PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Clinical Genetics10.1111/cge.12819201691179-85Utility of clinical high-depth next generation sequencing for somatic variant detection in thePIK3CA-related overgrowth spectrumV. Hucthagowder, A. Shenoy, M. Corliss, K.A. Vigh-Conrad, C. Storer, D.K. Grange, C.E. Cottrellhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fcge.12819, https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fcge.12819, http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.12819/fullpdf
The Journal of Molecular Diagnostics10.1016/j.jmoldx.2016.06.0042016186842-850Comparison of Next-Generation Sequencing Panels and Platforms for Detection and Verification of Somatic Tumor Variants for Clinical DiagnosticsMaksym Misyura, Tong Zhang, Mahadeo A. Sukhai, Mariam Thomas, Swati Garg, Suzanne Kamel-Reid, Tracy L. Stockleyhttps://api.elsevier.com/content/article/PII:S1525157816301325?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S1525157816301325?httpAccept=text/plain
Neuroscience10.1016/j.neuroscience.2019.08.0162019418291-310Clinical Application of Targeted Next-Generation Sequencing Panels and Whole Exome Sequencing in Childhood EpilepsyGregory Costain, Dawn Cordeiro, Diana Matviychuk, Saadet Mercimek-Andrewshttps://api.elsevier.com/content/article/PII:S030645221930572X?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S030645221930572X?httpAccept=text/plain
Clinical Lymphoma Myeloma and Leukemia10.1016/j.clml.2016.07.136201616S96Somatic Next Generation Sequencing Panels Identify Potentially Pathogenic Germline Variants in Genes Associated with Hereditary Myeloid MalignanciesMichael Drazer, Allison West, Madina Sukhanova, Simone Feurstein, Matthew Jones, Jeremy Segal, Jane Churpeck, Lucy Godleyhttps://api.elsevier.com/content/article/PII:S2152265016303172?httpAccept=text/plain, https://api.elsevier.com/content/article/PII:S2152265016303172?httpAccept=text/xml
The Plant Journal10.1111/j.1365-313x.2011.04627.x2011674736-745Large-scale detection of rare variants via pooled multiplexed next-generation sequencing: towards next-generation EcotillingFabio Marroni, Sara Pinosio, Eleonora Di Centa, Irena Jurman, Wout Boerjan, Nicoletta Felice, Federica Cattonaro, Michele Morgantehttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1365-313X.2011.04627.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-313X.2011.04627.x/fullpdf
Cancer Research and Treatment10.4143/crt.2019.036202052141-50Clinical Targeted Next-Generation sequencing Panels for Detection of Somatic Variants in GliomasHyemi Shin, Jason K. Sa, Joon Seol Bae, Harim Koo, Seonwhee Jin, Hee Jin Cho, Seung Won Choi, Jong Min Kyoung, Ja Yeon Kim, Yun Jee Seo, Je-Gun Joung, Nayoung K. D. Kim, Dae-Soon Son, Jongsuk Chung, Taeseob Lee, Doo-Sik Kong, Jung Won Choi, Ho Jun Seol, Jung-Il Lee, Yeon-Lim Suh, Woong-Yang Park, Do-Hyun Namhttp://e-crt.org/upload/pdf/crt-2019-036.pdf, http://e-crt.org/journal/view.php?doi=10.4143/crt.2019.036, http://e-crt.org/upload/pdf/crt-2019-036.pdf
Clinical Applications for Next-Generation Sequencing10.1016/b978-0-12-801739-5.00003-9201639-61Analysis of Structural Chromosome Variants by Next Generation Sequencing MethodsDariusz Plewczynski, Sławomir Gruca, Przemysław Szałaj, Krystian Gulik, Silviene Fabiana de Oliveira, Ankit Malhotrahttps://api.elsevier.com/content/article/PII:B9780128017395000039?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:B9780128017395000039?httpAccept=text/plain
Clinical Chemistry10.1373/clinchem.2019.3082132019661239-246Using Machine Learning to Identify True Somatic Variants from Next-Generation SequencingChao Wu, Xiaonan Zhao, Mark Welsh, Kellianne Costello, Kajia Cao, Ahmad Abou Tayoun, Marilyn Li, Mahdi Sarmadyhttp://academic.oup.com/clinchem/article-pdf/66/1/239/32233490/clinchem.2019.308213.pdf, http://academic.oup.com/clinchem/article-pdf/66/1/239/32233490/clinchem.2019.308213.pdf
Clinical Applications for Next-Generation Sequencing10.1016/b978-0-12-801739-5.00011-82016217-240Next Generation Sequencing in PharmacogenomicsUrszula Demkowhttps://api.elsevier.com/content/article/PII:B9780128017395000118?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:B9780128017395000118?httpAccept=text/plain
Journal of Allergy and Clinical Immunology10.1016/j.jaci.2021.12.12820221492AB29Diagnostic Utility of Targeted Next Generation Sequencing Panels in Inborn Errors of ImmunityKelli Williams, Yasmin Khan, Abigail Williams, Adam Bartholomeo, Samantha Minnicozzi, Larry Borish, Monica Lawrencehttps://api.elsevier.com/content/article/PII:S0091674921019515?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S0091674921019515?httpAccept=text/plain