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high throughput microarray platform illumina 27k array  (Illumina Inc)


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    Structured Review

    Illumina Inc high throughput microarray platform illumina 27k array
    High Throughput Microarray Platform Illumina 27k Array, supplied by Illumina 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/product/high+throughput+microarray+platforms/27k+array/pmc03763832-98-2-6
    Average 90 stars, based on 1 article reviews
    high throughput microarray platform illumina 27k array - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: A systematic review of the barcoding strategy that contributes to COVID-19 diagnostics at a population level
    Article Snippet: Amplicons prepared based on these methods are sequenced using Illumina sequencing platforms (iSeq, MiniSeq, MiSeq, NextSeq, NovaSeq).

    Article Title: Fluorescence activated cell sorting followed by small RNA sequencing reveals stable microRNA expression during cell cycle progression
    Article Snippet: Three high-throughput platforms (microarray, TaqMan Low Density Array and Illumina small RNA Sequencing) of miRNA expression were used to detect cell cycle dependent miRNA expression (Fig. , Panel a-d, Additional file : Figure S5).

    Article Title: Candidate genes linking maternal nutrient exposure to offspring health via DNA methylation: a review of existing evidence in humans with specific focus on one-carbon metabolism
    Article Snippet: The advent of high-throughput, genome-wide microarray platforms, such as the Illumina HumanMethylation 450 K and EPIC arrays, has helped in this regard, first by helping to standardize aspects of epigenome-wide association study (EWAS) design, and second by reducing the cost of genome-wide methylation assays required for adequately powered large studies.

    Article Title: Dissecting complex phenotypes using the genomics of twins
    Article Snippet: The fast development in high throughput SNP genotyping techniques using DNA microarray platforms, such as Illumina and Affymetrix, is revolutionizing the way we design and conduct genetic epidemiological studies of human complex traits or diseases.

    Article Title: Complementary genetic and genomic approaches help characterize the linkage group I seed protein QTL in soybean
    Article Snippet: In the present study, we leveraged a combination of resources - a NIL pair that differed substantially in seed protein [ ], transcript profiling by Affymetrix ® Soy GeneChip microarray, Illumina ® high-throughput transcriptome sequencing platforms, and the newly available soybean genome sequence--to assess genomic and genetic contributions to seed protein traits in soybean.

    High Throughput Screening Assay:

    Article Title: Twin-based DNA methylation analysis takes the center stage of studies of human complex diseases.
    Article Snippet: The etiology of complex diseases is characterized by the interaction between the genome and environmental conditions and the interface of epigenetics may be a central mechanism.. Current technologies already allow us high-throughput profiling of epigenetic patterns at genome level.. However, our understanding of the epigenetic processes remains limited.

    Microarray:

    Article Title: Twin-based DNA methylation analysis takes the center stage of studies of human complex diseases.
    Article Snippet: The etiology of complex diseases is characterized by the interaction between the genome and environmental conditions and the interface of epigenetics may be a central mechanism.. Current technologies already allow us high-throughput profiling of epigenetic patterns at genome level.. However, our understanding of the epigenetic processes remains limited.

    Next-Generation Sequencing:

    Article Title: Twin-based DNA methylation analysis takes the center stage of studies of human complex diseases.
    Article Snippet: The etiology of complex diseases is characterized by the interaction between the genome and environmental conditions and the interface of epigenetics may be a central mechanism.. Current technologies already allow us high-throughput profiling of epigenetic patterns at genome level.. However, our understanding of the epigenetic processes remains limited.



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    Number of present miRNAs at different stages (day 0, day 12, day 19 and day 26) during cardiomyocyte specific differentiation and <t> maturation. </t>
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    Image Search Results


    Number of present miRNAs at different stages (day 0, day 12, day 19 and day 26) during cardiomyocyte specific differentiation and  maturation.

    Journal: PLoS ONE

    Article Title: MicroRNA Profiling during Cardiomyocyte-Specific Differentiation of Murine Embryonic Stem Cells Based on Two Different miRNA Array Platforms

    doi: 10.1371/journal.pone.0025809

    Figure Lengend Snippet: Number of present miRNAs at different stages (day 0, day 12, day 19 and day 26) during cardiomyocyte specific differentiation and maturation.

    Article Snippet: In the present manuscript paper, a transgenic mouse ES cell clone was used to generate uniform Cor.At® cardiomyocytes. miRNAs were profiled for undifferentiated transgenic ES cells (day 0) and at time points day 12, day 19 and day 26 during cardiomyocyte-specific differentiation and maturation using 2 high throughput microarray platforms provided from Affymetrix and Febit.

    Techniques:

    The number of up/down regulated miRNAs at different maturation stages (day 12, day 19 and day 26) compared to undifferentiated ES cells were denoted with arrows up/down.

    Journal: PLoS ONE

    Article Title: MicroRNA Profiling during Cardiomyocyte-Specific Differentiation of Murine Embryonic Stem Cells Based on Two Different miRNA Array Platforms

    doi: 10.1371/journal.pone.0025809

    Figure Lengend Snippet: The number of up/down regulated miRNAs at different maturation stages (day 12, day 19 and day 26) compared to undifferentiated ES cells were denoted with arrows up/down.

    Article Snippet: In the present manuscript paper, a transgenic mouse ES cell clone was used to generate uniform Cor.At® cardiomyocytes. miRNAs were profiled for undifferentiated transgenic ES cells (day 0) and at time points day 12, day 19 and day 26 during cardiomyocyte-specific differentiation and maturation using 2 high throughput microarray platforms provided from Affymetrix and Febit.

    Techniques: