Whole-genome sequencing (WGS) is a comprehensive method that uses NGS technology for analyzing the entire genome in organisms. This genomic data is instrumental for identification of inherited disorders, characterization of cancer progression, and has a potential to offer precise molecular diagnosis and medicine. Bioinformatics analysis of WGS involves Controlling the quality of raw data , Sequencing depth and coverage statistics , SNP/InDel/SV/CNV calling, de novo assembly, reference genome mapping ,Statistics and annotation , Analysis of athway enrichment and Analyses of population genetics.

Advantages of Whole Genome Sequencing

  • Phylogenetic studies and Population evolution
  • Single base-pair resolution
  • Genome-wide mutation characterization and De novo sequencing
  • Drug discovery and development and Disease research

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