Long-read RNA sequencing (RNA-seq) technologies have revolutionized transcriptomic research by enabling the sequencing of full-length RNA molecules, thus providing a more accurate characterization of ...
A third of disease-causing variants are estimated to disrupt mRNA splicing [1, 2]. Splice-affecting variants are often missed and are under-ascertained in clinical variant databases, as these are not ...
Short-read RNA-seq provides robust gene-level expression but is limited in resolving full-length transcripts and splice variants. Long-read sequencing addresses these limitations by capturing complete ...
Here, Aaron Wenger, Principal Scientist – Bioinformatics at PacBio (CA, USA), explores how advances in accuracy, throughput and cost are making long-read sequencing more accessible at scale. Advances ...
Shareef A. Nahas brings deep expertise in genomics and laboratory operations, with senior leadership experience at Rady Children’s Institute for Genomic Medicine, Genoptix (Novartis), and Ambry ...
Researchers at the University of California San Diego have identified new genetic variants associated with autism spectrum disorder (ASD) by using long-read whole genome sequencing (LR-WGS), an ...
The single-cell genomics industry does not stop advancing, with a steady stream of new companies, kits, acquisitions, and more. One new company, ArgenTag, was founded in Argentina during the COVID-19 ...
In just a few decades, DNA sequencing technologies evolved from slow, manual processes to rapid, automated ones, making ...
Long-read sequencing is transforming the landscape of genomic research, offering exceptional resolution and accuracy in the analysis of complex genetic structures. From research in genetic analysis to ...
GREENWOOD, SC, UNITED STATES, April 15, 2026 /EINPresswire.com/ -- The Greenwood Genetic Center (GGC) Diagnostic Laboratory today announced the launch of long-read ...
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