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Regeneron inc exome sequencing data
Exome Sequencing Data, supplied by Regeneron inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sequencing+data/exome+sequencing+data/pmc06592771-187-3-21
Average 90 stars, based on 1 article reviews
exome sequencing data - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Variant Assay:

Article Title: Errors and Delays in Diagnosing Keratitis Fugax Hereditaria.
Article Snippet: Purpose: To study errors and delays in diagnosing keratitis fugax hereditaria (KFH), an autosomal-dominant periodic corneal autoinflammatory disease caused by the NLRP3 variant c.61G>C, by reviewing the medical records of genetically confirmed Finnish patients with KFH and by determining the frequency of the c.61G>C variant in selected biobank samples.. Design: A retrospective cohort and a cross-sectional biobank study.

Article Title: Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis.
Article Snippet: © Author(s) (or their employer(s)) 2025.. Reuse permitted under CC BYNC.. No commercial reuse.

Sequencing:

Article Title: Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis
Article Snippet: The purified amplicons were Sanger sequenced by Azenta Life Sciences, South Plainfield, NJ 07080. .. Exome sequence data for MyCode participants were generated through the Geisinger-Regeneron DiscovEHR collaboration [ 27 ]. ..

Article Title: The Phenotypic Spectrum of COL4A3 Heterozygotes
Article Snippet: .. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: This research was approved by the Geisinger Clinic Institutional Review Board and included participants in the MyCode Health Initiative who have exome sequencing data obtained as part of the Geisinger-Regeneron DiscovEHR collaboration. ..

Article Title: The Phenotypic Spectrum of COL4A3 Heterozygotes
Article Snippet: .. Ethics Declaration: This research was approved by the Geisinger Clinic Institutional Review Board and included participants in the MyCode Health Initiative who have exome sequencing data obtained as part of the Geisinger-Regeneron DiscovEHR collaboration. ..

Article Title: Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism
Article Snippet: .. There are no major differences in allele frequency in individuals of other European ancestries, as seen in exome sequencing data from the Regeneron Genetic Center (accept terms and search for “2:233718890:C:A”), which holds data from 821,979 unrelated individuals (Response Figure 2). ..

Article Title: Influence of family history on penetrance of hereditary cancers in a population setting
Article Snippet: .. Exome sequencing data were available on 454,712 individuals (246,591 women), generated externally by Regeneron. ..

Article Title: The Phenotypic Spectrum of COL4A3 Heterozygotes
Article Snippet: .. This research was approved by the Geisinger Clinic Institutional Review Board and included participants in the MyCode Health Initiative who have exome sequencing data obtained as part of the Geisinger-Regeneron DiscovEHR collaboration. ..

Article Title: Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis.
Article Snippet: © Author(s) (or their employer(s)) 2025.. Reuse permitted under CC BYNC.. No commercial reuse.

Generated:

Article Title: Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis
Article Snippet: The purified amplicons were Sanger sequenced by Azenta Life Sciences, South Plainfield, NJ 07080. .. Exome sequence data for MyCode participants were generated through the Geisinger-Regeneron DiscovEHR collaboration [ 27 ]. ..

Article Title: Influence of family history on penetrance of hereditary cancers in a population setting
Article Snippet: .. Exome sequencing data were available on 454,712 individuals (246,591 women), generated externally by Regeneron. ..

Article Title: Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis.
Article Snippet: © Author(s) (or their employer(s)) 2025.. Reuse permitted under CC BYNC.. No commercial reuse.



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