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About the Help category
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0
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221
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July 8, 2019
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Calculate_qc_metrics gene count
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0
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6
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December 2, 2021
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Do we need to redo scv.pp.filter_and_normalize() if using the Scanpy processed data?
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0
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8
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November 23, 2021
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Adata obs not consistent after merge
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0
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17
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November 23, 2021
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How to set the figure width and height for the output figure?
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1
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16
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November 22, 2021
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How to show the downregulated marker genes by sc.pl.rank_genes_groups?
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0
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16
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November 18, 2021
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Genes changing across pseudotime
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0
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16
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November 17, 2021
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UMAP incorrectly installed?
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6
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60
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November 17, 2021
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Feature Plot Showing Gene Co-expression
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0
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29
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November 15, 2021
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Distances between different cell types
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1
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55
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November 4, 2021
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Why we cannot tranfer adata along with functions?
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0
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9
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November 1, 2021
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Which data should be used for finding marker genes?
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0
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28
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November 1, 2021
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.obsp annotations lost
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0
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13
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October 29, 2021
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Customize dotplot function to group by multiple .obs columns
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0
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30
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October 25, 2021
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Change the sc.pl.paga edge color
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0
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14
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October 20, 2021
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Concatenate won't work
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1
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67
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October 18, 2021
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Correction versus Integration
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0
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33
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October 14, 2021
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Ingest on diffmap
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0
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29
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October 12, 2021
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When to perform batch correction?
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4
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936
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October 5, 2021
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Issue with the spatial transcriptomics tutorial
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3
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45
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October 1, 2021
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Getting Cells for list of genes ~ covid
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5
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507
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September 30, 2021
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Highly variable genes - best practice?
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5
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1714
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September 27, 2021
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Is is possible to export dendrograms to R
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0
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35
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September 11, 2021
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Error while using sc.pp.calculate_qc_metrics
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0
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37
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September 10, 2021
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Error while using read_10x_mtx
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4
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1193
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September 9, 2021
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Where's the raw count matrix in the anndata
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0
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85
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September 8, 2021
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Subsetting cells based on gene expression
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1
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69
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September 2, 2021
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Wilcoxon testing on a specific gene set
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0
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45
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August 25, 2021
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Difference between n_genes and n_genes_by_counts
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0
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60
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August 25, 2021
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Normalizing data based on spike-in cells
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0
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33
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August 24, 2021
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