Here, we will work with FASTQ files, the standard format output used by modern sequencers. You will learn how to work with quality scores per base and also consider the variations in output coming from different sequencing machines and databases. This is the first recipe that will use real data (big data) from the Human 1,000 Genomes Project. We will start with a brief description of the project.
Working with modern sequence formats
Getting ready
The Human 1,000 Genomes Project aims to catalog worldwide human genetic variation and takes advantage of modern sequencing technology to do WGS. This project makes all data publicly available, which includes output from sequencers, sequence alignments, and SNP calls, among many other...