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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Generate SuperSigs (supervised mutational signatures) from single nucleotide variants in the cancer genome. Functions included in the package allow the user to learn supervised mutational signatures from their data and apply them to new data. The methodology is based on the one described in Afsari (2021, ELife).
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Preprocess mutation data, build a trinucleotide feature matrix, and train a supervised mutational signature (SuperSig).
library(supersigs)
library(VariantAnnotation)
library(BSgenome.Hsapiens.UCSC.hg19)
library(dplyr)
# 1. Read VCF and add patient age to colData
fl <- system.file("extdata", "chr22.vcf.gz", package="VariantAnnotation")
vcf <- VariantAnnotation::readVcf(fl, "hg19")
vcf <- vcf[, 1]
positions <- geno(vcf)$GT != "0|0"
vcf <- vcf[positions[, 1],]
colData(vcf)$age <- 50
# 2. Process VCF to a simplified data frame
dt <- process_vcf(vcf)
# 3. Transform mutations into a trinucleotide matrix
input_dt <- make_matrix(dt)
# 4. Add the indicator variable (IndVar)
input_dt <- input_dt %>%
mutate(IndVar = c(1, 1, 1, 0, 0)) %>%
relocate(IndVar)
# 5. Train the supervised signature
set.seed(1)
supersig <- get_signature(data = input_dt, factor = "Smoking")
# 6. Simplify the signature for visualization
features <- simplify_signature(object = supersig, iupac = FALSE)
Note: Input is a VCF object or a data frame of mutations with sample IDs, ages, and genomic coordinates; output is a trained SuperSig S4 object and simplified signature features.
Remove the contribution of a supervised signature from a mutation data frame to adjust for a confounding factor.
library(supersigs)
# Adjust the mutation matrix by removing the signature's contribution
adjusted_dt <- partial_signature(data = input_dt, object = supersig)
Note: Input is a feature count data frame and a trained SuperSig object; output is an adjusted mutation feature data frame.
Apply a trained or pre-trained SuperSig to a new dataset to predict classification scores.
library(supersigs)
library(dplyr)
# Apply a trained SuperSig to a new dataset
newdata <- predict_signature(supersig, newdata = input_dt, factor = "Smoking")
# Or use a pre-trained signature from supersig_ls
newdata_pretrained <- predict_signature(supersig_ls[["SMOKING (LUAD)"]], newdata = input_dt, factor = "Smoking")
Note: Input is a trained SuperSig object (or pre-trained from supersig_ls) and a new feature count data frame; output is a data frame containing predicted classification scores and feature counts.
get_signature).predict_signature, supersig_ls).partial_signature).sample_id, age, chromosome, position, ref, and alt columns.BSgenome.Hsapiens.UCSC.hg19 or BSgenome.Hsapiens.UCSC.hg38) for trinucleotide context extraction.IndVar, sample_id, age, and 96 trinucleotide mutation count columns in get_signature.get_signature and predict_signature.SuperSig S4 object in simplify_signature and partial_signature.simplify_signature.predict_signature.colData(vcf)$age before calling process_vcf.set.seed) before running get_signature to ensure reproducibility of cross-validation folds.simplify_signature(..., iupac = TRUE) to group trinucleotide features into more interpretable IUPAC representations for plotting.partial_signature before learning other signatures.get_signature requires a logical/numeric indicator variable named IndVar in the input data frame. Fix: Add and relocate the IndVar column using dplyr::mutate and dplyr::relocate.make_matrix. Fix: Ensure the correct BSgenome package is loaded and matches the coordinates in your mutation data.まだレビューはありません。使ってみた感想をお寄せください。
概要と使いどころ
The package contains functions for exploratory oligonucleotide array analysis. The dependence on tkWidgets only concerns few convenience functions. 'affy' is fully functional without it.
日本語の概要は準備中です。原文の説明を表示しています。
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
日本語の概要は準備中です。原文の説明を表示しています。
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).
日本語の概要は準備中です。原文の説明を表示しています。
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
日本語の概要は準備中です。原文の説明を表示しています。