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Personalizing Whole Genome Sequencing Doubles Diagnosis of Rare Diseases

Tailoring the analysis of whole genome sequencing to individual patients could double the diagnostic rates of rare diseases.

Posted by Andy Lundin | Nov 2, 2022 | Pancreatic |

Bluestar Genomics announced the results of a validation study for its early pancreatic cancer detection test.

Posted by Andy Lundin | Nov 1, 2022 | Pancreatic |

Pancreatic cancer could be identified in patients up to three years earlier than current diagnoses, new research suggests.

Posted by Andy Lundin | Oct 27, 2022 | Covid 19, Research |

Bruker launched PhenoRisk PACS RuO, a research-use-only NMR test for molecular phenomics research on Long COVID patients’ blood samples.

Multiple instruments as the core of testing provides a number of advantages and complexities for clinical laboratories.