Getting Started with Targeted NGS with TruSeq® Custom Amplicon Low-Input on the MiniSeqTM System

2017년 3월 6일

Getting started with targeted next-generation sequencing (NGS) is simple using the TruSeq® Custom Amplicon solution, a streamlined workflow for your targeted NGS studies. Ivan Godinez, Senior Technical Application Scientist at Illumina, walks through the entire process, from creating your design in DesignStudioTM to prepping your libraries, to sequencing on the MiniSeq System to analyzing your data on BaseSpace® Sequence Hub. Learn more https://www.illumina.com/tgrs A global genomics leader, Illumina provides comprehensive next-generation sequencing solutions to the research, clinical, and applied markets. Illumina technology is responsible for generating more than 90% of the world’s sequencing data.* Through collaborative innovation, Illumina is fueling groundbreaking advancements in oncology, reproductive health, genetic disease, microbiology, agriculture, forensic science, and beyond. *Data calculations on file. Illumina, Inc., 2015. Subscribe to the Illumina video channel http://www.youtube.com/subscription_center?add_user=IlluminaInc View customer spotlight videos https://www.youtube.com/playlist?list=PLKRu7cmBQlajfheLzgbI4S7xBn7IDbt79 View Illumina webinars https://www.youtube.com/playlist?list=PLKRu7cmBQlahpXlnrrXlQw9itVJ8yHwUZ View Illumina product videos https://www.youtube.com/playlist?list=PLKRu7cmBQlaj6YuZmkfxZcT9twqDgP2Xd View Illumina support videos https://www.youtube.com/playlist?list=PLKRu7cmBQlajbm2KGsICWb-JOnusJfYvM

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