All analysis and scoring functions only use the -4 to +4 flanking positions instead of -7 to +7.
There are now file checks for data inputs for main functions to ensure all files are formatted properly prior to analysis.
multi_screener()
now outputs a list containing relevant analysis settings
(e.g. method
, pval_corr
, etc) which will be automatically used by all
downstream functions that take screener as an input. It is no longer necessary
to manually specify these in any function that requires screener. Example
functions this applies to:
generate_substrates()
score_candidates()
multi_candidate_screener()
multi_candidate_screener
now accepts an boolean(T/F) value to screen against
a kinase family instead of the full screener library.
multi_candidate_screener()
and multi_screener()
now include percent progress
bars.
multi_screener()
now provides ROC curves labeled with the optimal cutpoint
for every kinase in the screener library.
multi_screener()
now accepts a user-defined specificity constraint using
variable constrain
. The default remains 90% specificity.
generate_substrates()
now allows user to manually curate amino acid residues
when a maximum number of permutations (currently 250,000) is exceeded.
Manual installation of Bioconductor is no longer necessary.
multi_screener()
now accepts any user-generated screener and uniprot files
rather than only the package-provided ones.
substrate_fisher_test()
now works with amino acid properties.
Vignette no longer requires the motifStack
package to render properly.
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