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Separate Novel from Previously Published Mutations in Minutes!

"How to Identify Genetic Disorders" Using NGS Bioinformatics
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Since sequencing produces thousands of variants, the first step in understanding the genetic basis of any disease is to identify previously described variants in addition to any disease associations attributed to these same variants.

Download your introductory copy of the primer on "How to Identify Genetic Disorders" and learn more about how clinicians and scientists can apply bioinformatic tools to the discovery of the causal agents of disease.

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Don't forget to receive your copy of a complimentary NGS Bioinformatics primer by completing the form below.

For up-to-date information and product-specific disclaimers, see the respective QIAGEN kit handbooks or user manual. QIAGEN kit handbooks and user manuals are avaliable at www.qiagen.com or can be requested from QIAGEN Technical Services or your locale distributer.

"How to Identify Genetic Disorders" Using NGS BioinformaticsComplete the form to receive your complimentary copy

"How to Identify Genetic Disorders" Using NGS Bioinformatics
Complete the form to receive your complimentary copy