Biocview "Transcriptomics"

A CAusal Reasoning tool for Network Identification (from gene expression data) using Integer VALue programming
A CAusal Reasoning tool for Network Identification (from gene expression data) using Integer VALue programming
A CAusal Reasoning tool for Network Identification (from gene expression data) using Integer VALue programming
Access matrix-like HDF5 server content or BigQuery content through a SummarizedExperiment interface
Access matrix-like HDF5 server content or BigQuery content through a SummarizedExperiment interface
Access matrix-like HDF5 server content or BigQuery content through a SummarizedExperiment interface
A dimensionality reduction tool using gene detection pattern to mitigate noisy expression profile of scRNA-seq
A dimensionality reduction tool using gene detection pattern to mitigate noisy expression profile of scRNA-seq
A dimensionality reduction tool using gene detection pattern to mitigate noisy expression profile of scRNA-seq
An alignment and integration method for single cell genomics
An alignment and integration method for single cell genomics
Analysis of Cap Analysis of Gene Expression (CAGE) data using Bioconductor
Analysis of Cap Analysis of Gene Expression (CAGE) data using Bioconductor
Analysis Of Differential Abundance Taking Sample Variation Into Account
Analysis Of Differential Abundance Taking Sample Variation Into Account
Analyze Transcription Factor Enrichment
Analyze Transcription Factor Enrichment
An R package for the analysis and result reporting of RNA-Seq data by combining multiple statistical algorithms
An R package for the analysis and result reporting of RNA-Seq data by combining multiple statistical algorithms
An R package for the analysis and result reporting of RNA-Seq data by combining multiple statistical algorithms
A search tool for single cell RNA-seq data by gene lists
A search tool for single cell RNA-seq data by gene lists
Assigning scRNA-seq to clone-of-origin using copy number from ultra-low-depth scDNA-seq
A Supervised Approach for **P**r**e**dicting **c**ell Cycle Pr**o**gression using scRNA-seq data
A Supervised Approach for **P**r**e**dicting **c**ell Cycle Pr**o**gression using scRNA-seq data
A tool for differential expression analysis and DEGs based investigation to complex diseases by bi-clustering analysis
A tool for unsupervised projection of single cell RNA-seq data
A tool for unsupervised projection of single cell RNA-seq data
AUCell: Analysis of 'gene set' activity in single-cell RNA-seq data (e.g. identify cells with specific gene signatures)
AUCell: Analysis of 'gene set' activity in single-cell RNA-seq data (e.g. identify cells with specific gene signatures)
Automated functions for comparing various omic data from cbioportal.org
Automated functions for comparing various omic data from cbioportal.org
Automated functions for comparing various omic data from cbioportal.org
Automated, probabilistic assignment of scRNA-seq to cell types
Bayesian Analysis of Single-Cell Sequencing data
Bayesian Analysis of Single-Cell Sequencing data
BEARscc (Bayesian ERCC Assesstment of Robustness of Single Cell Clusters)
BEARscc (Bayesian ERCC Assesstment of Robustness of Single Cell Clusters)
Calculate JCC Scores
Cancer Clone Finder
Cancer Clone Finder
Casc
Causal network analysis methods
CB2: A cluster-based approach for distinguishing cells from background barcodes in 10x Genomics data
Cell-Cycle using Mixture Models
Classify Samples From RNA-Seq Datasets
Client for the Reactome Analysis Service for comparative multi-omics gene set analysis
Client for the Reactome Analysis Service for comparative multi-omics gene set analysis
Clone Identification from Single Cell Data
Clone Identification from Single Cell Data
Cluster analysis of Spatial Transcriptomics data
Cluster analysis of Spatial Transcriptomics data
Co-expression Modules identification Tool
Co-expression Modules identification Tool
Compendium of human transcriptome sequences
Computational pipeline for computing probability of modification from structure probing experiment data
Computational pipeline for computing probability of modification from structure probing experiment data
Controlling bias and inflation in association studies using the empirical null distribution
Conversion between the Workflow4metabolomics tabulated format and the ExpressionSet bioconductor class
Covariate Assisted Large-scale Multiple testing
Covariate Assisted Large-scale Multiple testing
Cross omic genetic fingerprinting
Cross omic genetic fingerprinting
Decomposing Heterogeneous Cohorts using Omic Data Profiling
Decomposing Heterogeneous Cohorts using Omic Data Profiling
Delineate outstanding genomic zones of differential gene activity
Delineate outstanding genomic zones of differential gene activity
DEsingle for detecting three types of differential expression in single-cell RNA-seq data
DEsingle for detecting three types of differential expression in single-cell RNA-seq data
Determination of essential phenotypic elements of clusters in high-dimensional entities
Determination of essential phenotypic elements of clusters in high-dimensional entities
Differential Expression Analysis for RNA-seq data through a robust variance component test
Empirical Analysis of Digital Gene Expression Data in R
Enjoy Analyzing And Integrating The Results From Differential Expression Analysis And Functional Enrichment Analysis
Enjoy Analyzing And Integrating The Results From Differential Expression Analysis And Functional Enrichment Analysis
Evaluate Cellspecific Mixing
Evaluate Cellspecific Mixing
Exon-Intron Split Analysis (EISA) in R
Exon-Intron Split Analysis (EISA) in R
explore metrics for sample annotation for genomic experiments
explore metrics for sample annotation for genomic experiments
Exposome and omic data associatin and integration analysis
Exposome and omic data associatin and integration analysis
Factorial Latent Variable Modeling of Single-Cell RNA-Seq Data
Factorial Latent Variable Modeling of Single-Cell RNA-Seq Data
Factorial Latent Variable Modeling of Single-Cell RNA-Seq Data
Fast, Sensitive, and Accurate Integration of Single Cell Data
FCBF-based Co-Expression Networks for Single Cells
FCBF-based Co-Expression Networks for Single Cells
FCBF-based Co-Expression Networks for Single Cells
Functional interpretation of single cell RNA-seq latent manifolds
Functional interpretation of single cell RNA-seq latent manifolds
Gene expression-based subtype classification for high-grade serous ovarian cancer
Gene expression-based subtype classification for high-grade serous ovarian cancer
Gene expression changes in three biological conditions
Gene expression changes in three biological conditions
Gene Expression Meta-analysis Visualization Tool
Gene Expression Meta-analysis Visualization Tool
Gene regulator enrichment analysis
Global Test for Counts
Global Test for Counts
Graphical Interface for Alternative Splicing Quantification, Analysis and Visualisation
Graphical Interface for Alternative Splicing Quantification, Analysis and Visualisation
Identification of candidate causal perturbations from differential gene expression data
Identification of candidate causal perturbations from differential gene expression data
Identify, Annotate and Visualize Alternative Splicing and Isoform Switches with Functional Consequences from both short- and long-read RNA-seq data.
Identify, Annotate and Visualize Alternative Splicing and Isoform Switches with Functional Consequences from both short- and long-read RNA-seq data.
Identify Different Architectures of Sequence Elements
Identify genes associated with multiple expression phenotypes in single-cell CRISPR screening data
Identify genes associated with multiple expression phenotypes in single-cell CRISPR screening data
ILoReg enables high-precision cell population identification from scRNA-Seq data
Import and summarize transcript-level estimates for transcript- and gene-level analysis
Import and summarize transcript-level estimates for transcript- and gene-level analysis
Improving replicability in single-cell RNA-Seq cell type discovery
Improving replicability in single-cell RNA-Seq cell type discovery
Infer Copy Number Variation from Single-Cell RNA-Seq Data
Infer Copy Number Variation from Single-Cell RNA-Seq Data
Infer Copy Number Variation from Single-Cell RNA-Seq Data
Inferring the Tree of Cells
Infers biological signatures from gene expression data
In-Silico Annotation of Doublets for Single Cell RNA Sequencing Data
In-Silico Annotation of Doublets for Single Cell RNA Sequencing Data
Integrating Cap Enrichment with Transcript Expression Analysis
Integrating Cap Enrichment with Transcript Expression Analysis
Integrative Pathway Analysis with Modern PCA Methodology and Gene Selection
Integrative Pathway Analysis with Modern PCA Methodology and Gene Selection
Interactive SummarizedExperiment Explorer
Interactive SummarizedExperiment Explorer
Interactive SummarizedExperiment Explorer
Interactive SummarizedExperiment Explorer
Interactive visualization of scRNA-seq data with Cerebro
Interpretable marker-based single-cell pseudotime using Bayesian parametric models
Interpretable marker-based single-cell pseudotime using Bayesian parametric models
iSEE Universe
iSEE Universe
iSEE Universe
KnowSeq R/Bioc package: Beyond the traditional Transcriptomic pipeline
KnowSeq R/Bioc package: Beyond the traditional Transcriptomic pipeline
Landscape Single Cell Entropy
Learn and Apply Cell Type Signatures
Learn and Apply Cell Type Signatures
Linear Models for Microarray Data
Log fold change distribution tools for working with ratios of counts
Log fold change distribution tools for working with ratios of counts
Long gene expression as a metric for neuronal identity
Mapping Alternative Splicing Events to pRoteins
Mapping Alternative Splicing Events to pRoteins
Maximum Likelihood Decay Modeling of RNA Degradation Data
Maximum Likelihood Decay Modeling of RNA Degradation Data
Methods for Single-Cell RNA-Seq Data Analysis
Methods for Single-Cell RNA-Seq Data Analysis
Michaelis-Menten Modelling of Dropouts in single-cell RNASeq
Michaelis-Menten Modelling of Dropouts in single-cell RNASeq
Michaelis-Menten Modelling of Dropouts in single-cell RNASeq
Mini-batch K-means Clustering for Single-Cell RNA-seq
Mini-batch K-means Clustering for Single-Cell RNA-seq
Minimized Single-Cell Consensus Clustering
Minimized Single-Cell Consensus Clustering
Model-based Analysis of Single Cell Transcriptomics
Model-based Analysis of Single Cell Transcriptomics
Molecular Degree of Perturbation calculates scores for transcriptome data samples based on their perturbation from controls
Molecular Degree of Perturbation calculates scores for transcriptome data samples based on their perturbation from controls
Molecular Degree of Perturbation calculates scores for transcriptome data samples based on their perturbation from controls
Multi-Contrast Gene Set Enrichment Analysis
Multi-Contrast Gene Set Enrichment Analysis
Multi-Contrast Gene Set Enrichment Analysis
Multi Omic Master Regulator Analysis
Multi Omic Master Regulator Analysis
NanoString data normalization and differential gene expression analysis
Network Analysis Supported by Boosting
Network Perturbation Amplitude
Network Perturbation Amplitude
Network smoothing for scRNAseq
Network smoothing for scRNAseq
Object design (S4) for AMARETTO
Omics Longitudinal Differential Analysis
Omics Longitudinal Differential Analysis
ontological exploration of scRNA-seq of 1.3 million mouse neurons from 10x genomics
ontological exploration of scRNA-seq of 1.3 million mouse neurons from 10x genomics
Outlier Analysis for pairwise differential comparison
Outlier Analysis for pairwise differential comparison
Outlier Analysis for pairwise differential comparison
OUTRIDER - OUTlier in RNA-Seq fInDER
OUTRIDER - OUTlier in RNA-Seq fInDER
PCA, PLS(-DA) and OPLS(-DA) for multivariate analysis and feature selection of omics data
PCA, PLS(-DA) and OPLS(-DA) for multivariate analysis and feature selection of omics data
Phenotypic EMD for comparison of single-cell samples
Phenotypic EMD for comparison of single-cell samples
Phenotypic EMD for comparison of single-cell samples
pipeComp pipeline benchmarking framework
Pipeline for augmented co-expression analysis
Pipelines for Bi-Clustering Using Matrix Factorization
Plots and annotation for choosing BrainFlow target probe sequence
Plots and annotation for choosing BrainFlow target probe sequence
PolyA counting and differential transcript usage analysis for scRNA-seq data
Quality Control for Single-Cell RNA-seq Data
Quality Control for Single-Cell RNA-seq Data
Quality Control for Single-Cell RNA-seq Data
Quantify and interpret divers of variation in multilevel gene expression experiments
Quantify and interpret divers of variation in multilevel gene expression experiments
RcisTarget: Identify transcription factor binding motifs enriched on a gene list
RcisTarget: Identify transcription factor binding motifs enriched on a gene list
Reference-Based Single-Cell RNA-Seq Annotation
Reference-Based Single-Cell RNA-Seq Annotation
Reference Index for Cell Types
Regulation Simulator of Interaction between miRNA and Competing RNAs (ceRNA)
Regulation Simulator of Interaction between miRNA and Competing RNAs (ceRNA)
Retrieves Condition-Specific Variants in RNA-Seq Data
Retrieves Condition-Specific Variants in RNA-Seq Data
RiboseQC, a Comprehensive Ribo-Seq Analysis Tool
RNA Centric Annotation System
RNA Centric Annotation System
RNA-seq analysis using multiple algorithms
RNA-seq analysis using multiple algorithms
R package for RIVER (RNA-Informed Variant Effect on Regulation)
R package for RIVER (RNA-Informed Variant Effect on Regulation)
R package for RIVER (RNA-Informed Variant Effect on Regulation)
SAFE-clustering:Single-cell Aggregated (From Ensemble) Clustering for Single-cell RNA-seq Data
SAME: Single-cell RNA-seq Aggregated clustering via Mixture model Ensemble for Single-cell RNA-seq Data
SCANVIS - a tool for SCoring, ANnotating and VISualizing splice junctions
SCANVIS - a tool for SCoring, ANnotating and VISualizing splice junctions
scMerge: Merging multiple batches of scRNA-seq data
scMerge: Merging multiple batches of scRNA-seq data
scRecover for imputation of single-cell RNA-seq data
scRecover for imputation of single-cell RNA-seq data
scRecover for imputation of single-cell RNA-seq data
Selecting transcript model using PRO-seq
Selecting transcript model using PRO-seq
Signature-based Clustering for Diagnostic Purposes
Signature-based Clustering for Diagnostic Purposes
Signature-based Clustering for Diagnostic Purposes
Signature discovery from omics data
Simple Simulation of Single-cell RNA Sequencing Data
Simple Simulation of Single-cell RNA Sequencing Data
Simple Simulation of Single-cell RNA Sequencing Data
Simple Simulation of Single-cell RNA Sequencing Data
Single-cell analysis toolkit for gene expression data in R
Single-Cell Analysis Toolkit for Gene Expression Data in R
Single-Cell Analysis Toolkit for Gene Expression Data in R
Single-Cell Batch Correction Methods
Single-Cell Batch Correction Methods
Single-Cell Consensus Clustering
Single-Cell Consensus Clustering
single-cell higher order testing
single-cell higher order testing
Single Cell Overview of Normalized Expression data
Single Cell Overview of Normalized Expression data
Single cell replicability analysis
Single cell replicability analysis
Single Cell Shiny Application for Analysing Single Cell Transcriptomics Data
Single-cell Targetted Network Inference
Small-Count Analysis Methods for High-Dimensional Data
Small-Count Analysis Methods for High-Dimensional Data
SMNN: Batch Effect Correction for Single-cell RNA-seq data with Supervised Mutual Nearest Neighbor Detection
Sparse Partial Correlations On Gene Expression
Sparse Partial Correlations On Gene Expression
Sparse Partial Correlations On Gene Expression
Spatial Reconstruction of Tissues from scRNA-seq Data
Spatial Transcriptomics Analysis
Spatial Transcriptomics Analysis
ssPATHS: Single Sample PATHway Score
ssPATHS: Single Sample PATHway Score
Suffix Array Kernel Smoothing for discovery of correlative sequence motifs and multi-motif domains
Switch-like differential expression across single-cell trajectories
Switch-like differential expression across single-cell trajectories
text mining for msigdb sets construed as documents
TFutils
TFutils
TFutils
the R package for analyzing expression evolution based on RNA-seq data
Tidy Meta Profiles using Bioconductor and the Tidyverse
Tools for ordering single-cell sequencing
Tools for ordering single-cell sequencing
Tools for spliced gene structure manipulation and analysis
Tools for spliced gene structure manipulation and analysis
Tools to work with a Compendium of 181000 human transcriptome sequencing studies
Tools to work with a Compendium of 181000 human transcriptome sequencing studies
Top Confident Effect Sizes
Top Confident Effect Sizes
trajectory-based differential expression analysis for sequencing data
trajectory-based differential expression analysis for sequencing data
Transcriptional Data Guided fMRI Network Classification
Transcript Quantification Import with Automatic Metadata
Transcript Quantification Import with Automatic Metadata
Translational control assessment from ribosome footprint and total RNA libraries
User Friendly Single-Cell and Bulk RNA Sequencing Visualization
User Friendly Single-Cell and Bulk RNA Sequencing Visualization
User Friendly Single-Cell and Bulk RNA Sequencing Visualization
Utilities for Handling Single-Cell Droplet Data
Utilities for Handling Single-Cell Droplet Data
Varying-Censoring Aware Matrix Factorization
Visual and interactive gene expression analysis
Visual and interactive gene expression analysis
Visual and interactive gene expression analysis
Visual Exploration of Omic Datasets Using a Shiny App
Visual Exploration of Omic Datasets Using a Shiny App
Visual Exploration of Omic Datasets Using a Shiny App
Weighted matrix manipulation, finding components of variation with weighted or sparse data
Weighted matrix manipulation, finding components of variation with weighted or sparse data
What the Package Does TODOELI
Zero-Inflated Negative Binomial Model for RNA-Seq Data
Zero-Inflated Negative Binomial Model for RNA-Seq Data