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Bringing together two leaders: AmpliSeqTM for Illumina®

7618 views | 6 years ago

Leaders from Illumina and Thermo-Fisher Scientific discuss their collaboration on AmpliSeq for Illumina, the latest in amplicon sequencing. Hear them share insights on the partnership and their commitment...

Meet Your New Lab Partner

7359 views | 6 years ago

Introducing the iSeq 100, the latest advancement in the world of next-generation sequencing (NGS) from Illumina. The iSeq 100 instrument leverages Illumina technological advances in its smallest and...

Custom Content Creation: AmpliSeqTM for Illumina®

1063 views | 6 years ago

Create custom content on the AmpliSeq for Illumina solution—the new workflow for your targeted next-generation sequencing (NGS) studies. Learn how to design custom panels with our DesignStudio software,...

Sequencing amplified: AmpliSeq™ for Illumina®

5412 views | 6 years ago

The latest addition to the Illumina library prep portfolio, the AmpliSeq for Illumina solution provides a simple, fast, and robust amplicon sequencing option to achieve high-confidence data from even...

Data Analysis with Local Run Manager: AmpliSeqTM for Illumina®

492 views | 6 years ago

Accelerate your research with the AmpliSeq for Illumina solution—the new workflow for your targeted next-generation sequencing (NGS) studies. Learn how to perform on-premises amplicon analysis using...

Selective Advances in Cattle Breeding | Adventures in Genomics

1894 views | 7 years ago

The world population is continuously growing. As the second largest producer and largest exporter of beef in the world, Brazil has an important role in feeding such a population. Jacques and Irene from...

アルツハイマー病の秘密を解き明かす | ゲノミクスにおける冒険

1352 views | 7 years ago

アルツハイマー病は、個人の脳内に局面や絡まりが存在することが特徴です。この明確な病理学的定義にもかかわらず、これらのプラークや変化の素因や影響は不明です。このゲノミクスにおける冒険のエピソードでは、JacquesとIreneがマイアミ大学のAmanda Myers氏と話します。Amanda Myers氏は、ゲノミクス、トランスクリプトミクス、プロテオミクスを組み合わせてデータのネットワークを特定し、この疾患の複雑さを説明しています。イルミナのサブスクリプション:http://bit.ly/IlluminaYouTubeFor...

Sophia’s iHope Story: Diagnosing a Rare De Novo Mutation

1802 views | 7 years ago

Sophia and her family spent years in search of a diagnosis for her condition. Finally, a de novo mutation was discovered through a clinical whole genome sequencing (cWGS) test she received from the...