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knockoutDirection() predicts whether each gene goes up or
down after a knockout, from the heat kernel of the WT gene-gene
correlation matrix of log1p(CPM) expression.
scTenifoldKnk() reports it by default
(dr_direction = TRUE, dr_directionT = 5) as
the direction and directionScore columns of
diffRegulation, and as perturbationDirections
in transcriptome-wide mode.
dr_directionRegressLibSize = TRUE (off by default)
regresses log library size out of each gene first, for data sets in
which nearly all genes are predicted down.hkManifoldAlignment() computes the heat kernel of the WT
network once (heatKernel()) and reads every knockout from
it, so the cost of a transcriptome-wide screen no longer scales with the
number of knockouts. Selected with ma_method = "heat"
(ma_heatT = 10).perturbationMap() ranks the knockouts
of a transcriptome-wide run by the similarity of their signed profiles
to a reference signature, such as a disease-vs-control comparison of the
same cell type, and draws them on a map.diffRegulation has eight columns instead of six
(direction, directionScore). Set
dr_direction = FALSE for the 1.x table.transcriptomeWide = TRUE) uses
the heat manifold alignment by default, so its distances differ from
1.x. Set ma_method = "manifold" to recover them. Single and
multi-gene knockouts still use the manifold alignment by default and
give the same distances, Z-scores and p-values as 1.1.5.dRegulation().gKO are knocked
out together (#47).plotKO() enrichment works without attaching enrichR
(#43); data.frame input is rejected (#44).seed argument for reproducible results (#48); warning
when the knocked-out genes have no outgoing edges.These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.