1
Sequencing Technologies its applications, Introduction to NGS and DNA seq,
1 Hour
2
Basic Terminologies in NGS
1 Hour
3
Understanding of SRA database
1 Hour
4
Tools installation in Linux for Variation Calling
1 Hour
5
Quality control (FastQC)
1 Hour
6
Trimming of Reads (Trimmomatic)
1 Hour
7
Indexing of Genome (BWA) and Alignment of Reads (BWA)
1 Hour
8
Variation calling using GATK
1 Hour
9
Variant Effect Prediction(VEP)
1 Hour
10
Variation Visualization (IGV)
1 Hour