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The Center for Genomics and Transcriptomics in Tübingen, Germany has launched next-generation sequencing panels for the diagnosis of ataxia, hereditary spastic paraplegia, spinal muscular atrophy, choreatic movement disorders, and leukodystrophy/leukoencephalopathy.

It has also launched panels for inherited kidney diseases. The comprehensive panel covers 145 genes associated with both isolated and syndromic nephropathies. It can also be run as 21 different subpanels.

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St. Jude Children's Research Hospital scientists have treated infants with X-linked severe combined immunodeficiency using gene therapy in an early phase study.

Bloomberg reports that the DNA-for-cash deal reported in Kentucky might be a more widespread scam.

St. Louis Public Radio reports that some African Americans are turning to DNA ancestry testing to help guide genealogical searches.

In Nature this week: a genomic analysis of the snailfish Pseudoliparis swirei, ancient DNA analysis gives insight into the introduction of farming to England, and more.

Apr
30
Sponsored by
Lexogen

This webinar will discuss novel long-read transcript sequencing (LRTseq) methods for transcriptome annotation that could increase the efficiency and accuracy of future sequencing projects.

May
08
Sponsored by
Sysmex Inostics

This webinar will present recent evidence that demonstrates how incorporating circulating tumor DNA (ctDNA) assessments into real-world patient management can influence patient care decisions, alter radiographic interpretations, and impact clinical outcomes.