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dna fingerprint java application analysis software  (SourceForge net)

 
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    SourceForge net dna fingerprint java application analysis software
    RAPD genotyping of the strains. ( a ) Combined RAPD patterns of 23 clinical Acinetobacter isolates obtained after electrophoresis of the PCRs with five different primers individually. For each primer, five RAPD gels were combined into one image. ( b ) RAPD dendrogram was constructed with <t>GelJ</t> cluster analysis software by Unweighted Pair Group Method with Arithmetic Mean UPGMA). Percentages of similarity and primers used as presented in on the top line of the dendrogram. RAPD type and strain code as in and strain numbers as presented in a appear on the right (between parenthesis).
    Dna Fingerprint Java Application Analysis Software, supplied by SourceForge net, 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/java+software+applications/dna+fingerprint+java+application+analysis+software/pmc07558960-226-4-15
    Average 90 stars, based on 1 article reviews
    dna fingerprint java application analysis software - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Antibiogram, Prevalence of OXA Carbapenemase Encoding Genes, and RAPD-Genotyping of Multidrug-Resistant Acinetobacter baumannii Incriminated in Hidden Community-Acquired Infections"

    Article Title: Antibiogram, Prevalence of OXA Carbapenemase Encoding Genes, and RAPD-Genotyping of Multidrug-Resistant Acinetobacter baumannii Incriminated in Hidden Community-Acquired Infections

    Journal: Antibiotics

    doi: 10.3390/antibiotics9090603

    RAPD genotyping of the strains. ( a ) Combined RAPD patterns of 23 clinical Acinetobacter isolates obtained after electrophoresis of the PCRs with five different primers individually. For each primer, five RAPD gels were combined into one image. ( b ) RAPD dendrogram was constructed with GelJ cluster analysis software by Unweighted Pair Group Method with Arithmetic Mean UPGMA). Percentages of similarity and primers used as presented in on the top line of the dendrogram. RAPD type and strain code as in and strain numbers as presented in a appear on the right (between parenthesis).
    Figure Legend Snippet: RAPD genotyping of the strains. ( a ) Combined RAPD patterns of 23 clinical Acinetobacter isolates obtained after electrophoresis of the PCRs with five different primers individually. For each primer, five RAPD gels were combined into one image. ( b ) RAPD dendrogram was constructed with GelJ cluster analysis software by Unweighted Pair Group Method with Arithmetic Mean UPGMA). Percentages of similarity and primers used as presented in on the top line of the dendrogram. RAPD type and strain code as in and strain numbers as presented in a appear on the right (between parenthesis).

    Techniques Used: Electrophoresis, Construct, Software

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    other:

    Article Title: Proteomic characterization of murine hematopoietic stem progenitor cells reveals dynamic fetal-to-adult changes in metabolic-related pathways.
    Article Snippet: Hematopoietic stem progenitor cells (HSPCs) give rise to the hematopoietic system, maintain hematopoiesis throughout the lifespan, and undergo molecular and functional changes during their development and aging.. The importance of hematopoietic stem cell (HSC) biology has led to their extensive characterization at genomic and transcriptomic levels.. However, the proteomics of HSPCs throughout the murine lifetime still needs to be fully completed.

    Article Title: Regulatory mechanism of plnC in Lactiplantibacillus plantarum B1 on Plantaricin biosynthesis
    Article Snippet: The PlnC encoded by plnC is an essential response regulator in Plantaricin biosynthesis 17 well-studied in Lactiplantibacillus plantarum.. Since the known effects of plnC are not exhaustive, it 18 is crucial to perfect a precise regulatory mechanism for plnC.. Overexpression of plnC was found to 19 transiently reduce bacterial activity during the logarithmic growth phase, however, it significantly 20 increased the expression levels of bacteriocin genes within the pln locus by 1.45 to 2.35 times.

    Software:

    Article Title: Oxidative metabolism mechanism of terpenoid compound ZQ-8 by cytochrome P450 enzyme in Helicoverpa armigera.
    Article Snippet: In our previous research, we identified that treatment of Helicoverpa armigera with ZQ-8 led to upregulation of CYP450 genes.. To clarify the metabolic pathway of ZQ-8, this study analyzed the expression of CYP450 genes and proteins in H. armigera after ZQ-8 treatment through transcriptomics and proteomics.. Molecular docking, recombinant protein expression, and surface plasmon resonance techniques were employed to investigate the interactions between ZQ-8 and P450 proteins.

    Article Title: Combined protein and transcriptomics identifies DCTPP1 as a putative biomarkers for predicting immunotherapy responsiveness in gastric cancer patients
    Article Snippet: This study aimed to screen the changes after overexpression of dCTP pyrophosphatase 1 (DCTPP1) in human gastric adenocarcinoma cells (AGS) cells by proteome and transcriptome sequencing.. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis were performed to explore the functional significance of the differentially expressed DCTPP1 in gastric cancer (GC).. Cell Counting Kit-8 (CCK-8) assay was used to detect the proliferation of cells.

    Article Title: Effect of Corticosterone on Gene Expression in the Context of Global Hippocampal Transcription
    Article Snippet: .. The examples of genes with highly repeatable responses to corticosterone are shown in , while all clusters are available in (files cort cluster.cdt, cort cluster.gtr, and cort cluster.jtv) for visualization in Java TreeView software ( https://sourceforge.net/projects/jtreeview/files/ (accessed on 9 April 2019) following guidelines provided at https://data.mendeley.com/datasets/dghdbmggc4/4/files/bc38268a-c54b-48bc-85b4-bf0fc52994d2 (accessed on 17 November 2021). ..

    Article Title: Multi-targeted olink proteomics analyses of cerebrospinal fluid from patients with aneurysmal subarachnoid hemorrhage
    Article Snippet: .. Cluster 3.0 ( http://bonsai.hgc.jp/mdehoon/software/cluster/software.htm ) and Java Treeview software ( http://jtreeview.sourceforge.net ) were used to perform hierarchical clustering analysis. ..

    Article Title: Effect of Corticosterone on Gene Expression in the Context of Global Hippocampal Transcription.
    Article Snippet: .. The examples of genes with highly repeatable responses to corticosterone are shown in Figure 9, while all clusters are available in Supplementary Data S5 (files cort cluster.cdt, cort cluster.gtr, and cort cluster.jtv) for visualization in Java TreeView software (https://sourceforge.net/projects/jtreeview/files/ (accessed on 9 April 2019) following guidelines provided at https://data.mendeley.com/ datasets/dghdbmggc4/4/files/bc38268a-c54b-48bc-85b4-bf0fc52994d2 (accessed on 17 November 2021). ..



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    RAPD genotyping of the strains. ( a ) Combined RAPD patterns of 23 clinical Acinetobacter isolates obtained after electrophoresis of the PCRs with five different primers individually. For each primer, five RAPD gels were combined into one image. ( b ) RAPD dendrogram was constructed with <t>GelJ</t> cluster analysis software by Unweighted Pair Group Method with Arithmetic Mean UPGMA). Percentages of similarity and primers used as presented in on the top line of the dendrogram. RAPD type and strain code as in and strain numbers as presented in a appear on the right (between parenthesis).
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    (A) Principal component analysis of monocyte- and fibroblast-specific gene expression. (B) Heatmap diagram of monocyte- and fibroblast-specific gene expression. (C–E) The enrichment plot in the monocytic gene set of KDOE, OE-only, and KD-only. (F–H) Gene set enrichment analysis in the fibroblastic gene set of KDOE, KD-only, and OE-only.
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    Image Search Results


    RAPD genotyping of the strains. ( a ) Combined RAPD patterns of 23 clinical Acinetobacter isolates obtained after electrophoresis of the PCRs with five different primers individually. For each primer, five RAPD gels were combined into one image. ( b ) RAPD dendrogram was constructed with GelJ cluster analysis software by Unweighted Pair Group Method with Arithmetic Mean UPGMA). Percentages of similarity and primers used as presented in on the top line of the dendrogram. RAPD type and strain code as in and strain numbers as presented in a appear on the right (between parenthesis).

    Journal: Antibiotics

    Article Title: Antibiogram, Prevalence of OXA Carbapenemase Encoding Genes, and RAPD-Genotyping of Multidrug-Resistant Acinetobacter baumannii Incriminated in Hidden Community-Acquired Infections

    doi: 10.3390/antibiotics9090603

    Figure Lengend Snippet: RAPD genotyping of the strains. ( a ) Combined RAPD patterns of 23 clinical Acinetobacter isolates obtained after electrophoresis of the PCRs with five different primers individually. For each primer, five RAPD gels were combined into one image. ( b ) RAPD dendrogram was constructed with GelJ cluster analysis software by Unweighted Pair Group Method with Arithmetic Mean UPGMA). Percentages of similarity and primers used as presented in on the top line of the dendrogram. RAPD type and strain code as in and strain numbers as presented in a appear on the right (between parenthesis).

    Article Snippet: For cluster analysis, a DNA fingerprint java application analysis software (GelJ) was used (downloaded from https://sourceforge.net/projects/gelj/ ) [ ].

    Techniques: Electrophoresis, Construct, Software

    METTL3 expression was associated with altered glucose metabolism in HCC cases. A, Illustration of enzymes involved the key steps in glucose metabolic flux. B, Heatmap with cluster analysis of METT3 expression and glucose metabolism related genes revealed a co‐expression trend between METTL3 and genes involved in glycolysis. C, D, GSEA plot of two predefined gene sets based on the METTL3 expression revealed genes involved in normal glucose metabolism were significantly enriched in HCC cases with lower METTL3 expression, which suggesting that normal glucose metabolism was preserved in these cases. E, A heatmap displaying the Spearman rank correlation test results which implied positive correlation between METTL3 expression and glycolysis‐related genes and negative correlation between METTL3 expression and glycogenesis‐related genes, the bar indicates the value of spearman correlation coefficient

    Journal: Cancer Medicine

    Article Title: METTL3 expression is associated with glycolysis metabolism and sensitivity to glycolytic stress in hepatocellular carcinoma

    doi: 10.1002/cam4.2918

    Figure Lengend Snippet: METTL3 expression was associated with altered glucose metabolism in HCC cases. A, Illustration of enzymes involved the key steps in glucose metabolic flux. B, Heatmap with cluster analysis of METT3 expression and glucose metabolism related genes revealed a co‐expression trend between METTL3 and genes involved in glycolysis. C, D, GSEA plot of two predefined gene sets based on the METTL3 expression revealed genes involved in normal glucose metabolism were significantly enriched in HCC cases with lower METTL3 expression, which suggesting that normal glucose metabolism was preserved in these cases. E, A heatmap displaying the Spearman rank correlation test results which implied positive correlation between METTL3 expression and glycolysis‐related genes and negative correlation between METTL3 expression and glycogenesis‐related genes, the bar indicates the value of spearman correlation coefficient

    Article Snippet: Java GSEA Desktop Application software (V3.0, Broad Institute) was used.

    Techniques: Expressing

    Correlation between METTL3 expression and activity of mTORC1 activity. A, GSEA plot of mTOR signal pathway based on METTL3 expression levels in TCGA cases. B, HCC cell lines were treated with siRNA oligonucleotides or not, then the indicated proteins were detected by WB. (C‐G) The HCC cell lines were treated with rapamycin or co‐treated with siRNA oligonucleotides, for 48 h followed by immunoblotting for mTOR phosphorylation levels (C), glucose uptake assays in HCC cells Huh‐7 (D) and SMMC‐7721 (E), and lactate production assays in Huh‐7 cell line (F) and SMMC‐7721 cell line (G). H, I, Gene‐specific m6A‐IP‐qPCR results showing the relative methylation levels of five RNAs in the HCC cell lines treated with siRNA oligonucleotides compared to those normal control cells

    Journal: Cancer Medicine

    Article Title: METTL3 expression is associated with glycolysis metabolism and sensitivity to glycolytic stress in hepatocellular carcinoma

    doi: 10.1002/cam4.2918

    Figure Lengend Snippet: Correlation between METTL3 expression and activity of mTORC1 activity. A, GSEA plot of mTOR signal pathway based on METTL3 expression levels in TCGA cases. B, HCC cell lines were treated with siRNA oligonucleotides or not, then the indicated proteins were detected by WB. (C‐G) The HCC cell lines were treated with rapamycin or co‐treated with siRNA oligonucleotides, for 48 h followed by immunoblotting for mTOR phosphorylation levels (C), glucose uptake assays in HCC cells Huh‐7 (D) and SMMC‐7721 (E), and lactate production assays in Huh‐7 cell line (F) and SMMC‐7721 cell line (G). H, I, Gene‐specific m6A‐IP‐qPCR results showing the relative methylation levels of five RNAs in the HCC cell lines treated with siRNA oligonucleotides compared to those normal control cells

    Article Snippet: Java GSEA Desktop Application software (V3.0, Broad Institute) was used.

    Techniques: Expressing, Activity Assay, Western Blot, Phospho-proteomics, Methylation, Control

    Up- and downregulated metabolic gene sets in KO compared to WT based on the  GSEA  method.

    Journal: Scientific Reports

    Article Title: Transcriptome analysis suggests a compensatory role of the cofactors coenzyme A and NAD + in medium-chain acyl-CoA dehydrogenase knockout mice

    doi: 10.1038/s41598-019-50758-0

    Figure Lengend Snippet: Up- and downregulated metabolic gene sets in KO compared to WT based on the GSEA method.

    Article Snippet: Gene-set enrichment analysis (GSEA) was performed according to Subramanian et al . 2005 using the GSEA desktop Java application software (version 2.2.4, Broad Institute).

    Techniques: Phospho-proteomics

    Up- and downregulated metabolic gene sets in KO compared to WT based on the Alternative  GSEA  method.

    Journal: Scientific Reports

    Article Title: Transcriptome analysis suggests a compensatory role of the cofactors coenzyme A and NAD + in medium-chain acyl-CoA dehydrogenase knockout mice

    doi: 10.1038/s41598-019-50758-0

    Figure Lengend Snippet: Up- and downregulated metabolic gene sets in KO compared to WT based on the Alternative GSEA method.

    Article Snippet: Gene-set enrichment analysis (GSEA) was performed according to Subramanian et al . 2005 using the GSEA desktop Java application software (version 2.2.4, Broad Institute).

    Techniques:

    (A) Principal component analysis of monocyte- and fibroblast-specific gene expression. (B) Heatmap diagram of monocyte- and fibroblast-specific gene expression. (C–E) The enrichment plot in the monocytic gene set of KDOE, OE-only, and KD-only. (F–H) Gene set enrichment analysis in the fibroblastic gene set of KDOE, KD-only, and OE-only.

    Journal: PLoS ONE

    Article Title: Asymmetric Regulation of Peripheral Genes by Two Transcriptional Regulatory Networks

    doi: 10.1371/journal.pone.0160459

    Figure Lengend Snippet: (A) Principal component analysis of monocyte- and fibroblast-specific gene expression. (B) Heatmap diagram of monocyte- and fibroblast-specific gene expression. (C–E) The enrichment plot in the monocytic gene set of KDOE, OE-only, and KD-only. (F–H) Gene set enrichment analysis in the fibroblastic gene set of KDOE, KD-only, and OE-only.

    Article Snippet: We used the java GSEA Desktop Application software from the Broad Institute Gene Set Enrichment Analysis website ( http://software.broadinstitute.org/gsea/downloads.jsp ).

    Techniques: Gene Expression