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Dideoxy DNA sequencing

Quality Score Based Identification and Correction of Pyrosequencing Errors

Shyamala Iyer, Heather Bouzek, [ ... ], James I. Mullins

Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

Denise Yan, Guangxin Xiang, [ ... ], Xue Zhong Liu

Next-Generation Sequencing of Aquatic Oligochaetes: Comparison of Experimental Communities

Régis Vivien, Franck Lejzerowicz, Jan Pawlowski

Exome Sequencing and Functional Analysis Identifies a Novel Mutation in EXT1 Gene That Causes Multiple Osteochondromas

Feng Zhang, Jinlong Liang, [ ... ], Jun Wang

Fanconi-BRCA pathway mutations in childhood T-cell acute lymphoblastic leukemia

Gayle P. Pouliot, James Degar, [ ... ], Alejandro Gutierrez

Prevalence and Evolution of Low Frequency HIV Drug Resistance Mutations Detected by Ultra Deep Sequencing in Patients Experiencing First Line Antiretroviral Therapy Failure

Marie-Anne Vandenhende, Pantxika Bellecave, [ ... ], Bernard Masquelier

Improvement in detecting cytomegalovirus drug resistance mutations in solid organ transplant recipients with suspected resistance using next generation sequencing

Rubén López-Aladid, Alba Guiu, [ ... ], Maria Ángeles Marcos

Comparison of the abilities of universal, super, and specific DNA barcodes to discriminate among the original species of Fritillariae cirrhosae bulbus and its adulterants

Qi Chen, Xiaobo Wu, Dequan Zhang

Whole-Exome Sequencing to Decipher the Genetic Heterogeneity of Hearing Loss in a Chinese Family with Deaf by Deaf Mating

Jie Qing, Denise Yan, [ ... ], Xue Zhong Liu

Rapid Screening of Complex DNA Samples by Single-Molecule Amplification and Sequencing

Jiaqi Huang, Zongli Zheng, [ ... ], Weimin Ye

Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness

Zied Riahi, Crystel Bonnet, [ ... ], Christine Petit

Comprehensive Molecular Profiling of Archival Bone Marrow Trephines Using a Commercially Available Leukemia Panel and Semiconductor-Based Targeted Resequencing

Stephan Bartels, Elisa Schipper, Hans Heinrich Kreipe, Ulrich Lehmann

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions

Neng-Li Wang, Yu-Lan Lu, [ ... ], Jian-She Wang

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