Tutorials

Perl Script to Split FASTA Files Extract Matching Data from Two Files Using Python Variant Annotation Pipeline Tutorial Using BWA to align sequenced reads to reference genome A simple python tool to calculate GC content directly SRA-toolkit (Using SRA to download and process sequencing data from NCBI database) Extracting Variants Using SnpSift Convert vcf to hapmap format Analysis of vcf file tutorial Writing a bash script Population genetic analysis