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10.1080/14737159.2016.1209411 http://scihub22266oqcxt.onion/10.1080/14737159.2016.1209411 C5040519!5040519!27388938     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Expert+Rev+Mol+Diagn 2016 ; 16 (9): 987-99 Nephropedia Template TP {{tp|p=27388938|t=2016. Sequencing-based diagnostics for pediatric genetic diseases: progress and potential |pdf=|usr=}}{{27388938}} gab.com Text Sequencing-based diagnostics for pediatric genetic diseases: progress and potential JO: Expert Rev Mol Diagn http://www.kidney.de/pget.php?&tw=1&pmid=27388938 #FOAvip Introduction: The last two decades have witnessed revolutionary changes in clinical diagnostics, fueled by the Human Genome Project and advances in high throughput, Next Generation Sequencing (NGS). We review the current state of sequencing-based pediatric diagnostics, associated challenges, and future prospects. Areas Covered: We present an overview of genetic disease in children, review the technical aspects of Next Generation Sequencing and the strategies to make molecular diagnoses for children with genetic disease. We discuss the challenges of genomic sequencing including incomplete current knowledge of variants, lack of data about certain genomic regions, mosaicism, and the presence of regions with high homology. Expert Commentary: NGS has been a transformative technology and the gap between the research and clinical communities has never been so narrow. Therapeutic interventions are emerging based on genomic findings and the applications of NGS are progressing to prenatal genetics, epigenomics and transcriptomics. Twit Text FOAVip Sequencing-based diagnostics for pediatric genetic diseases: progress and potential ????Expert Rev Mol Diagn http://www.kidney.de/pget.php?&tw=1&pmid=27388938 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27388938 #FOAvip English Wikipedia <ref>{{Cite pmid|27388938}}</ref> Sequencing-based diagnostics for pediatric genetic diseases: progress and potential #MMPMID27388938 Tayoun AA; Krock B; Spinner NB Expert Rev Mol Diagn 2016[Sep]; 16 (9): 987-99 PMID27388938show ga Introduction: The last two decades have witnessed revolutionary changes in clinical diagnostics, fueled by the Human Genome Project and advances in high throughput, Next Generation Sequencing (NGS). We review the current state of sequencing-based pediatric diagnostics, associated challenges, and future prospects. Areas Covered: We present an overview of genetic disease in children, review the technical aspects of Next Generation Sequencing and the strategies to make molecular diagnoses for children with genetic disease. We discuss the challenges of genomic sequencing including incomplete current knowledge of variants, lack of data about certain genomic regions, mosaicism, and the presence of regions with high homology. Expert Commentary: NGS has been a transformative technology and the gap between the research and clinical communities has never been so narrow. Therapeutic interventions are emerging based on genomic findings and the applications of NGS are progressing to prenatal genetics, epigenomics and transcriptomics. äSequencing-based diagnostics for pediatric genetic diseases: progress (epmc).pdf DeepDyve Pubget Overpricing