SNP calling exercise part 1: Revision history

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29 November 2024

  • curprev 14:3614:36, 29 November 2024‎ Gabre talk contribs‎ 6,331 bytes +67‎ No edit summary
  • curprev 14:3314:33, 29 November 2024‎ Gabre talk contribs‎ 6,264 bytes +6,264‎ Created page with "<H2>Overview</H2> First: <OL> <LI>Navigate to your home directory: <LI>Create a directory called "variant_call" <LI>Navigate to the directory you just created. </OL> We will: <OL> <LI>Genotype some whole-genome sequencing data. <LI>Get acquainted with VCF files <LI>Soft filtering <LI>Hard filtering <LI> Annotation of variants </OL> ---- <H2>Genotyping</H2> We will genotype a chromosome from a BAM file that has been processed using the steps we detailed before. It i..."
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