WGS 30 x average sequencing depth , 100 Gb/sample

Whole genome sequencing (WGS) is a molecular biology technique used to sequence and analyze the complete DNA sequence of an organism, including all of its genes, regulatory regions, and non-coding regions. WGS can provide a comprehensive view of an organism's genome, including information on gene content, gene expression, and genomic variation. WGS involves the use of next-generation sequencing (NGS) technologies to generate millions of short reads from the genome. The resulting sequence data can be analyzed to identify single nucleotide variations (SNVs), small insertions or deletions (indels), structural variations (SVs), and other genomic features. WGS has numerous applications in various fields of research, including human genetics, microbial genomics, and evolutionary biology. In human genetics, WGS can be used to identify disease-causing mutations, investigate the genetic basis of complex diseases, and develop personalized treatment strategies. In microbial genomics, WGS can be used to identify virulence factors, antibiotic resistance genes, and other genomic features that contribute to microbial pathogenesis. In evolutionary biology, WGS can be used to investigate the genetic diversity and population history of different species. WGS is a powerful tool for comprehensive genetic analysis, providing insights into the molecular mechanisms underlying various biological processes and diseases.