Simple simulation of single-cell RNA sequencing data
PyChem-Pro: 100% Python API, fast, flexible & programmable molecular viewer - 2D and 3D, molecular docking pose viewer, cheminformatics library, molec...
A universal toolkit for upstream processing of long RNA reads
Nature Communications | BASALT (Binning Across a Series of Assemblies Toolkit) for binning and refinement of short- and long-read sequencing data
A collection of scripts and notes related to genomics and bioinformatics
Clone with Python! Data structures for double stranded DNA & simulation of homologous recombination, Gibson assembly, cut & paste cloning.
goleft is a collection of bioinformatics tools distributed under MIT license in a single static binary
Metadata and website for the Open Bio Ontologies Foundry Ontology Registry
Ten Quick Tips for Deep Learning in Biology
Fast alignment and preprocessing of chromatin profiles
:rocket: A sequencing simulator
:package: :whale: Dockerfiles and documentation on tools for public health bioinformatics
A framework for state-of-the-art pre-trained bio foundation models on genomics and transcriptomics modalities.
R package for the analysis of massive SNP arrays.
Earl Grey: A fully automated TE curation and annotation pipeline
Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Application and Python module for average nucleotide identity analyses of microbes.
CodonTransformer (2M+ Downloads); The tool for codon optimization, optimizing DNA for protein expression
INDRA (Integrated Network and Dynamical Reasoning Assembler) is an automated model assembly system interfacing with NLP systems and databases to colle...
Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
A fully reproducible and state-of-the-art ancient DNA analysis pipeline
Clustering scRNAseq by genotypes
Bioinformatics Workbook repository
MetaEuk - sensitive, high-throughput gene discovery and annotation for large-scale eukaryotic metagenomics
Constructing a pangenome gene graph
TOGA (Tool to infer Orthologs from Genome Alignments): implements a novel paradigm to infer orthologous genes. TOGA integrates gene annotation, inferr...
PhysiCell: Scientist end users should use latest release! Developers please fork the development branch and submit PRs to the dev branch. Thanks!
🔬 Bioinformatics Notebook. Scripts for bioinformatics pipelines, with quick start guides for programs and video demonstrations.
课题组每周研讨会
Differential expression analysis for single-cell RNA-seq data.
A structural variation pipeline for short-read sequencing
Tutorials on machine learning, artificial intelligence, data science with math explanation and reusable code (in python and R)
Fast indexing and search of discontinuous motifs in protein structures
Aligns short reads using dynamic seed size with strobemers
Scans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
Population-scale genotyping using pangenome graphs
C-library for calculating Solvent Accessible Surface Areas
Make Picrust2 Output Analysis and Visualization Easier
CLI tool for flexible and fast adaptive sampling on ONT sequencers
viral-ngs: command line tools and wrappers for processing raw viral genomic data
MSA(Multiple Sequence Alignment) visualization python package for sequence analysis
Work with bioinformatic files using Arrow, Polars, and/or DuckDB
A Python library for Gene–environment interaction analysis via deep learning
tools for working with Bisulfite Sequencing data while preserving reads intrinsic dependencies
Genomic interval operations on Pandas DataFrames
AWS for Bioinformatics Researchers
The uncompromising Snakemake code formatter
Compressing protein structures effectively with torsion angles
A visualization grammar and GPU-accelerated toolkit for genomic data
chromatin Variability Across Regions (of the genome!)