rsem
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public |
RSEM is a software package for estimating gene and isoform expression levels from RNA-Seq data.
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2024-12-16 |
bamcmp
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public |
Tools for deconvolving host and graft reads using full-length alignments and their scores.
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2024-12-16 |
dna-nn
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public |
Model and predict short DNA sequence features with neural networks.
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2024-12-16 |
pasa
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public |
PASA, acronym for Program to Assemble Spliced Alignments (and pronounced 'pass-uh'), is a eukaryotic genome annotation tool that exploits spliced alignments of expressed transcript sequences to automatically model gene structures, and to maintain gene structure annotation consistent with the most recently available experimental sequence data. PASA also identifies and classifies all splicing variations supported by the transcript alignments.
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2024-12-16 |
nextpolish2
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public |
Repeat-aware polishing genomes assembled using HiFi long reads.
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2024-12-16 |
namfinder
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public |
Finds Non-overlapping Approximate Matches (NAMs) between query and reference sequences using strobemers
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2024-12-16 |
bioconductor-rhdf5lib
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public |
hdf5 library as an R package
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2024-12-16 |
seshat
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public |
Tools for programmatically annotating VCFs with the Seshat TP53 database.
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2024-12-16 |
sentieon
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public |
Accelerated performance bioinformatics tools for mapping and variant calling
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2024-12-16 |
sylph
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public |
sylph quickly enables querying of genomes against even low-coverage shotgun metagenomes to find nearest neighbour ANI.
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2024-12-16 |
ms-entropy
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public |
This package provides a Python implementation of calculating spectral entropy, entropy similarity, and Flash entropy search for mass spectrometry data.
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2024-12-16 |
purge_dups
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public |
Purge_dups is a package used to purge haplotigs and overlaps in an assembly based on read depth
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2024-12-16 |
edta
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public |
Extensive de-novo TE Annotator
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2024-12-16 |
bioconductor-iterativebma
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public |
The Iterative Bayesian Model Averaging (BMA) algorithm
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2024-12-16 |
bioconductor-generecommender
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public |
A gene recommender algorithm to identify genes coexpressed with a query set of genes
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2024-12-16 |
paf2chain
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public |
convert PAF format to CHAIN format
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2024-12-16 |
bioconductor-subseq
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public |
Subsampling of high-throughput sequencing count data
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2024-12-16 |
softsv
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public |
SoftSV is a tool for the detection of small and large deletions, inversions, tandem duplications and translocations from paired-end sequencing data.
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2024-12-16 |
bioconductor-geneclassifiers
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public |
Application of gene classifiers
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2024-12-16 |
bioconductor-rols
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public |
An R interface to the Ontology Lookup Service
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2024-12-16 |
bioconductor-specond
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public |
Condition specific detection from expression data
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2024-12-16 |
megadepth
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public |
Megadepth is an efficient tool for extracting coverage related information from RNA and DNA-seq BAM and BigWig files. It supports reading whole-genome coverage from BAM files and writing either indexed TSV or BigWig files, as well as efficient region coverage summary over intervals from both types of files.
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2024-12-16 |
bioconductor-pandar
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public |
PANDA Algorithm
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2024-12-16 |
wiggletools
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public |
The WiggleTools package allows genomewide data files to be manipulated as numerical functions, equipped with all the standard functional analysis operators (sum, product, product by a scalar, comparators), and derived statistics (mean, median, variance, stddev, t-test, Wilcoxon's rank sum test, etc).
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2024-12-16 |
bioconductor-coveb
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public |
Empirical Bayes estimate of block diagonal covariance matrices
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2024-12-16 |
superstr
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public |
A lightweight, alignment-free utility for detecting repeat-containing reads in short-read WGS, WES and RNA-seq data.
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2024-12-16 |
bioconductor-rmagpie
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public |
MicroArray Gene-expression-based Program In Error rate estimation
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2024-12-16 |
cyvcf2
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public |
A cython wrapper around htslib built for fast parsing of Variant Call Format (VCF) files
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2024-12-16 |
bioconductor-a4core
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public |
Automated Affymetrix Array Analysis Core Package
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2024-12-16 |
expansionhunter
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public |
A tool for estimating repeat sizes
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2024-12-16 |
bioconductor-normalize450k
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public |
Preprocessing of Illumina Infinium 450K data
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2024-12-16 |
bioconductor-ecolitk
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public |
Meta-data and tools for E. coli
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2024-12-16 |
dicey
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public |
In-silico PCR and variant primer design
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2024-12-16 |
bioconductor-reactomegsa
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public |
Client for the Reactome Analysis Service for comparative multi-omics gene set analysis
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2024-12-16 |
cvlr
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public |
Clustering and Visualization of Long Reads
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2024-12-16 |
bioconductor-biodist
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public |
Different distance measures
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2024-12-16 |
ngslca
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public |
ngsLCA: fast and flexible taxonomic classification of DNA reads aligned to reference databases
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2024-12-16 |
r-mgsz
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public |
Performs gene set analysis based on GSZ scoring function and asymptotic p-value. It is different from GSZ in that it implements asymptotic p-values instead of empirical p-values. Asymptotic p-values are calculated by fitting suitable distribution model to the null distribution. Unlike empirical p-values, resolution of asymptotic p-values are independent of the number of permutations and hence requires considerably fewer permutations. In addition, this package allows gene set analysis with seven other popular gene set analysis methods.
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2024-12-16 |
vcfdist
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public |
vcfdist: benchmarking phased germline variant calls in VCF format
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2024-12-16 |
leviosam
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public |
lift-over of alignments for variant-aware references
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2024-12-16 |
hecatomb
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public |
Hecatomb: and end-to-end platform for viral metagenomics
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2024-12-16 |
mashpit
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public |
Sketch-based surveillance platform.
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2024-12-16 |
bioconductor-progeny
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public |
Pathway RespOnsive GENes for activity inference from gene expression
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2024-12-16 |
ataqv
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public |
ataqv is a toolkit for measuring and comparing ATAC-seq results. It was written to help understand how well ATAC-seq assays have worked, and to make it easier to spot differences that might be caused by library prep or sequencing.
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2024-12-16 |
bioconductor-plpe
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public |
Local Pooled Error Test for Differential Expression with Paired High-throughput Data
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2024-12-16 |
bioconductor-bayesknockdown
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public |
BayesKnockdown: Posterior Probabilities for Edges from Knockdown Data
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2024-12-16 |
methpipe
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public |
A pipeline for analyzing DNA methylation data from bisulfite sequencing.
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2024-12-16 |
bioconductor-river
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public |
R package for RIVER (RNA-Informed Variant Effect on Regulation)
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2024-12-16 |
samtools
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public |
Tools for dealing with SAM, BAM and CRAM files
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2024-12-16 |
bioconductor-mipp
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public |
Misclassification Penalized Posterior Classification
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2024-12-16 |