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96.96 dynamic arraystm  (fluidigm)


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    fluidigm 96.96 dynamic arraystm
    96.96 Dynamic Arraystm, supplied by fluidigm, 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/96.96 dynamic arraystm/product/fluidigm
    Average 90 stars, based on 1 article reviews
    96.96 dynamic arraystm - by Bioz Stars, 2026-06
    90/100 stars

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    Boxplots display the counts of errors or missing data over sample sets across all scorable <t>SNP</t> loci. The bars within boxplots represent medians, while data points show single samples that appear as outliers. (A) Error rates - allelic dropouts (blue) and false alleles (red). (B) Rates of missing data resulting from invalidation of whole SNP loci or whole sample genotypes during scoring (orange) or lack of genotype signal for single samples at single loci, e.g. no calls (grey). (C) Number of loci that produced scorable genotype data (light grey, numbers) or failed in <t>genotyping</t> (dark grey). 1 n = 92 reference samples (high-DNA, Table 1) with known genotypes; 2 n = 90 duplicated tissue samples from various European wildcat populations; 3 n = 30 triplicated hair samples from genetic wildcat monitoring in Germany; single failing marker was later successfully substituted for the final panel.
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    Boxplots display the counts of errors or missing data over sample sets across all scorable SNP loci. The bars within boxplots represent medians, while data points show single samples that appear as outliers. (A) Error rates - allelic dropouts (blue) and false alleles (red). (B) Rates of missing data resulting from invalidation of whole SNP loci or whole sample genotypes during scoring (orange) or lack of genotype signal for single samples at single loci, e.g. no calls (grey). (C) Number of loci that produced scorable genotype data (light grey, numbers) or failed in genotyping (dark grey). 1 n = 92 reference samples (high-DNA, Table 1) with known genotypes; 2 n = 90 duplicated tissue samples from various European wildcat populations; 3 n = 30 triplicated hair samples from genetic wildcat monitoring in Germany; single failing marker was later successfully substituted for the final panel.

    Journal: Molecular ecology resources

    Article Title: Applying genomic data in wildlife monitoring: development guidelines for genotyping degraded samples with reduced single nucleotide polymorphism (SNP) panels

    doi: 10.1111/1755-0998.13136

    Figure Lengend Snippet: Boxplots display the counts of errors or missing data over sample sets across all scorable SNP loci. The bars within boxplots represent medians, while data points show single samples that appear as outliers. (A) Error rates - allelic dropouts (blue) and false alleles (red). (B) Rates of missing data resulting from invalidation of whole SNP loci or whole sample genotypes during scoring (orange) or lack of genotype signal for single samples at single loci, e.g. no calls (grey). (C) Number of loci that produced scorable genotype data (light grey, numbers) or failed in genotyping (dark grey). 1 n = 92 reference samples (high-DNA, Table 1) with known genotypes; 2 n = 90 duplicated tissue samples from various European wildcat populations; 3 n = 30 triplicated hair samples from genetic wildcat monitoring in Germany; single failing marker was later successfully substituted for the final panel.

    Article Snippet: 96.96 Dynamic Array TM SNP genotyping SNP genotyping was performed on 96.96 Dynamic ArraysTM (Fluidigm) with integrated fluidic circuits (IFCs, Wang et al., 2009 ).

    Techniques: Produced, Marker

    Clinical and demographic patient data from the Biocruces Bizkaia cohort samples. Samples used for SNP validation analysis by  genotyping.

    Journal: International Journal of Molecular Sciences

    Article Title: BIRC6 Is Associated with Vulnerability of Carotid Atherosclerotic Plaque

    doi: 10.3390/ijms21249387

    Figure Lengend Snippet: Clinical and demographic patient data from the Biocruces Bizkaia cohort samples. Samples used for SNP validation analysis by genotyping.

    Article Snippet: SNP genotyping was performed using the Fluidigm 96.96 IFC Dynamic ArraysTM for Genotyping (Fluidigm, San Francisco, CA, USA).

    Techniques: Biomarker Discovery