bioconductor-genomicdatacommons
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public |
NIH / NCI Genomic Data Commons Access
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2024-12-19 |
bioconductor-gdrstyle
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public |
A package with style requirements for the gDR suite
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2024-12-19 |
bioconductor-nanostringnctools
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public |
NanoString nCounter Tools
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2024-12-19 |
bioconductor-loci2path
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public |
Loci2path: regulatory annotation of genomic intervals based on tissue-specific expression QTLs
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2024-12-19 |
bioconductor-tfarm
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public |
Transcription Factors Association Rules Miner
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2024-12-19 |
bioconductor-target
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public |
Predict Combined Function of Transcription Factors
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2024-12-19 |
bioconductor-brain
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public |
Baffling Recursive Algorithm for Isotope distributioN calculations
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2024-12-19 |
fraggenescan
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public |
FragGeneScan is an application for finding (fragmented) genes in short reads.
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2024-12-19 |
r-quilt
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public |
Rapid and accurate genotype imputation from low coverage short read, long read, and cell free DNA sequence.
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2024-12-19 |
mgkit
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public |
Metagenomics Framework
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2024-12-19 |
tinker
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public |
The Tinker molecular modeling software is a complete and general package for molecular mechanics and dynamics, with some special features for biopolymers
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2024-12-19 |
amplicontyper
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public |
Tool for training model and classifying reads from environmental ONT amplicon sequencing.
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2024-12-19 |
mirscore
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public |
miRScore: A rapid and precise microRNA validation tool
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2024-12-19 |
bioconductor-clustall
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public |
ClustAll: Data driven strategy to robustly identify stratification of patients within complex diseases
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2024-12-19 |
bioconductor-bioccheck
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public |
Bioconductor-specific package checks
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2024-12-19 |
hostile
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public |
Hostile: accurate host decontamination
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2024-12-19 |
svtk
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public |
Utilities for consolidating, filtering, resolving, and annotating structural variants.
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2024-12-19 |
bioconductor-crimage
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public |
CRImage a package to classify cells and calculate tumour cellularity
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2024-12-19 |
r-deconcell
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public |
DeconCell is an statitsical framework for generating cell proportions predictive models using bulk expresion data. It currently has pre-calculated models
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2024-12-19 |
bioconductor-spectra
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public |
Spectra Infrastructure for Mass Spectrometry Data
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2024-12-19 |
bioconductor-pvca
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public |
Principal Variance Component Analysis (PVCA)
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2024-12-19 |
ntlink
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public |
Genome assembly scaffolder using long reads and minimizers
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2024-12-19 |
bioconductor-spia
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public |
Signaling Pathway Impact Analysis (SPIA) using combined evidence of pathway over-representation and unusual signaling perturbations
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2024-12-19 |
r-nanostringnorm
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public |
A set of tools for normalizing, diagnostics and visualization of NanoString nCounter data.
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2024-12-19 |
bioconductor-cola
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public |
A Framework for Consensus Partitioning
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2024-12-19 |
bioconductor-doscheda
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public |
A DownStream Chemo-Proteomics Analysis Pipeline
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2024-12-19 |
pygtftk
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public |
The gtftk suite providing facilities to manipulate genomic annotations in gtf format.
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2024-12-19 |
bioconductor-interactivecomplexheatmap
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public |
Make Interactive Complex Heatmaps
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2024-12-19 |
bioconductor-rvs
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public |
Computes estimates of the probability of related individuals sharing a rare variant
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2024-12-19 |
bioconductor-lpnet
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public |
Linear Programming Model for Network Inference
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2024-12-19 |
clair3-trio
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public |
Clair3-Trio is a variants caller tailored for family trios from nanopore long-reads. Clair3-Trio employs a Trio-to-Trio deep neural network model that allows it to input all trio’s sequencing information and output all trio’s predicted variants within a single model, to perform far better variant calling. We also present MCVLoss, the first loss function that can improve variants calling in trios by leveraging the explicitly encoding of the priors of the Mendelian inheritance in trios. Clair3-Trio showed comprehensive improvement in experiments. It predicted much fewer Mendelian inheritance violation variations than current state-of-the-art methods.
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2024-12-19 |
bioconductor-affycontam
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public |
structured corruption of affymetrix cel file data
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2024-12-19 |
ntsynt
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public |
Detecting multi-genome synteny blocks using minimizer graph mapping
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2024-12-19 |
bioconductor-flowdensity
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public |
Sequential Flow Cytometry Data Gating
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2024-12-19 |
bioconductor-optimalflow
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public |
optimalFlow
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2024-12-19 |
bioconductor-rcwlpipelines
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public |
Bioinformatics pipelines based on Rcwl
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2024-12-19 |
tigmint
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public |
Correct misassemblies using linked or long reads
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2024-12-19 |
bioconductor-trio
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public |
Testing of SNPs and SNP Interactions in Case-Parent Trio Studies
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2024-12-19 |
bioconductor-simona
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public |
Semantic Similarity on Bio-Ontologies
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2024-12-19 |
bioconductor-flowtrans
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public |
Parameter Optimization for Flow Cytometry Data Transformation
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2024-12-19 |
ntjoin
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public |
Genome assembly scaffolder using minimizer graphs
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2024-12-19 |
tiny-count
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public |
\ A precision counting tool for hierarchical classification and quantification of small RNA-seq reads. tiny-count is part of the tinyRNA analysis pipeline.
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2024-12-19 |
clair3
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public |
Clair3 is a small variant caller for long-reads. Compare to PEPPER (r0.4), Clair3 (v0.1) shows a better SNP F1-score with ≤30-fold of ONT data (precisionFDA Truth Challenge V2), and a better Indel F1-score, while runs generally four times faster. Clair3 makes the best of both worlds of using pileup or full-alignment as input for deep-learning based long-read small variant calling. Clair3 is simple and modular for easy deployment and integration.
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2024-12-19 |
bioconductor-rexposome
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public |
Exposome exploration and outcome data analysis
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2024-12-19 |
r-conos
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public |
Wires together large collections of single-cell RNA-seq datasets, which allows for both the identification of recurrent cell clusters and the propagation of information between datasets in multi-sample or atlas-scale collections. 'Conos' focuses on the uniform mapping of homologous cell types across heterogeneous sample collections. For instance, users could investigate a collection of dozens of peripheral blood samples from cancer patients combined with dozens of controls, which perhaps includes samples of a related tissue such as lymph nodes. This package interacts with data available through the 'conosPanel' package, which is available in a 'drat' repository. To access this data package, see the instructions at <https://github.com/kharchenkolab/conos>. The size of the 'conosPanel' package is approximately 12 MB.
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2024-12-19 |
bioconductor-cardinalworkflows
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public |
Datasets and workflows for the Cardinal MSI
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2024-12-19 |
bioconductor-ccplotr
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public |
Plots For Visualising Cell-Cell Interactions
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2024-12-19 |
bioconductor-flowmerge
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public |
Cluster Merging for Flow Cytometry Data
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2024-12-19 |
bioconductor-cnorfeeder
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public |
Integration of CellNOptR to add missing links
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2024-12-19 |
bioconductor-ncigraph
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public |
Pathways from the NCI Pathways Database
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2024-12-19 |