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the innoscan 300 microarray scanner  (Innopsys Inc)

 
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    Innopsys Inc the innoscan 300 microarray scanner
    The Innoscan 300 Microarray Scanner, supplied by Innopsys 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/result/the innoscan 300 microarray scanner/product/Innopsys Inc
    Average 90 stars, based on 1 article reviews
    the innoscan 300 microarray scanner - by Bioz Stars, 2026-05
    90/100 stars

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    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 .
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    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