aliview
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public |
AliView is an intuitive and fast alignment viewer and editor for DNA and amino acid sequences.
|
2025-03-10 |
cleanifier
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public |
A fast lightweight tool to remove contamination using k-mers.
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2025-03-10 |
severus
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public |
A tool for somatic structural variant calling using long reads
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2025-03-10 |
hmftools-esvee
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public |
Structural variant caller specialised for breakend-breakpoint calling.
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2025-03-10 |
hmftools-linx
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public |
LINX is an annotation, interpretation and visualisation tool for structural variants.
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2025-03-10 |
hmftools-pave
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public |
PAVE annotates SNV/MNV/INDEL calls with consequence on corresponding genes, transcripts, and proteins.
|
2025-03-10 |
r-pathosurveilr
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public |
Utilities for interacting with the pathogensurveillance pipeline.
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2025-03-10 |
grepq
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public |
Quickly filter FASTQ files.
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2025-03-09 |
olivar
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public |
Olivar PCR tiling design
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2025-03-09 |
captus
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public |
Captus: Assembly of Phylogenomic Datasets from High-Throughput Sequencing data
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2025-03-09 |
artic
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public |
ARTIC pipeline - a bioinformatics pipeline for working with virus sequencing data sequenced with nanopore.
|
2025-03-09 |
pybwa
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public |
Pybwa is a python module that makes it easy to align sequence data. It is a lightweight wrapper of bwa.
|
2025-03-08 |
galaxy-data
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public |
The Galaxy models, datatype framework, and datatype implementations.
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2025-03-08 |
galaxy-files
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public |
The Galaxy file sources framework and default plugins.
|
2025-03-08 |
galaxy-objectstore
|
public |
The Galaxy object store framework and default implementations
|
2025-03-08 |
galaxy-schema
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public |
The Galaxy API schema objects.
|
2025-03-08 |
postmaster
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public |
Postmaster is a tool for annotating transcriptome alignments with posterior alignment probabilities derived from salmon quantifications.
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2025-03-08 |
danbing-tk
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public |
Toolkit for VNTR genotyping and repeat-pan genome graph construction
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2025-03-08 |
longbow
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public |
A Python program for nanopore sequencing basecalling configuration prediction
|
2025-03-08 |
miniprot
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public |
Miniprot aligns a protein sequence against a genome with affine gap penalty, splicing and frameshift.
It is primarily intended for annotating protein-coding genes in a new species using known genes from other species.
|
2025-03-08 |
last
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public |
LAST finds & aligns related regions of sequences.
|
2025-03-07 |
gmap
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public |
Genomic mapping and alignment program for mRNA and EST sequences.
|
2025-03-07 |
callingcardstools
|
public |
An API and collection of cmd line tools to work with calling cards sequencing data
|
2025-03-07 |
taxtastic
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public |
Tools for taxonomic naming and annotation
|
2025-03-07 |
r-signac
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public |
A framework for the analysis and exploration of single-cell chromatin data. The 'Signac' package contains functions for quantifying single-cell chromatin data, computing per-cell quality control metrics, dimension reduction and normalization, visualization, and DNA sequence motif analysis. Reference: Stuart and Butler et al. (2019) <doi:10.1016/j.cell.2019.05.031>.
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2025-03-07 |
cctk
|
public |
Tools to identify and compare CRISPR arrays.
|
2025-03-07 |
r-psminer
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public |
Utilities for interacting with the pathogensurveillance pipeline.
|
2025-03-07 |
busco
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public |
Assessment of assembly completeness using Universal Single Copy Orthologs.
|
2025-03-07 |
omark
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public |
OMArk - Proteome quality assesment based on OMAmer placements
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2025-03-07 |
perl-bio-phylo-forest-dbtree
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public |
DBIx::Class-backed, Bio::Phylo-like API for large phylogenies.
|
2025-03-07 |
wfmash
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public |
a pangenome-scale aligner
|
2025-03-07 |
te-aid
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public |
Annotation helper tool for the manual curation of transposable element consensus sequences
|
2025-03-07 |
bioblend
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public |
A Python library for interacting with the Galaxy API.
|
2025-03-07 |
hmftools-cuppa
|
public |
Predict tissue of origin for tumor samples from WGTS data.
|
2025-03-07 |
pegas
|
public |
PeGAS is a Snakemake pipeline for genome analysis
|
2025-03-07 |
snakemake-executor-plugin-kubernetes
|
public |
A snakemake executor plugin for submission of jobs to Kubernetes
|
2025-03-07 |
ebolaseq
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public |
Tool for downloading and analyzing Ebola virus sequences
|
2025-03-07 |
bioconductor-dada2
|
public |
Accurate, high-resolution sample inference from amplicon sequencing data
|
2025-03-07 |
centrifuger
|
public |
Lossless compression of microbial genomes for efficient and accurate metagenomic sequence classification.
|
2025-03-07 |
resistify
|
public |
A resistance gene annotation tool.
|
2025-03-07 |
plannotate
|
public |
Webserver and command line tool for annotating engineered plasmids
|
2025-03-07 |
viroconstrictor
|
public |
ViroConstrictor is a flexible pipeline for analysis of targeted viral sequencing data
|
2025-03-07 |
snp2cell
|
public |
A package for finding enriched regulatory networks from GWAS and single cell data.
|
2025-03-07 |
savana
|
public |
SAVANA: a somatic structural variant caller for long-read data
|
2025-03-07 |
bioconductor-glmgampoi
|
public |
Fit a Gamma-Poisson Generalized Linear Model
|
2025-03-06 |
gmap-fusion
|
public |
GMAP-fusion is a utility for identifying candidate fusion transcripts based on transcript sequences reconstructed via RNA-Seq de novo transcriptome assembly.
|
2025-03-06 |
transdecoder
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public |
TransDecoder identifies candidate coding regions within transcript sequences, such as those generated by de novo RNA-Seq transcript assembly using Trinity, or constructed based on RNA-Seq alignments to the genome using Tophat and Cufflinks.
|
2025-03-06 |
fusion-filter
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public |
FusionFilter provides a common fusion-finding, filtering, and annotation framework for the Trinity Cancer Transcriptome Analysis Toolkit (CTAT).
|
2025-03-06 |
fusion-inspector
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public |
FusionInspector is a component of the Trinity Cancer Transcriptome Analysis Toolkit (CTAT). FusionInspector assists in fusion transcript discovery by performing a supervised analysis of fusion predictions, attempting to recover and re-score evidence for such predictions. - https://github.com/FusionInspector/FusionInspector/wiki
|
2025-03-06 |
flexynesis
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public |
A deep-learning-based multi-omics bulk sequencing data integration suite with a focus on (pre-)clinical endpoint prediction.
|
2025-03-06 |