Publications by authors named "E I Spriggs"

The Canadian NTRK (CANTRK) study is an interlaboratory comparison ring study to optimize testing for neurotrophic receptor tyrosine kinase (NTRK) fusions in Canadian laboratories. Sixteen diagnostic laboratories used next-generation sequencing (NGS) for NTRK1, NTRK2, or NTRK3 fusions. Each laboratory received 12 formalin-fixed, paraffin-embedded tumor samples with unique NTRK fusions and two control non-NTRK fusion samples (one ALK and one ROS1).

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Article Synopsis
  • The document outlines key considerations and recommendations for Canadian clinical laboratories involved in next-generation sequencing (NGS)-based tumor testing for ovarian cancers, covering pre-analytical, analytical, and post-analytical aspects.
  • It was created by the Canadian College of Medical Geneticists’ somatic BRCA Ad Hoc Working Group and incorporates feedback from CCMG members before receiving board approval.
  • The guidelines serve as a resource for laboratories but do not encompass all necessary information for the effective validation and use of NGS in this context.
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Nonimmune hydrops fetalis, the excessive accumulation of serous fluid in the subcutaneous tissues and serous cavities of the fetus, has many possible etiologies, providing a diagnostic challenge for the physician. Lysosomal storage diseases have been reported in up to 5%-16% of nonimmune hydrops fetalis pregnancies. Infantile free sialic acid storage disease (ISSD) (OMIM #269920) is a severe form of autosomal recessive sialic acid storage disease.

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Premise: Although chestnuts and chinquapins are some of the best known and most widely loved of any plants in North America, relatively little genomic sequencing has been done, and much is still unknown about their evolution.

Methods: We used double-digest restriction-site-associated DNA (ddRAD) sequencing data to infer the species-level phylogeny for Castanea and assess the phylogeography of the North American species using samples collected from populations that span the full extent of the species' ranges. We also constructed species distribution models using digitized herbarium specimens and observational data from field surveys.

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Article Synopsis
  • The study focused on resolving conflicting interpretations of genetic variants among Canadian clinical laboratories through the Canadian Open Genetics Repository (COGR).
  • Using the Franklin Genoox platform, laboratories could upload their variant classifications and received reports highlighting discrepancies for reassessment.
  • The results showed a significant reduction in discordant variants after reassessment, supporting the effectiveness of COGR in promoting standardized interpretations and enhancing the quality of genetic testing in clinical practices.
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