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MetWare Ltd kegg pathway enrichment analysis
Kegg Pathway Enrichment Analysis, supplied by MetWare Ltd, 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/result/kegg pathway enrichment analysis/product/MetWare Ltd
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MetWare Ltd kegg pathway enrichment analysis
Kegg Pathway Enrichment Analysis, supplied by MetWare Ltd, 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/result/kegg pathway enrichment analysis/product/MetWare Ltd
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A Pie chart of quantified metabolite categories. Colors represent different compound super-classes; coloration follows the legend counterclockwise per each pie chart. B Volcano plot analysis performed on early-ESCC tissue samples vs. normal controls. P -values were determined by two-sided t -test without adjustments. Differentially-expressed metabolites are indicated by blue dots (down-regulation relative to normal controls) and red dots (up-regulation relative to normal controls), respectively. Gray dots indicate no significant difference. C Treemap of the most enriched <t>KEGG</t> pathways in early-ESCC tissue samples. Relative betweenness centrality was the selected node importance measure for pathway topological analysis. Each square represents <t>a</t> <t>metabolic</t> pathway; the square size represents the impact factor in the topological analysis; the color of the squares indicates the p -value of the enrichment analysis; and the darker the color, the more significant the enrichment. D O2PLS loading plots of the key differential metabolites analyzed by NMR-based and MS-based metabolomics. The top 30 metabolites in early-ESCC tissues detected by NMR and MS are labeled in purple and blue, respectively. Source data are provided as a Source Data file.
Kegg Metabolic Pathway Enrichment Analysis, supplied by Biofluids Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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A Pie chart of quantified metabolite categories. Colors represent different compound super-classes; coloration follows the legend counterclockwise per each pie chart. B Volcano plot analysis performed on early-ESCC tissue samples vs. normal controls. P -values were determined by two-sided t -test without adjustments. Differentially-expressed metabolites are indicated by blue dots (down-regulation relative to normal controls) and red dots (up-regulation relative to normal controls), respectively. Gray dots indicate no significant difference. C Treemap of the most enriched <t>KEGG</t> pathways in early-ESCC tissue samples. Relative betweenness centrality was the selected node importance measure for pathway topological analysis. Each square represents <t>a</t> <t>metabolic</t> pathway; the square size represents the impact factor in the topological analysis; the color of the squares indicates the p -value of the enrichment analysis; and the darker the color, the more significant the enrichment. D O2PLS loading plots of the key differential metabolites analyzed by NMR-based and MS-based metabolomics. The top 30 metabolites in early-ESCC tissues detected by NMR and MS are labeled in purple and blue, respectively. Source data are provided as a Source Data file.
Kegg Pathway Enrichment Analysis, supplied by Guangyuan Capital Water Co Ltd, 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/result/kegg pathway enrichment analysis/product/Guangyuan Capital Water Co Ltd
Average 90 stars, based on 1 article reviews
kegg pathway enrichment analysis - by Bioz Stars, 2026-04
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Bioinformatics analysis. ( A ) The gene expression in GSE101639 was subjected to quantile normalization. ( B ) DEGs in normal group and sepsis group. ( C ) It was found in GSE154918 that the expression of PIK3CA was down-regulated in sepsis compared with that in normal samples. ( D ) The upstream miRNAs of PIK3CA were evaluated through miRDB, starBase and TargetScan, and the DEG <t>of</t> <t>miR-506,</t> a key regulator of PIK3CA, was obtained from the intersection. ( E ) miR-506 of PIK3CA had a targeted binding region. ( F ) GO enrichment analysis was performed using the online tool DAVID. A total of 37 down-regulated pathways were enriched, including autophagy, transcription elongation from RNA polymerase II promoter and regulation of blood pressure. ( G ) 30 up-regulated pathways, including protein SUMOylation, glucose homeostasis and negative regulation of protein kinase activity. ( H ) <t>KEGG</t> pathway analysis was conducted on the integrated DEGs using DAVID. ( I ) The hub gene was obtained by Cytoscape.
Kegg Pathway Enrichment Analysis, supplied by RStudio, 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/result/kegg pathway enrichment analysis/product/RStudio
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Bioinformatics analysis. ( A ) The gene expression in GSE101639 was subjected to quantile normalization. ( B ) DEGs in normal group and sepsis group. ( C ) It was found in GSE154918 that the expression of PIK3CA was down-regulated in sepsis compared with that in normal samples. ( D ) The upstream miRNAs of PIK3CA were evaluated through miRDB, starBase and TargetScan, and the DEG <t>of</t> <t>miR-506,</t> a key regulator of PIK3CA, was obtained from the intersection. ( E ) miR-506 of PIK3CA had a targeted binding region. ( F ) GO enrichment analysis was performed using the online tool DAVID. A total of 37 down-regulated pathways were enriched, including autophagy, transcription elongation from RNA polymerase II promoter and regulation of blood pressure. ( G ) 30 up-regulated pathways, including protein SUMOylation, glucose homeostasis and negative regulation of protein kinase activity. ( H ) <t>KEGG</t> pathway analysis was conducted on the integrated DEGs using DAVID. ( I ) The hub gene was obtained by Cytoscape.
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Bioinformatics analysis. ( A ) The gene expression in GSE101639 was subjected to quantile normalization. ( B ) DEGs in normal group and sepsis group. ( C ) It was found in GSE154918 that the expression of PIK3CA was down-regulated in sepsis compared with that in normal samples. ( D ) The upstream miRNAs of PIK3CA were evaluated through miRDB, starBase and TargetScan, and the DEG <t>of</t> <t>miR-506,</t> a key regulator of PIK3CA, was obtained from the intersection. ( E ) miR-506 of PIK3CA had a targeted binding region. ( F ) GO enrichment analysis was performed using the online tool DAVID. A total of 37 down-regulated pathways were enriched, including autophagy, transcription elongation from RNA polymerase II promoter and regulation of blood pressure. ( G ) 30 up-regulated pathways, including protein SUMOylation, glucose homeostasis and negative regulation of protein kinase activity. ( H ) <t>KEGG</t> pathway analysis was conducted on the integrated DEGs using DAVID. ( I ) The hub gene was obtained by Cytoscape.
Gene Ontology (Go) And Kyoto Encyclopedia Of Genes And Genomes (Kegg) Pathway Enrichment Analysis, supplied by RStudio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bioinformatics analysis. ( A ) The gene expression in GSE101639 was subjected to quantile normalization. ( B ) DEGs in normal group and sepsis group. ( C ) It was found in GSE154918 that the expression of PIK3CA was down-regulated in sepsis compared with that in normal samples. ( D ) The upstream miRNAs of PIK3CA were evaluated through miRDB, starBase and TargetScan, and the DEG <t>of</t> <t>miR-506,</t> a key regulator of PIK3CA, was obtained from the intersection. ( E ) miR-506 of PIK3CA had a targeted binding region. ( F ) GO enrichment analysis was performed using the online tool DAVID. A total of 37 down-regulated pathways were enriched, including autophagy, transcription elongation from RNA polymerase II promoter and regulation of blood pressure. ( G ) 30 up-regulated pathways, including protein SUMOylation, glucose homeostasis and negative regulation of protein kinase activity. ( H ) <t>KEGG</t> pathway analysis was conducted on the integrated DEGs using DAVID. ( I ) The hub gene was obtained by Cytoscape.
Kegg Pathway Enrichment Analysis, supplied by Kaneka Corp, 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/result/kegg pathway enrichment analysis/product/Kaneka Corp
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Bioinformatics analysis. ( A ) The gene expression in GSE101639 was subjected to quantile normalization. ( B ) DEGs in normal group and sepsis group. ( C ) It was found in GSE154918 that the expression of PIK3CA was down-regulated in sepsis compared with that in normal samples. ( D ) The upstream miRNAs of PIK3CA were evaluated through miRDB, starBase and TargetScan, and the DEG <t>of</t> <t>miR-506,</t> a key regulator of PIK3CA, was obtained from the intersection. ( E ) miR-506 of PIK3CA had a targeted binding region. ( F ) GO enrichment analysis was performed using the online tool DAVID. A total of 37 down-regulated pathways were enriched, including autophagy, transcription elongation from RNA polymerase II promoter and regulation of blood pressure. ( G ) 30 up-regulated pathways, including protein SUMOylation, glucose homeostasis and negative regulation of protein kinase activity. ( H ) <t>KEGG</t> pathway analysis was conducted on the integrated DEGs using DAVID. ( I ) The hub gene was obtained by Cytoscape.
Kegg Pathway Enrichment Analysis, supplied by Broad Institute 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/result/kegg pathway enrichment analysis/product/Broad Institute Inc
Average 90 stars, based on 1 article reviews
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Bioinformatics analysis. ( A ) The gene expression in GSE101639 was subjected to quantile normalization. ( B ) DEGs in normal group and sepsis group. ( C ) It was found in GSE154918 that the expression of PIK3CA was down-regulated in sepsis compared with that in normal samples. ( D ) The upstream miRNAs of PIK3CA were evaluated through miRDB, starBase and TargetScan, and the DEG <t>of</t> <t>miR-506,</t> a key regulator of PIK3CA, was obtained from the intersection. ( E ) miR-506 of PIK3CA had a targeted binding region. ( F ) GO enrichment analysis was performed using the online tool DAVID. A total of 37 down-regulated pathways were enriched, including autophagy, transcription elongation from RNA polymerase II promoter and regulation of blood pressure. ( G ) 30 up-regulated pathways, including protein SUMOylation, glucose homeostasis and negative regulation of protein kinase activity. ( H ) <t>KEGG</t> pathway analysis was conducted on the integrated DEGs using DAVID. ( I ) The hub gene was obtained by Cytoscape.
Kegg Pathway Enrichment Analysis, supplied by Bioplanet, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bioinformatics analysis. ( A ) The gene expression in GSE101639 was subjected to quantile normalization. ( B ) DEGs in normal group and sepsis group. ( C ) It was found in GSE154918 that the expression of PIK3CA was down-regulated in sepsis compared with that in normal samples. ( D ) The upstream miRNAs of PIK3CA were evaluated through miRDB, starBase and TargetScan, and the DEG <t>of</t> <t>miR-506,</t> a key regulator of PIK3CA, was obtained from the intersection. ( E ) miR-506 of PIK3CA had a targeted binding region. ( F ) GO enrichment analysis was performed using the online tool DAVID. A total of 37 down-regulated pathways were enriched, including autophagy, transcription elongation from RNA polymerase II promoter and regulation of blood pressure. ( G ) 30 up-regulated pathways, including protein SUMOylation, glucose homeostasis and negative regulation of protein kinase activity. ( H ) <t>KEGG</t> pathway analysis was conducted on the integrated DEGs using DAVID. ( I ) The hub gene was obtained by Cytoscape.
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A Pie chart of quantified metabolite categories. Colors represent different compound super-classes; coloration follows the legend counterclockwise per each pie chart. B Volcano plot analysis performed on early-ESCC tissue samples vs. normal controls. P -values were determined by two-sided t -test without adjustments. Differentially-expressed metabolites are indicated by blue dots (down-regulation relative to normal controls) and red dots (up-regulation relative to normal controls), respectively. Gray dots indicate no significant difference. C Treemap of the most enriched KEGG pathways in early-ESCC tissue samples. Relative betweenness centrality was the selected node importance measure for pathway topological analysis. Each square represents a metabolic pathway; the square size represents the impact factor in the topological analysis; the color of the squares indicates the p -value of the enrichment analysis; and the darker the color, the more significant the enrichment. D O2PLS loading plots of the key differential metabolites analyzed by NMR-based and MS-based metabolomics. The top 30 metabolites in early-ESCC tissues detected by NMR and MS are labeled in purple and blue, respectively. Source data are provided as a Source Data file.

Journal: Nature Communications

Article Title: NMR and MS reveal characteristic metabolome atlas and optimize esophageal squamous cell carcinoma early detection

doi: 10.1038/s41467-024-46837-0

Figure Lengend Snippet: A Pie chart of quantified metabolite categories. Colors represent different compound super-classes; coloration follows the legend counterclockwise per each pie chart. B Volcano plot analysis performed on early-ESCC tissue samples vs. normal controls. P -values were determined by two-sided t -test without adjustments. Differentially-expressed metabolites are indicated by blue dots (down-regulation relative to normal controls) and red dots (up-regulation relative to normal controls), respectively. Gray dots indicate no significant difference. C Treemap of the most enriched KEGG pathways in early-ESCC tissue samples. Relative betweenness centrality was the selected node importance measure for pathway topological analysis. Each square represents a metabolic pathway; the square size represents the impact factor in the topological analysis; the color of the squares indicates the p -value of the enrichment analysis; and the darker the color, the more significant the enrichment. D O2PLS loading plots of the key differential metabolites analyzed by NMR-based and MS-based metabolomics. The top 30 metabolites in early-ESCC tissues detected by NMR and MS are labeled in purple and blue, respectively. Source data are provided as a Source Data file.

Article Snippet: KEGG metabolic pathway enrichment analysis was further performed (Fig. ), and we found that ‘Alanine, aspartate and glutamate metabolism’ consistently exhibited the most significant changes from tumor-bearing to tumor-resected phase and to healthy status in biofluids (Supplementary Fig. ).

Techniques: Labeling

Bioinformatics analysis. ( A ) The gene expression in GSE101639 was subjected to quantile normalization. ( B ) DEGs in normal group and sepsis group. ( C ) It was found in GSE154918 that the expression of PIK3CA was down-regulated in sepsis compared with that in normal samples. ( D ) The upstream miRNAs of PIK3CA were evaluated through miRDB, starBase and TargetScan, and the DEG of miR-506, a key regulator of PIK3CA, was obtained from the intersection. ( E ) miR-506 of PIK3CA had a targeted binding region. ( F ) GO enrichment analysis was performed using the online tool DAVID. A total of 37 down-regulated pathways were enriched, including autophagy, transcription elongation from RNA polymerase II promoter and regulation of blood pressure. ( G ) 30 up-regulated pathways, including protein SUMOylation, glucose homeostasis and negative regulation of protein kinase activity. ( H ) KEGG pathway analysis was conducted on the integrated DEGs using DAVID. ( I ) The hub gene was obtained by Cytoscape.

Journal: Aging (Albany NY)

Article Title: miR-506-3p induces autophagy of renal tubular epithelial cells in sepsis through targeting PI3K pathway

doi: 10.18632/aging.204759

Figure Lengend Snippet: Bioinformatics analysis. ( A ) The gene expression in GSE101639 was subjected to quantile normalization. ( B ) DEGs in normal group and sepsis group. ( C ) It was found in GSE154918 that the expression of PIK3CA was down-regulated in sepsis compared with that in normal samples. ( D ) The upstream miRNAs of PIK3CA were evaluated through miRDB, starBase and TargetScan, and the DEG of miR-506, a key regulator of PIK3CA, was obtained from the intersection. ( E ) miR-506 of PIK3CA had a targeted binding region. ( F ) GO enrichment analysis was performed using the online tool DAVID. A total of 37 down-regulated pathways were enriched, including autophagy, transcription elongation from RNA polymerase II promoter and regulation of blood pressure. ( G ) 30 up-regulated pathways, including protein SUMOylation, glucose homeostasis and negative regulation of protein kinase activity. ( H ) KEGG pathway analysis was conducted on the integrated DEGs using DAVID. ( I ) The hub gene was obtained by Cytoscape.

Article Snippet: Furthermore, KEGG pathway enrichment analysis using R-Studio showed that miR-506-3p had a targeted regulatory effect on PIK3CA, a key gene in the PI3K-Akt signaling pathway.

Techniques: Gene Expression, Expressing, Binding Assay, Activity Assay