Genome Wide Association Studies (GWAS) training/workshop is to introduce researchers to the basic principles of analyzing genotyping individuals at common variants across the genome using genome wide SNP by next-gen sequencing approaches.
The most important NGS file formats (fastq, sam/bam, bigWig, etc.) are introduced and one proceeds with first hands-on analyses (QC, mapping, visualization).
Goals :
In this hands-on session we will align example data from an GWAS experiment against the genome, variation calling and statistical GWAS analysis with significant pvalue for highly associated mutations filtration.
Also combining Computer aided drug designing techniques to validate in-silico for wild type and mutant mutation detected with highly associated mutation from GWAS.
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