Package 'scanMiRApp'

Title: scanMiR shiny application
Description: A shiny interface to the scanMiR package. The application enables the scanning of transcripts and custom sequences for miRNA binding sites, the visualization of KdModels and binding results, as well as browsing predicted repression data. In addition contains the IndexedFst class for fast indexed reading of large GenomicRanges or data.frames, and some utilities for facilitating scans and identifying enriched miRNA-target pairs.
Authors: Pierre-Luc Germain [cre, aut] , Michael Soutschek [aut], Fridolin Gross [ctb]
Maintainer: Pierre-Luc Germain <[email protected]>
License: GPL-3
Version: 1.13.0
Built: 2024-11-21 06:13:33 UTC
Source: https://github.com/bioc/scanMiRApp

Help Index


enrichedMirTxPairs

Description

Identifies pairs of miRNA and target transcripts that have an unexpectedly high number of sites.

Usage

enrichedMirTxPairs(m, minSites = 5, max.binom.p = 0.001)

Arguments

m

A GRanges of matches, as produced by findSeedMatches. This will be filtered down to only 8mer and 7mer sites.

minSites

The minimum number of sites for a given miRNA-target pair to be considered.

max.binom.p

The maximum binomial p-value of miRNA-target pairs.

Value

A data.frame of top combinations, including number of sites and the log-transformed binomial p-value.

Examples

# we create a dummy scan (see `runFullScan`)
library(scanMiR)
seqs <- getRandomSeq(n=10)
mirs <- c("TTGTATAA","AGCATTAA")
m <- findSeedMatches(seqs,mirs,verbose=FALSE)
# we look for enriched pairs
res <- enrichedMirTxPairs(m, minSites=1, max.binom.p=1)
res

Example 'fake' TxDb object

Description

A fake transcript database used for examples.

Value

a named character vector of length 1.


getTranscriptSequence

Description

Utility wrapper to extracts the sequence of a given transcript (UTR or CDS+UTR).

Usage

getTranscriptSequence(
  tx = NULL,
  annotation,
  annoFilter = NULL,
  extract = c("UTRonly", "withORF", "exons"),
  ...
)

Arguments

tx

The ensembl ID of the transcript(s)

annotation

A ScanMiRAnno object.

annoFilter

An optional 'AnnotationFilter' or 'AnnotationFilterList' to further filter the set of transcripts to be extracted

extract

Which parts of the transcripts to extract. For 'UTRonly' (default) only the 3' UTR regions are extracted, 'withORF' additionally extracts the coding regions, and 'exons' extracts all exons

...

Passed to AnnotationHub

Value

A DNAStringSet.

Examples

anno <- ScanMiRAnno("fake")
seq <- getTranscriptSequence( tx="ENSTFAKE0000056456", annotation=anno )

IndexedFst

Description

Objects of the IndexedFst class enable fast named random access to FST files. This is particularly appropriate for large data.frames which often need to be accessed according to the (e.g. factor) value of a particular column.

Usage

## S4 method for signature 'IndexedFst'
show(object)

## S4 method for signature 'IndexedFst'
summary(object)

## S4 method for signature 'IndexedFst'
names(x)

## S4 method for signature 'IndexedFst'
length(x)

## S4 method for signature 'IndexedFst'
lengths(x)

## S4 method for signature 'IndexedFst'
nrow(x)

## S4 method for signature 'IndexedFst'
ncol(x)

## S4 method for signature 'IndexedFst'
colnames(x)

## S4 method for signature 'IndexedFst,ANY,ANY'
x[[i, j = NULL, ...]]

## S4 method for signature 'IndexedFst,ANY,ANY,ANY'
x[i, j = NULL, ..., drop = TRUE]

## S4 method for signature 'IndexedFst'
x$name

## S4 method for signature 'IndexedFst'
head(x, n = 6L, ...)

## S4 method for signature 'IndexedFst'
as.data.frame(x, name)

Arguments

object

an IndexedFst object

x

an IndexedFst object

i

the desired index (either numeric or name)

j, drop

ignored

...

ignored

name

the indexed name to fetch

n

the desired number of rows

Value

Depends on the method

Author(s)

Pierre-Luc Germain, [email protected]

See Also

saveIndexedFst, loadIndexedFst

Examples

# we first create and save an indexed FST file
tmp <- tempdir()
f <- system.file(tmp, "test")
d <- data.frame( category=sample(LETTERS[1:4], 10000, replace=TRUE),
                 var2=sample(LETTERS, 10000, replace=TRUE),
                 var3=runif(10000) )
format(object.size(d),units="Kb")
saveIndexedFst(d, "category", f)
rm(d)
# we then load the index, and can use category names for random access:
d <- loadIndexedFst(f)
format(object.size(d),units="Kb")
nrow(d)
names(d)
head(d$A)

Saving and loading IndexedFst

Description

Functions to save or load and indexed fst file

Saves a data.frame (or GRanges object) into an indexed FST file.

Usage

loadIndexedFst(file, nthreads = 1)

saveIndexedFst(
  d,
  index.by,
  file.prefix,
  nthreads = 1,
  index.properties = NULL,
  add.info = list(),
  ...
)

Arguments

file

Path to the fst file, it's index (.idx), or their prefix.

nthreads

Number of threads to use for reading (default 1). This does not affect the loading of the index itself, but will affect all downstream reading operations performed on the object. If NULL, will use 'fst::threads_fst()'.

d

A data.frame or GRanges object

index.by

A column of 'd' by which it should be indexed.

file.prefix

Path and prefix of the output files.

index.properties

An optional data.frame of properties, with the levels of 'index.by' as row names.

add.info

An optional list of additional information to save.

...

Passed to 'write.fst'

Value

'loadIndexedFst' returns an object of class IndexedFst-class, and 'saveIndexedFst' returns nothing.

See Also

IndexedFst-class

IndexedFst-class

Examples

# we first create and save an indexed FST file
tmp <- tempdir()
f <- system.file(tmp, "test")
d <- data.frame( category=sample(LETTERS[1:4], 10000, replace=TRUE),
                 var2=sample(LETTERS, 10000, replace=TRUE),
                 var3=runif(10000) )
saveIndexedFst(d, "category", f)
# we then load the index, and can use category names for random access:
d <- loadIndexedFst(f)

plotSitesOnUTR

Description

Wrapper function with minimal arguments to plot scanMiR-Binding sites on 3'UTRs of specified transcripts. The red dashed line indicates the background threshhold is indicated, the lightblue dashed line shows the average 8mer dissociation rate of the given miRNA

Usage

plotSitesOnUTR(
  tx,
  annotation,
  miRNA = NULL,
  label_6mers = FALSE,
  label_notes = FALSE,
  verbose = TRUE,
  ...
)

Arguments

tx

An ensembl TranscriptID

annotation

A ScanMiRAnno object.

miRNA

A miRNA name in the mirbase format (eg. "hsa-miR-485-5p"), a 'KdModel', or a miRNA sequence or target seed.

label_6mers

Logical whether to label 6mer sites in the plot

label_notes

Logical whether to label special sites in the plot (as TDMD or Slicing)

verbose

Logical; whether to print updates on the processing

...

Any further arguments passed to findSeedMatches

Value

Returns a ggplot.

Examples

anno <- ScanMiRAnno("fake")
plotSitesOnUTR( tx="ENSTFAKE0000056456", annotation=anno,
                miRNA="hsa-miR-155-5p" )

runFullScan

Description

Runs a full miRNA scan on all protein-coding transcripts (or UTRs) of an annotation.

Usage

runFullScan(
  annotation,
  mods = NULL,
  annoFilter = NULL,
  extract = c("UTRonly", "withORF", "exons"),
  onlyCanonical = TRUE,
  shadow = 15,
  cores = 1,
  maxLogKd = c(-1, -1.5),
  save.path = NULL,
  ...
)

Arguments

annotation

A ScanMiRAnno object

mods

An optional 'KdModelList' (defaults to the one in 'annotation')

annoFilter

An optional 'AnnotationFilter' or 'AnnotationFilterList' to filter the set of transcripts to be extracted

extract

Which parts of the transcripts to extract. For 'UTRonly' (default) only the 3' UTR regions are extracted, 'withORF' additionally extracts the coding regions, and 'exons' extracts all exons

onlyCanonical

passed to findSeedMatches

shadow

The size of the ribosomal shadow at the UTR starts

cores

The number of threads to use. Alternatively accepts a BiocParallelParam-class, as for instance produced by MulticoreParam.

maxLogKd

The maximum log_kd of sites to report

save.path

Optional, the path to which to save the results

...

Arguments passed to findSeedMatches

Value

A 'GRanges' object

Examples

anno <- ScanMiRAnno("fake")
m <- runFullScan( annotation=anno )
m

ScanMiRAnno

Description

ScanMiRAnno

Usage

ScanMiRAnno(
  species = NULL,
  genome = NULL,
  ensdb = NULL,
  models = NULL,
  scan = NULL,
  aggregated = NULL,
  version = NULL,
  addDBs = list(),
  ...
)

Arguments

species

The species/build acronym for automatic construction; if omitted, 'genome' and 'ensdb' should be given. Current possible values are: GRCh38, GRCm38, GRCm39, Rnor_6.

genome

A BSgenome-class, or a TwoBitFile

ensdb

An EnsDb-class (or a TxDb-class) object

models

An optional KdModelList

scan

An optional full scan (IndexedFst or GRanges)

aggregated

An optional per-transcript aggregation (IndexedFst or data.frame)

version

optional ensembl version

addDBs

A named list of additional tx-miRNA databases, each of which should be a data.frame with the columns 'transcript', 'miRNA', and 'score'.

...

Arguments passed to 'AnnotationHub'

Value

A 'ScanMiRAnno' object

Examples

anno <- ScanMiRAnno(species="fake")
anno

Methods for the ScanMiRAnno class

Description

Methods for the ScanMiRAnno class

Usage

## S4 method for signature 'ScanMiRAnno'
summary(object)

## S4 method for signature 'ScanMiRAnno'
show(object)

Arguments

object

An object of class ScanMiRAnno

Value

Depends on the method.

See Also

ScanMiRAnno


scanMiRApp A wrapper for launching the scanMiRApp shiny app

Description

scanMiRApp A wrapper for launching the scanMiRApp shiny app

Usage

scanMiRApp(annotations = NULL, ...)

Arguments

annotations

A named list of ScanMiRAnno objects. If omitted, will use the base ones.

...

Passed to scanMiRserver

Value

A shiny app

Examples

if(interactive()){
  anno <- ScanMiRAnno("fake")
  scanMiRApp(list(fakeAnno=anno))
}

scanMiRserver

Description

Server function for the scanMiR shiny app. Most users are expected to use scanMiRApp instead.

Usage

scanMiRserver(
  annotations = list(),
  modlists = NULL,
  maxCacheSize = 10 * 10^6,
  BP = SerialParam()
)

Arguments

annotations

A named list of ScanMiRAnno object.

modlists

A named list of 'KdModelList' objects. If omitted, will fetch it from the annotation objects.

maxCacheSize

Maximum cache size in bytes.

BP

BPPARAM for multithreading

Value

A shiny server function

Examples

# we'd normally fetch a real annotation:
# anno <- ScanMiRAnno("Rnor_6")
# here we'll use a fake one:
anno <- ScanMiRAnno("fake")
srv <- scanMiRserver(list(fake=anno))

scanMiRui

Description

UI for the scanMiR app.

Usage

scanMiRui()

Value

A shiny ui

Examples

ui <- scanMiRui()