ngs brochure
Brochure

Newborn sequencing research

Inside this brochure, we highlight the technologies and software that power our end-to-end, newborn sequencing research workflow. Includes details surrounding sample collection, extraction, quality control, library preparation, sequencing, and our coinciding software suite – packed with a gene panel of 390+ genes. A configurable solution, the workflow is designed to maximize compatibility with your laboratory. Reimagine the possibilities for your newborn sequencing research today.

For research use only. Not for use in diagnostic procedures.

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Newborn sequencing research

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