A flexible Nextflow-based framework for the definition of sequencing data processing pipelines
an R/Shiny application for interactive creation of non-circular plots of whole genomes
Afternotes for the attended courses at Ca' Foscari University, master in Data Management and Analytics.
A fast constructor of the compressed de Bruijn graph from many genomes
Fast calculations of linkage-disequilibrium in large-scale human cohorts
Fast and Versatile Alignments for Python
Gene Expression Omnibus Analysis with Shiny :microscope:
Examples using Clustergrammer2 to explore high-dimensional datasets.
Benchmarking common tasks on proteins in various languages and packages
Biological Engineering Test Code for Worm Analysis: https://stackoverflow.com/q/37820629/293195
⛰ covtobed | Convert the coverage track from a BAM file into a BED file
Eyes on your (genomic) data
Viral infection diagnostics using next-generation sequencing
SINA - Reference based multiple sequence alignment
Digital Expression Explorer 2 (DEE2): a repository of uniformly processed RNA-seq data
Efficiently keep track of changes to genomes
SARS-CoV-2 workflow for nanopore sequence data
TEsorter: an accurate and fast method to classify LTR-retrotransposons in plant genomes
[DEPRECATED, see https://immunarch.com/] tcR: an R package for immune receptor repertoire advanced data analysis.
💧Bionode-Watermill: A (Not Yet Streaming) Workflow Engine
Htmlwidgets binding R commands to the BioCircos.js library
Go / Golang Bioinformatics Library
StochPy is a versatile stochastic modeling package which is designed for stochastic simulation of molecular control networks
An open-source, cloud-ready web application for simplified deployment of big data workflows.
Genomic neighbor typing of bacterial pathogens using MinHash :rat:
For live demo, see http://lh3lh3.users.sourceforge.net/bioseq.shtml
Bioinformatics tool outputs converter to JSON or YAML
:hatching_chick: locally query the ncbi taxonomy
An attempt to help anyone interested in using Perl for Bioinformatics
An opinionated Cromwell orchestration manager.
Predict plasmids from uncorrected long read data
Deprecated see https://github.com/MHH-RCUG/nf_wochenende : A whole Genome/Metagenome Sequencing Alignment Pipeline in Python3
Next-Gen Sequencing tools from the Horvath Lab
OmicSelector - Environment, docker-based application and R package for biomarker signiture selection (feature selection) & deep learning diagnostic to...
Elastic, reproducible, and reusable genomic data science tools from R backed by cloud resources
Datastructures and algorithms for working with genetic variation
Curation and analysis of metabolic models
Repositório do grupo de estudo de Bioinformática da rede de comunidades das PyLadies Brasil.
An Artificial Neural Network-based discriminator for validating clinically significant genomic variants
A web based visualization tool for process description maps in SBGN
2017_2018 single cell RNA sequencing Workshop UCD_UCB_UCSF
An experimental tool to estimate the similarity between all pairs of contigs
simple viewer for variant call format using htslib
Tokenization, sentence segmentation, POS tagging and dependency parsing for biomedical texts (BMC Bioinformatics 2019)
A simplified pipeline for ctDNA sequencing data analysis
DCC uses output from the STAR read mapper to systematically detect back-splice junctions in next-generation sequencing data. DCC applies a series of f...
Seven Bridges API Client, CWL Schema, Meta Schema, and SDK Helper in R
Data visualization library for creating interactive graphs and dashboards for bioinformatics etc.
the z in bioinformatics
R wrappers to connect Python dimensional reduction tools and single cell data objects (Seurat, SingleCellExperiment, etc...)