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Targeted polymerase chain reaction-based enrichment and next generation sequencing for diagnostic testing of congenital disorders of glycosylation de réir Melanie A. Jones, Shruti Bhide, Ephrem Chin, Bobby G. Ng, Devin Rhodenizer, Victor Wei Zhang, Jessica Sun, Alice Tanner, Hudson H. Freeze, Madhuri Hegde

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Cancer Driver Log (CanDL) de réir Senthilkumar Damodaran, Jharna Miya, Esko A. Kautto, Eliot Y. Zhu, Eric Samorodnitsky, Jharna Datta, Julie W. Reeser, Sameek Roychowdhury

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Development and Validation of a Next-Generation Sequencing Assay for BRCA1 and BRCA2 Variants for the Clinical Laboratory de réir Charles M. Strom, Steven Rivera, Christopher Elzinga, Taraneh Angeloni, Sun Hee Rosenthal, Dana M. Goos-Root, Martin Siaw, Jamie L. Platt, Cory Braastadt, Linda Cheng, David A. Ross, Weimin Sun

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Massively parallel high-order combinatorial genetics in human cells de réir Alan S.L. Wong, Gigi C.G. Choi, Allen A. Cheng, Oliver Purcell, Timothy K. Lu

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Validation of next-generation sequencing for comprehensive chromosome screening of embryos de réir A. Kung, S. Munné, Brandon Bankowski, A. Coates, Dagan Wells

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STAG3 truncating variant as the cause of primary ovarian insufficiency de réir Polona Le Quesne Stabej, Hywel Williams, Chela James, Mehmet Tekman, Horia Stanescu, Robert Kleta, Louise Ocaka, Francesco Lescai, Helen L. Storr, Maria Bitner‐Glindzicz, Chiara Bacchelli, Gerard S. Conway

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Mitochondrial Sequence Analysis for Forensic Identification Using Pyrosequencing Technology de réir H. Andréasson, A. Asp, Anders Alderborn, U. Gyllensten, Maxine Allen

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Underlying Data for Sequencing the Mitochondrial Genome with the Massively Parallel Sequencing Platform Ion Torrent™ PGM™ de réir Seung Bum Seo, Xiangpei Zeng, Jonathan L. King, Bobby LaRue, Mourad Assidi, Mohamed H. Alqahtani, Antti Sajantila, Bruce Budowle

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Benefits and limitations of whole genome versus targeted approaches for noninvasive prenatal testing for fetal aneuploidies de réir Elles M. J. Boon, Brigitte H. W. Faas

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Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell‐free DNA from maternal plasma de réir Amin R. Mazloom, Željko Džakula, Paul Oeth, Huiquan Wang, Taylor J. Jensen, John A. Tynan, Ron McCullough, Juan‐Sebastian Saldivar, Mathias Ehrich, Dirk van den Boom, Allan T. Bombard, Margo Maeder, Graham McLennan, Wendy S. Meschino, Glenn E. Palomaki, Jacob A. Canick, Cosmin Deciu

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Preparation of Single‐Cell RNA‐Seq Libraries for Next Generation Sequencing de réir John J. Trombetta, David Gennert, Diana Lu, Rahul Satija, Alex K. Shalek, Aviv Regev

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Construction of Normalized RNA‐seq Libraries for Next‐Generation Sequencing Using the Crab Duplex‐Specific Nuclease de réir Danos C. Christodoulou, Joshua M. Gorham, Daniel S. Herman, Jonathan G. Seidman

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Brief Report: Whole‐Exome Sequencing Revealing Somatic <i>NLRP3</i> Mosaicism in a Patient With Chronic Infantile Neurologic, Cutaneous, Articular Syndrome de réir Ebun Omoyinmi, Sónia Gomes, Ariane Standing, Dorota Rowczenio, Despina Eleftheriou, Nigel Klein, Juan I. Aróstegui, Helen J. Lachmann, Philip N. Hawkins, Paul Brogan

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Noninvasive fetal genotyping of human platelet antigen‐1a using targeted massively parallel sequencing de réir Sandra Wienzek‐Lischka, Annika Krautwurst, V Fröhner, Holger Hackstein, Stefan Gattenlöhner, Andreas Bräuninger, R Axt-Fliedner, J Degenhardt, Christina Deisting, Sentot Santoso, Ulrich J. Sachs, Gregor Bein

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Determination of the allelic frequency in Smith–Lemli–Opitz syndrome by analysis of massively parallel sequencing data sets de réir Jennifer L. Cross, James Iben, Claire L. Simpson, Audrey Thurm, Susan E. Swedo, Elaine Tierney, Joan E. Bailey‐Wilson, Leslie G. Biesecker, Forbes D. Porter, Christopher A. Wassif

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<i><scp>KRAS</scp></i> (but not <i><scp>BRAF</scp></i>) mutations in ovarian serous borderline tumour are associated with recurrent low‐grade serous carcinoma de réir Yvonne T.M. Tsang, Michael T. Deavers, Charlotte C. Sun, Suet‐Yan Kwan, Eric Kuo, Anaís Malpica, Samuel C. Mok, David M. Gershenson, Kwong‐Kwok Wong

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Clinical applications of next generation sequencing in cancer: from panels, to exomes, to genomes de réir Tony S. Shen, Stefan Hans Pajaro-Van de Stadt, Nai Chien Yeat, Jimmy Lin

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Non‐invasive prenatal testing for aneuploidy: current status and future prospects de réir Peter Benn, Howard Cuckle, Eugene Pergament

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Dynamics in Transcriptomics: Advancements in RNA-seq Time Course and Downstream Analysis de réir Daniel Spies, Constance Ciaudo

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Progress and prospects of next-generation sequencing testing for inherited retinal dystrophy de réir John Chiang, Tina M. Lamey, Terri L. McLaren, Jennifer A. Thompson, H. C. Montgomery, John N. De Roach

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