Targeted panels · Exome · Genome · RNA-seq

Next-Generation Sequencing Services

Validated oncology panels, custom panel development, and sequencing from library prep to curated report — in our CLIA-certified, CAP-accredited laboratory.

Validated panels

Ready-to-run oncology panels

Illumina

TruSight Oncology 500

Content

SNVs, indels, CNVs, and fusions across 523 genes, plus TMB and MSI

Sample types

Solid tumor FFPE, and plasma ctDNA for liquid biopsy

Illumina

TruSight Tumor 170

Content

DNA and RNA variants targeted in one comprehensive assay

Sample type

DNA and RNA from the same FFPE sample

Comprehensive services

Every step of the sequencing workflow

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Library preparation

  • Optimized extraction for nearly any sample type
  • Protocols for ultra-low nucleic acid input
  • Concurrent RNA and DNA extraction from FFPE and other challenging samples
  • Exosome capture
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Sequencing modalities

  • RNA-seq
  • Exome and genome
  • Oncology panels
  • Exosome RNA-seq and microRNA-seq
  • Long-read sequencing
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Capture technologies

  • IDT
  • Twist
  • Agilent
  • Qiagen
  • Illumina
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Sequencing panels

  • TSO 500 solid tumor (FFPE)
  • TSO 500 ctDNA for liquid biopsy
  • TruSight Tumor 170
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Custom panel development

  • Small panels (under 20 targets)
  • Medium panels (20–200 targets)
  • Large panels (200–22,000 targets)
  • Hybrid capture or amplicon designs
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EXO-NET® exosome sequencing

As a certified EXO-NET provider, we offer validated exosome RNA-seq, microRNA-seq, total RNA, and total DNA from plasma, serum, urine, saliva, and cell-conditioned medium.

Flexible bioinformatics & data storage

Choose your data deliverable

1

Wet lab only

Raw BCL and FASTQ files.

2

Wet lab & QC

BCL, FASTQ, aligned BAM files, and sequencing QC reports.

3

Variant reporting

Standard output plus variant calls in VCF and gVCF.

4

Full reports

Curated genomic interpretation reports, with options such as QIAGEN Ingenuity Variant Analysis and custom annotation.

Need a custom panel?

Schedule a consultation to discuss your next-generation sequencing needs.