Whole-genome sequencing (WGS)

Whole-genome sequencing (WGS) is a comprehensive method for analyzing entire genomes. Genomic information has been instrumental in identifying inherited disorders, characterizing the mutations that drive cancer progression, and tracking disease outbreaks. 
 
Advantages of whole-genome sequencing
Provides a high-resolution, base-by-base view of the genome
Captures both large and small variants that might be missed with targeted approaches
Identifies potential causative variants for further follow-up studies of gene expression and regulation mechanisms
Undiagnosed Conditions - In cases where no diagnosis has been made, but clinical presentation is suggestive of a genetic condition.
Ideal for targeted management of complex & rare syndromes.
To end the Diagnostic Odyssey.
Whole-genome sequencing can detect single nucleotide variants, insertions/deletions, copy number changes, and large structural variants. Due to recent technological innovations, the latest genome sequencers can perform whole-genome sequencing more efficiently than ever. 
Sample type - Whole Blood.
45days Turn around time