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matlab compiler version 8 4  (MathWorks Inc)


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    MathWorks Inc matlab compiler version 8 4
    (A) OXER1 phylogenetic tree. (B) Relative expression levels of hcar1–3 and hcar1–4 mRNA in leukocytes compared with the rest of the body determined by FACS-sorting of dissociated neutrophil (left panel, TG( lyz :pm2-mk2)) or macrophage (right panel, TG( mpeg1: eGFP )) reporter zebrafish larvae and qRT-PCR. Error bars, SD of three different pools of zebrafish leukocytes. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., p > 0.05; Student’s t test (two tailed, two sample unequal variance test). (C) Top left panel: experimental cartoon scheme. This figure was created with BioRender. Bottom left panel: Venn diagram of zebrafish genes with ENSEMBL orthologs (ENSEMBL release 107) in human, cat, mouse, and rat. Red number, number of DIOPT-filtered NRNM genes (see ). Right panel: sorted sGCA heatmap of significantly regulated mRNA-seq expression profiles (fold-regulation > 2, p adj < 0.05 by Benjamini and Hochberg method) with high similarity to the respective binary expression phenotypes (correlation distance < 0.25, , also see and <t>MATLAB</t> sGCA script). Color scale, mRNA-seq profiles are row-scaled between 0 (blue) and 1 (pink). Shown are three biological replicates per experimental condition. Heatmap inset: significant (p adj < 0.05) fold-upregulation of select inflammatory receptor mRNAs 2 and 4 h after PA infection as calculated by DEseq2. DIOPT-filtered NRNM genes are marked on the left side of the heatmap (zebrafish gene/human ortholog). NRNM genes with “high”-ranked (criteria see ) human orthologs are printed in bold. (D) Heatmap of row-scaled lipid concentrations as measured by LIPIDMAPS full panel eicosanoid mass spectroscopical analysis. Color scale, relative lipid concentrations are row-scaled between 0 (blue) and 1 (orange). Boxed numbers, absolute lipid concentrations in pmol/mg tissue (~μM). Note that the color scale does not represent these absolute lipid concentrations, but that it highlights the relative changes for each lipid. Shown are three biological replicates (i.e., ~400 3 dpf zebrafish larvae per pool) per experimental condition. Numbers right of heatmap, p values of Student’s t test (two tailed, two sample unequal variance test) comparing 0 h PA vs. 2 h PA. See also and and .
    Matlab Compiler Version 8 4, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 96/100, based on 324 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/compiler+version+8%2E4/MATLAB+Compiler/pmc09973399-68-0-0
    Average 96 stars, based on 324 article reviews
    matlab compiler version 8 4 - by Bioz Stars, 2026-10
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    1) Product Images from "Oxoeicosanoid signaling mediates early antimicrobial defense in zebrafish"

    Article Title: Oxoeicosanoid signaling mediates early antimicrobial defense in zebrafish

    Journal: Cell reports

    doi: 10.1016/j.celrep.2022.111974

    (A) OXER1 phylogenetic tree. (B) Relative expression levels of hcar1–3 and hcar1–4 mRNA in leukocytes compared with the rest of the body determined by FACS-sorting of dissociated neutrophil (left panel, TG( lyz :pm2-mk2)) or macrophage (right panel, TG( mpeg1: eGFP )) reporter zebrafish larvae and qRT-PCR. Error bars, SD of three different pools of zebrafish leukocytes. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., p > 0.05; Student’s t test (two tailed, two sample unequal variance test). (C) Top left panel: experimental cartoon scheme. This figure was created with BioRender. Bottom left panel: Venn diagram of zebrafish genes with ENSEMBL orthologs (ENSEMBL release 107) in human, cat, mouse, and rat. Red number, number of DIOPT-filtered NRNM genes (see ). Right panel: sorted sGCA heatmap of significantly regulated mRNA-seq expression profiles (fold-regulation > 2, p adj < 0.05 by Benjamini and Hochberg method) with high similarity to the respective binary expression phenotypes (correlation distance < 0.25, , also see and MATLAB sGCA script). Color scale, mRNA-seq profiles are row-scaled between 0 (blue) and 1 (pink). Shown are three biological replicates per experimental condition. Heatmap inset: significant (p adj < 0.05) fold-upregulation of select inflammatory receptor mRNAs 2 and 4 h after PA infection as calculated by DEseq2. DIOPT-filtered NRNM genes are marked on the left side of the heatmap (zebrafish gene/human ortholog). NRNM genes with “high”-ranked (criteria see ) human orthologs are printed in bold. (D) Heatmap of row-scaled lipid concentrations as measured by LIPIDMAPS full panel eicosanoid mass spectroscopical analysis. Color scale, relative lipid concentrations are row-scaled between 0 (blue) and 1 (orange). Boxed numbers, absolute lipid concentrations in pmol/mg tissue (~μM). Note that the color scale does not represent these absolute lipid concentrations, but that it highlights the relative changes for each lipid. Shown are three biological replicates (i.e., ~400 3 dpf zebrafish larvae per pool) per experimental condition. Numbers right of heatmap, p values of Student’s t test (two tailed, two sample unequal variance test) comparing 0 h PA vs. 2 h PA. See also and and .
    Figure Legend Snippet: (A) OXER1 phylogenetic tree. (B) Relative expression levels of hcar1–3 and hcar1–4 mRNA in leukocytes compared with the rest of the body determined by FACS-sorting of dissociated neutrophil (left panel, TG( lyz :pm2-mk2)) or macrophage (right panel, TG( mpeg1: eGFP )) reporter zebrafish larvae and qRT-PCR. Error bars, SD of three different pools of zebrafish leukocytes. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., p > 0.05; Student’s t test (two tailed, two sample unequal variance test). (C) Top left panel: experimental cartoon scheme. This figure was created with BioRender. Bottom left panel: Venn diagram of zebrafish genes with ENSEMBL orthologs (ENSEMBL release 107) in human, cat, mouse, and rat. Red number, number of DIOPT-filtered NRNM genes (see ). Right panel: sorted sGCA heatmap of significantly regulated mRNA-seq expression profiles (fold-regulation > 2, p adj < 0.05 by Benjamini and Hochberg method) with high similarity to the respective binary expression phenotypes (correlation distance < 0.25, , also see and MATLAB sGCA script). Color scale, mRNA-seq profiles are row-scaled between 0 (blue) and 1 (pink). Shown are three biological replicates per experimental condition. Heatmap inset: significant (p adj < 0.05) fold-upregulation of select inflammatory receptor mRNAs 2 and 4 h after PA infection as calculated by DEseq2. DIOPT-filtered NRNM genes are marked on the left side of the heatmap (zebrafish gene/human ortholog). NRNM genes with “high”-ranked (criteria see ) human orthologs are printed in bold. (D) Heatmap of row-scaled lipid concentrations as measured by LIPIDMAPS full panel eicosanoid mass spectroscopical analysis. Color scale, relative lipid concentrations are row-scaled between 0 (blue) and 1 (orange). Boxed numbers, absolute lipid concentrations in pmol/mg tissue (~μM). Note that the color scale does not represent these absolute lipid concentrations, but that it highlights the relative changes for each lipid. Shown are three biological replicates (i.e., ~400 3 dpf zebrafish larvae per pool) per experimental condition. Numbers right of heatmap, p values of Student’s t test (two tailed, two sample unequal variance test) comparing 0 h PA vs. 2 h PA. See also and and .

    Techniques Used: Expressing, Quantitative RT-PCR, Two Tailed Test, Infection


    Figure Legend Snippet:

    Techniques Used: Virus, Recombinant, Saline, cDNA Synthesis, Software, Imaging, Microscopy

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    (A) OXER1 phylogenetic tree. (B) Relative expression levels of hcar1–3 and hcar1–4 mRNA in leukocytes compared with the rest of the body determined by FACS-sorting of dissociated neutrophil (left panel, TG( lyz :pm2-mk2)) or macrophage (right panel, TG( mpeg1: eGFP )) reporter zebrafish larvae and qRT-PCR. Error bars, SD of three different pools of zebrafish leukocytes. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., p > 0.05; Student’s t test (two tailed, two sample unequal variance test). (C) Top left panel: experimental cartoon scheme. This figure was created with BioRender. Bottom left panel: Venn diagram of zebrafish genes with ENSEMBL orthologs (ENSEMBL release 107) in human, cat, mouse, and rat. Red number, number of DIOPT-filtered NRNM genes (see ). Right panel: sorted sGCA heatmap of significantly regulated mRNA-seq expression profiles (fold-regulation > 2, p adj < 0.05 by Benjamini and Hochberg method) with high similarity to the respective binary expression phenotypes (correlation distance < 0.25, , also see and <t>MATLAB</t> sGCA script). Color scale, mRNA-seq profiles are row-scaled between 0 (blue) and 1 (pink). Shown are three biological replicates per experimental condition. Heatmap inset: significant (p adj < 0.05) fold-upregulation of select inflammatory receptor mRNAs 2 and 4 h after PA infection as calculated by DEseq2. DIOPT-filtered NRNM genes are marked on the left side of the heatmap (zebrafish gene/human ortholog). NRNM genes with “high”-ranked (criteria see ) human orthologs are printed in bold. (D) Heatmap of row-scaled lipid concentrations as measured by LIPIDMAPS full panel eicosanoid mass spectroscopical analysis. Color scale, relative lipid concentrations are row-scaled between 0 (blue) and 1 (orange). Boxed numbers, absolute lipid concentrations in pmol/mg tissue (~μM). Note that the color scale does not represent these absolute lipid concentrations, but that it highlights the relative changes for each lipid. Shown are three biological replicates (i.e., ~400 3 dpf zebrafish larvae per pool) per experimental condition. Numbers right of heatmap, p values of Student’s t test (two tailed, two sample unequal variance test) comparing 0 h PA vs. 2 h PA. See also and and .
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    (A) OXER1 phylogenetic tree. (B) Relative expression levels of hcar1–3 and hcar1–4 mRNA in leukocytes compared with the rest of the body determined by FACS-sorting of dissociated neutrophil (left panel, TG( lyz :pm2-mk2)) or macrophage (right panel, TG( mpeg1: eGFP )) reporter zebrafish larvae and qRT-PCR. Error bars, SD of three different pools of zebrafish leukocytes. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., p > 0.05; Student’s t test (two tailed, two sample unequal variance test). (C) Top left panel: experimental cartoon scheme. This figure was created with BioRender. Bottom left panel: Venn diagram of zebrafish genes with ENSEMBL orthologs (ENSEMBL release 107) in human, cat, mouse, and rat. Red number, number of DIOPT-filtered NRNM genes (see ). Right panel: sorted sGCA heatmap of significantly regulated mRNA-seq expression profiles (fold-regulation > 2, p adj < 0.05 by Benjamini and Hochberg method) with high similarity to the respective binary expression phenotypes (correlation distance < 0.25, , also see and <t>MATLAB</t> sGCA script). Color scale, mRNA-seq profiles are row-scaled between 0 (blue) and 1 (pink). Shown are three biological replicates per experimental condition. Heatmap inset: significant (p adj < 0.05) fold-upregulation of select inflammatory receptor mRNAs 2 and 4 h after PA infection as calculated by DEseq2. DIOPT-filtered NRNM genes are marked on the left side of the heatmap (zebrafish gene/human ortholog). NRNM genes with “high”-ranked (criteria see ) human orthologs are printed in bold. (D) Heatmap of row-scaled lipid concentrations as measured by LIPIDMAPS full panel eicosanoid mass spectroscopical analysis. Color scale, relative lipid concentrations are row-scaled between 0 (blue) and 1 (orange). Boxed numbers, absolute lipid concentrations in pmol/mg tissue (~μM). Note that the color scale does not represent these absolute lipid concentrations, but that it highlights the relative changes for each lipid. Shown are three biological replicates (i.e., ~400 3 dpf zebrafish larvae per pool) per experimental condition. Numbers right of heatmap, p values of Student’s t test (two tailed, two sample unequal variance test) comparing 0 h PA vs. 2 h PA. See also and and .
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    (A) OXER1 phylogenetic tree. (B) Relative expression levels of hcar1–3 and hcar1–4 mRNA in leukocytes compared with the rest of the body determined by FACS-sorting of dissociated neutrophil (left panel, TG( lyz :pm2-mk2)) or macrophage (right panel, TG( mpeg1: eGFP )) reporter zebrafish larvae and qRT-PCR. Error bars, SD of three different pools of zebrafish leukocytes. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., p > 0.05; Student’s t test (two tailed, two sample unequal variance test). (C) Top left panel: experimental cartoon scheme. This figure was created with BioRender. Bottom left panel: Venn diagram of zebrafish genes with ENSEMBL orthologs (ENSEMBL release 107) in human, cat, mouse, and rat. Red number, number of DIOPT-filtered NRNM genes (see ). Right panel: sorted sGCA heatmap of significantly regulated mRNA-seq expression profiles (fold-regulation > 2, p adj < 0.05 by Benjamini and Hochberg method) with high similarity to the respective binary expression phenotypes (correlation distance < 0.25, , also see and <t>MATLAB</t> sGCA script). Color scale, mRNA-seq profiles are row-scaled between 0 (blue) and 1 (pink). Shown are three biological replicates per experimental condition. Heatmap inset: significant (p adj < 0.05) fold-upregulation of select inflammatory receptor mRNAs 2 and 4 h after PA infection as calculated by DEseq2. DIOPT-filtered NRNM genes are marked on the left side of the heatmap (zebrafish gene/human ortholog). NRNM genes with “high”-ranked (criteria see ) human orthologs are printed in bold. (D) Heatmap of row-scaled lipid concentrations as measured by LIPIDMAPS full panel eicosanoid mass spectroscopical analysis. Color scale, relative lipid concentrations are row-scaled between 0 (blue) and 1 (orange). Boxed numbers, absolute lipid concentrations in pmol/mg tissue (~μM). Note that the color scale does not represent these absolute lipid concentrations, but that it highlights the relative changes for each lipid. Shown are three biological replicates (i.e., ~400 3 dpf zebrafish larvae per pool) per experimental condition. Numbers right of heatmap, p values of Student’s t test (two tailed, two sample unequal variance test) comparing 0 h PA vs. 2 h PA. See also and and .
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    Journal: Cell reports

    Article Title: Oxoeicosanoid signaling mediates early antimicrobial defense in zebrafish

    doi: 10.1016/j.celrep.2022.111974

    Figure Lengend Snippet:

    Article Snippet: MATLAB Compiler Version 8.4 (R2022a) , Mathworks Inc., USA , http://mathworks.com.

    Techniques: Recombinant, Software, Imaging, Microscopy

    (A) OXER1 phylogenetic tree. (B) Relative expression levels of hcar1–3 and hcar1–4 mRNA in leukocytes compared with the rest of the body determined by FACS-sorting of dissociated neutrophil (left panel, TG( lyz :pm2-mk2)) or macrophage (right panel, TG( mpeg1: eGFP )) reporter zebrafish larvae and qRT-PCR. Error bars, SD of three different pools of zebrafish leukocytes. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., p > 0.05; Student’s t test (two tailed, two sample unequal variance test). (C) Top left panel: experimental cartoon scheme. This figure was created with BioRender. Bottom left panel: Venn diagram of zebrafish genes with ENSEMBL orthologs (ENSEMBL release 107) in human, cat, mouse, and rat. Red number, number of DIOPT-filtered NRNM genes (see ). Right panel: sorted sGCA heatmap of significantly regulated mRNA-seq expression profiles (fold-regulation > 2, p adj < 0.05 by Benjamini and Hochberg method) with high similarity to the respective binary expression phenotypes (correlation distance < 0.25, , also see and MATLAB sGCA script). Color scale, mRNA-seq profiles are row-scaled between 0 (blue) and 1 (pink). Shown are three biological replicates per experimental condition. Heatmap inset: significant (p adj < 0.05) fold-upregulation of select inflammatory receptor mRNAs 2 and 4 h after PA infection as calculated by DEseq2. DIOPT-filtered NRNM genes are marked on the left side of the heatmap (zebrafish gene/human ortholog). NRNM genes with “high”-ranked (criteria see ) human orthologs are printed in bold. (D) Heatmap of row-scaled lipid concentrations as measured by LIPIDMAPS full panel eicosanoid mass spectroscopical analysis. Color scale, relative lipid concentrations are row-scaled between 0 (blue) and 1 (orange). Boxed numbers, absolute lipid concentrations in pmol/mg tissue (~μM). Note that the color scale does not represent these absolute lipid concentrations, but that it highlights the relative changes for each lipid. Shown are three biological replicates (i.e., ~400 3 dpf zebrafish larvae per pool) per experimental condition. Numbers right of heatmap, p values of Student’s t test (two tailed, two sample unequal variance test) comparing 0 h PA vs. 2 h PA. See also and and .

    Journal: Cell reports

    Article Title: Oxoeicosanoid signaling mediates early antimicrobial defense in zebrafish

    doi: 10.1016/j.celrep.2022.111974

    Figure Lengend Snippet: (A) OXER1 phylogenetic tree. (B) Relative expression levels of hcar1–3 and hcar1–4 mRNA in leukocytes compared with the rest of the body determined by FACS-sorting of dissociated neutrophil (left panel, TG( lyz :pm2-mk2)) or macrophage (right panel, TG( mpeg1: eGFP )) reporter zebrafish larvae and qRT-PCR. Error bars, SD of three different pools of zebrafish leukocytes. *p < 0.05, **p < 0.01, ***p < 0.001, n.s., p > 0.05; Student’s t test (two tailed, two sample unequal variance test). (C) Top left panel: experimental cartoon scheme. This figure was created with BioRender. Bottom left panel: Venn diagram of zebrafish genes with ENSEMBL orthologs (ENSEMBL release 107) in human, cat, mouse, and rat. Red number, number of DIOPT-filtered NRNM genes (see ). Right panel: sorted sGCA heatmap of significantly regulated mRNA-seq expression profiles (fold-regulation > 2, p adj < 0.05 by Benjamini and Hochberg method) with high similarity to the respective binary expression phenotypes (correlation distance < 0.25, , also see and MATLAB sGCA script). Color scale, mRNA-seq profiles are row-scaled between 0 (blue) and 1 (pink). Shown are three biological replicates per experimental condition. Heatmap inset: significant (p adj < 0.05) fold-upregulation of select inflammatory receptor mRNAs 2 and 4 h after PA infection as calculated by DEseq2. DIOPT-filtered NRNM genes are marked on the left side of the heatmap (zebrafish gene/human ortholog). NRNM genes with “high”-ranked (criteria see ) human orthologs are printed in bold. (D) Heatmap of row-scaled lipid concentrations as measured by LIPIDMAPS full panel eicosanoid mass spectroscopical analysis. Color scale, relative lipid concentrations are row-scaled between 0 (blue) and 1 (orange). Boxed numbers, absolute lipid concentrations in pmol/mg tissue (~μM). Note that the color scale does not represent these absolute lipid concentrations, but that it highlights the relative changes for each lipid. Shown are three biological replicates (i.e., ~400 3 dpf zebrafish larvae per pool) per experimental condition. Numbers right of heatmap, p values of Student’s t test (two tailed, two sample unequal variance test) comparing 0 h PA vs. 2 h PA. See also and and .

    Article Snippet: MATLAB Compiler Version 8.4 (R2022a) , Mathworks Inc., USA , http://mathworks.com.

    Techniques: Expressing, Quantitative RT-PCR, Two Tailed Test, Infection

    Journal: Cell reports

    Article Title: Oxoeicosanoid signaling mediates early antimicrobial defense in zebrafish

    doi: 10.1016/j.celrep.2022.111974

    Figure Lengend Snippet:

    Article Snippet: MATLAB Compiler Version 8.4 (R2022a) , Mathworks Inc., USA , http://mathworks.com.

    Techniques: Virus, Recombinant, Saline, cDNA Synthesis, Software, Imaging, Microscopy