Tools#
Quantification#
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Calculate the proportion of colocalized transcripts for each gene. |
Estimate a neighbor-distance radius from the local geometry of a sample of cells. |
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Find and visualize the smallest neighbor count |
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Classify transcripts by local-density enrichment relative to a Bayesian cell/background model. |
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Identify extracellular RNA structures, quantify their morphology, and assign them to parent cells. |
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Compute spatial variability of extracellular RNA using Moran's I (or another autocorrelation statistic). |
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Create the |
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Quantify gene overexpression relative to a Poisson noise model derived from control codewords. |
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Compute the proportion of extracellular vs. |
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Compute the proportion of spatially colocalized extracellular transcripts per gene. |
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Compute the correlation between intracellular and extracellular gene expression. |
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Compare the spatial distribution of intracellular and extracellular transcripts per gene. |
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Cluster transcripts without relying on pre-defined cell or tissue segmentations. |
Calculate the mean expression of each feature (gene) per cell type. |
Source, target and communication#
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Score extracellular transcripts against nearby cells using an adaptive neighborhood size. |
Score extracellular transcripts against nearby cells using a chunked, numba-accelerated kernel. |
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Find the nearest cell to each transcript and annotate it with that cell's ID, type, and distance. |
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Compute, for every extracellular transcript, a per-cell-type target score plus its closest cell. |
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Compute the per-gene proportion of extracellular transcripts assigned to each cell type. |
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Cluster genes by the distribution of their transcripts' distances to source cells. |
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Compute cell-type x cell-type contact-count matrices based on spatial and uRNA-mediated neighborhoods. |
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Compute a cell-type x cell-type contact matrix from the spatial proximity of "owned" transcripts. |
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Compute and plot the interaction strength between source and target cell types for one gene. |
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Compute a 3D interaction strength matrix by multiplying per-transcript source and target scores. |
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Aggregate per-transcript interaction scores into gene-level mean interaction matrices. |
Cell scores#
Compute a normalised extracellular RNA (uRNA) contribution score for each cell. |
Factor analysis#
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Project extracellular-RNA factor loadings onto the cellular table for shared genes. |
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Apply latent factor identification (NMF, LDA, or DRVI) to reduce the dimensionality of gene expression data. |
Multimodal quantication#
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Extract image intensities at transcript locations and store them as a new table. |