Aila(AI超元域): The premier AI integration tool for Windows, macOS, and Android. Ask once, get answers from 10+ AIs like ChatGPT, Gemini, Claude3, Copilot, Poe, perplexity and more. Features customiza…

为GPT/GLM等LLM大语言模型提供实用化交互接口，特别优化论文阅读/润色/写作体验，模块化设计，支持自定义快捷按钮&函数插件，支持Python和C++等项目剖析&自译解功能，PDF/LaTex论文翻译&总结功能，支持并行问询多种LLM模型，支持chatglm3等本地模型。接入通义千问, deepseekcoder, 讯飞星火, 文心一言, llama2, rwkv, claude2, m…

A Snakemake pipeline to perform BSA-seq to identify causal the recessive mutation(s) underlying a mutant phenotype

MutMap pipeline to identify causative mutations responsible for a phenotype

Multple methods for BSA Pipeline

The analysis pipeline of BSA-seq. Just for information purposes. Not a fully fledged container

zUMIs: A fast and flexible pipeline to process RNA sequencing data with UMIs

RNAseq analysis notes from Ming Tang

Informatics for RNA-seq: A web resource for analysis on the cloud. Educational tutorials and working pipelines for RNA-seq analysis including an introduction to: cloud computing, critical file form…

RNA sequencing analysis pipeline using STAR, RSEM, HISAT2 or Salmon with gene/isoform counts and extensive quality control.

A repository for setting up a RNAseq workflow

QTLseqr is an R package for QTL mapping using NGS Bulk Segregant Analysis

A novel algorithm with high detection power for BSA-Seq data analysis - the significant structural variant method

Data for use with QTLseqr vignette

Scripts used to perform bulk segregant analysis in Brassica napus

This repository including scripts for Bulk Segregant Analysis with B.napus

This repository including scripts for Bulk Segregant Analysis with B.napus

lab manual for MCB160L bulk segregant mapping lab

DeepBSA is a novel bulked segregant analysis (BSA) software for the dissection of complex traits.

Bulked segregation analysis tools for outbreeding species(BSATOS)

Tutorial for bulk segregant analysis using Python

Graph-based Sequence Assembly Toolkit

Bulked-Segregant Analysis using vcf file with or without parents

Phylogenetic orthology inference for comparative genomics

Code repository for O'Reilly book

NOVOPlasty - The organelle assembler and heteroplasmy caller

MitoDNA extending assembler from NGS data

Sequence analysis following the BioStars handbook

Quickly search, compare, and analyze genomic and metagenomic data sets.

Making bioinformatics fun again