... other databases, such as RefSeq and Vega, and non-codingfunctional elements such as untranslated and regulatory regions. The number of variants per base pair (variantdensity) and our ability ... which are approxi mately 70% GC, had appro xi-mately half of the sequence depth of coverage as the CCDS regions, approximately 50% GC. When comparedto WGS (non-capture) data the same general biaseswere ... identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy. Nat Genet 2010, 42:840-850.9. Bilguvar K, Ozturk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnizoglu D,Tuysuz B, Caglayan AO,...