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Starred repositories

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Jupyter Notebook 5 1 Updated Jan 25, 2025

Hidden State Speciation and Extinction

R 6 6 Updated Feb 3, 2025

This repo includes ChatGPT prompt curation to use ChatGPT and other LLM tools better.

JavaScript 126,243 16,793 Updated May 16, 2025

The second version of the Kraken taxonomic sequence classification system

C++ 789 286 Updated Apr 23, 2025

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

Python 150 24 Updated Aug 8, 2024

Tools for data handling and analysis in macroecology

R 29 7 Updated May 15, 2025

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

R 13 3 Updated Feb 5, 2025

Phylogenetic orthology inference for comparative genomics

Python 767 193 Updated Oct 22, 2024

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 336 31 Updated May 15, 2025

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

C++ 424 154 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 28 5 Updated May 22, 2025

A structural variation pipeline for short-read sequencing

Python 188 75 Updated May 22, 2025

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

Java 18 4 Updated Nov 18, 2023

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

C++ 412 41 Updated Dec 26, 2024

deep learning prediction of geographic location from individual genome sequences

Python 50 18 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 99 22 Updated May 9, 2025

Tools to work with variant call format files

R 259 53 Updated Feb 21, 2025

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

Nextflow 169 83 Updated May 16, 2025

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

Python 47 19 Updated Apr 2, 2025

The next version of bwa-mem

C++ 754 102 Updated Aug 5, 2024

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

C++ 441 121 Updated Mar 13, 2024

k-mer based assembly evaluation

Shell 310 20 Updated Jun 28, 2024

Transcript assembly and quantification for RNA-Seq

C++ 435 80 Updated May 12, 2025

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

Python 3,403 751 Updated May 16, 2025

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

JavaScript 1,302 619 Updated May 22, 2025

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

HTML 170 90 Updated Mar 23, 2021

R Port of psmc

C 15 4 Updated Mar 16, 2023

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

Objective-C 15,963 1,226 Updated May 23, 2025
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