FASTQ to Annotation (Part 4)
Posted on Tue 06 October 2020 in Unix • Tagged with Bioinformatics, genomic variation, entrez-direct, EDirect
Introduction
In a previous post, I showed how to configure an Ubuntu system to install Bioinformatics programs.
Now, using the environment I created, I will demonstrate a bash script, FastQ_to_Annotation.sh
that takes next generation sequencing (NGS) raw reads from human whole genome sequencing as input and produces …
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