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target region  (Addgene inc)


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    Structured Review

    Addgene inc target region
    Target Region, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/target region/product/Addgene inc
    Average 93 stars, based on 9 article reviews
    target region - by Bioz Stars, 2026-04
    93/100 stars

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    Image Search Results


    The distribution of A, T, G and C bases. ( a ) compares Nanopore whole-genome and Illumina whole-exome sequencing. ( b ) also includes the Nanopore exome results.

    Journal: International Journal of Molecular Sciences

    Article Title: Methodological Comparison of Short-Read and Long-Read Sequencing Methods on Colorectal Cancer Samples

    doi: 10.3390/ijms26189254

    Figure Lengend Snippet: The distribution of A, T, G and C bases. ( a ) compares Nanopore whole-genome and Illumina whole-exome sequencing. ( b ) also includes the Nanopore exome results.

    Article Snippet: Therefore, no statistically significant differences in mean VAF values can be established between the two platforms for mutations commonly detected within the Illumina exome panel target regions.

    Techniques: Sequencing

    SNP transitions across all morphological groups using the results of Nanopore whole-genome and Illumina whole-exome sequencing analyses.

    Journal: International Journal of Molecular Sciences

    Article Title: Methodological Comparison of Short-Read and Long-Read Sequencing Methods on Colorectal Cancer Samples

    doi: 10.3390/ijms26189254

    Figure Lengend Snippet: SNP transitions across all morphological groups using the results of Nanopore whole-genome and Illumina whole-exome sequencing analyses.

    Article Snippet: Therefore, no statistically significant differences in mean VAF values can be established between the two platforms for mutations commonly detected within the Illumina exome panel target regions.

    Techniques: Sequencing

    Variant allele frequency (VAF) values from Illumina exome panel restrictions using Nanopore and Illumina platforms. ( a ) displays results for the NEG group. ( b ) displays results for the NAT group, and ( c ) for CRC morphological classifications. The x-axis represents gene–mutation pairs, while the y-axis shows their corresponding VAF values. Blue circles indicate data from Nanopore sequencing, and red circles represent Illumina-derived values. Arrows indicate the direction of VAF differences: upward when Illumina VAF is greater than Nanopore, and downward when it is lower.

    Journal: International Journal of Molecular Sciences

    Article Title: Methodological Comparison of Short-Read and Long-Read Sequencing Methods on Colorectal Cancer Samples

    doi: 10.3390/ijms26189254

    Figure Lengend Snippet: Variant allele frequency (VAF) values from Illumina exome panel restrictions using Nanopore and Illumina platforms. ( a ) displays results for the NEG group. ( b ) displays results for the NAT group, and ( c ) for CRC morphological classifications. The x-axis represents gene–mutation pairs, while the y-axis shows their corresponding VAF values. Blue circles indicate data from Nanopore sequencing, and red circles represent Illumina-derived values. Arrows indicate the direction of VAF differences: upward when Illumina VAF is greater than Nanopore, and downward when it is lower.

    Article Snippet: Therefore, no statistically significant differences in mean VAF values can be established between the two platforms for mutations commonly detected within the Illumina exome panel target regions.

    Techniques: Variant Assay, Mutagenesis, Nanopore Sequencing, Derivative Assay