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Next-generation sequencing

Improved detection of SBDS gene mutation by a new method of next-generation sequencing analysis based on the Chinese mutation spectrum

Dong Wu, Li Zhang, Yuzhen Qiang, Kaiyu Wang

Frequency of occurrence of HIV-1 dual infection in a Belgian MSM population

Laura Hebberecht, Leen Vancoillie, [ ... ], Chris Verhofstede

Positive selection in coding regions and motif duplication in regulatory regions of bottlenose dolphin MHC class II genes

Heidi J. T. Pagán, Tatiana Ferrer, Greg O’Corry-Crowe

Detection of MYD88 L265P mutation by next-generation deep sequencing in peripheral blood mononuclear cells of Waldenström’s macroglobulinemia and IgM monoclonal gammopathy of undetermined significance

Ayako Nakamura, Chikako Ohwada, [ ... ], Emiko Sakaida

Immunoglobulin gene rearrangement in Koreans with multiple myeloma: Clonality assessment and repertoire analysis using next-generation sequencing

Miyoung Kim, Kibum Jeon, [ ... ], Young Kyung Lee

Inferring Short-Range Linkage Information from Sequencing Chromatograms

Bastian Beggel, Maria Neumann-Fraune, [ ... ], Thomas Lengauer

Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis

Maria Teresa Pagliari, Andrea Cairo, [ ... ], Flora Peyvandi

SparkGA2: Production-quality memory-efficient Apache Spark based genome analysis framework

Hamid Mushtaq, Nauman Ahmed, Zaid Al-Ars

Simulation-guided tunable DNA probe design for mismatch tolerant hybridization

Pallavi Bugga, Vishwaratn Asthana, Rebekah Drezek

Gene selection tool (GST): A R-based tool for genetic disorders based on the sliding-window proportion test using whole-exome sequencing data

Sugi Lee, Minah Jung, [ ... ], Dae-soo Kim

Evaluation of serverless computing for scalable execution of a joint variant calling workflow

Aji John, Kathleen Muenzen, Kristiina Ausmees

Application of Multi-Objective Optimization to Pooled Experiments of Next Generation Sequencing for Detection of Rare Mutations

Julius Žilinskas, Algirdas Lančinskas, Mario Rosario Guarracino

Design of DNA Pooling to Allow Incorporation of Covariates in Rare Variants Analysis

Weihua Guan, Chun Li

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