Studying genome accessibility and filtering SNP data

While previous recipes were focused on giving an overview of Python libraries to deal with alignment and variant call data, we concentrate on actually using them with a clear purpose in mind here.

If you are using NGS data, chances are that your most important file to analyze is a VCF file, produced by a genotype caller such as samtools mpileup, or GATK. The quality of your VCF calls may need to be assessed and filtered. Here, we will put in place a framework to filter SNP data. Rather than giving you filtering rules (an impossible task to be performed in a general way), we give you procedures to assess the quality of your data. With this, you can devise your own filters.

Getting ready

In the best-case ...

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