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All in NGS Applications
Twist Exome 2.0: A new and powerful exome panel with best-in-class performance for translational research and more
With flu season approaching, labs are contemplating new, more efficient ways to differentiate between respiratory viruses. Multiplex, PCR-based tests could save both labs and patients significant heartache.
In the milieu of rushing blood, plasma, and cells, small wayward bits of DNA are easy to overlook. But stored within these scraps of genetic material, known as cell-free DNA (cfDNA), is information offering the earliest glimpses of cancer development. Being able to detect and understand these signals could dramatically improve our ability to detect and treat cancer before the disease has developed.
A conversation with Dan Landau, core faculty member of the New York Genome Center and associate professor of medicine at Weill Cornell Medicine.
RNA-seq is an essential research tool that holds exciting prospects for the early detection of cancer. However, in clinical samples highly abundant mRNA and rRNA sequences obscure rarer RNA subtypes that may hold the keys to early cancer detection, such as long non-coding RNA. Here we dive into recent research from the University of Ghent outlining the use of targeted RNA-seq to enrich lncRNA from various sample types and discuss how recent advances make target enrichment an invaluable tool for high-resolution RNA-seq experiments.
In this article, we highlight how quality library preparation reduces sequencing error rates while providing high-yield sequencing libraries. Twist has just upgraded its suite of library preparation tools by creating the Library Preparation Enzymatic Fragmentation (EF) Kit 2.0. We detail how this kit has been built to help you achieve better quality library preparation for better sequencing results.
