant to research design and analysis, including genotyping, NIPT, transplant rejection, and more.
This product is a complete kit that includes all elements necessary to generate multiplex libraries compatible with Illumina™ sequencing platforms, including primer pairs and indexed sequencing adapters.
Features:
Single-tube assay
Ready-to-sequence libraries in 2 hours
Inputs as low as 10 ng
104 amplicons: 95 for exonic SNPs and 9 for gender ID
Validated with cfDNA and FFPE
Benefits:
Easily track samples within and between studies
Ideal for validating tumor/normal pairs
Power of discrimination over 1 in 85,000
Robust calling of germline variants
Compliments WGS or exome sequencing for sample tracking
On-target specificity and coverage uniformity > 95%
Leverages the high fidelity performance of Illumina platforms
Complete library generation in a single kit
Reduce sequencing cost with 384 indexing
The Accel-Amplicon Sample_ID panel is a streamlined amplicon
NGS library prep kit that offers 95 primer pairs targeting exonic
single nucleotide polymorphisms (SNPs) with high minor allele
frequency (MAF) and 9 amplicons to determine gender.