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KNIME GmbH pca plot
<t>PCA</t> analysis of N-glycan profiles from heart <t>tissue</t> <t>homogenate</t> (n=3), primary enriched CM (donor matched, n=3), and hiPSC-CM (n=3 for each time-point). A PCA plot of total N-glycome profiles for all sample types covering 93% of all observed variation. B Loading plot showing major N-glycan structure contributors to each cluster plotted with vectors (line length and angle) proportional to PCA dimension contribution strength and direction.
Pca Plot, supplied by KNIME GmbH, 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/pca+plot/pmc07852319-123-1-22?v=KNIME+GmbH
Average 90 stars, based on 1 article reviews
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Images

1) Product Images from "Reference glycan structure libraries of primary human cardiomyocytes and pluripotent stem cell-derived cardiomyocytes reveal cell-type and culture stage-specific glycan phenotypes"

Article Title: Reference glycan structure libraries of primary human cardiomyocytes and pluripotent stem cell-derived cardiomyocytes reveal cell-type and culture stage-specific glycan phenotypes

Journal: Journal of molecular and cellular cardiology

doi: 10.1016/j.yjmcc.2019.12.012

PCA analysis of N-glycan profiles from heart tissue homogenate (n=3), primary enriched CM (donor matched, n=3), and hiPSC-CM (n=3 for each time-point). A PCA plot of total N-glycome profiles for all sample types covering 93% of all observed variation. B Loading plot showing major N-glycan structure contributors to each cluster plotted with vectors (line length and angle) proportional to PCA dimension contribution strength and direction.
Figure Legend Snippet: PCA analysis of N-glycan profiles from heart tissue homogenate (n=3), primary enriched CM (donor matched, n=3), and hiPSC-CM (n=3 for each time-point). A PCA plot of total N-glycome profiles for all sample types covering 93% of all observed variation. B Loading plot showing major N-glycan structure contributors to each cluster plotted with vectors (line length and angle) proportional to PCA dimension contribution strength and direction.

Techniques Used: Glycoproteomics



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Image Search Results


a , Whole-cell liver lysates collected at 1 day, 5 days, and 10 weeks post-exposure were analyzed by western blot for phosho-p53. Band intensities normalized to TPS and saline WT controls. n = 4 per group (2 males, 2 females). b , Liver lysates from identical timepoints were immunoblotted for p21, normalized as above. n = 4 per group (2 males, 2 females). c , Liver lysates from identical timepoints were immunoblotted for RAD51, normalized as above. n = 4 per group (2 males, 2 females). d , e , Principal Component Analysis (PCA) of phosphoproteomics at 1 day ( d ) and 10 weeks ( e ) post-exposure displayed distinct sample clustering by treatment group and genotype. n = 4 (2 males and 2 females). f , g , Heatmaps show the most differentially expressed phosphorylated proteins at 1 day ( f ) and 10 weeks ( g ) post-exposure, identified by phosphoproteomics. DNA repair proteins are highlighted in bold ( f ). Protein selection based on multi-group ANOVA by treatment (p < 0.05), with standard deviation < 0.05; 354 total proteins ( f ), 214 total proteins ( g ). h , Phosphoproteomic quantification of gH2AX (combined S140 and S137 sites) at 1 day post-exposure. n ≥ 2 per group. i, STRING database analysis of top-expressed phosphoproteins at 1 day and 10 weeks post-exposure. Functional enrichment at 1 day highlights DNA repair clusters; 10 weeks displays enrichment for non-DNA repair biological processes from gene ontology. Statistical comparisons performed using one-way ANOVA with Šídák’s multiple comparisons test ( a – c , h ). Data are presented as mean ± s.e.m. Statistical significance: *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. NS, not significant.

Journal: bioRxiv

Article Title: Persistent interferon signaling and clonal expansion mark early events in DNA methylation damage-induced liver cancer

doi: 10.1101/2025.10.01.679856

Figure Lengend Snippet: a , Whole-cell liver lysates collected at 1 day, 5 days, and 10 weeks post-exposure were analyzed by western blot for phosho-p53. Band intensities normalized to TPS and saline WT controls. n = 4 per group (2 males, 2 females). b , Liver lysates from identical timepoints were immunoblotted for p21, normalized as above. n = 4 per group (2 males, 2 females). c , Liver lysates from identical timepoints were immunoblotted for RAD51, normalized as above. n = 4 per group (2 males, 2 females). d , e , Principal Component Analysis (PCA) of phosphoproteomics at 1 day ( d ) and 10 weeks ( e ) post-exposure displayed distinct sample clustering by treatment group and genotype. n = 4 (2 males and 2 females). f , g , Heatmaps show the most differentially expressed phosphorylated proteins at 1 day ( f ) and 10 weeks ( g ) post-exposure, identified by phosphoproteomics. DNA repair proteins are highlighted in bold ( f ). Protein selection based on multi-group ANOVA by treatment (p < 0.05), with standard deviation < 0.05; 354 total proteins ( f ), 214 total proteins ( g ). h , Phosphoproteomic quantification of gH2AX (combined S140 and S137 sites) at 1 day post-exposure. n ≥ 2 per group. i, STRING database analysis of top-expressed phosphoproteins at 1 day and 10 weeks post-exposure. Functional enrichment at 1 day highlights DNA repair clusters; 10 weeks displays enrichment for non-DNA repair biological processes from gene ontology. Statistical comparisons performed using one-way ANOVA with Šídák’s multiple comparisons test ( a – c , h ). Data are presented as mean ± s.e.m. Statistical significance: *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. NS, not significant.

Article Snippet: Qlucore software was used to generate heatmaps and PCA plots.

Techniques: Western Blot, Saline, Phospho-proteomics, Selection, Standard Deviation, Functional Assay

a , PCA of Mgmt −/− liver samples collected at days 1, 2, and 5 post-saline or NDMA exposure shows clear clustering separation by treatment group. RNA was extracted from liver tissue and analyzed by RNA-seq; n ≥ 7 per group (males and females combined). b , Bar graphs depict the number of differentially expressed RNA transcripts (up- and downregulated) in WT and Mgmt −/− liver following NDMA exposure across indicated timepoints. c , Venn diagrams compare overlap of significantly up- and downregulated genes across genotypes and timepoints. d , Pathway enrichment analysis of persistently up- and downregulated genes (intersected across all timepoints from panel c , red circles) in Mgmt −/− samples using Enrichr for MSigDB Hallmark gene sets. The top 8 pathways are displayed, ranked by Fisher exact test p-value. Pathways involved in IFN response are marked with an asterisk (*). e , Volcano plots display the most differentially expressed genes in Mgmt −/− livers comparing NDMA vs saline treatment at 1 day, 5 days, and 10 weeks. Plots show –log 10 p-value versus log 2 fold change. Genes from the GSEA Hallmark p53 pathway are circled in red or black; Cyp2e1 downregulation is circled in blue. f , i , Bar graphs quantify the number of up- and downregulated genes within the pre-curated IFN ( f ) and DNA repair ( i ) gene lists, comparing NDMA effects between WT and Mgmt −/− across the time course. g , h , Heatmaps show expression profiles for curated IFN response genes ( g ) and DNA repair genes ( h ) in response to NDMA treatment in WT and Mgmt −/− livers at days 1, 2, and 5 post-exposure. Color scale reflects relative gene expression intensity. Statistical analysis: All comparisons use thresholds of adjusted p-value < 0.05 and absolute log 2 fold change > 0.58 ( b – i ).

Journal: bioRxiv

Article Title: Persistent interferon signaling and clonal expansion mark early events in DNA methylation damage-induced liver cancer

doi: 10.1101/2025.10.01.679856

Figure Lengend Snippet: a , PCA of Mgmt −/− liver samples collected at days 1, 2, and 5 post-saline or NDMA exposure shows clear clustering separation by treatment group. RNA was extracted from liver tissue and analyzed by RNA-seq; n ≥ 7 per group (males and females combined). b , Bar graphs depict the number of differentially expressed RNA transcripts (up- and downregulated) in WT and Mgmt −/− liver following NDMA exposure across indicated timepoints. c , Venn diagrams compare overlap of significantly up- and downregulated genes across genotypes and timepoints. d , Pathway enrichment analysis of persistently up- and downregulated genes (intersected across all timepoints from panel c , red circles) in Mgmt −/− samples using Enrichr for MSigDB Hallmark gene sets. The top 8 pathways are displayed, ranked by Fisher exact test p-value. Pathways involved in IFN response are marked with an asterisk (*). e , Volcano plots display the most differentially expressed genes in Mgmt −/− livers comparing NDMA vs saline treatment at 1 day, 5 days, and 10 weeks. Plots show –log 10 p-value versus log 2 fold change. Genes from the GSEA Hallmark p53 pathway are circled in red or black; Cyp2e1 downregulation is circled in blue. f , i , Bar graphs quantify the number of up- and downregulated genes within the pre-curated IFN ( f ) and DNA repair ( i ) gene lists, comparing NDMA effects between WT and Mgmt −/− across the time course. g , h , Heatmaps show expression profiles for curated IFN response genes ( g ) and DNA repair genes ( h ) in response to NDMA treatment in WT and Mgmt −/− livers at days 1, 2, and 5 post-exposure. Color scale reflects relative gene expression intensity. Statistical analysis: All comparisons use thresholds of adjusted p-value < 0.05 and absolute log 2 fold change > 0.58 ( b – i ).

Article Snippet: Qlucore software was used to generate heatmaps and PCA plots.

Techniques: Saline, RNA Sequencing, Expressing, Gene Expression

Effect of photoperiod on serum bile acid profile in Taihe silky fowls. (A) PCA plot; (B) Bile acid clustering heatmap; (C) Bar chart of differentially abundant bile acids fold changes; (D) KEGG enrichment plot of differentially abundant bile acids. Data are presented as means ± SEM ( n = 6).

Journal: Poultry Science

Article Title: Molecular mechanisms of photoperiod regulation of bile acid metabolism in Taihe silky fowls based on the gut-liver axis

doi: 10.1016/j.psj.2025.105489

Figure Lengend Snippet: Effect of photoperiod on serum bile acid profile in Taihe silky fowls. (A) PCA plot; (B) Bile acid clustering heatmap; (C) Bar chart of differentially abundant bile acids fold changes; (D) KEGG enrichment plot of differentially abundant bile acids. Data are presented as means ± SEM ( n = 6).

Article Snippet: Effect of photoperiod on serum bile acid profile in Taihe silky fowls. (A) PCA plot; (B) Bile acid clustering heatmap; (C) Bar chart of differentially abundant bile acids fold changes; (D) KEGG enrichment plot of differentially abundant bile acids.

Techniques:

Effects of photoperiod on liver gene expression in Taihe silky fowls. (A) PCA plot; (B) Bar chart of differentially expressed genes; (C) Volcano plot of differentially expressed genes; (D) GO enrichment analysis bubble plot of differentially expressed genes; (E) KEGG enrichment analysis bubble plot of differentially expressed genes. Data are presented as means ± SEM ( n = 3).

Journal: Poultry Science

Article Title: Molecular mechanisms of photoperiod regulation of bile acid metabolism in Taihe silky fowls based on the gut-liver axis

doi: 10.1016/j.psj.2025.105489

Figure Lengend Snippet: Effects of photoperiod on liver gene expression in Taihe silky fowls. (A) PCA plot; (B) Bar chart of differentially expressed genes; (C) Volcano plot of differentially expressed genes; (D) GO enrichment analysis bubble plot of differentially expressed genes; (E) KEGG enrichment analysis bubble plot of differentially expressed genes. Data are presented as means ± SEM ( n = 3).

Article Snippet: Effect of photoperiod on serum bile acid profile in Taihe silky fowls. (A) PCA plot; (B) Bile acid clustering heatmap; (C) Bar chart of differentially abundant bile acids fold changes; (D) KEGG enrichment plot of differentially abundant bile acids.

Techniques: Gene Expression

Comparative bioinformatic analyses of immune cell enrichment in the PTB + T2DM and HC groups. ( A - B ) Enrichment scores of 22 distinct immune cell types in the two groups (PTB with T2DM vs. Healthy control and PTB with T2DM vs. T2DM group). ( C ) Correlation analysis between six key genes in PTB + T2DM and various immune cell types. ( D ) PCA was performed using the PCA expression plot feature in RStudio, data dimensionality of the data set was reduced, allowing the creation of a two-dimensional scatter plot for an initial sample distribution assessment. ( E ) Spearman’s correlation analysis of C1QA and LINC00278 expression with M2 macrophages. The values on the x-axis represent the relative enrichment level of M2 macrophages, and the values on the y-axis represent the expression levels of C1QA and LINC00278.

Journal: Scientific Reports

Article Title: A bioinformatics-driven approach to identify biomarkers and elucidate the pathogenesis of type 2 diabetes concurrent with pulmonary tuberculosis

doi: 10.1038/s41598-025-00928-0

Figure Lengend Snippet: Comparative bioinformatic analyses of immune cell enrichment in the PTB + T2DM and HC groups. ( A - B ) Enrichment scores of 22 distinct immune cell types in the two groups (PTB with T2DM vs. Healthy control and PTB with T2DM vs. T2DM group). ( C ) Correlation analysis between six key genes in PTB + T2DM and various immune cell types. ( D ) PCA was performed using the PCA expression plot feature in RStudio, data dimensionality of the data set was reduced, allowing the creation of a two-dimensional scatter plot for an initial sample distribution assessment. ( E ) Spearman’s correlation analysis of C1QA and LINC00278 expression with M2 macrophages. The values on the x-axis represent the relative enrichment level of M2 macrophages, and the values on the y-axis represent the expression levels of C1QA and LINC00278.

Article Snippet: Healthy control and PTB with T2DM vs. T2DM group). ( C ) Correlation analysis between six key genes in PTB + T2DM and various immune cell types. ( D ) PCA was performed using the PCA expression plot feature in RStudio, data dimensionality of the data set was reduced, allowing the creation of a two-dimensional scatter plot for an initial sample distribution assessment. ( E ) Spearman’s correlation analysis of C1QA and LINC00278 expression with M2 macrophages.

Techniques: Control, Expressing