wwwkkk83 发表于 2016-10-21 07:32:43

The Journal of Molecular Diagnostics: Nov-2016

Special Article

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Emerging and Future Applications of Matrix-Assisted Laser Desorption Ionization Time-of-Flight (MALDI-TOF) Mass Spectrometry in the Clinical Microbiology Laboratory
Christopher D. Doern, Susan M. Butler-Wu

Review

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Clinical Performance Evaluation of Molecular Diagnostic Tests
Bipasa Biswas

Commentary

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Next-Generation Sequencing in Cancer Diagnostics
Christopher L. Corless

Technical Advances

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Improved Diagnosis of Inherited Retinal Dystrophies by High-Fidelity PCR of ORF15 followed by Next-Generation Sequencing
Jianli Li, Jia Tang, Yanming Feng, Mingchu Xu, Rui Chen, Xuan Zou, Ruifang Sui, Emmanuel Y. Chang, Richard A. Lewis, Victor W. Zhang, Jing Wang, Lee-Jun C. Wong

Improving Accuracy of Urinary miRNA Quantification in Heparinized Patients Using Heparinase I Digestion
Henk P. Roest, Cornelia J. Verhoeven, Jubi E. de Haan, Jeroen de Jonge, Jan N.M. IJzermans, Luc J.W. van der Laan

Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array
Laila C. Schenkel, Charles Schwartz, Cindy Skinner, David I. Rodenhiser, Peter J. Ainsworth, Guillaume Pare, Bekim Sadikovic

Regular Articles

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Comparison of Next-Generation Sequencing Panels and Platforms for Detection and Verification of Somatic Tumor Variants for Clinical Diagnostics
Maksym Misyura, Tong Zhang, Mahadeo A. Sukhai, Mariam Thomas, Swati Garg, Suzanne Kamel-Reid, Tracy L. Stockley
Open Access   
Reliable Next-Generation Sequencing of Formalin-Fixed, Paraffin-Embedded Tissue Using Single Molecule Tags
Astrid Eijkelenboom, Eveline J. Kamping, Annemiek W. Kastner-van Raaij, Sandra J. Hendriks-Cornelissen, Kornelia Neveling, Roland P. Kuiper, Alexander Hoischen, Marcel R. Nelen, Marjolijn J.L. Ligtenberg, Bastiaan B.J. Tops
Open Access   
The Clinical Implications of Inconsistently Methylated Results from Glioblastoma MGMT Testing by Replicate Methylation-Specific PCR
Daniel Xia, David A. Reardon, Jacqueline L. Bruce, Neal I. Lindeman

CNV-RF Is a Random Forest–Based Copy Number Variation Detection Method Using Next-Generation Sequencing
Getiria Onsongo, Linda B. Baughn, Matthew Bower, Christine Henzler, Matthew Schomaker, Kevin A.T. Silverstein, Bharat Thyagarajan

Multiplexed Reference Materials as Controls for Diagnostic Next-Generation Sequencing
Emily M. Kudalkar, Naif A.M. Almontashiri, Catherine Huang, Bharathi Anekella, Mark Bowser, Elizabeth Hynes, Russell Garlick, Birgit H. Funke

Validation of a Clinical-Grade Assay to Measure Donor-Derived Cell-Free DNA in Solid Organ Transplant Recipients
Marica Grskovic, David J. Hiller, Lane A. Eubank, John J. Sninsky, Cindy Christopherson, John P. Collins, Kathryn Thompson, Mindy Song, Yue S. Wang, David Ross, Mitchell J. Nelles, James P. Yee, Judith C. Wilber, Maria G. Crespo-Leiro, Susan L. Scott, Robert N. Woodward
Open Access   
Clinical Application of Picodroplet Digital PCR Technology for Rapid Detection of EGFR T790M in Next-Generation Sequencing Libraries and DNA from Limited Tumor Samples
Laetitia Borsu, Julie Intrieri, Linta Thampi, Helena Yu, Gregory Riely, Khedoudja Nafa, Raghu Chandramohan, Marc Ladanyi, Maria E. Arcila

Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel
Francesca Boaretto, Deborah Snijders, Cecilia Salvoro, Ambra Spalletta, Maria Luisa Mostacciuolo, Mirella Collura, Salvatore Cazzato, Donatella Girosi, Michela Silvestri, Giovanni Arturo Rossi, Angelo Barbato, Giovanni Vazza

Sanger Confirmation Is Required to Achieve Optimal Sensitivity and Specificity in Next-Generation Sequencing Panel Testing
Wenbo Mu, Hsiao-Mei Lu, Jefferey Chen, Shuwei Li, Aaron M. Elliott



ms003 发表于 2016-10-22 21:45:27

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