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illumina iscan microarray scanner  (Illumina Inc)


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    Structured Review

    Illumina Inc illumina iscan microarray scanner
    Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal <t>microarray</t> analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .
    Illumina Iscan Microarray Scanner, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 97/100, based on 1711 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/illumina+iscan+microarray+scanner/iScan+System/pmc12739554-93-8-8
    Average 97 stars, based on 1711 article reviews
    illumina iscan microarray scanner - by Bioz Stars, 2026-09
    97/100 stars

    Images

    1) Product Images from "RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series"

    Article Title: RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series

    Journal: Frontiers in Medicine

    doi: 10.3389/fmed.2025.1657054

    Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .
    Figure Legend Snippet: Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .

    Techniques Used: Microarray

    Related Articles

    Microarray:

    Article Title: RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series
    Article Snippet: Chromosomal microarray analysis (CMA) was performed for P1 using Infinium ® CytoSNP-850 K BeadChip v1.2 (Illumina, San Diego, USA) according to the manufacturer’s instructions at the MGZ Munich. .. Scanning and image acquisition were performed using an Illumina iScan microarray scanner. .. Data analysis was performed using BlueFuse Multi software v4.5 (Illumina, San Diego, USA).

    Article Title: Clinical and Molecular Characteristics of 100 Atypical Teratoid Rhabdoid Tumor Patients from Low- and Middle-Income Countries
    Article Snippet: Bisulfite-converted DNA was restored using the Infinium HD FFPE DNA Restore Kit (WG-321-1002, Illumina Inc., San Deiago, CA, USA), followed by hybridization to Illumina Infinium Human Methylation EPIC 850K bead chips. .. Hybridized chips were then scanned using the Illumina iScan microarray scanner according to the manufacturer’s recommendations (Illumina Inc., San Deiago, CA, USA). ..

    Article Title: Genomic analysis of spermatocytic tumors demonstrates recurrent molecular alterations in cases with malignant clinical behavior.
    Article Snippet: The DNA was processed for hybridization and fluorescence staining on the Infinium MethylationEPIC (850 k) BeadChip array (Illumina, San Diego, CA, USA) following the manufacturer’s recommendations. .. Arrays were scanned in an Illumina iScan microarray scanner (Illumina), and the raw idat files were analyzed in R (R Foundation for Statistical Computing, Vienna, Austria). ..

    Article Title: MicroRNA-371-373 cluster and methylome analysis suggests that a subset of 'somatic-type' malignancies arising in germ cell tumors may originate in yolk sac tumor components.
    Article Snippet: The DNA was then processed for hybridization and fluorescence staining using the Infinium MethylationEPIC (850k) BeadChip array (Illumina, San Diego, CA, USA) following the manufacturer’s protocol. .. The arrays were scanned using the Illumina iScan microarray scanner (Illumina). ..

    Article Title: MicroRNA ‐371–373 cluster and methylome analysis suggests that a subset of ‘somatic‐type’ malignancies arising in germ cell tumors may originate in yolk sac tumor components
    Article Snippet: The DNA was then processed for hybridization and fluorescence staining using the Infinium MethylationEPIC (850k) BeadChip array (Illumina, San Diego, CA, USA) following the manufacturer's protocol. .. The arrays were scanned using the Illumina iScan microarray scanner (Illumina). ..

    Article Title: Methylation changes and INS-IGF2 expression predict progression in early-stage Wilms tumor
    Article Snippet: Bisulfite-converted FFPE DNA was then restored with Infinium HD FFPE DNA Restore Kit (WG-321-1002, Illumina Inc.). .. Restored bisulfite-modified DNA samples were hybridized to the Illumina Infinium Human Methylation EPIC bead chips and scanned using the Illumina iScan microarray scanner (Illumina Inc.) according to the manufacturer’s recommendations. .. The bioinformatics workflow is summarized in Fig. . R software (v4.3.1) and minfi R package (v1.44.0) [ ] were used to load the Illumina Human Methylation EPIC intensity data files (IDAT) and check their quality.

    Article Title: Methylation changes and INS-IGF2 expression predict progression in early-stage Wilms tumor.
    Article Snippet: Bisulfite-converted FFPE DNA was then restored with Infinium HD FFPE DNA Restore Kit (WG-321-1002, Illumina Inc.). .. Restored bisulfite-modified DNA samples were hybridized to the Illumina Infinium Human Methylation EPIC bead chips and scanned using the Illumina iScan microarray scanner (Illumina Inc.) according to the manufacturer’s recommendations. ..

    Article Title: Multi-omic atlas of the parahippocampal gyrus in Alzheimer's disease.
    Article Snippet: Next, DNA samples were fragmented and hybridized to Infinium MethylEPIC BeadChips33 (Illumina, catalog# WG-317-1001). .. Lastly, hybridization signals were obtained through the Illumina iScan microarray scanner (Illumina, catalog# SY-202-1001). ..

    Methylation:

    Article Title: Methylation changes and INS-IGF2 expression predict progression in early-stage Wilms tumor
    Article Snippet: Bisulfite-converted FFPE DNA was then restored with Infinium HD FFPE DNA Restore Kit (WG-321-1002, Illumina Inc.). .. Restored bisulfite-modified DNA samples were hybridized to the Illumina Infinium Human Methylation EPIC bead chips and scanned using the Illumina iScan microarray scanner (Illumina Inc.) according to the manufacturer’s recommendations. .. The bioinformatics workflow is summarized in Fig. . R software (v4.3.1) and minfi R package (v1.44.0) [ ] were used to load the Illumina Human Methylation EPIC intensity data files (IDAT) and check their quality.

    Article Title: Methylation changes and INS-IGF2 expression predict progression in early-stage Wilms tumor.
    Article Snippet: Bisulfite-converted FFPE DNA was then restored with Infinium HD FFPE DNA Restore Kit (WG-321-1002, Illumina Inc.). .. Restored bisulfite-modified DNA samples were hybridized to the Illumina Infinium Human Methylation EPIC bead chips and scanned using the Illumina iScan microarray scanner (Illumina Inc.) according to the manufacturer’s recommendations. ..

    Hybridization:

    Article Title: Multi-omic atlas of the parahippocampal gyrus in Alzheimer's disease.
    Article Snippet: Next, DNA samples were fragmented and hybridized to Infinium MethylEPIC BeadChips33 (Illumina, catalog# WG-317-1001). .. Lastly, hybridization signals were obtained through the Illumina iScan microarray scanner (Illumina, catalog# SY-202-1001). ..



    Similar Products

    97
    Illumina Inc illumina iscan microarray scanner
    Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal <t>microarray</t> analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .
    Illumina Iscan Microarray Scanner, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/illumina+iscan+microarray+scanner/iScan+System/pmc12739554-93-8-8
    Average 97 stars, based on 1 article reviews
    illumina iscan microarray scanner - by Bioz Stars, 2026-09
    97/100 stars
      Buy from Supplier

    Image Search Results


    Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .

    Journal: Frontiers in Medicine

    Article Title: RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series

    doi: 10.3389/fmed.2025.1657054

    Figure Lengend Snippet: Pedigree and genetic analysis for family 1. (A) Genetic pedigree of family 1; black circle II.1 indicates the affected child (P1). (B) SeqPilot ® CNV analysis: reduced copy number for the RUNX1 exons for the index patient (green columns) compared to the patients analyzed in the same enrichment (blue), indicating a heterozygous RUNX1 -gene deletion. (C) Chromosomal microarray analysis: 1.56 Mb deletion (21q22.11q22.12 shown as a red bar) including RUNX1 .

    Article Snippet: Scanning and image acquisition were performed using an Illumina iScan microarray scanner.

    Techniques: Microarray