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Next generation sequencing articles
xGen™ Adaptase™ and Normalase™ technology: 6 key facts to understand
Next generation sequencing (NGS) library preparation workflows can be complicated. xGen Adaptase and Normalase technologies can simplify your library prep by streamlining adapter ligation and library normalization. This DECODED provides a description of these novel technologies as well as outlines how you can incorporate them into your next library prep workflow.
- xGen™ Adaptase™ and Normalase™ technology: 6 key facts to understand
- Comprehensive genomic profiling—what, why, and its future
- How to improve SNV and indel detection in an exome NGS assay
- Mechanical vs. enzymatic fragmentation approaches: Which method best improves library quality?
- Why library prep is essential to sequencing
- What you need to know about gene fusions
- What is library prep in sequencing?
- RNA-seq: Basics, applications, and protocols
- How DNA ligation works
- Methyl-seq analysis of the human ‘methylome’ provides a resource for biomarker and gene regulation research
- Viral surveillance using wastewater
- A fusion gene identification strategy using CRISPR-Cas9 and long read nanopore sequencing
- CRISPR-based depletion of unwanted sequences improves targeted next generation sequencing
- Tips for designing spike-in controls for next generation sequencing analysis
- Beginner’s guide to next generation sequencing
- Targeted sequencing: Hybridization capture or amplicon sequencing?
- Using CRISPR-Cas9 technology for targeted nanopore sequencing
- Protocol tips to boost your NGS target capture success
- Multiplexed targeted next generation sequencing coverage
- ve-SEQ: An improved approach to high throughput, whole genome viral sequencing
