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GeneWorks is an independent Australian service provider to the local and international research community. We aim to provide the highest level of service, confidentiality and customer support, working with our customers to reach their goals. Our Next Gen Sequencing services are fully backed by GeneWorks’ ISO 9001 and Illumina CSPro certification.
With the 2007 installation of our first Illumina Genome Analyzer, GeneWorks now has over three years experience with this versatile technology and a proven history of providing quality outcomes for all major applications (see our Testimonials page) direct from our Adelaide laboratories.
GeneWorks offers short (35b), intermediate (65b) and long (90b or longer) reads with guaranteed sequence yields per lane. Read length and data volume is likely to further increase with introduction of improved chemistries and data analysis.
Genome Analyzer II(x) technology is a powerful tool for exploring genetic variation and gene expression. The process starts with generation of a library of DNA fragments containing Illumina-specific sequences at either end. Our different sample preparation methods allow libraries to be generated for a wide range of research applications. For more information please read below or navigate to our Service Options and Pricing page.
GeneWorks has experience in many newly published applications and works with our customers to develop new methodologies. Please enquire.
If you have any questions, or require advice, please contact our experienced customer and technical support team:
Tel (INT) +61-8-8234 2644 Tel (NZ) 0800 450 001 Tel (AUS) 1800 882 555 or 08 8234 2644 Fax +61-8-8234 2699 E-mail firstname.lastname@example.org
Sanger (capillary) Sequencing
To complement our Next Generation Sequencing services, GeneWorks has teamed up with 1st BASE in Singapore to provide high quality, affordable Sanger sequencing. Using Applied Biosystems 3730xl capillary sequencers, 1st BASE provides high quality, long read (850b) sequencing of plasmids and PCR products. For more information on this service and how to access it via GeneWorks please refer to our 1st BASE Sequencing page.
BEST OF BOTH WORLDS!
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