Sequencing and Custom Data Analysis to Guide Decision Making

Rely on our experienced genomics services to deliver high quality, interpretable results using highly sensitive PCR-based, real-time PCR, and NGS technologies and advanced data analytics. All your genomics research needs can be accommodated through our highly flexible and customizable platform, as well as our long standing experience in analyzing preclinical study samples:

Streamline your preclinical workflow by integrating genomics services into your existing in vitro or in vivo studies
Leverage state-of-the-art platforms to meet your sequencing needs from short to long-read sequencing and detection of structural variants using Illumina NovaSeq 6000, BGI MGISEQ-2000, PacBio^® Sequel II, and the Bionano^® Genomics Saphyr System
Explore and validate drug mechanism with advanced genomic analyses
Identify genetic features associated with drug response through genomic profiling of your preclinical samples
Understand drug resistance by interrogating the immunogenomics of tumor-immune interactions
Take advantage of our proprietary tools and model data including our large database of NGS-characterized models and algorithm for biomarker discovery utilizing NGS data.

Genomics Service Solutions for Your Every Research Need

Our genomics services cover nucleic acid extraction, sequencing, bioinformatics analysis, reports, and visualization and can be utilized as a standalone service or as part of an integrated preclinical project. We accept various RUO sample types including fresh and frozen cells and tissue, FFPE, biopsies, and mouth swabs.

You can customize your analyses as well as using our standard genomic services including:

Single genes and pathway gene expressions
Virus copy numbers
Gene mutations
Gene fusion validations
SNP genotyping
Differential and tissue specific gene expression
Functional annotation of differentially expressed genes
Pathway and network analysis of differentially expressed genes

Driver mutation prediction
Tumor purity analysis
Molecular subtyping analysis
Co-expression network analysis
Comparative analysis with published human tumor samples (e.g. TCGA)
Copy number variant identification
Large structural variants
Epigenomics
Target gene methylation analysis
Single cell sequencing

Choose from two secure and convenient reporting options:

Tier 1: FASTQ (raw data)
Tier 2: FASTQ, processed data (i.e. expression, mutation, copy number, gene fusion), and comprehensive report
Consultation included with all tiers
Secure data transfer via Amazon Web Services
1 year storage included with service pricing
Long-term storage available

Global Gene Expression of Cell Lines