Abstract: Disclosed herein include systems, devices, methods, and spillover editor for displaying and editing spillover values. A view of a spillover editor can comprise a triangular grid of rows and columns, representing flourophores, each comprising at least one display area and two spillover values. After receiving an adjusted spillover value, an adjusted view of the spillover editor can comprise adjusted plots determined using the adjusted spillover value.

Abstract: Disclosed herein include systems, devices, methods, and spillover editor for displaying and editing spillover values. A view of a spillover editor can comprise a triangular grid of rows and columns, representing flourophores, each comprising at least one display area and two spillover values. After receiving an adjusted spillover value, an adjusted view of the spillover editor can comprise adjusted plots determined using the adjusted spillover value.

Abstract: Disclosed herein include systems, devices, methods, and spillover editor for displaying and editing spillover values. A view of a spillover editor can comprise a triangular grid of rows and columns, representing flourophores, each comprising at least one display area and two spillover values. After receiving an adjusted spillover value, an adjusted view of the spillover editor can comprise adjusted plots determined using the adjusted spillover value.

Abstract: Data visualization features are described that provide synchronized displaying of interactive visualizations for high parameter data. The visualization features include graphically representing multiple parameters simultaneously with the associated statistical data for each parameter in an interactive way that maintains the contextual relationships between parameters and the related cell population. The visualization features may be used for displaying high parameter multi-color flow cytometry or genomic data sets.

Abstract: Disclosed herein include systems, devices, methods, and spillover editor for displaying and editing spillover values. A view of a spillover editor can comprise a triangular grid of rows and columns, representing flourophores, each comprising at least one display area and two spillover values. After receiving an adjusted spillover value, an adjusted view of the spillover editor can comprise adjusted plots determined using the adjusted spillover value.

Abstract: Data visualization features are described that provide synchronized displaying of interactive visualizations for high parameter data. The visualization features include graphically representing multiple parameters simultaneously with the associated statistical data for each parameter in an interactive way that maintains the contextual relationships between parameters and the related cell population. The visualization features may be used for displaying high parameter multi-color flow cytometry or genomic data sets.

Abstract: Data visualization features are described that provide a fast and accurate tool for displaying visualizations of high parameter data. The visualization features include graphically representing multiple parameters simultaneously with the associated statistical data for each parameter in an interactive way that maintains the contextual relationships between parameters and the related cell population. The visualization may be dynamically generated based on the measurements for the cell population and the resources available to the display device. The visualization features may be used for displaying high parameter multi-color flow cytometry or genomic data sets.

Abstract: Data visualization features are described that provide a fast and accurate tool for displaying visualizations of high parameter data. The visualization features include graphically representing multiple parameters simultaneously with the associated statistical data for each parameter in an interactive way that maintains the contextual relationships between parameters and the related cell population. The visualization may be dynamically generated based on the measurements for the cell population and the resources available to the display device. The visualization features may be used for displaying high parameter multi-color flow cytometry or genomic data sets.

Abstract: Data visualization features are described that provide synchronized displaying of interactive visualizations for high parameter data. The visualization features include graphically representing multiple parameters simultaneously with the associated statistical data for each parameter in an interactive way that maintains the contextual relationships between parameters and the related cell population. The visualization features may be used for displaying high parameter multi-color flow cytometry or genomic data sets.

Abstract: Data visualization features are described that provide synchronized displaying of interactive visualizations for high parameter data. The visualization features include graphically representing multiple parameters simultaneously with the associated statistical data for each parameter in an interactive way that maintains the contextual relationships between parameters and the related cell population. The visualization features may be used for displaying high parameter multi-color flow cytometry or genomic data sets.

Abstract: When manually drawing gates on plots of flow cytometric data, how the underlying data is rendered can cause inaccuracies and/or inefficiencies in the drawing. The present application is directed to graphics control features for dynamically adjusting attributes of the plot such as event color or plot style (e.g., dot plot, contour plot) while drawing a gate. The adjustments may be triggered by the gate, by the area being gated, or a trigger (e.g., mouse or key stroke event) while drawing the gate.

Abstract: Systems and methods of using the same for sorting cells are provided. The systems may include a cell sorter including a deflector capable of deflecting an analyzed droplet to a deflected droplet receiving location, a support stage including a container and configured to continuously move in two dimensions. The systems and methods of using the same find use in a variety of different applications.

Abstract: When manually drawing gates on plots of flow cytometric data, how the underlying data is rendered can cause inaccuracies and/or inefficiencies in the drawing. The present application is directed to graphics control features for dynamically adjusting attributes of the plot such as event color or plot style (e.g., dot plot, contour plot) while drawing a gate. The adjustments may be triggered by the gate, by the area being gated, or a trigger (e.g., mouse or key stroke event) while drawing the gate.