☆92Nov 19, 2025Updated 4 months ago
Alternatives and similar repositories for PromoterAI
Users that are interested in PromoterAI are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- A deep learning approach to predicting transcription initiation from sequence at single nucleotide resolution☆14Feb 24, 2026Updated last month
- ☆19Jul 28, 2025Updated 7 months ago
- ☆16May 22, 2025Updated 10 months ago
- ☆16Feb 15, 2026Updated last month
- Analyses related to the Borzoi paper.☆25Dec 14, 2025Updated 3 months ago
- DigitalOcean Gradient AI Platform • AdBuild production-ready AI agents using customizable tools or access multiple LLMs through a single endpoint. Create custom knowledge bases or connect external data.
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆92Oct 30, 2025Updated 4 months ago
- RNA-seq prediction with deep convolutional neural networks.☆232Aug 28, 2025Updated 6 months ago
- ☆24Jan 9, 2026Updated 2 months ago
- An online database of variants functionally demonstrated to affect (or not affect) splicing.☆11Mar 20, 2025Updated last year
- Computational Optimization of DNA Activity (CODA)☆67Apr 3, 2025Updated 11 months ago
- ☆11Oct 4, 2021Updated 4 years ago
- An end-to-end computational pipeline for large Perturb-seq screens☆15Apr 25, 2025Updated 11 months ago
- Orthrus is a mature RNA model for RNA property prediction. It uses a mamba encoder backbone, a variant of state-space models specifical…☆90Dec 10, 2025Updated 3 months ago
- ☆41Jun 16, 2025Updated 9 months ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- ☆32Updated this week
- Clinical machine-learning based interpreter of germline mutations.☆11Mar 13, 2025Updated last year
- Machine learning methods for DNA sequence analysis.☆60Feb 27, 2026Updated 3 weeks ago
- deep learning-inspired explainable sequence model for transcription initiation☆103Mar 3, 2025Updated last year
- ☆73Mar 13, 2026Updated last week
- ☆36Feb 20, 2026Updated last month
- Pangolin is a deep-learning method for predicting splice site strengths.☆85Jun 17, 2024Updated last year
- ☆623Mar 13, 2024Updated 2 years ago
- Introme prioritises coding and noncoding splice-altering variants for clinical variant interpretation☆22Dec 18, 2025Updated 3 months ago
- DigitalOcean Gradient AI Platform • AdBuild production-ready AI agents using customizable tools or access multiple LLMs through a single endpoint. Create custom knowledge bases or connect external data.
- scGRO-seq analyses codes☆13Jan 9, 2024Updated 2 years ago
- This pipeline is used to distinguish allotetraploid subgenomes.☆11Apr 8, 2024Updated last year
- Variant Annotation, Segregation and Exclusion for family or cohort based rare-disease sequencing studies.☆12Jun 2, 2022Updated 3 years ago
- This repository hosts a minimal version of a Python API for BPNet.☆55Jan 24, 2026Updated 2 months ago
- exploratory scripts for clustering ccs amplicon data☆11Feb 2, 2021Updated 5 years ago
- (WIP) best-practices workflow for rare disease☆62Jul 1, 2024Updated last year
- Rare Disease variant reanalysis tool☆31Mar 5, 2026Updated 2 weeks ago
- Automated ACMG/AMP classification for human variants associated with congenital hearing loss☆11May 14, 2025Updated 10 months ago
- scripts to automatically update ANNOVAR db☆18Nov 17, 2021Updated 4 years ago
- Virtual machines for every use case on DigitalOcean • AdGet dependable uptime with 99.99% SLA, simple security tools, and predictable monthly pricing with DigitalOcean's virtual machines, called Droplets.
- Transformer-based sequence correction method for genome assembly polishing☆99Mar 11, 2025Updated last year
- This is the official development repository for BaseVar, which call variants for large-scale ultra low-pass (<1.0x) WGS data, especially …☆27Jul 28, 2025Updated 7 months ago
- Flow2Spatial reconstructs spatial proteomics through transfer learning.☆22May 16, 2025Updated 10 months ago
- Tests Allelic Expression data for extreme imbalance w.r.t. population☆11Oct 8, 2021Updated 4 years ago
- Calibrated clustering with artificial variables to avoid over-clustering in single-cell RNA-sequencing☆18Nov 18, 2025Updated 4 months ago
- Genomic Pre-trained Network☆331Updated this week
- Curated list of resources for variant prioritization☆14Nov 18, 2025Updated 4 months ago