Whole Genome Sequencing Data Analysis
Whole-genome sequencing provides a comprehensive view of entire genome. Whole genome sequencing (WGS) or genome resequencing are ideally suited for genome wide variant identifications and structural variation detection. These SNPs and insertion or deletions constitute the major disease biomarker for human and complex genomes.
Genome Sequencing Overview
Latest sequencing instruments like NovaSeq and HiSeq have a high output making whole genome sequencing cost effective. Such improvements in the sequencing throughput are making Whole-genome sequencing a powerful tool in hands of geneticists and clinicians to in identify inherited disorders, characterize clinically relevant biomarkers that drive cancer progression, and tracking disease outbreaks. Whole-genome sequencing has been applied not only to study human genomes but is highly effective method of choice to study economically important livestock and plant genomes along with their diseases causing pathogens.
Key Advantages of Whole Genome Resequencing?
- Comprehensive view of genetic variations
- Capture point mutations and large structural variations
- Provide high resolution assemblies
- Identify clinically relevant biomarkers for disease studies
- Rapidly identify infectious and disease causing viruses, bacteria and pathogens
- Study evolutionary changes in a species or related
Whole Genome Resequencing Data Analysis Overview
Here is a peek at our whole genome resequencing data analysis pipeline. We have optimised various tools and parameters to detect SNPs, INDELS and CNVs in whole genome resequencing data.
Whole Genome Sequencing Service Deliverables
Unleash the Power of Genomics: Explore 1010Genome's Whole Genome Analysis Services!
Are you a researcher, academic, or clinician ready to make groundbreaking discoveries and unlock the secrets hidden within whole genomes? Look no further! At 1010Genome, we're your trusted partner in Whole Genome Analysis.