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DNA sequencing

An extended KASP-SNP resource for molecular breeding in Chinese cabbage(Brassica rapa L. ssp. pekinensis)

Shuangjuan Yang, Wentao Yu, [ ... ], Xiaowei Zhang

Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci

Johannes Jernqvist Gaare, Gonzalo Nido, [ ... ], Charalampos Tzoulis

Novel variant in the CNNM2 gene associated with dominant hypomagnesemia

Alejandro García-Castaño, Leire Madariaga, [ ... ], Sonia Gaztambide

Lower DNA methylation levels in CpG island shores of CR1, CLU, and PICALM in the blood of Japanese Alzheimer’s disease patients

Risa Mitsumori, Kazuya Sakaguchi, [ ... ], Nobuyoshi Shimoda

A comparative study of single nucleotide variant detection performance using three massively parallel sequencing methods

Linea Christine Trudsø, Jeppe Dyrberg Andersen, [ ... ], Niels Morling

Evaluation of the GenoType NTM-DR assay performance for the identification and molecular detection of antibiotic resistance in Mycobacterium abscessus complex

Nicolas Bouzinbi, Olivier Marcy, [ ... ], Sylvain Godreuil

Sensitive and reliable evaluation of single-cut sgRNAs to restore dystrophin by a GFP-reporter assay

Pin Lyu, Kyung Whan Yoo, [ ... ], Baisong Lu

Genetic testing offer for inherited neuromuscular diseases within the EURO-NMD reference network: A European survey study

Borut Peterlin, Francesca Gualandi, [ ... ], Alessandra Ferlini

Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing

Rowida Almomani, Margherita Marchi, [ ... ], on behalf on the PROPANE Study Group

A genetic analysis of a Spanish population with early onset Parkinson’s disease

Tejera-Parrado Cristina, Mir Pablo, [ ... ], Pilar Gómez-Garre

An approach to increase the success rate of cultivation of soil bacteria based on fluorescence-activated cell sorting

Laura Espina

The clinical significance of stringent complete response in multiple myeloma is surpassed by minimal residual disease measurements

Maria-Teresa Cedena, Estela Martin-Clavero, [ ... ], Joaquin Martinez-Lopez

Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome

Geeta Madathil Govindaraj, Abhinav Jain, [ ... ], Vinod Scaria

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