Internal functions used by EventPointer in the different steps of the algorithm
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 | annotateEvents(Events, PSR_Gene, Junc_Gene, Gxx)
annotateEventsMultipath(Events, PSR_Gene, Junc_Gene, Gxx, paths)
AnnotateEvents_RNASeq(Events)
AnnotateEvents_RNASeq_MultiPath(Events, paths)
AnnotateEvents_KLL(Events, Gxx, GenI)
ClassifyEvents(SG, Events, twopaths)
estimateAbsoluteConc(Signal1, Signal2, SignalR, lambda)
estimateAbsoluteConcmultipath(datos, lambda = 0.1)
findTriplets(randSol, tol = 1e-08)
findTriplets2(Incidence, paths = 2, randSol)
GetCounts(Events, sg_txiki, type = "counts")
GetCountsMP(Events, sg_txiki, type = "counts")
getEventPaths(Events, SG)
getEventMultiPaths(Events, SG, twopaths, paths)
GetIGVPaths(EventInfo, SG_Edges)
getPSI(ExFit, lambda = 0.1)
getPSI_RNASeq(Result, lambda = 0.1)
getPSI_RNASeq_MultiPath(Result, lambda = 0.1)
getRandomFlow(Incidence, ncol = 1)
IHsummarization(Pv1, t1, Pv2, t2, coherence = "Opposite")
pdist2(X, Y)
PrepareCountData(Result)
PrepareProbes(Probes, Class)
PrepareOutput(Result, Final)
SG_Info(SG_Gene)
SG_creation(SG_Gene)
SG_creation_RNASeq(SG_Gene)
WriteGTF(PATH, Data, Probes, Paths)
WriteGTF_RNASeq(PATH, Data, Paths)
flat2Cdf(file, chipType, tags = NULL, rows = 2560, cols = 2560,
verbose = 10, xynames = c("X", "Y"), gcol = 5, ucol = 6,
splitn = 4, col.class = c("integer", "character")[c(1, 1, 1, 2, 2,
2)], Directory = getwd(), ...)
uniquefast(X)
filterimagine(Info, paths)
transfromedge(SG, SG_Gene)
sacartranscritos(edgetr, events)
convertToSGFeatures2(x, coerce = FALSE, merge = FALSE)
processFeatures2(features, coerce = FALSE, merge = FALSE)
annotate2(query, subject)
annotateFeatures2(query, subject)
mergeExonsTerminal2(features, min_n_sample = 1)
get_beta(combboots, incrPSI_original, ncontrastes)
get_table(PSI_arrayP, nevents, totchunk, chunk, nsamples, incrPSI_original,
V, nboot, nbootin, ncontrastes)
get_YB(PSI_arrayS, l, nsamples, I, J, CTEind)
getInfo(table, ncontrast)
PrimerSequenceGeneral(taqman, FinalExons, generaldata, SG, Dir, nPrimers,
Primer3Path = Sys.which("primer3_core"), maxLength, minsep, wminsep,
valuethreePpenalty, wnpaths, qualityfilter)
PrimerSequenceTwo(FinalExons, SG, generaldata, n, thermo.param,
Primer3Path, settings)
ProbesSequence(SG, FinalSeq, generaldata, Dir,
Primer3Path = Sys.which("primer3_core"), nProbes)
sort.exons(namesPath, decreasing = FALSE)
all_simple_paths2(wg, from, to, ...)
callPrimer3(seq, threeprimers = FALSE, pr, reverse = FALSE,
size_range = "150-500", Tm = c(57, 59, 62), name = "Primer1",
Primer3Path = "primer3-2.3.7/bin/primer3_core",
thermo.param = "primer3-2.3.7/src/primer3_config/",
sequence_target = NULL,
settings = "primer3-2.3.7/primer3web_v4_0_0_default_settings.txt")
callPrimer3probes(seq, name = "Primer1",
Primer3Path = "primer3-2.3.7/bin/primer3_core",
thermo.param = "primer3-2.3.7/src/primer3_config/",
sequence_target = NULL,
settings = "primer3-2.3.7/primer3web_v4_0_0_default_settings.txt")
CreateSequenceforProbe(SG, Exons, FinalSeq, n)
findPotencialExons(D, namesPath, maxLength, SG, minexonlength)
fullExons(namesPath)
includeaexons(Forward)
genreverse(FinalInfo)
getDistanceseachPath(Exon1, Exon2, generaldata, distinPrimers, SG)
getDominants2(PrimersTwo, Primers1, commonForward, commonReverse, namesRef,
D, numberOfPaths, nprimerstwo, ED, wNpaths = 1000, wP12inRef = 1000)
getDominantsFor(Primers1, Primers2, commonForward, namesRef, D,
numberOfPaths, Event, ncommonForward, ED, wNpaths = 1000,
wP12inRef = 1000)
getDominantsRev(Primers1, Primers2, commonReverse, namesRef, D,
numberOfPaths, Event, ncommonReverse, ED, wNpaths = 1000,
wP12inRef = 1000)
getExonsFullSignal(namesPath, SG)
getFinalExons(generaldata, maxLength, nPrimerstwo, ncommonForward,
ncommonReverse, nExons, minsep, wminsep, valuethreePpenalty,
minexonlength)
getgeneraldata(SG, Event, shortdistpenalty)
getrankexons(SG, Dominants, nt, wg, items, minsep, wminsep,
valuethreePpenalty, D)
getranksequence(taqman, Fdata, maxLength, minsep, wminsep,
valuethreePpenalty, wnpaths, qualityfilter)
PrimerSequenceCommonFor(FinalExons, SG, generaldata, n, thermo.param,
Primer3Path, settings)
PrimerSequenceCommonRev(FinalExons, SG, generaldata, n, thermo.param,
Primer3Path, settings)
|
Internal outputs
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.