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 package is a implementation of biclustering ensemble method MoSBi (Molecular signature Identification from Biclustering). MoSBi provides standardized interfaces for biclustering results and can combine their results with a multi-algorithm ensemble approach to compute robust ensemble biclusters on molecular omics data. This is done by computing similarity networks of biclusters and filtering for overlaps using a custom error model. After that, the louvain modularity it used to extract biclus
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Run multiple biclustering algorithms on a data matrix, construct a similarity network with an error model, extract robust communities, and generate consensus ensemble biclusters.
library(mosbi)
# 1. Prepare data matrix
data(mouse_data)
mouse_data_sub <- mouse_data[c(grep("metabolite_identification", colnames(mouse_data)), grep("^X", colnames(mouse_data)))]
# Simple mock matrix for runnable demonstration
data_matrix <- matrix(rnorm(1000), nrow = 100, ncol = 10)
rownames(data_matrix) <- paste0("M", 1:100)
colnames(data_matrix) <- paste0("S", 1:10)
# 2. Run Biclustering Algorithms
fb <- mosbi::run_fabia(data_matrix)
BCisa <- mosbi::run_isa(data_matrix)
BCplaid <- mosbi::run_plaid(data_matrix)
BCqubic <- mosbi::run_qubic(data_matrix)
all_bics <- c(fb, BCisa, BCplaid, BCqubic)
# 3. Compute Bicluster Similarity Network with Error Model
bic_net <- mosbi::bicluster_network(all_bics, data_matrix, n_randomizations = 5, MARGIN = "both", metric = 4)
# 4. Extract Louvain Communities
coms <- mosbi::get_louvain_communities(bic_net, min_size = 3, bics = all_bics)
# 5. Generate Consensus Ensemble Biclusters
ensemble_bicluster_list <- mosbi::ensemble_biclusters(coms, all_bics, data_matrix, row_threshold = 0.1, col_threshold = 0.1)
Input: A numeric data matrix; Output: A list of robust ensemble biclusters.
run_fabia, ISA via run_isa, Plaid via run_plaid, QUBIC via run_qubic) and combine their results.bicluster_network.get_louvain_communities and generate consensus ensemble biclusters via ensemble_biclusters.biclust or fabia can be used directly.data_matrix in the vignette derived from mouse_data using log2 and z-score normalization).bicluster_network.bicluster_network.bicluster_network.bicluster_network.bicluster_network.get_louvain_communities.colhistogram and rowhistogram (or a helper like bicluster_histo).plot_edge_dist = TRUE in bicluster_network.plot or plot_algo_network to inspect how different algorithms contribute to communities.get_louvain_communities with a min_size that is too high, resulting in zero saved communities. Fix: Lower min_size (e.g., to 3).biclust for running individual biclustering algorithms like Plaid.fabia for Fabia biclustering.QUBIC for QUBIC biclustering.isa2 for ISA biclustering.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.
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。
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
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。