Genetic Analysis Services
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We provide “For Research Use” genetic analysis, discovery and confirmatory sequencing services
Our sequencing laboratories are CLIA-certified and CAP-accredited
Our analysis team is based in the U.S.
We follow ACMG guidelines in our clinical interpretation services
Our process and workflow are HIPAA compliant
All client samples are destroyed after projects have been completed
De-identified data is stored, redundantly-backed up and protected at our CLIA-certified and CAP-accredited laboratories.
DNA and RNA sequencing
Whole genome, whole exome, RNA, methylation, single-cell and Sanger sequencing services
Microbiome analysis
Deep Exome Sequencing and Transcriptome Sequencing of Tumor and Matching Normal Pairs
Whole exome analysis comprehensively characterize tumor driver and germline mutations, using tumor and matching normal samples, respectively
Identify gene expression signatures and mutational profiles at the transcriptome level
Pinpoint variants that regulate cancer gene expressions
Profile gene fusions arising from chromosomal translocations
Complementary to routine tumor profile testing by providing additional therapy candidates and clinical outcome predictions
Data Analysis
Primary, secondary and tertiary data analysis services
Interpretation
Interpretation and variant classification of causative variants detected from whole genome, whole exome, panel, RNA and Sanger sequencing data
Include SNVs, indels, CNVs, intronic and mosaic mutations
Pharmacogenomics
Gene-drug interactions
Drug-drug interactions
Analysis of challenging mutations Coupled with our Confirmatory sequencing services
Copy number variants (CNVs), including intragenic and multi-gene CNVs
Approach: Whole genome and long-read sequencing and high-resolution (1.6Kb) microarray
Intronic mutations, including deep intronic variants
Approach: Whole genome and RNA sequencing
Mosaic mutations, including mosaic CNVs
Approach: Whole genome, MLPA and Sanger sequencing
Splice site variants
Approach: Whole genome and RNA sequencing
Reports
We provide provisional report for institutions for further review and signing off by their medical directors
We also provide “For Research Use” analysis reports
Our Genetic Analysis Services are “For Research Use Only. Not For Use in Diagnostic Procedures”
For diagnostic testing, please refer to our menu of Clinical genetic tests