Next-Generation Sequencing – Multimedia

In this Teach Me in 10 we are joined by senior field application scientist Nick Hapshe.

Download this listicle to explore how proteomics is being applied in drug discovery and biomedical research, food industry, agriculture, environmental science and forensics.

In this eBook, we highlight developments in cancer research through a selection of articles, interviews and graphics.

Target enrichment allows researchers to selectively capture, sequence and study specific genes or genomic regions. Carefully designed target enrichment probes that hybridize with high specificity and coverage are essential to ensuring workflow efficiency and data quality.

In this episode we discuss how the combination of both genetic and epigenetic information within a single DNA sample can provide key insights on the dynamic interactions that are occurring, offering significant advantages in many research areas.

In this Teach me in 10 episode we will explore how simultaneous sequencing of genetic and epigenetic bases in cfDNA allows for early cancer detection.

Unique molecular identifiers (UMIs) now present a solution that can reduce quantitative bias, distinguish between PCR duplicates, and recognize sequencing errors.

The ability to study transcript isoforms in detail could have a significant impact on our understanding of health and disease. However, most commonly, bulk sequencing is the selected method that only provides an average of the transcripts expressed across your sample of cells.

The Alissa Clinical Informatics Platform offers integrated sequencing analysis solutions to manage data, helping you to identify, triage and classify variants and generate customizable reports for clinical NGS and CGH.

This eBook has been compiled with this in mind, and has everything you need to know about PCR, including tips on PCT to aid your success, how to set up a PCR lab from scratch plus reducing protocol for PCR.