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Prior to performing trajectory analysis, you should: 

1) Normalize the data

Trajectory analysis requires normalized counts as the input data. We recommend our default "CPM, Add 1, Log 2" normalization for most scRNA-Seq data.

2) Filter to cells that belong in the same trajectory

Trajectory analysis will built a single branching trajectory for all input cells. Consequently, only cells that share the biological process being studied should be included. For example, a trajectory describing progression through T cell activation should not include monocytes that do not undergo T cell activation. 

3) Filter to genes that characterize the trajectory

The trajectory should be built using a set of genes that increase or decrease as a function of progression through the biological processes being modeled. One example is using differentially expressed genes between cells collected at the beginning of the process to cells collected at the end of the process. If you have no prior knowledge about the process being studied, you can try identifying genes that are differentially expressed between clusters of cells or genes that are highly variable within the data set. Generally, you should try to filter to 1,000 to 3,000 informative genes prior to running Trajectory analysis. The list manager functionality in Partek Flow is useful for creating a list of genes to use in the filter. 

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