axiom array cel files Search Results


cel microarray image files  (Thermo Fisher)
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Thermo Fisher cel microarray image files
Complementary methods for detecting genetic variants associated with T1D. ( a ) The effect size of any given variant on T1D risk is inversely related to the frequency of the variant . ( b ) To detect more commonly observed variants, DNA samples from nPOD donors were probed for the presence of SNPs previously reported in T1D GWAS efforts using the UFDIchip, yielding <t>CEL</t> <t>microarray</t> image files (modified from Affymetrix Axiom website: https://www.affymetrix.com/products_services/arrays/specific/axiom_mydesign.affx ). ( c ) To detect rare or novel variants, whole exome sequencing (WES) was performed on DNA from nPOD donors (modified from Roche NimbleGen SeqCap EZ Exome Library workflow ). Diagrams created in BioRender.
Cel Microarray Image Files, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Complementary methods for detecting genetic variants associated with T1D. ( a ) The effect size of any given variant on T1D risk is inversely related to the frequency of the variant . ( b ) To detect more commonly observed variants, DNA samples from nPOD donors were probed for the presence of SNPs previously reported in T1D GWAS efforts using the UFDIchip, yielding CEL microarray image files (modified from Affymetrix Axiom website: https://www.affymetrix.com/products_services/arrays/specific/axiom_mydesign.affx ). ( c ) To detect rare or novel variants, whole exome sequencing (WES) was performed on DNA from nPOD donors (modified from Roche NimbleGen SeqCap EZ Exome Library workflow ). Diagrams created in BioRender.

Journal: Scientific Data

Article Title: A genomic data archive from the Network for Pancreatic Organ donors with Diabetes

doi: 10.1038/s41597-023-02244-6

Figure Lengend Snippet: Complementary methods for detecting genetic variants associated with T1D. ( a ) The effect size of any given variant on T1D risk is inversely related to the frequency of the variant . ( b ) To detect more commonly observed variants, DNA samples from nPOD donors were probed for the presence of SNPs previously reported in T1D GWAS efforts using the UFDIchip, yielding CEL microarray image files (modified from Affymetrix Axiom website: https://www.affymetrix.com/products_services/arrays/specific/axiom_mydesign.affx ). ( c ) To detect rare or novel variants, whole exome sequencing (WES) was performed on DNA from nPOD donors (modified from Roche NimbleGen SeqCap EZ Exome Library workflow ). Diagrams created in BioRender.

Article Snippet: Fig. 1 Complementary methods for detecting genetic variants associated with T1D. ( a ) The effect size of any given variant on T1D risk is inversely related to the frequency of the variant . ( b ) To detect more commonly observed variants, DNA samples from nPOD donors were probed for the presence of SNPs previously reported in T1D GWAS efforts using the UFDIchip, yielding CEL microarray image files (modified from Affymetrix Axiom website: https://www.affymetrix.com/products_services/arrays/specific/axiom_mydesign.affx ). ( c ) To detect rare or novel variants, whole exome sequencing (WES) was performed on DNA from nPOD donors (modified from Roche NimbleGen SeqCap EZ Exome Library workflow ).

Techniques: Variant Assay, Microarray, Modification, Sequencing