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microarray raw intensities limma package r v2.13.0 software  (Agilent technologies)


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    Agilent technologies microarray raw intensities limma package r v2.13.0 software
    Microarray Raw Intensities Limma Package R V2.13.0 Software, supplied by Agilent technologies, 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/microarray+software+packages/pmc09643439-255-42-45
    Average 90 stars, based on 1 article reviews
    microarray raw intensities limma package r v2.13.0 software - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Gene Expression:

    Article Title: CDKN1A is a target for phagocytosis-mediated cellular immunotherapy in acute leukemia
    Article Snippet: The RT-qPCR data were analyzed with qPCR CFX Maestro Version 4.0.2325.0418. (Biorad). .. Gene expression analysis of Phago - MDMs and Phago + MDMs was performed with an Agilent® SurePrint G3 Human GE 8x60K Microarray (Agilent Technologies, AMADID 28004) using Microarray images Extraction software version (10.7.3.1) (Agilent Technologies) and Microarray raw intensities limma package for R v2.13.0 software (Agilent Technologies), with two technical replicates for each sample. ..

    Microarray:

    Article Title: CDKN1A is a target for phagocytosis-mediated cellular immunotherapy in acute leukemia
    Article Snippet: The RT-qPCR data were analyzed with qPCR CFX Maestro Version 4.0.2325.0418. (Biorad). .. Gene expression analysis of Phago - MDMs and Phago + MDMs was performed with an Agilent® SurePrint G3 Human GE 8x60K Microarray (Agilent Technologies, AMADID 28004) using Microarray images Extraction software version (10.7.3.1) (Agilent Technologies) and Microarray raw intensities limma package for R v2.13.0 software (Agilent Technologies), with two technical replicates for each sample. ..

    Extraction:

    Article Title: CDKN1A is a target for phagocytosis-mediated cellular immunotherapy in acute leukemia
    Article Snippet: The RT-qPCR data were analyzed with qPCR CFX Maestro Version 4.0.2325.0418. (Biorad). .. Gene expression analysis of Phago - MDMs and Phago + MDMs was performed with an Agilent® SurePrint G3 Human GE 8x60K Microarray (Agilent Technologies, AMADID 28004) using Microarray images Extraction software version (10.7.3.1) (Agilent Technologies) and Microarray raw intensities limma package for R v2.13.0 software (Agilent Technologies), with two technical replicates for each sample. ..

    Software:

    Article Title: CDKN1A is a target for phagocytosis-mediated cellular immunotherapy in acute leukemia
    Article Snippet: The RT-qPCR data were analyzed with qPCR CFX Maestro Version 4.0.2325.0418. (Biorad). .. Gene expression analysis of Phago - MDMs and Phago + MDMs was performed with an Agilent® SurePrint G3 Human GE 8x60K Microarray (Agilent Technologies, AMADID 28004) using Microarray images Extraction software version (10.7.3.1) (Agilent Technologies) and Microarray raw intensities limma package for R v2.13.0 software (Agilent Technologies), with two technical replicates for each sample. ..



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    A, Electrophoresis of whole serum (WS) or fractionated serum IgG derived from a systemic lupus erythematosus (SLE) patient (L) and a normal subject (N). Molecular weight marker (M) is shown at the right. B, Scatterplot of entire gene set considered by <t>microarray</t> analysis to be expressed in podocytes (P < 0.05). The position of each dot on the scatterplot corresponds to the normalized average signal intensity (log scale) of a single gene. The normalized average signal intensity after exposure to SLE IgG and normal IgG is shown on the x and y axes, respectively. Broken red lines represent normal IgG:SLE IgG ratios of 2.0 (top; 2-fold greater expression in normal IgG) and 0.5 (bottom; 2-fold greater expression in SLE IgG). Black broken line is the mean.
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    Image Search Results


    A, Electrophoresis of whole serum (WS) or fractionated serum IgG derived from a systemic lupus erythematosus (SLE) patient (L) and a normal subject (N). Molecular weight marker (M) is shown at the right. B, Scatterplot of entire gene set considered by microarray analysis to be expressed in podocytes (P < 0.05). The position of each dot on the scatterplot corresponds to the normalized average signal intensity (log scale) of a single gene. The normalized average signal intensity after exposure to SLE IgG and normal IgG is shown on the x and y axes, respectively. Broken red lines represent normal IgG:SLE IgG ratios of 2.0 (top; 2-fold greater expression in normal IgG) and 0.5 (bottom; 2-fold greater expression in SLE IgG). Black broken line is the mean.

    Journal: Arthritis & rheumatology (Hoboken, N.J.)

    Article Title: Lupus Nephritis IgG Induction of Calcium/Calmodulin-Dependent Protein Kinase IV Expression in Podocytes and Alteration of Their Function

    doi: 10.1002/art.39499

    Figure Lengend Snippet: A, Electrophoresis of whole serum (WS) or fractionated serum IgG derived from a systemic lupus erythematosus (SLE) patient (L) and a normal subject (N). Molecular weight marker (M) is shown at the right. B, Scatterplot of entire gene set considered by microarray analysis to be expressed in podocytes (P < 0.05). The position of each dot on the scatterplot corresponds to the normalized average signal intensity (log scale) of a single gene. The normalized average signal intensity after exposure to SLE IgG and normal IgG is shown on the x and y axes, respectively. Broken red lines represent normal IgG:SLE IgG ratios of 2.0 (top; 2-fold greater expression in normal IgG) and 0.5 (bottom; 2-fold greater expression in SLE IgG). Black broken line is the mean.

    Article Snippet: Scan data images were analyzed using the Microarray Data Analysis Tool software package (Filgen), a comprehensive program that also produced the gene ontology and Z score reports.

    Techniques: Electrophoresis, Derivative Assay, Molecular Weight, Marker, Microarray, Expressing