Clinical Exome Sequencing – Identifying Underlying Genetic Disorders or Phenotypic Change Resulting from Exon Variation
The genome sequencing consists of exon and intron sequences but only the exons are spliced together to form genes that encode for various proteins. Any variation or mutation in the protein-encoding genes can result in genetic disorder, phenotypic change, or inherit the condition to the offspring. Clinical exome sequencing is a targeted and powerful diagnostic technique that […]