Skip to main content
. 2022 Mar 7;23:73. doi: 10.1186/s13059-022-02629-7

Fig. 2.

Fig. 2

TraSig workflow. Top left: For a scRNA-Seq dataset, we use the reconstructed pseudotime trajectory and the expression data as inputs. Bottom left: We next determine expression profiles for genes along each of the edges (clusters) using sliding windows and compute dot product scores for pairs of genes in edges. Right: Finally, we use permutation tests to assign significance levels to the scores we computed