Baylor Genetics, a leading diagnostic genomics partner offering a full spectrum of comprehensive genetic tests and diagnostic services, today announced it will be participating in the Patient-centered ...
Quintara Biosciences today announced the launch of AmpValue, a new high-throughput nanopore-based amplicon sequencing service. AmpValue delivers full-length reads at a flat price of $4.99 per sample, ...
A new report has found that the Darwin Tree of Life project, which aims to sequence the genomes of all complex life in the UK and Ireland, could generate billions of pounds for the global economy. It ...
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 ...
Stanford develops protein-to-DNA method enabling high-throughput protein sequencing Technique detects up to 1,000 times more ...
The US Food and Drug Administration (FDA) has released draft guidance on how sponsors can utilize next-generation sequencing ...
Explore how advances in accuracy, throughput and cost are making long-read sequencing more accessible at scale.
Researchers from Children's Hospital of Philadelphia (CHOP) developed a new RNA sequencing strategy that can reveal how ...
Bone-only, osteoblastic disease and the absence of prior ARPI exposure define the optimal radium-223 candidate, while ...
In a striking example of nature's ingenuity, a collaborative research team has revealed that a bioluminescent fish glows not ...
Sanger sequencing is the unsung workhorse of molecular biology, one whose value has long been undermined by the tedious nature of processing its data. Converting files of raw sequencing data into a ...
Long read sequencing improves detection of structural variants in paediatric leukaemia, identifying missed gene fusions and ...
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