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 whole-genome sequencing approach shows early promise over current commercial methods for identifying more patients likely ...
Due to its high accuracy and fast, simple workflow, capillary electrophoresis (CE) is a foundational technology for clinical applications. CE is an invaluable tool used to detect genetic variations ...
Around 15% of hereditary diseases and cancers are associated with alternative RNA splicing, while the development of 1 in 6 cancers is driven by gene fusions. Isolating RNA from individual cells is a ...
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 ...
April 14, 2025 – Genome Research (https://genome.org) publishes a second special issue highlighting advances in long-read sequencing applications in biology and medicine. In this second Special Issue, ...
The global DNA methylation market size was valued at US$ 1.9 Bn in 2025 and is projected to reach US$ 7.7 Bn by 2036, growing ...
A new study published in Addiction has identified genetic factors that influence both a person's risk of developing an addiction and their educational attainment. Researchers found that some genetic ...
Key opportunities lie in next-generation sequencing methods, with hospitals as major end-users and North America as a ...
Physicians classify brain tumors and determine treatment options, in part, by the genes they express. According to World Health Organization standards, the abnormal activation of oncogene FOXR2 only ...
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