8000 lucventurini (Luca Venturini) / Starred · GitHub
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Jupyter Notebook 37 9 Updated Sep 29, 2026

Highly cited and useful papers related to machine learning, deep learning, AI, game theory, reinforcement learning

2,968 801 Updated Feb 18, 2023

Genomics Extension for SQLite

C++ 171 12 Updated Nov 10, 2026

The labyrinth king judges your gene models.

Python 10 Updated Apr 30, 2026

Genome scaffolding based on HiC data in heterozygous and high ploidy genomes

Jupyter Notebook 60 13 Updated Oct 28, 2026

Fast and flexible ORF finder

Python 84 10 Updated Jan 17, 2022

Mikado is a lightweight Python3 pipeline whose purpose is to facilitate the identification of expressed loci from RNA-Seq data and to select the best models in each locus.

Python 6 2 Updated Mar 15, 2021

Wavefront alignment algorithm (WFA): Fast and exact gap-affine pairwise alignment

C 199 15 Updated Mar 8, 2022

Deep learning infrastructure for genomics

Jupyter Notebook 258 34 Updated Sep 29, 2021

Monet: An open-source Python package for analyzing scRNA-Seq data using PCA-based latent spaces

Python 41 10 Updated Sep 17, 2021

Statistical power studies for multi-omics experiments.

R 35 10 Updated Jan 18, 2025

Awesome free machine learning and AI courses with video lectures.

3,118 318 Updated Dec 12, 2024

PacBio BAM C++ library

C++ 20 17 Updated Aug 14, 2023
Rust 58 3 Updated Aug 11, 2022

oushujun / EDTA

Extensive de-novo TE Annotator

Perl 474 94 Updated Nov 11, 2026

Ultrafast GPU-enabled QTL mapper

Python 221 68 Updated Jun 29, 2025

Coding Genome Reconstruction using Iso-Seq data

Python 60 17 Updated Oct 20, 2021

A collection of various deep learning architectures, models, and tips

Jupyter Notebook 17,635 4,090 Updated Sep 26, 2026

A package which efficiently applies any function to a pandas dataframe or series in the fastest available manner

Python 2,630 104 Updated Mar 20, 2024

Clair: Exploring the limit of using deep neural network on pileup data for germline variant calling

Python 105 12 Updated Sep 1, 2022

fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing

Nim 880 108 Updated Oct 29, 2026

HiCExplorer is a powerful and easy to use set of tools to process, normalize and visualize Hi-C data.

C++ 282 76 Updated Nov 10, 2026

Graph-based mapping of long sequences, noisy or HiFi.

Perl 55 2 Updated Oct 5, 2020

De novo clustering of long transcript reads into genes

Python 83 9 Updated Oct 2, 2026

Ultrafast consensus module for raw de novo genome assembly of long uncorrected reads

C++ 244 34 Updated Dec 29, 2023

SUPPA: Fast quantification of splicing and differential splicing

Python 307 62 Updated Nov 6, 2025

Transcript assembly and quantification for RNA-Seq

C++ 536 91 Updated Nov 11, 2026

De novo assembler for single molecule sequencing reads using repeat graphs

C 956 193 Updated Apr 3, 2026

Genome assembly soft-masking using Red (REpeat Detector)

Python 18 4 Updated Dec 7, 2018

Open workflow definitions for genomic analysis from MGI at WUSM.

Common Workflow Language 107 55 Updated Jun 23, 2025
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