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    MathWorks Inc core dbscan matlab code
    (a) (Upper panel) A schematic of acute depletion of Cohesin in mouse ESCs by the auxin-induced protein depletion system. The mini auxin-inducible degron (mAID)-HaloTag was bi-allelically knocked into the C-terminus of Rad21 gene (Cohesin subunit) by CRISPR/Cas9 in mESCs stably expressing the plant derived E3 ligase adaptor protein osTir1. (Lower panel) Adding plant derived hormone analogue (auxin) triggers rapid degradation of target protein RAD21 as revealed by single cell fluorescence imaging (HaloTag ligand JF 549 ). OCT4 immunostaining was used as a control. Scale bar, 5 μm. (b) Single-cell illustration of 3D ATAC-PALM localizations upon RAD21 depletion. A wild type control cell is also shown in the upper left corner. The color bar indicates localization density calculated by using a canopy radius of 250 nm. The experiments have been independently repeated for four times. Also see the 3D rotatory presentation in . Scale bar, 2 μm. (c) RAD21 depletion promotes global increase of accessible chromatin clustering measured by pair auto-correlation function, which describes the similarity among observations. The top panel shows a simplified two-dimensional scheme for distribution of localizations in uniform (black dots, left) or wild type (green dots, middle) or RAD21 depleted (green dots, right) conditions. g(r) represents the pair autocorrelation function of distance r calculated from a given origin point inside the space. The error bar represents standard error (SE) of the mean and two-sided Mann-Whitney U test was applied for comparing data points at g(0) . (d) The violin plot of normalized radius (upper panel) or localization density (lower panel) of top 100 ranked <t>ACDs</t> among 4 individual cells for Control and RAD21 depleted conditions. The localization density was determined by the total number of ATAC-PALM localizations within a 250nm(radius) spherical region. The black bar indicates the median value for each data set. (e) 3D iso -surface reconstruction of ACDs (green) identified by using <t>the</t> <t>DBSCAN</t> algorithm for Control (left panel) and RAD21 depletion (right panel) conditions. The iso -surface in grey outlines the nuclear envelope. The lower panels show 4× magnification of local regions under each condition. Scale bar, 1 μm. (f ) Enhanced clustering of transcription factor (TF) SOX2 stable binding sites upon RAD21 depletion. The pair auto-correlation function g(r) for stable SOX2 binding sites was calculated before and after RAD21 depletion. SOX2 binding events with dwell times longer than 4s were considered as stable binding events (see ). The error bars represent standard error (SE) of the mean. The two-sided Mann-Whitney U test was used for statistical testing. The inset illustrates the 3D TF binding between specific (green) and non-specific (blue) binding sites.
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    1) Product Images from "BRD2 Compartmentalizes the Accessible Genome"

    Article Title: BRD2 Compartmentalizes the Accessible Genome

    Journal: Nature genetics

    doi: 10.1038/s41588-022-01044-9

    (a) (Upper panel) A schematic of acute depletion of Cohesin in mouse ESCs by the auxin-induced protein depletion system. The mini auxin-inducible degron (mAID)-HaloTag was bi-allelically knocked into the C-terminus of Rad21 gene (Cohesin subunit) by CRISPR/Cas9 in mESCs stably expressing the plant derived E3 ligase adaptor protein osTir1. (Lower panel) Adding plant derived hormone analogue (auxin) triggers rapid degradation of target protein RAD21 as revealed by single cell fluorescence imaging (HaloTag ligand JF 549 ). OCT4 immunostaining was used as a control. Scale bar, 5 μm. (b) Single-cell illustration of 3D ATAC-PALM localizations upon RAD21 depletion. A wild type control cell is also shown in the upper left corner. The color bar indicates localization density calculated by using a canopy radius of 250 nm. The experiments have been independently repeated for four times. Also see the 3D rotatory presentation in . Scale bar, 2 μm. (c) RAD21 depletion promotes global increase of accessible chromatin clustering measured by pair auto-correlation function, which describes the similarity among observations. The top panel shows a simplified two-dimensional scheme for distribution of localizations in uniform (black dots, left) or wild type (green dots, middle) or RAD21 depleted (green dots, right) conditions. g(r) represents the pair autocorrelation function of distance r calculated from a given origin point inside the space. The error bar represents standard error (SE) of the mean and two-sided Mann-Whitney U test was applied for comparing data points at g(0) . (d) The violin plot of normalized radius (upper panel) or localization density (lower panel) of top 100 ranked ACDs among 4 individual cells for Control and RAD21 depleted conditions. The localization density was determined by the total number of ATAC-PALM localizations within a 250nm(radius) spherical region. The black bar indicates the median value for each data set. (e) 3D iso -surface reconstruction of ACDs (green) identified by using the DBSCAN algorithm for Control (left panel) and RAD21 depletion (right panel) conditions. The iso -surface in grey outlines the nuclear envelope. The lower panels show 4× magnification of local regions under each condition. Scale bar, 1 μm. (f ) Enhanced clustering of transcription factor (TF) SOX2 stable binding sites upon RAD21 depletion. The pair auto-correlation function g(r) for stable SOX2 binding sites was calculated before and after RAD21 depletion. SOX2 binding events with dwell times longer than 4s were considered as stable binding events (see ). The error bars represent standard error (SE) of the mean. The two-sided Mann-Whitney U test was used for statistical testing. The inset illustrates the 3D TF binding between specific (green) and non-specific (blue) binding sites.
    Figure Legend Snippet: (a) (Upper panel) A schematic of acute depletion of Cohesin in mouse ESCs by the auxin-induced protein depletion system. The mini auxin-inducible degron (mAID)-HaloTag was bi-allelically knocked into the C-terminus of Rad21 gene (Cohesin subunit) by CRISPR/Cas9 in mESCs stably expressing the plant derived E3 ligase adaptor protein osTir1. (Lower panel) Adding plant derived hormone analogue (auxin) triggers rapid degradation of target protein RAD21 as revealed by single cell fluorescence imaging (HaloTag ligand JF 549 ). OCT4 immunostaining was used as a control. Scale bar, 5 μm. (b) Single-cell illustration of 3D ATAC-PALM localizations upon RAD21 depletion. A wild type control cell is also shown in the upper left corner. The color bar indicates localization density calculated by using a canopy radius of 250 nm. The experiments have been independently repeated for four times. Also see the 3D rotatory presentation in . Scale bar, 2 μm. (c) RAD21 depletion promotes global increase of accessible chromatin clustering measured by pair auto-correlation function, which describes the similarity among observations. The top panel shows a simplified two-dimensional scheme for distribution of localizations in uniform (black dots, left) or wild type (green dots, middle) or RAD21 depleted (green dots, right) conditions. g(r) represents the pair autocorrelation function of distance r calculated from a given origin point inside the space. The error bar represents standard error (SE) of the mean and two-sided Mann-Whitney U test was applied for comparing data points at g(0) . (d) The violin plot of normalized radius (upper panel) or localization density (lower panel) of top 100 ranked ACDs among 4 individual cells for Control and RAD21 depleted conditions. The localization density was determined by the total number of ATAC-PALM localizations within a 250nm(radius) spherical region. The black bar indicates the median value for each data set. (e) 3D iso -surface reconstruction of ACDs (green) identified by using the DBSCAN algorithm for Control (left panel) and RAD21 depletion (right panel) conditions. The iso -surface in grey outlines the nuclear envelope. The lower panels show 4× magnification of local regions under each condition. Scale bar, 1 μm. (f ) Enhanced clustering of transcription factor (TF) SOX2 stable binding sites upon RAD21 depletion. The pair auto-correlation function g(r) for stable SOX2 binding sites was calculated before and after RAD21 depletion. SOX2 binding events with dwell times longer than 4s were considered as stable binding events (see ). The error bars represent standard error (SE) of the mean. The two-sided Mann-Whitney U test was used for statistical testing. The inset illustrates the 3D TF binding between specific (green) and non-specific (blue) binding sites.

    Techniques Used: CRISPR, Stable Transfection, Expressing, Derivative Assay, Fluorescence, Imaging, Immunostaining, Control, MANN-WHITNEY, Binding Assay



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    MathWorks Inc core dbscan matlab code
    (a) (Upper panel) A schematic of acute depletion of Cohesin in mouse ESCs by the auxin-induced protein depletion system. The mini auxin-inducible degron (mAID)-HaloTag was bi-allelically knocked into the C-terminus of Rad21 gene (Cohesin subunit) by CRISPR/Cas9 in mESCs stably expressing the plant derived E3 ligase adaptor protein osTir1. (Lower panel) Adding plant derived hormone analogue (auxin) triggers rapid degradation of target protein RAD21 as revealed by single cell fluorescence imaging (HaloTag ligand JF 549 ). OCT4 immunostaining was used as a control. Scale bar, 5 μm. (b) Single-cell illustration of 3D ATAC-PALM localizations upon RAD21 depletion. A wild type control cell is also shown in the upper left corner. The color bar indicates localization density calculated by using a canopy radius of 250 nm. The experiments have been independently repeated for four times. Also see the 3D rotatory presentation in . Scale bar, 2 μm. (c) RAD21 depletion promotes global increase of accessible chromatin clustering measured by pair auto-correlation function, which describes the similarity among observations. The top panel shows a simplified two-dimensional scheme for distribution of localizations in uniform (black dots, left) or wild type (green dots, middle) or RAD21 depleted (green dots, right) conditions. g(r) represents the pair autocorrelation function of distance r calculated from a given origin point inside the space. The error bar represents standard error (SE) of the mean and two-sided Mann-Whitney U test was applied for comparing data points at g(0) . (d) The violin plot of normalized radius (upper panel) or localization density (lower panel) of top 100 ranked <t>ACDs</t> among 4 individual cells for Control and RAD21 depleted conditions. The localization density was determined by the total number of ATAC-PALM localizations within a 250nm(radius) spherical region. The black bar indicates the median value for each data set. (e) 3D iso -surface reconstruction of ACDs (green) identified by using <t>the</t> <t>DBSCAN</t> algorithm for Control (left panel) and RAD21 depletion (right panel) conditions. The iso -surface in grey outlines the nuclear envelope. The lower panels show 4× magnification of local regions under each condition. Scale bar, 1 μm. (f ) Enhanced clustering of transcription factor (TF) SOX2 stable binding sites upon RAD21 depletion. The pair auto-correlation function g(r) for stable SOX2 binding sites was calculated before and after RAD21 depletion. SOX2 binding events with dwell times longer than 4s were considered as stable binding events (see ). The error bars represent standard error (SE) of the mean. The two-sided Mann-Whitney U test was used for statistical testing. The inset illustrates the 3D TF binding between specific (green) and non-specific (blue) binding sites.
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    (a) (Upper panel) A schematic of acute depletion of Cohesin in mouse ESCs by the auxin-induced protein depletion system. The mini auxin-inducible degron (mAID)-HaloTag was bi-allelically knocked into the C-terminus of Rad21 gene (Cohesin subunit) by CRISPR/Cas9 in mESCs stably expressing the plant derived E3 ligase adaptor protein osTir1. (Lower panel) Adding plant derived hormone analogue (auxin) triggers rapid degradation of target protein RAD21 as revealed by single cell fluorescence imaging (HaloTag ligand JF 549 ). OCT4 immunostaining was used as a control. Scale bar, 5 μm. (b) Single-cell illustration of 3D ATAC-PALM localizations upon RAD21 depletion. A wild type control cell is also shown in the upper left corner. The color bar indicates localization density calculated by using a canopy radius of 250 nm. The experiments have been independently repeated for four times. Also see the 3D rotatory presentation in . Scale bar, 2 μm. (c) RAD21 depletion promotes global increase of accessible chromatin clustering measured by pair auto-correlation function, which describes the similarity among observations. The top panel shows a simplified two-dimensional scheme for distribution of localizations in uniform (black dots, left) or wild type (green dots, middle) or RAD21 depleted (green dots, right) conditions. g(r) represents the pair autocorrelation function of distance r calculated from a given origin point inside the space. The error bar represents standard error (SE) of the mean and two-sided Mann-Whitney U test was applied for comparing data points at g(0) . (d) The violin plot of normalized radius (upper panel) or localization density (lower panel) of top 100 ranked <t>ACDs</t> among 4 individual cells for Control and RAD21 depleted conditions. The localization density was determined by the total number of ATAC-PALM localizations within a 250nm(radius) spherical region. The black bar indicates the median value for each data set. (e) 3D iso -surface reconstruction of ACDs (green) identified by using <t>the</t> <t>DBSCAN</t> algorithm for Control (left panel) and RAD21 depletion (right panel) conditions. The iso -surface in grey outlines the nuclear envelope. The lower panels show 4× magnification of local regions under each condition. Scale bar, 1 μm. (f ) Enhanced clustering of transcription factor (TF) SOX2 stable binding sites upon RAD21 depletion. The pair auto-correlation function g(r) for stable SOX2 binding sites was calculated before and after RAD21 depletion. SOX2 binding events with dwell times longer than 4s were considered as stable binding events (see ). The error bars represent standard error (SE) of the mean. The two-sided Mann-Whitney U test was used for statistical testing. The inset illustrates the 3D TF binding between specific (green) and non-specific (blue) binding sites.
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    (a) (Upper panel) A schematic of acute depletion of Cohesin in mouse ESCs by the auxin-induced protein depletion system. The mini auxin-inducible degron (mAID)-HaloTag was bi-allelically knocked into the C-terminus of Rad21 gene (Cohesin subunit) by CRISPR/Cas9 in mESCs stably expressing the plant derived E3 ligase adaptor protein osTir1. (Lower panel) Adding plant derived hormone analogue (auxin) triggers rapid degradation of target protein RAD21 as revealed by single cell fluorescence imaging (HaloTag ligand JF 549 ). OCT4 immunostaining was used as a control. Scale bar, 5 μm. (b) Single-cell illustration of 3D ATAC-PALM localizations upon RAD21 depletion. A wild type control cell is also shown in the upper left corner. The color bar indicates localization density calculated by using a canopy radius of 250 nm. The experiments have been independently repeated for four times. Also see the 3D rotatory presentation in . Scale bar, 2 μm. (c) RAD21 depletion promotes global increase of accessible chromatin clustering measured by pair auto-correlation function, which describes the similarity among observations. The top panel shows a simplified two-dimensional scheme for distribution of localizations in uniform (black dots, left) or wild type (green dots, middle) or RAD21 depleted (green dots, right) conditions. g(r) represents the pair autocorrelation function of distance r calculated from a given origin point inside the space. The error bar represents standard error (SE) of the mean and two-sided Mann-Whitney U test was applied for comparing data points at g(0) . (d) The violin plot of normalized radius (upper panel) or localization density (lower panel) of top 100 ranked <t>ACDs</t> among 4 individual cells for Control and RAD21 depleted conditions. The localization density was determined by the total number of ATAC-PALM localizations within a 250nm(radius) spherical region. The black bar indicates the median value for each data set. (e) 3D iso -surface reconstruction of ACDs (green) identified by using <t>the</t> <t>DBSCAN</t> algorithm for Control (left panel) and RAD21 depletion (right panel) conditions. The iso -surface in grey outlines the nuclear envelope. The lower panels show 4× magnification of local regions under each condition. Scale bar, 1 μm. (f ) Enhanced clustering of transcription factor (TF) SOX2 stable binding sites upon RAD21 depletion. The pair auto-correlation function g(r) for stable SOX2 binding sites was calculated before and after RAD21 depletion. SOX2 binding events with dwell times longer than 4s were considered as stable binding events (see ). The error bars represent standard error (SE) of the mean. The two-sided Mann-Whitney U test was used for statistical testing. The inset illustrates the 3D TF binding between specific (green) and non-specific (blue) binding sites.
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    (a) (Upper panel) A schematic of acute depletion of Cohesin in mouse ESCs by the auxin-induced protein depletion system. The mini auxin-inducible degron (mAID)-HaloTag was bi-allelically knocked into the C-terminus of Rad21 gene (Cohesin subunit) by CRISPR/Cas9 in mESCs stably expressing the plant derived E3 ligase adaptor protein osTir1. (Lower panel) Adding plant derived hormone analogue (auxin) triggers rapid degradation of target protein RAD21 as revealed by single cell fluorescence imaging (HaloTag ligand JF 549 ). OCT4 immunostaining was used as a control. Scale bar, 5 μm. (b) Single-cell illustration of 3D ATAC-PALM localizations upon RAD21 depletion. A wild type control cell is also shown in the upper left corner. The color bar indicates localization density calculated by using a canopy radius of 250 nm. The experiments have been independently repeated for four times. Also see the 3D rotatory presentation in . Scale bar, 2 μm. (c) RAD21 depletion promotes global increase of accessible chromatin clustering measured by pair auto-correlation function, which describes the similarity among observations. The top panel shows a simplified two-dimensional scheme for distribution of localizations in uniform (black dots, left) or wild type (green dots, middle) or RAD21 depleted (green dots, right) conditions. g(r) represents the pair autocorrelation function of distance r calculated from a given origin point inside the space. The error bar represents standard error (SE) of the mean and two-sided Mann-Whitney U test was applied for comparing data points at g(0) . (d) The violin plot of normalized radius (upper panel) or localization density (lower panel) of top 100 ranked <t>ACDs</t> among 4 individual cells for Control and RAD21 depleted conditions. The localization density was determined by the total number of ATAC-PALM localizations within a 250nm(radius) spherical region. The black bar indicates the median value for each data set. (e) 3D iso -surface reconstruction of ACDs (green) identified by using <t>the</t> <t>DBSCAN</t> algorithm for Control (left panel) and RAD21 depletion (right panel) conditions. The iso -surface in grey outlines the nuclear envelope. The lower panels show 4× magnification of local regions under each condition. Scale bar, 1 μm. (f ) Enhanced clustering of transcription factor (TF) SOX2 stable binding sites upon RAD21 depletion. The pair auto-correlation function g(r) for stable SOX2 binding sites was calculated before and after RAD21 depletion. SOX2 binding events with dwell times longer than 4s were considered as stable binding events (see ). The error bars represent standard error (SE) of the mean. The two-sided Mann-Whitney U test was used for statistical testing. The inset illustrates the 3D TF binding between specific (green) and non-specific (blue) binding sites.
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    Simulation results. (A) Left hand side of the figure shows simulated site activity without noise added in blue, and independent components derived from noisy wire outputs in red. The four different spike shapes can be detected in this figure. On the right hand side of the figure, a site level collision is observed, and preserved by ICA. The activation scale and signal scale differ but the correlation coefficient of the reconstruction is 0.99. (B) <t>DBSCAN</t> method showing recovery of only clean non-colliding spikes. <t>(C)</t> <t>Plexon</t> Offline Sorter (POS) extracted spikes showing variation in spikes shapes caused by presence of spike collisions that are being assigned to spike clusters.
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    MathWorks Inc code density-based algorithm for discovering clusters (dbscan)
    Simulation results. (A) Left hand side of the figure shows simulated site activity without noise added in blue, and independent components derived from noisy wire outputs in red. The four different spike shapes can be detected in this figure. On the right hand side of the figure, a site level collision is observed, and preserved by ICA. The activation scale and signal scale differ but the correlation coefficient of the reconstruction is 0.99. (B) <t>DBSCAN</t> method showing recovery of only clean non-colliding spikes. <t>(C)</t> <t>Plexon</t> Offline Sorter (POS) extracted spikes showing variation in spikes shapes caused by presence of spike collisions that are being assigned to spike clusters.
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    Simulation results. (A) Left hand side of the figure shows simulated site activity without noise added in blue, and independent components derived from noisy wire outputs in red. The four different spike shapes can be detected in this figure. On the right hand side of the figure, a site level collision is observed, and preserved by ICA. The activation scale and signal scale differ but the correlation coefficient of the reconstruction is 0.99. (B) <t>DBSCAN</t> method showing recovery of only clean non-colliding spikes. <t>(C)</t> <t>Plexon</t> Offline Sorter (POS) extracted spikes showing variation in spikes shapes caused by presence of spike collisions that are being assigned to spike clusters.
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    (a) (Upper panel) A schematic of acute depletion of Cohesin in mouse ESCs by the auxin-induced protein depletion system. The mini auxin-inducible degron (mAID)-HaloTag was bi-allelically knocked into the C-terminus of Rad21 gene (Cohesin subunit) by CRISPR/Cas9 in mESCs stably expressing the plant derived E3 ligase adaptor protein osTir1. (Lower panel) Adding plant derived hormone analogue (auxin) triggers rapid degradation of target protein RAD21 as revealed by single cell fluorescence imaging (HaloTag ligand JF 549 ). OCT4 immunostaining was used as a control. Scale bar, 5 μm. (b) Single-cell illustration of 3D ATAC-PALM localizations upon RAD21 depletion. A wild type control cell is also shown in the upper left corner. The color bar indicates localization density calculated by using a canopy radius of 250 nm. The experiments have been independently repeated for four times. Also see the 3D rotatory presentation in . Scale bar, 2 μm. (c) RAD21 depletion promotes global increase of accessible chromatin clustering measured by pair auto-correlation function, which describes the similarity among observations. The top panel shows a simplified two-dimensional scheme for distribution of localizations in uniform (black dots, left) or wild type (green dots, middle) or RAD21 depleted (green dots, right) conditions. g(r) represents the pair autocorrelation function of distance r calculated from a given origin point inside the space. The error bar represents standard error (SE) of the mean and two-sided Mann-Whitney U test was applied for comparing data points at g(0) . (d) The violin plot of normalized radius (upper panel) or localization density (lower panel) of top 100 ranked ACDs among 4 individual cells for Control and RAD21 depleted conditions. The localization density was determined by the total number of ATAC-PALM localizations within a 250nm(radius) spherical region. The black bar indicates the median value for each data set. (e) 3D iso -surface reconstruction of ACDs (green) identified by using the DBSCAN algorithm for Control (left panel) and RAD21 depletion (right panel) conditions. The iso -surface in grey outlines the nuclear envelope. The lower panels show 4× magnification of local regions under each condition. Scale bar, 1 μm. (f ) Enhanced clustering of transcription factor (TF) SOX2 stable binding sites upon RAD21 depletion. The pair auto-correlation function g(r) for stable SOX2 binding sites was calculated before and after RAD21 depletion. SOX2 binding events with dwell times longer than 4s were considered as stable binding events (see ). The error bars represent standard error (SE) of the mean. The two-sided Mann-Whitney U test was used for statistical testing. The inset illustrates the 3D TF binding between specific (green) and non-specific (blue) binding sites.

    Journal: Nature genetics

    Article Title: BRD2 Compartmentalizes the Accessible Genome

    doi: 10.1038/s41588-022-01044-9

    Figure Lengend Snippet: (a) (Upper panel) A schematic of acute depletion of Cohesin in mouse ESCs by the auxin-induced protein depletion system. The mini auxin-inducible degron (mAID)-HaloTag was bi-allelically knocked into the C-terminus of Rad21 gene (Cohesin subunit) by CRISPR/Cas9 in mESCs stably expressing the plant derived E3 ligase adaptor protein osTir1. (Lower panel) Adding plant derived hormone analogue (auxin) triggers rapid degradation of target protein RAD21 as revealed by single cell fluorescence imaging (HaloTag ligand JF 549 ). OCT4 immunostaining was used as a control. Scale bar, 5 μm. (b) Single-cell illustration of 3D ATAC-PALM localizations upon RAD21 depletion. A wild type control cell is also shown in the upper left corner. The color bar indicates localization density calculated by using a canopy radius of 250 nm. The experiments have been independently repeated for four times. Also see the 3D rotatory presentation in . Scale bar, 2 μm. (c) RAD21 depletion promotes global increase of accessible chromatin clustering measured by pair auto-correlation function, which describes the similarity among observations. The top panel shows a simplified two-dimensional scheme for distribution of localizations in uniform (black dots, left) or wild type (green dots, middle) or RAD21 depleted (green dots, right) conditions. g(r) represents the pair autocorrelation function of distance r calculated from a given origin point inside the space. The error bar represents standard error (SE) of the mean and two-sided Mann-Whitney U test was applied for comparing data points at g(0) . (d) The violin plot of normalized radius (upper panel) or localization density (lower panel) of top 100 ranked ACDs among 4 individual cells for Control and RAD21 depleted conditions. The localization density was determined by the total number of ATAC-PALM localizations within a 250nm(radius) spherical region. The black bar indicates the median value for each data set. (e) 3D iso -surface reconstruction of ACDs (green) identified by using the DBSCAN algorithm for Control (left panel) and RAD21 depletion (right panel) conditions. The iso -surface in grey outlines the nuclear envelope. The lower panels show 4× magnification of local regions under each condition. Scale bar, 1 μm. (f ) Enhanced clustering of transcription factor (TF) SOX2 stable binding sites upon RAD21 depletion. The pair auto-correlation function g(r) for stable SOX2 binding sites was calculated before and after RAD21 depletion. SOX2 binding events with dwell times longer than 4s were considered as stable binding events (see ). The error bars represent standard error (SE) of the mean. The two-sided Mann-Whitney U test was used for statistical testing. The inset illustrates the 3D TF binding between specific (green) and non-specific (blue) binding sites.

    Article Snippet: The density-based clustering algorithm DBSCAN (Density-Based Spatial Clustering of Applications with Noise) was adopted to map and visualize individual local ACDs (core DBSCAN MATLAB code from http://yarpiz.com/255/ypml110-dbscan-clustering ) as we previously described .

    Techniques: CRISPR, Stable Transfection, Expressing, Derivative Assay, Fluorescence, Imaging, Immunostaining, Control, MANN-WHITNEY, Binding Assay

    Simulation results. (A) Left hand side of the figure shows simulated site activity without noise added in blue, and independent components derived from noisy wire outputs in red. The four different spike shapes can be detected in this figure. On the right hand side of the figure, a site level collision is observed, and preserved by ICA. The activation scale and signal scale differ but the correlation coefficient of the reconstruction is 0.99. (B) DBSCAN method showing recovery of only clean non-colliding spikes. (C) Plexon Offline Sorter (POS) extracted spikes showing variation in spikes shapes caused by presence of spike collisions that are being assigned to spike clusters.

    Journal: Frontiers in Neuroscience

    Article Title: Highly Flexible Precisely Braided Multielectrode Probes and Combinatorics for Future Neuroprostheses

    doi: 10.3389/fnins.2019.00613

    Figure Lengend Snippet: Simulation results. (A) Left hand side of the figure shows simulated site activity without noise added in blue, and independent components derived from noisy wire outputs in red. The four different spike shapes can be detected in this figure. On the right hand side of the figure, a site level collision is observed, and preserved by ICA. The activation scale and signal scale differ but the correlation coefficient of the reconstruction is 0.99. (B) DBSCAN method showing recovery of only clean non-colliding spikes. (C) Plexon Offline Sorter (POS) extracted spikes showing variation in spikes shapes caused by presence of spike collisions that are being assigned to spike clusters.

    Article Snippet: To sort individual unit activity at each site, we used two approaches: (1) Density based spatial clustering of applications with noise (DBSCAN), a density based clustering algorithm first described in and implemented in the DBSCAN code on Matlab file exchange. (2) Plexon POS using K-Means or contour results as templates.

    Techniques: Activity Assay, Derivative Assay, Activation Assay