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
- Siang Li lisiang.darcy@gmail.com Developer
Blood Diseases Hospital, Peking Union Medical College, China
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Summary
Accession | BT007293 |
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Tool Type | Pipeline & Protocol |
Category | Demultiplexing |
Platforms | Linux/Unix |
Technologies | Python3 |
User Interface | Terminal Command Line |
Input Data | FASTA, FASTQ |
Download Count | 0 |
Submitted By | Siang Li |