eBooks

Sponsor: Molecular MDCodevelopment is an intermittent and uncertain process. Adopting an agnostic approach to the challenges associated with platform and method selection provide added degrees of freedom for strategic development and selection of the most appropriate clinical trial assay.

Sponsor: PerkinElmerRNA and sequencing technologies have the potential to unlock the mystery of our every dynamic transcriptome.

Sponsor: QiagenToday genetic innovation is advancing at breakneck pace. Despite incredible advances in sequencing technology, most notable being next-generation sequencing (NGS), genetic has only recently become a clinical application. The challenge is no longer how to sequence DNA, but how to interpret a patient’s genetic variation in a meaningful and actionable way. In this eBook Qiagen looks at three trends that will change how NGS tests for inherited disorders are analyzed and interpreted in the future.

Sponsor: MolecularMDDownload this eBook to learn how MolecularMD helped usher in a new era of CML treatment now prescribed by progressive clinicians.

Sponsor: IsoPlexisIsoPlexis’ next generation systems provide actionable potency, safety, and patient difference metrics by detecting highly potent single cell functional subsets for the first time.

Sponsor: Advanced Analytical2015 was a phenomenal year full of new developments for the structures and mechanisms of CRISPR systems.

Sponsor: DNAnexusThe challenges of incorporating NGS into clinical trials is being addressed through the adoption of robust technology solutions.

Sponsor: TakedaTakeda has taken great strides in incorporating a patient-centric approach to drug development through the use of minimally invasive and less frequent testing procedures while maintaining the power and rigor of the clinical trial.

Sponsor: MolecularMDIn this eBook learn how MolecularMD is harnessing the company's unique capabilities to address diagnostic needs within immuno-oncology.

Sponsor: Oxford NanoporeOxford Nanopore’s DNA/RNA sequencing technology delivers ultra-long reads (up to 2 Mb), enabling rapid and comprehensive analysis of variants. With devices scalable from portable to benchtop, nanopore sequencing offers a cost-effective solution to the challenges faced by traditional sequencing platforms.