Whole genome sequencing
Whole genome sequencing (WGS) is a comprehensive method that involves determining the complete DNA sequence of an organism’s genome at a single time.
Whole exome sequencing (WES) is a powerful genomic technique that focuses on sequencing
the protein-coding regions of genes in a genome, known as the exome.
Single gene tests look for any genetic changesin
one gene.Then a Segregation analysis is performed which a statistical method to determine if a trait, continuous or binary, has a transmission pattern
in pedigrees that is consistent with Mendelian segregation.
Gene panel sequencing targets a curated set of genes known to be associated with specific conditions or clinical symptoms.
Carrier detection uses targeted sequencing to identify asymptomatic mutation carriers for family planning and risk assessment.
Array comparative genomic hybridization (Array CGH) is an effective tool for examining an entire genome for regions exhibiting DNA gains
and losses.
Array comparative genomic hybridization (Array CGH) is an effective tool for examining an entire genome for regions exhibiting DNA gains
and losses.
Array comparative genomic hybridization (Array CGH) is an effective tool for examining an entire genome for regions exhibiting DNA gains
and losses.
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