The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it.
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The ORFhunteR package is a R and C++ library for an automatic determination and annotation of open reading frames (ORF) in a large set of RNA molecules. It efficiently implements the machine learning model based on vectorization of nucleotide sequences and the random forest classification algorithm. The ORFhunteR package consists of a set of functions written in the R language in conjunction with C++. The efficiency of the package was confirmed by the examples of the analysis of RNA molecules fr
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library(ORFhunteR)
trans <- system.file("extdata", "Set.trans_sequences.fasta", package = "ORFhunteR")
model <- "http://www.sstcenter.com/download/ORFhunteR/classRFmodel_1.rds"
# Predict ORFs
ORFs <- predictORF(tr = trans, model = model, prThr = 0)
# Write coordinates to a temporary file for downstream functions
orfs_path <- tempfile(fileext = ".txt")
write.table(ORFs, file = orfs_path, sep = "\t", row.names = FALSE, quote = FALSE)
# Extract sequences
seq_orfs <- getSeqORFs(orfs = orfs_path, tr = trans, genome = "BSgenome.Hsapiens.UCSC.hg38")
# Find PTCs
gtf_path <- system.file("extdata", "Set.trans_sequences.gtf", package = "ORFhunteR")
ptcs <- findPTCs(orfs = orfs_path, gtf = gtf_path)
# Translate ORFs
seq_orf_path <- system.file("extdata", "Set.trans_ORFs.sequences.fasta", package = "ORFhunteR")
prot_seqs <- translateORFs(seqORFs = seq_orf_path)
# Annotate ORFs
prts_path <- system.file("extdata", "Set.trans_proteins.sequences.fasta", package = "ORFhunteR")
anno_orfs <- annotateORFs(orfs = orfs_path, tr = trans, gtf = gtf_path, prts = prts_path)
Input: FASTA file of transcript sequences and a pre-trained Random Forest model.
Output: Predicted ORFs, extracted sequences, PTC status, translated proteins, and a comprehensive annotation table.
library(ORFhunteR)
# Load pseudo-ORFs (lncRNAs) and true ORFs (mRNAs)
fileORFLncRNAs <- "http://www.sstcenter.com/download/ORFhunteR/NCBI_RefSeq_release_109_GRCh38.p12_ORF_candidates_sequences_lncRNAs.fasta.gz"
ORFLncRNAs <- loadTrExper(tr = fileORFLncRNAs)
fileORFmRNAs <- "http://www.sstcenter.com/download/ORFhunteR/NCBI_RefSeq_release_109_GRCh38.p12_ORFs_true_sequences_mRNAs.fasta.gz"
ORFmRNAs <- loadTrExper(tr = fileORFmRNAs)
# Train the Random Forest classifier
clt <- classifyORFsCandidates(
ORFLncRNAs = ORFLncRNAs[1:10],
ORFmRNAs = ORFmRNAs[1:10],
pLearn = 0.75,
nTrees = 10
)
Input: Lists of pseudo-ORFs and true coding ORFs.
Output: A trained randomForest classifier object.
library(ORFhunteR)
trans <- system.file("extdata", "Set.trans_sequences.fasta", package = "ORFhunteR")
model <- "http://www.sstcenter.com/download/ORFhunteR/classRFmodel_1.rds"
# 1. Predict true ORFs
ORFs <- predictORF(tr = trans, model = model, prThr = 0)
# 2. Extract nucleotide sequences of predicted ORFs
orfs_path <- system.file("extdata", "Set.trans_ORFs.coordinates.txt", package = "ORFhunteR")
seq_orfs <- getSeqORFs(orfs = orfs_path, tr = trans, genome = "BSgenome.Hsapiens.UCSC.hg38")
# 3. Detect premature termination codons (PTCs)
gtf_path <- system.file("extdata", "Set.trans_sequences.gtf", package = "ORFhunteR")
ptcs <- findPTCs(orfs = orfs_path, gtf = gtf_path)
# 4. Translate predicted ORFs into amino acid sequences
seq_orf_path <- system.file("extdata", "Set.trans_ORFs.sequences.fasta", package = "ORFhunteR")
prot_seqs <- translateORFs(seqORFs = seq_orf_path)
# 5. Generate a comprehensive annotation table
prts_path <- system.file("extdata", "Set.trans_proteins.sequences.fasta", package = "ORFhunteR")
anno_orfs <- annotateORFs(orfs = orfs_path, tr = trans, gtf = gtf_path, prts = prts_path)
Input: Transcript sequences, coordinates of ORFs, GTF file, and protein sequences.
Output: Annotated ORF table containing molecular weight, isoelectric point, and potential protein interaction index.
vectorizeORFs.classifyORFsCandidates.translateORFs.StringTie or Scallop instead.InterProScan or AlphaFold.fasta or fa format (or gtf/gff format with a corresponding BSgenome package like BSgenome.Hsapiens.UCSC.hg38).predictORF).gtf or gff format for PTC detection.0): Probability threshold for the winning class of ORFs."ATG"): Start codon to scan for in findORFs.0.75): Fraction of ORFs used for the training set in classifyORFsCandidates.500): Number of trees to grow in the Random Forest model."BSgenome.Hsapiens.UCSC.hg38"): Name of the pre-installed BSgenome data package.loadTrExper to safely load and parse transcript sequences from FASTA or GTF files.prThr (e.g., 0.9) in predictORF to reduce false positives.orfs), transcript sequences (tr), and GTF file (gtf) match exactly when running annotateORFs or findPTCs.getSeqORFs or predictORF with GTF/GFF inputs fails if the specified genome package is not installed. Fix: Install the required BSgenome package (e.g., BSgenome.Hsapiens.UCSC.hg38) before running.nTrees to at least 500 in classifyORFsCandidates.아직 리뷰가 없습니다. 사용해 본 소감을 남겨 주세요.
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The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it.
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This tool uses the label-tree function from HyPhy to annotate a phylogenetic tree. It allows users to select a subset of leaves using either a regular expression or a list of sequence names, and then apply a specified label to these selecte
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This package provides a client for the Bioconductor AnnotationHub web resource. The AnnotationHub web resource provides a central location where genomic files (e.g., VCF, bed, wig) and other resources from standard locations (e.g., UCSC, En
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apeglm provides Bayesian shrinkage estimators for effect sizes for a variety of GLM models, using approximation of the posterior for individual coefficients.
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ASURAT is a software for single-cell data analysis. Using ASURAT, one can simultaneously perform unsupervised clustering and biological interpretation in terms of cell type, disease, biological process, and signaling pathway activity. Inputting a single-cell RNA-seq data and knowledge-based databases, such as Cell Ontology, Gene Ontology, KEGG, etc., ASURAT transforms gene expression tables into original multivariate tables, termed sign-by-sample matrices (SSMs).
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AUCell allows to identify cells with active gene sets (e.g. signatures, gene modules...) in single-cell RNA-seq data. AUCell uses the "Area Under the Curve" (AUC) to calculate whether a critical subset of the input gene set is enriched with
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