fuzzy logic toolbox v2 9 Search Results


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Carefusion carefusion nicvue v2.9.3
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Illumina Inc strelka2 v2.9.7
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Overview of the AtOM elements constituting the mouse, rat and human brain atlas versions currently supported by the EBRAINS research infrastructure.
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Illumina Inc cutadapt
Overview of the AtOM elements constituting the mouse, rat and human brain atlas versions currently supported by the EBRAINS research infrastructure.
Cutadapt, supplied by Illumina 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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Oxford Nanopore flye v2.9

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Becton Dickinson flowsom v2.9
Analysis of B cells phenotype by mass cytometry in systemic lupus erythematosus (SLE) in comparison to healthy controls (HC) using unsupervised clustering analysis. ( A ) Merged t-SNE plots incorporating 120 k B cells from 30 SLE and 120 k B cells from 30 HC and showing B cell clusters identified by <t>FlowSOM</t> unsupervised clustering analysis (each color represents a different cluster). (B) Frequency of each B cell clusters in 30 SLE patients compared to 30 HC. Bar plots represents mean ± SD. Statistical analysis were performed on log-transformed data (to obtain normal distributions) using a student t-test followed by Bonferroni’s correction. ***p value < 0.001. ( C ) Heatmap showing B cell clusters and their scaled mean level of expression of each surface markers used for FlowSOM analysis. ( D ) tSNE plots showing the expression of surface markers (arcsin transformed) in SLE and HC. SF1 = SLAMF1, SF7 = SLAMF7. Analysis and figures were performed using GraphPad Prism version 8.0.0 for Windows (GraphPad Software, San Diego, California USA, www.graphpad.com ) ( A , C , D ) and FlowJo™ Software version 10.7.1 (Becton, Dickinson and Company; 2019 ) by exploiting the following FlowJo™ plugins: DownSample v3.3 and FlowSOM <t>v2.9</t> ( B ).
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Millar Inc micromanometer catheter spr 839
Analysis of B cells phenotype by mass cytometry in systemic lupus erythematosus (SLE) in comparison to healthy controls (HC) using unsupervised clustering analysis. ( A ) Merged t-SNE plots incorporating 120 k B cells from 30 SLE and 120 k B cells from 30 HC and showing B cell clusters identified by <t>FlowSOM</t> unsupervised clustering analysis (each color represents a different cluster). (B) Frequency of each B cell clusters in 30 SLE patients compared to 30 HC. Bar plots represents mean ± SD. Statistical analysis were performed on log-transformed data (to obtain normal distributions) using a student t-test followed by Bonferroni’s correction. ***p value < 0.001. ( C ) Heatmap showing B cell clusters and their scaled mean level of expression of each surface markers used for FlowSOM analysis. ( D ) tSNE plots showing the expression of surface markers (arcsin transformed) in SLE and HC. SF1 = SLAMF1, SF7 = SLAMF7. Analysis and figures were performed using GraphPad Prism version 8.0.0 for Windows (GraphPad Software, San Diego, California USA, www.graphpad.com ) ( A , C , D ) and FlowJo™ Software version 10.7.1 (Becton, Dickinson and Company; 2019 ) by exploiting the following FlowJo™ plugins: DownSample v3.3 and FlowSOM <t>v2.9</t> ( B ).
Micromanometer Catheter Spr 839, supplied by Millar 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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Illumina Inc ariba v2.9.4
Analysis of B cells phenotype by mass cytometry in systemic lupus erythematosus (SLE) in comparison to healthy controls (HC) using unsupervised clustering analysis. ( A ) Merged t-SNE plots incorporating 120 k B cells from 30 SLE and 120 k B cells from 30 HC and showing B cell clusters identified by <t>FlowSOM</t> unsupervised clustering analysis (each color represents a different cluster). (B) Frequency of each B cell clusters in 30 SLE patients compared to 30 HC. Bar plots represents mean ± SD. Statistical analysis were performed on log-transformed data (to obtain normal distributions) using a student t-test followed by Bonferroni’s correction. ***p value < 0.001. ( C ) Heatmap showing B cell clusters and their scaled mean level of expression of each surface markers used for FlowSOM analysis. ( D ) tSNE plots showing the expression of surface markers (arcsin transformed) in SLE and HC. SF1 = SLAMF1, SF7 = SLAMF7. Analysis and figures were performed using GraphPad Prism version 8.0.0 for Windows (GraphPad Software, San Diego, California USA, www.graphpad.com ) ( A , C , D ) and FlowJo™ Software version 10.7.1 (Becton, Dickinson and Company; 2019 ) by exploiting the following FlowJo™ plugins: DownSample v3.3 and FlowSOM <t>v2.9</t> ( B ).
Ariba V2.9.4, supplied by Illumina 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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Image Search Results


Overview of the AtOM elements constituting the mouse, rat and human brain atlas versions currently supported by the EBRAINS research infrastructure.

Journal: Scientific Data

Article Title: AtOM, an ontology model to standardize use of brain atlases in tools, workflows, and data infrastructures

doi: 10.1038/s41597-023-02389-4

Figure Lengend Snippet: Overview of the AtOM elements constituting the mouse, rat and human brain atlas versions currently supported by the EBRAINS research infrastructure.

Article Snippet: , 2.9 , Julich-Brain Cytoarchitectonic Atlas v2.9, MNI Colin 27 , MNI Colin 27 v1998 template , MNI Colin 27 v1998 space , Whole-brain PM and MPM v2.9 , , Julich-Brain terminology v2.9 , RRID:SCR_023277 , , ; .

Techniques:

Journal: Cell Genomics

Article Title: Centromeric transposable elements and epigenetic status drive karyotypic variation in the eastern hoolock gibbon

doi: 10.1016/j.xgen.2025.100808

Figure Lengend Snippet:

Article Snippet: Flye (v2.9) was used to assemble the raw Oxford Nanopore reads using an estimated genome size of 2.9 Gb, the size of the previously assembled Nomascus leucogenys genome.

Techniques: Purification, Produced, Recombinant, DNA Extraction, Cell Culture, DNA Sequencing, Proximity Ligation Assay, DNA Purification, Polymerase Chain Reaction, Multiplex Assay, Sequencing, Software

Analysis of B cells phenotype by mass cytometry in systemic lupus erythematosus (SLE) in comparison to healthy controls (HC) using unsupervised clustering analysis. ( A ) Merged t-SNE plots incorporating 120 k B cells from 30 SLE and 120 k B cells from 30 HC and showing B cell clusters identified by FlowSOM unsupervised clustering analysis (each color represents a different cluster). (B) Frequency of each B cell clusters in 30 SLE patients compared to 30 HC. Bar plots represents mean ± SD. Statistical analysis were performed on log-transformed data (to obtain normal distributions) using a student t-test followed by Bonferroni’s correction. ***p value < 0.001. ( C ) Heatmap showing B cell clusters and their scaled mean level of expression of each surface markers used for FlowSOM analysis. ( D ) tSNE plots showing the expression of surface markers (arcsin transformed) in SLE and HC. SF1 = SLAMF1, SF7 = SLAMF7. Analysis and figures were performed using GraphPad Prism version 8.0.0 for Windows (GraphPad Software, San Diego, California USA, www.graphpad.com ) ( A , C , D ) and FlowJo™ Software version 10.7.1 (Becton, Dickinson and Company; 2019 ) by exploiting the following FlowJo™ plugins: DownSample v3.3 and FlowSOM v2.9 ( B ).

Journal: Scientific Reports

Article Title: Measurement of circulating CD21 − CD27 − B lymphocytes in SLE patients is associated with disease activity independently of conventional serological biomarkers

doi: 10.1038/s41598-022-12775-4

Figure Lengend Snippet: Analysis of B cells phenotype by mass cytometry in systemic lupus erythematosus (SLE) in comparison to healthy controls (HC) using unsupervised clustering analysis. ( A ) Merged t-SNE plots incorporating 120 k B cells from 30 SLE and 120 k B cells from 30 HC and showing B cell clusters identified by FlowSOM unsupervised clustering analysis (each color represents a different cluster). (B) Frequency of each B cell clusters in 30 SLE patients compared to 30 HC. Bar plots represents mean ± SD. Statistical analysis were performed on log-transformed data (to obtain normal distributions) using a student t-test followed by Bonferroni’s correction. ***p value < 0.001. ( C ) Heatmap showing B cell clusters and their scaled mean level of expression of each surface markers used for FlowSOM analysis. ( D ) tSNE plots showing the expression of surface markers (arcsin transformed) in SLE and HC. SF1 = SLAMF1, SF7 = SLAMF7. Analysis and figures were performed using GraphPad Prism version 8.0.0 for Windows (GraphPad Software, San Diego, California USA, www.graphpad.com ) ( A , C , D ) and FlowJo™ Software version 10.7.1 (Becton, Dickinson and Company; 2019 ) by exploiting the following FlowJo™ plugins: DownSample v3.3 and FlowSOM v2.9 ( B ).

Article Snippet: Analysis and figures were performed using GraphPad Prism version 8.0.0 for Windows (GraphPad Software, San Diego, California USA, www.graphpad.com ) ( A , C , D ) and FlowJo™ Software version 10.7.1 (Becton, Dickinson and Company; 2019 ) by exploiting the following FlowJo™ plugins: DownSample v3.3 and FlowSOM v2.9 ( B ).

Techniques: Mass Cytometry, Transformation Assay, Expressing, Software