AlphaFold
DeepMind's protein-structure prediction system, with open AlphaFold 2 code and a public database of predicted structures.
RESEARCH CATEGORY
Work with biological data, proteins, and medical imaging. The database currently includes 78 tools, models, databases, or infrastructure entries in this category.
DeepMind's protein-structure prediction system, with open AlphaFold 2 code and a public database of predicted structures.
A cloud platform for biotechnology research that combines electronic lab records, sequence tools, and research data management.
An open-source Python library for applying machine learning to drug discovery, quantum chemistry, biology, and materials problems.
A collection of frameworks, models, and deployment tools for generative AI in biomolecular and drug research.
A trainable open-source implementation of AlphaFold 2 intended for protein-structure research and model development.
An open-source workflow that combines accelerated sequence search with AlphaFold-based structure prediction.
NCBI sequence-search tools for finding local similarity between nucleotide or protein queries and sequence databases.
An open web platform for running, documenting, and sharing reproducible computational biology workflows.
Open-source software for building pipelines that measure cellular and other biological features in microscopy images.
An open-source framework built on PyTorch for developing and deploying deep-learning workflows in medical imaging.
An open-source Python toolkit for computational biology, including sequence, structure, database, and file-format operations.
An open-source Python toolkit for preprocessing, reducing, clustering, and visualizing single-cell gene-expression data.
An open-source Python package that provides probabilistic generative models and a shared interface for single-cell omics.
An open-source workflow system for portable and scalable computational pipelines, widely used in bioinformatics.
An open-source workflow manager that expresses analysis steps and their dependencies as rules.
A community project that maintains Nextflow pipelines under shared development, testing, and release practices.
An open-source pipeline that uses a deep neural network to call genetic variants from aligned sequencing reads.
Open-source deep-learning software for segmenting cells and other objects in microscopy images.
An open-source desktop application for interactive machine-learning workflows such as pixel and object classification.
An open-source Python viewer for inspecting, annotating, and analyzing multidimensional scientific images.
Open-source desktop software for digital pathology and whole-slide image analysis.
A distribution of ImageJ bundled with plugins and update sites for scientific image analysis, especially in life sciences.
An open platform for managing, viewing, sharing, and analyzing microscopy images with their metadata.
An open-source R package for quality control, analysis, integration, and visualization of single-cell transcriptomic data.
An open bioinformatics software ecosystem built around R, with analysis, annotation, experiment-data, and workflow packages.
An open-source genomics toolkit from the Broad Institute focused on variant discovery, genotyping, and related sequencing-data processing.
Open-source software that uses a deep neural network to call somatic variants from tumor-normal or tumor-only sequencing data.
An open-source splice-aware aligner designed for RNA sequencing reads.
An open-source command-line tool for estimating transcript abundance from RNA-seq data using selective alignment or sketching methods.
An open-source tool that uses pseudoalignment to estimate transcript abundance from bulk or single-cell RNA-seq data.
An open-source Python framework for scalable genomic data analysis across local, cloud, and Spark environments.
An open-source command-line toolset for genome-wide association studies, genotype quality control, and population-genetic analysis.
An open-source command-line suite for reading, converting, sorting, indexing, and summarizing SAM, BAM, and CRAM alignment files.
An open-source tool that aggregates outputs from many bioinformatics programs and samples into a unified quality-control report.
A set of 10x Genomics pipelines for processing Chromium single-cell data, including barcode handling, UMI counting, and selected immune-receptor analyses.
An open-source command-line suite for manipulating, querying, filtering, summarizing, and calling variants in VCF, BCF, and gVCF data.
An open-source Ensembl tool that annotates the potential consequences of genomic variants on transcripts, proteins, and regulatory regions.
An open research resource providing vertebrate genomes, gene annotation, comparative genomics, and variation data through browsers and programmatic interfaces.
A public knowledgebase that integrates protein sequences, functional information, and cross-references, with both reviewed and computationally annotated records.
A public resource that integrates protein signatures from member databases to classify families and identify domains and functional sites.
An open-source genome viewer for interactively examining sequencing, variation, annotation, and other data positioned on reference genomes.
Open-source deep-learning software for instance segmentation of approximately star-convex objects in two- and three-dimensional microscopy images.
Extensible open-source desktop software for displaying, processing, measuring, and analyzing scientific images.
Open-source software for controlling automated microscope hardware and running time-lapse, multichannel, and z-stack acquisitions.
An open-source Python tool for spatial molecular data analysis, including neighborhood graphs, spatial statistics, and tissue-image integration.
An open-source data framework, schema, and serialization format for representing, transforming, and querying uni- and multimodal spatial omics data.
An open-source command-line program that integrates convolutional-neural-network scoring and ligand optimization into molecular docking.
An open-source PyTorch toolbox for graph representation learning in drug discovery, with components for molecules, proteins, reactions, and knowledge graphs.
An open research resource and Python package providing therapeutic machine-learning tasks, datasets, evaluation functions, benchmarks, and leaderboards.
An open-source deep-learning toolkit for drug-target interaction, molecular-property, and related biomedical prediction tasks.
Open-source high-performance software for molecular-dynamics simulation, energy minimization, and trajectory analysis.
A free research service for submitting protein-small-molecule docking jobs through a web interface and examining candidate poses.
A free web tool that calculates molecular descriptors and predicts selected ADME, pharmacokinetic, and drug-likeness properties.
An open-source family of models and inference software for biomolecular complex structure and selected binding-affinity predictions.
Open-source research code and model weights for diffusion-based generation of protein backbones, motif scaffolds, and symmetric structures.
Proprietary modular software for visualizing, segmenting, tracking, and quantitatively measuring two- to four-dimensional microscopy images.
A proprietary digital-pathology platform for quantitative analysis of whole-slide images through configurable tissue, cell, and biomarker modules.
A proprietary platform for visualizing, segmenting, tracking, and phenotyping two- to five-dimensional microscopy images.
Proprietary software for visualizing, segmenting, and building repeatable analysis pipelines for large two-, three-, and four-dimensional microscopy datasets.
Open-source software for checking raw high-throughput sequencing data and producing modular plots, tables, and HTML reports.
An open-source command-line tool for quality control and preprocessing of short-read FASTQ data, including filtering, trimming, and HTML or JSON reporting.
An open-source tool that finds and removes specified adapters, primers, poly-A tails, and other unwanted sequences from high-throughput sequencing reads.
A cross-platform open-source command-line toolkit for querying, transforming, summarizing, sampling, and indexing FASTA and FASTQ files.
An open-source aligner for mapping DNA or mRNA sequences to a reference, with modes for long reads, short reads, spliced transcripts, and assembly comparison.
An open-source FM-index aligner for mapping sequencing reads to long reference sequences in local, end-to-end, gapped, and paired-end modes.
An open-source command-line suite for intersecting, merging, comparing, covering, and otherwise analyzing genomic intervals.
An optimized implementation of the BWA-MEM algorithm for aligning short-read DNA sequencing data to a reference genome and producing SAM output.
An open-source sequence aligner built on hierarchical graph FM indexes, with splice-aware alignment for RNA sequencing reads against genomes or transcript sets.
An open-source command-line suite for filtering, summarizing, and converting genetic-variant data in VCF format.
An open-source variant annotation program that predicts gene-, transcript-, and protein-level consequences using a selected genome annotation database.
An open-source Python toolkit for inferring and visualizing copy-number variation from targeted, exome, or whole-genome sequencing data.
An open-source Python toolkit for estimating RNA velocity, latent time, and transcriptional dynamics from spliced and unspliced counts in single-cell transcriptomic data.
An open-source R toolkit for clustering, trajectory reconstruction, pseudotime ordering, and differential analysis of single-cell RNA sequencing data.
An open-source Python tool that uses logistic-regression classifiers and built-in or custom reference models to predict cell types in single-cell RNA sequencing data.
An open-source biomedical image-segmentation framework that adapts preprocessing, U-Net configuration, training, and inference to a dataset.
An open-source deep-learning toolbox for markerless estimation of user-defined animal or object keypoints from video.
An open-source desktop application for navigating, annotating, and segmenting three-dimensional medical images through manual and semi-automatic methods.
An open-source cross-platform bioinformatics suite that combines sequence viewing, alignment, annotation, phylogenetics, and visual workflows.