Researchers developed STRIPE, a targeted long-read RNA sequencing tool that identifies disease-causing variants missed by ...
Traditional PCR systems require users to set a specified number of cycles according to the assay and the input amount. As a result, input material must be quantified, and samples of varying inputs ...
Researchers developed a new RNA sequencing strategy that can reveal how genetic variants disrupt gene function and improve the diagnosis of rare diseases. The study team demonstrated that this ...
Download this application note to learn more about targeted sequencing approaches such as RNA exome sequencing. Is the form ...
Recent advances in artificial intelligence are reshaping genomics, with new tools enabling faster, more accurate genome annotation, variant detection, and functional prediction across agriculture and ...
EMBL researchers created SDR-seq, a next-generation tool that decodes both DNA and RNA from the same cell. It finally opens access to non-coding regions, where most disease-associated genetic variants ...
New RNA-Seq innovations include a regional sequencing hub and an RNA preservation solution enabling ambient shipping. These advances reduce costs, improve turnaround times, and simplify workflows for ...
VIB-VUB researchers have developed a patient-relevant lung adenocarcinoma model combined with SEPARATE-Seq technology to ...
Bacteria aren’t just mindless microbes. Research by scientists at the Hebrew University of Jerusalem has revealed that single bacterial cells can carry a “memory” of their past environments—passing it ...
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