microarray image files Search Results


microarray imager software  (CombiMatrix)
90
CombiMatrix microarray imager software
Microarray Imager Software, supplied by CombiMatrix, 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/result/microarray imager software/product/CombiMatrix
Average 90 stars, based on 1 article reviews
microarray imager software - by Bioz Stars, 2026-05
90/100 stars
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microarray image files  (Molecular Devices LLC)
94
Molecular Devices LLC microarray image files
Microarray Image Files, supplied by Molecular Devices LLC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/microarray image files/product/Molecular Devices LLC
Average 94 stars, based on 1 article reviews
microarray image files - by Bioz Stars, 2026-05
94/100 stars
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dna microarray image analysis software  (Thermo Fisher)
99
Thermo Fisher dna microarray image analysis software
Dna Microarray Image Analysis Software, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/dna microarray image analysis software/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
dna microarray image analysis software - by Bioz Stars, 2026-05
99/100 stars
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cel microarray image files  (Thermo Fisher)
94
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
https://www.bioz.com/result/cel microarray image files/product/Thermo Fisher
Average 94 stars, based on 1 article reviews
cel microarray image files - by Bioz Stars, 2026-05
94/100 stars
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genomics suite software version 6.6  (Partek)
90
Partek genomics suite software version 6.6
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.
Genomics Suite Software Version 6.6, supplied by Partek, 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/result/genomics suite software version 6.6/product/Partek
Average 90 stars, based on 1 article reviews
genomics suite software version 6.6 - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier

Image Search Results


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