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openASO is a project designed to identify regulatory regions of an RNA that can be targeted by antisense oligonucleotides.

HTML 9 4 Updated Sep 30, 2021
Python 11 3 Updated Jul 2, 2024

Meditron is a suite of open-source medical Large Language Models (LLMs).

Python 2,041 196 Updated Apr 10, 2024
Python 42 2 Updated Sep 10, 2024

Alleloscope is a method for allele-specific copy number estimation that can be applied to single cell DNA and ATAC sequencing data (separately or in combination). Allele-specific estimation allows …

R 29 6 Updated Mar 10, 2023

counTR is a method to detect differential tandem repeat content between different groups of sequencing data

Python 1 1 Updated Mar 17, 2025

A library and tool for accessing remote BLOW5 files.

C 24 Updated Oct 9, 2024

Python application to generate self-contained pages embedding IGV visualizations, with no dependency on original input files.

Python 369 58 Updated Jun 17, 2025

A single-cell analysis toolkit to jointly analyze samples from distinct conditions

Python 31 Updated Apr 2, 2025

Official implementation for HyenaDNA, a long-range genomic foundation model built with Hyena

Assembly 700 100 Updated Apr 22, 2025

An m6A-aware basecalling model to detect m6A modifications at single nucleotide resolution in individual reads (Cruciani, Delgado-Tejedor, Pryszcz et al., BioRxiv 2023)

Jupyter Notebook 16 2 Updated Feb 25, 2025

RNA-seq prediction with deep convolutional neural networks.

Python 170 22 Updated Jun 10, 2025

Pipeline for generating reference and perturbed sequences for input into predictive models.

Jupyter Notebook 11 8 Updated Nov 15, 2024

Genomic Pre-trained Network

Jupyter Notebook 271 41 Updated Mar 30, 2025
Jupyter Notebook 89 19 Updated Oct 9, 2024

DeepSomatic is an analysis pipeline that uses a deep neural network to call somatic variants from tumor-normal and tumor-only sequencing data.

173 20 Updated May 17, 2025

Analyzing and visualizing KEGG information using the grammar of graphics

R 231 16 Updated Mar 29, 2025

Interactive multiscale visualization for structural variation in human genomes

TypeScript 70 7 Updated Jun 26, 2025

ILIAD: A suite of automated Snakemake workflows for processing genomic data for downstream applications

Python 28 2 Updated Dec 12, 2023

Small variant, structural variant, and short tandem repeat phasing tool for PacBio HiFi reads

Rust 76 4 Updated Mar 27, 2025

Additional themes, scales, and geoms for ggplot2

R 1,332 226 Updated Feb 14, 2024
Jupyter Notebook 16 1 Updated Sep 1, 2023

SHEPHERD: Few shot learning for phenotype-driven diagnosis of patients with rare genetic diseases

HTML 60 20 Updated Jul 1, 2025

TxGNN: Zero-shot prediction of therapeutic use with geometric deep learning and clinician centered design

Jupyter Notebook 213 50 Updated May 6, 2024

Pindel can detect breakpoints of large deletions, medium sized insertions, inversions, tandem duplications and other structural variants at single-based resolution from next-gen sequence data. It u…

C 3 1 Updated Feb 28, 2024

Spatially Resolved Gene Expression Prediction from H&E Histology Images via Bi-modal Contrastive Learning

Python 79 13 Updated Oct 22, 2024

molecular plots in Jupyter, powererd by Blender Geometry Nodes

Jupyter Notebook 55 8 Updated Mar 27, 2024

PyMOL-wasm port's binary and html/javascript code

HTML 26 1 Updated Nov 3, 2023
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