Focused sequencing panel to assess 15 genes that are commonly mutated in solid tumors in a single assay
A next-generation sequencing assay designed to cover 170 genes associated with common solid tumors
Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.
Targeted RNA-sequencing (RNA-Seq) is a highly accurate method for selecting and sequencing specific transcripts of interest and offers both quantitative and qualitative information.
TruSight Inherited Disease is a targeted sequencing panel that focuses on 552 genes associated with severe, recessive pediatric onset diseases.
This panel focuses on exonic regions harboring disease-causing variants. Labs can perform commonly ordered molecular assays on-site with one assay
A fully validated next-generation sequencing solution for PGS, providing accurate results in aneuploidy screening and extending future opportunities.
Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in less than 90 minutes, with a low DNA input requirement
Nextera DNA kits provide a fast and easy library prep workflow, delivering whole-genome sequencing libraries in under 90 min
This high-value solution for parentage testing of multiple beef and dairy cattle breeds includes genotyping of relevant traits in a single assay
This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depthsThis kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths
Converts bisulfite-treated, single-stranded DNA into an Illumina sequencing library. Enables comprehensive whole-genome DNA methylation analysis.