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Starred repositories

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Jupyter Notebook 6 1 Updated Nov 16, 2025

Hidden State Speciation and Extinction

R 6 6 Updated Aug 5, 2025

Share, discover, and collect prompts from the community. Free and open source — self-host for your organization with complete privacy.

TypeScript 142,207 18,867 Updated Jan 13, 2026

The second version of the Kraken taxonomic sequence classification system

C++ 858 296 Updated Jan 3, 2026

Effective selection of population size projection for construction of the site frequency spectrum. Convert VCF to dadi/fastsimcoal style SFS for demographic analysis

Python 166 24 Updated Aug 8, 2024

Tools for data handling and analysis in macroecology

R 29 7 Updated Nov 6, 2025

An R package for the calculation of taxonomic, phenotypic and phylogenetic metrics across grid cells.

R 15 3 Updated Aug 20, 2025

Phylogenetic orthology inference for comparative genomics

Python 822 201 Updated Jul 15, 2025

Telomere-to-telomere assembly of accurate long reads (PacBio HiFi, Oxford Nanopore Duplex, HERRO corrected Oxford Nanopore Simplex) and Oxford Nanopore ultra-long reads.

Python 377 34 Updated Jan 8, 2026

C++ API & command-line toolkit for working with BAM data

C++ 429 156 Updated May 18, 2025

Simulators of spatial genetic diversity: for non-programmers and researchers!

C++ 6 Updated Mar 20, 2022

Software to construct and analyse KewTreeOfLife (PAFTOL project)

5 1 Updated Aug 25, 2023

mapping pipeline for ancient DNA

Python 34 5 Updated Jan 2, 2026

A structural variation pipeline for short-read sequencing

Python 200 76 Updated Jan 12, 2026

A Java based tool to determine damage patterns on ancient DNA as a replacement for mapDamage

Java 18 3 Updated Nov 18, 2023

GFF/GTF utility providing format conversions, region filtering, FASTA sequence extraction and more

C++ 450 42 Updated Dec 26, 2024

deep learning prediction of geographic location from individual genome sequences

Python 52 16 Updated Jan 20, 2025

A flexible, scalable, and reproducible pipeline to automate variant calling from raw sequence reads, with lots of bells and whistles - for sampled individuals, and for pool sequencing.

Python 111 24 Updated Jun 24, 2025

Tools to work with variant call format files

R 265 53 Updated Oct 24, 2025

A fully reproducible and state-of-the-art ancient DNA analysis pipeline

Nextflow 195 87 Updated Nov 21, 2025

Pipelines and tools for the processing of ancient and modern HTS data.

Python 48 19 Updated Jan 4, 2026

The next version of bwa-mem

C++ 806 117 Updated Oct 15, 2025

RSEM: accurate quantification of gene and isoform expression from RNA-Seq data

C++ 455 126 Updated Mar 13, 2024

k-mer based assembly evaluation

Shell 335 23 Updated Jun 28, 2024

Transcript assembly and quantification for RNA-Seq

C++ 478 86 Updated Dec 26, 2025

DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

Python 3,592 767 Updated Oct 21, 2025

Aggregate results from bioinformatics analyses across many samples into a single report.

JavaScript 1,405 646 Updated Jan 13, 2026

This repository has teaching materials for a 2 and 3-day Introduction to RNA-sequencing data analysis workshop using the O2 Cluster

HTML 174 90 Updated Mar 23, 2021

R Port of psmc

C 17 4 Updated Mar 16, 2023

iTerm2 is a terminal emulator for Mac OS X that does amazing things.

Objective-C 16,782 1,276 Updated Jan 13, 2026
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