Description Usage Arguments Author(s)
Internal function to build a data table containing gene pairs and the correspoding transcriptomic/genomic feature values. The operon classifier trained/validated on the OPs and NOPs is used to predict the operon status of these gene pairs.
1 2 3 | select.pops(OPs, NOPs, genes.and.operons, transcCDSs, transcIGRs.pos,
transcIGRs.neg, minExprCDS = 0.1, minExprIGR = 0.25, maxLenIGR = 150,
POSSs, POESs, max.start.transc, max.end.transc, wseq, verbose = TRUE, ...)
|
OPs |
Data table including the confirmed operon pairs (OPs). See |
genes.and.operons |
Data table merging gene(s) and operon(s) annotations. See |
transcCDSs |
Transcription levels for the coding regions. See |
transcIGRs.pos |
Transcription levels for the intergenic regions (forard strand). See |
transcIGRs.neg |
Transcription levels for the intergenic regions (reverse strand). See |
minExprCDS |
Minimum expression level for the coding sequence regions (CDSs). Default values is 0.1. |
minExprIGR |
Minimum expression level for the intergenic regions (IGRs). Default values is 0.25. |
maxLenIGR |
Maximum length for the intergenic regions (IGRs). Default values is 150. |
POSSs |
Data table representing a set of putative operon start-points. |
POESs |
Data table representing a set of putative operon end-points. |
max.start.transc |
Cutoff values for the start transcription points. Default values is 0.1. |
max.end.transc |
Cutoff values for the end transcription points. Default values is 0.1. |
wseq |
Sequence genome. |
verbose |
Default logical value is TRUE. |
OPs |
Data table including the confirmed non-operon pairs (NOPs). See |
Vittorio Fortino select.pops()
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