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Genomic Services


TruSight Panels are designed to interrogate coding regions of known cancer and disease associated genes, as curated by leading professionals in each panel's respective field. Panels are optimized for quick turnaround, and affordable pricing whether you need to test a few samples or you have a large sample set. These panels are compatible with paired-end sequencing on the MiSeq platform.

Services / Applications

TruSight Rapid Capture Panels

Exome 7MB enrichment (Coding regions of genes associated with inherited disease – HGMD database)
Cancer Targets 284 SNPs within 94 genes known to be associated with cancer
Autism Targets 101 developmental delay genes linked specifically to autism.
Cardiomyopathy Designed to target 46 genes important in the research of inherited cardiomyopathies.
Inherited Disease Targeting 552 genes, including coding regions, intron-exon boundaries, and regions harboring pathogenic mutations.
Tumor Designed for deep sequencing of variants in solid tumors, enabling detection of low frequency variation (<5%) across 26 genes.

Benefits of Retrogen, Inc.'s NGS Services

  • Knowledgeable Technical Assistance
  • Fast Turnaround for Fixed Panels
  • Sequence with the depth of coverage that makes sense for your project
  • Multiplexing samples using validated indices lowers your costs
  • Library Construction
  • Multiple QC steps
  • High Quality Data
  • Cloud-Based Data Analysis

Platform Specifics

Input Quantity 50 ng input (25ng/µL)
Input Quality (A260.280) 1.8-2.0
Multiplexing Yes, up to 12 Samples per enrichment
Turnaround time 2 weeks