scanMiR is a bioconductor set of tools for working with miRNA affinity
models (KdModels), enabling efficient and flexible scanning for miRNA binding
sites and prediction of target repression.
This repository details the R package; for the web interface click here.
Getting started
Installation
BiocManager::install("ETHZ-INS/scanMiR")
Basic example usage
# accepts miRNA target seeds:
findSeedMatches(seqs, seeds="AAACCAC")
# full miRNA sequences:
findSeedMatches(seqs, seeds="UUAAUGCUAAUCGUGAUAGGGGUU")
# or KdModels:
findSeedMatches(seqs, seeds=model)
scanMiR can predict TDMD and circRNA slicing sites, and aggregate sites to
predict repression based on the biochemical model from
McGeary, Lin et al. (2019). For
more information, see our paper.
To learn more about the functionalities, see the package’s
vignettes.
To obtain predicted KdModels for all mouse, human and rat miRbase miRNAs, see the
scanMiRData pacakge.
For convenient wrappers connecting to AnnotationHub, fast out-of memory access
to large collections, or a web interface to scanMiR, see the
scanMiRApp package.
scanMiR
scanMiRis a bioconductor set of tools for working with miRNA affinity models (KdModels), enabling efficient and flexible scanning for miRNA binding sites and prediction of target repression.This repository details the R package; for the web interface click here.
Getting started
Installation
Basic example usage
The putative 3’ binding of each match can also be visualized:
scanMiRcan predict TDMD and circRNA slicing sites, and aggregate sites to predict repression based on the biochemical model from McGeary, Lin et al. (2019). For more information, see our paper.To learn more about the functionalities, see the package’s vignettes. To obtain predicted
KdModelsfor all mouse, human and rat miRbase miRNAs, see the scanMiRData pacakge.For convenient wrappers connecting to AnnotationHub, fast out-of memory access to large collections, or a web interface to scanMiR, see the scanMiRApp package.