The US Food and Drug Administration (FDA) has released draft guidance on how sponsors can utilize next-generation sequencing ...
The idea for the LRGASP Consortium was originally discussed among scientists at a conference in 2019.
Genetic variants that cause rare disorders may remain elusive even after expansive testing, such as exome sequencing. The diagnostic yield of genome sequencing, particularly after a negative ...
A new technology that analyzes gene expression in cells reveals new insights into immune cell activity. This new single-cell ...
What is Third-Generation Sequencing? Third-generation sequencing, also known as long-read sequencing, refers to the latest advancements in DNA sequencing technologies that enable the analysis of ...
Stanford develops protein-to-DNA method enabling high-throughput protein sequencing Technique detects up to 1,000 times more ...
Researchers from Children's Hospital of Philadelphia (CHOP) developed a new RNA sequencing strategy that can reveal how genetic variants disrupt gene function and improve the diagnosis of rare ...
Explore how advances in accuracy, throughput and cost are making long-read sequencing more accessible at scale.
In this webinar, we will hear from medical microbiologists and molecular scientists about their experiences detecting and tracking bacterial outbreaks using real-time nanopore sequencing and BugSeq ...
Long read sequencing improves detection of structural variants in paediatric leukaemia, identifying missed gene fusions and ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results