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Dideoxy DNA sequencing

A real-time PCR method to genotype mutant mouse models with altered affinity for cardiotonic steroids on the Na,K-ATPase

Peter W. Chomczynski, Kianna M. Vires, Michal Rymaszewski, Judith A. Heiny

Recurrent, low-frequency coding variants contributing to colorectal cancer in the Swedish population

Xiang Jiao, Wen Liu, [ ... ], Annika Lindblom

Modeling the structural implications of an alternatively spliced Exoc3l2, a paralog of the tunneling nanotube-forming M-Sec

Paul O’Callaghan, Yvette Zarb, Fredrik Noborn, Johan Kreuger

Repurposing a microfluidic formulation device for automated DNA construction

Garima Goyal, Nick Elsbree, [ ... ], Gregory Linshiz

Consecutive deletions in a unique Uruguayan SARS-CoV-2 lineage evidence the genetic variability potential of accessory genes

Yanina Panzera, Lucía Calleros, [ ... ], Ruben Pérez

Disease-associated variants of Gap Junction Beta 2 protein (GJB2) in the deaf population of Southern Punjab of Pakistan

Nabila Kausar, Asma Haque, [ ... ], Muhammad Qasim

Inferring Short-Range Linkage Information from Sequencing Chromatograms

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

Backward compatibility of whole genome sequencing data with MLVA typing using a new MLVAtype shiny application for Vibrio cholerae

Jérôme Ambroise, Léonid M. Irenge, [ ... ], Jean-Luc Gala

A novel method for the isolation of single cells mimicking circulating tumour cells adhered on Smart Bio Surface slides by Laser Capture Microdissection

Grazia Visci, Doron Tolomeo, [ ... ], Clelia Tiziana Storlazzi

Phylogenetic relationships of Atractylodes lancea, A. chinensis and A. macrocephala, revealed by complete plastome and nuclear gene sequences

Liqiang Wang, Hui Zhang, [ ... ], Chang Liu

The pathogenicity of novel GUCY2D mutations in Leber congenital amaurosis 1 assessed by HPLC-MS/MS

Xue Feng, Tianying Wei, [ ... ], Yinghui Ye

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

Analysis of POFUT1 Gene Mutation in a Chinese Family with Dowling-Degos Disease

Mingfei Chen, Yi Li, [ ... ], Furen Zhang

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