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  1. Whole exome sequencing of sporadic patients with Currarino Syndrome: A report of three trios
  2. cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data
  3. Identification of copy number variants from exome sequence data
  4. The Sri Lankan Personal Genome Project: an overview
  5. The Sri Lankan Genome Variation Database