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Chunk #35 — Online Methods — Analysis — Sample similarity tSNE

Source
chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data.
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For performing sample similarity tSNE, highly correlated motifs or kmers as well as motifs or kmers with variability below a certain threshold (1.5) were first removed from the bias corrected deviations matrix. The transpose of that matrix was then used as input to the Rtsne package28, with a perplexity parameter of 8 used for the down-sampled bulk hematopoiesis data and 25 for the single cell ATAC-seq data.