Exome Sequencing

OVERVIEW

Retrogen utilizes one of the industry’s top-rated platforms for Next Generation Sequencing (NGS), enabling massively parallel sequencing for almost any molecular genetics application. The flexible and scalable nature of the technology allows investigators to interrogate genomes, exomes, transcriptomes, or even just thousands of PCR amplicons in parallel, leading to significant data sets and decreased time to a conclusion. With the ability to multiplex using sample indices, your throughput will reach new speeds.

Retrogen uses Illumina’s sequencing by synthesis chemistry – compatible with the MiSeq and enabling small genome de novo or resequencing, SNP profiling, targeted enrichment, and amplicon sequencing. Additionally, Retrogen’s NGS offers workflows that support clinical diagnostics, prenatal testing, and women’s health, all available under a CLIA/CAP-regulated environment. Contact a sales representative today to bring your research into the next generation.

Types of Service

Molecular Diagnositcs
Amplicon sequencing
Library QC
Gene Expression
De Novo Sequencing
Exome Sequencing
Transcriptome Sequencing
AmpliSeq (Illumina)

BRCA Panel

Cancer Hotspot Panel v2

Childhood Cancer Panel

Comprehensive Cancer Panel

xGen Lockdown Panels (IDT)

Pan-Cancer Panel

Inherited Disease Panel

KAPA HyperPrep Kits for Library Construction

gDNA, mtDNA, and cDNA-derived Amplicons

Clone Checking

Transfection/Infection Checking

Mutagenesis

Vector/Plasmid Insert Sequencing

High-Sample Volume Genotyping

Metagenomics (16S rRNA)

Features & Benefits

Quality

Data routinely above Q30.

Scalable

Up to 30M PE reads (2×300).

Convenient

Local pickup available in select areas.

Quick Turnaround time

Starting from 1 week.

Support

Dedicated project management and excellent technical support to help you achieve your project goals.

Customizable

Depending on your project, a variety of sample types are accepted. Please consult your project manager for details and specifics.

Workflow

Design -> Review -> Confirm -> Order -> Sample QC -> Library Construction -> Sequencing QC -> Sequencing -> Data Analysis

How to Order

Refer to the sample submission guidelines for your application.
Once your samples are ready, log in to place your order, or call customer support at (858) 455-8411.