A simple control-flow library for Node.js targetted towards CoffeeScript developers.
CLI for GENI — a control plane for running Nextflow bioinformatics pipelines on AWS
This is a library used for common features in Nextflow apps.
Thư viện n8n node chuyên nghiệp cho tích hợp Zalo với mô hình kinh doanh freemium - Phát triển bởi NextFlow
Shared Zod schemas, node contracts, and node registry for nextflow
SDK tích hợp Zalo toàn diện cho hệ thống CRM AI Nextflow
This is a library used for common features in Nextflow apps.
AI-powered CLI for Seqera Platform - bioinformatics workflow management
A set of command line tools, NGS data analysis workflows [WDL, Nextflow, Snakemake, and Bpipe], and R shiny plugins/R markdown document for exploring next-generation sequencing data.
Stencil Component Starter
A example web component, as a number counter, built with stencil
ส่วนประกอบของข้อมูลสินค้า
An intelligent Claude Code agent for running nf-core bioinformatics pipelines via natural language.
n8n node for mobile app integration
AI-assisted troubleshooting for AWS HealthOmics genomic workflows with custom knowledge base support
A very simple data queue processing library.
CLI-based Bioinformatics Coding Agents - OpenCode plugin for bioinformatics workflows
based on R and JavaScript ecosystem.
Shows fastq stats using cprogs and python
Interface package for NEXT FlOW. You can use this package to build your own plugin that can control anything.
为 Next Flow 项目设计的高性能 UI 组件库。提供原生使用,及react使用两种版本。
Node-RED nodes for interacting with the Seqera Platform API
High-performance genomics I/O and interoperability layer
Extract byte ranges from BAM files and convert to interleaved FASTQ format for parallel processing
A rust framework to make using alevin-fry and alevin-fry-ATAC even simpler.
get sequences from 2bit/fa using bed/gtf/gff
ALPINE (Anachronistic Lineage and Persistent INfection Explorer) Core Utilities
A fast and memory efficient BED to GTF/GFF converter
A code highlighter giving the same output as VSCode
A project management tool for data science and bioinformatics
just get your chrom sizes
Accelerated DNA sequence search and [host] depletion using minimizers
Count the occurances of structured sequence reads and compare to an expected library
split FASTX into N chunks/files/headers
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