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Contemporary Approaches for Identifying Rare Bone Disease Causing Genes
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作者 Charles R.Farber Thomas L.Clemens 《Bone Research》 SCIE CAS 2013年第4期301-310,共10页
Recent improvements in the speed and accuracy of DNA sequencing, together with increasingly sophisti- cated mathematical approaches for annotating gene networks, have revolutionized the field of human genetics and mad... Recent improvements in the speed and accuracy of DNA sequencing, together with increasingly sophisti- cated mathematical approaches for annotating gene networks, have revolutionized the field of human genetics and made these once time consuming approaches assessable to most investigators. In the field of bone research, a particularly active area of gene discovery has occurred in patients with rare bone disorders such as osteogenesis imperfecta (OI) that are caused by mutations in single genes. In this perspective, we highlight some of these technological advances and describe how they have been used to identify the genetic determinants underlying two previously unexplained cases of OI. The widespread availability of advanced methods for DNA sequencing and bioinformatics analysis can be expected to greatly facilitate identification of novel gene networks that normally function to control bone formation and maintenance. 展开更多
关键词 exome sequencing genome sequencing BIOINFORMATICS osteogenesis imperfect pigment epithelium-derived factor (PEDF) bone restricted ifitm-like protein (bril
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