GREPore-seq A Robust Workflow to Detect Changes after Gene Editing through Long-range PCR and Nanopore Sequencing

Introduction

The package implements a pipeline consisting of a make reference module, Demultiplex module followed by Visualization module. The Demultiplex module takes raw reads(FASTQ) from a pooled multi-sample Oxford Nanopore sequencing run as input. Reads are demultiplexed into sample-specific FASTQs using Grepseq information.

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Credits

  1. Siang Li lisiang.darcy@gmail.com
    Developer

    Blood Diseases Hospital, Peking Union Medical College, China

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Summary
AccessionBT007293
Tool TypePipeline & Protocol
CategoryDemultiplexing
PlatformsLinux/Unix
TechnologiesPython3
User InterfaceTerminal Command Line
Input DataFASTA, FASTQ
Download Count0
Submitted BySiang Li