AlphaGenome
Research AI model / method · Research code or publication
Predicts genomic regulatory tracks and predicted functional effects of noncoding DNA variants.
Google DeepMind
Loading BioAtlas...
Loading BioAtlas...
Trouvez des modèles, des logiciels de recherche, des outils de support et du matériel. Utilisez des filtres pour le type d’entrée, le mode d’accès ou le rôle de l’IA.
28 produits correspondants · 28 produits sur la page 1. Les filtres s'appliquent à l'ensemble du catalogue.
Research AI model / method · Research code or publication
Predicts genomic regulatory tracks and predicted functional effects of noncoding DNA variants.
Google DeepMind
Classical/statistical scientific method · Confirm distribution and exact release
bcftools — germline-small-variant-calling / variant-calling
Research / method authors
Source-scoped research method · Confirm distribution and exact release
CADD — missense-pathogenicity-prioritization / regulatory-variant-prioritization
Research / method authors
Source-scoped research method · Confirm distribution and exact release
EVE — missense-pathogenicity-prioritization
Research / method authors
Classical/statistical scientific method · Confirm distribution and exact release
GATK HaplotypeCaller — germline-small-variant-calling / variant-calling
Research / method authors
Classical/statistical scientific method · Confirm distribution and exact release
GATK Mutect2 — somatic-small-variant-calling
Research / method authors
Source-scoped research method · Confirm distribution and exact release
Pangolin — splice-site-effect-prediction
Research / method authors
Source-scoped research method · Confirm distribution and exact release
REVEL — missense-pathogenicity-prioritization
Research / method authors
Open Source Model · Open Source
7-billion parameter long-context genomic transformer predicting and generating whole operons and plasmids
Arc Institute & Stanford University
AI Model · Open Source
Bi-directional state space model for long-range DNA sequence modeling
Stanford University & Princeton University
AI Model & Database · Open Access for Research
3D deep learning for human rare disease and clinical variant interpretation
Illumina Artificial Intelligence Lab
AI Model & Database · Open Access (Research)
Catalog of 71 million human missense mutations classified for clinical pathogenicity
Google DeepMind
Software Tool · Open Source
Transformer-based neural consensus caller for Pacific Biosciences HiFi sequencing
Google Health & PacBio
AI Model · Open Source
Long-range genomic foundation model handling context lengths up to 1 million base pairs
Stanford University (Hazy Research)
Research software / framework · Public code / project terms
Prediction of RNA-seq coverage from DNA sequence
Calico / Borzoi authors
Research software / framework · Public code / project terms
Base-resolution neural modeling of functional genomics
Kundaje laboratory
Research software / framework · Public code / project terms
Bias-aware deep learning of chromatin accessibility
Kundaje laboratory
Research software / model · Public code / project terms
Neural prediction of regulatory activity from sequence
Calico / Basenji contributors
Research software / model · Public code / project terms
Multi-species DNA sequence representation learning
MAGICS Lab / DNABERT-2 authors
Research software / model · Public code / project terms
Sequence-based prediction of gene-regulatory signals
Google DeepMind
Research software / model · Public code / project terms
Long-context DNA language modeling
Arc Institute / Evo contributors
Research software / model · Public code / project terms
Foundation models for genomic sequence representation
InstaDeep and collaborators
Research software / model · Public code / project terms
Deep-learning prediction of splice-altering variants
Illumina
Research software / framework · Public code
Basecalling for Oxford Nanopore sequencing
Oxford Nanopore Technologies
Research software / framework · Public code
Neural consensus polishing for nanopore data
Oxford Nanopore Technologies
Research software / framework · Public code
Deep-learning long-read variant calling
HKU BAL / Clair3 contributors
