Copy-number aberrations (CNAs) and whole-genome duplications (WGDs) are frequent somatic mutations in cancer but their quantification from DNA sequencing of bulk tumor samples is challenging. Standard ...
The Genome Diagnostics lab of the Human Genetics Dept. at Radboud UMC provides rapid whole exome sequencing since 2017, with a max turnaround time of 15 days (from sample to report). With the ...
Moss enables high sensitivity single-nucleotide variant calling from multiple bulk DNA tumor samples
Intra-tumor heterogeneity renders the identification of somatic single-nucleotide variants (SNVs) a challenging problem. In particular, low-frequency SNVs are hard to distinguish from sequencing ...
(Boston) - Clinicians rely on laboratory tests to monitor the progression or remission of disease, or to identify pathologic alterations in physiology that may precede clinical events. Monitoring ...
A method for quickly detecting signs of multiple sclerosis has been developed. The discovery, using advanced mass spectrometry techniques, offers a diagnostic tool that enables the detection of ...
Laser-driven thermoviscous flows provide contact-free rotation, transport or stabilization of delicate samples such as ...
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