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Copy number variation

The copy number variation and stroke (CaNVAS) risk and outcome study

John W. Cole, Taiwo Adigun, [ ... ], Caspar Grond-Ginsbach

Prognostic value of integrated cytogenetic, somatic variation, and copy number variation analyses in Korean patients with newly diagnosed multiple myeloma

Nuri Lee, Sung-Min Kim, [ ... ], Dong Soon Lee

Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia

Maroua Boujemaa, Yosr Hamdi, [ ... ], Mohamed Samir Boubaker

Identification of a 6-gene signature for the survival prediction of breast cancer patients based on integrated multi-omics data analysis

Wenju Mo, Yuqin Ding, [ ... ], Xiaowen Ding

Homogeneity among glyphosate-resistant Amaranthus palmeri in geographically distant locations

William T. Molin, Eric L. Patterson, Christopher A. Saski

Whole genome detection of sequence and structural polymorphism in six diverse horses

Mohammed Ali Al Abri, Heather Marie Holl, [ ... ], Samantha A. Brooks

Comparing genome-scale DNA methylation and CNV marks between adult human cultured ITGA6+ testicular cells and seminomas to assess in vitro genomic stability

Robert B. Struijk, Lambert C. J. Dorssers, [ ... ], Ans M. M. van Pelt

CalPen (Calculator of Penetrance), a web-based tool to estimate penetrance in complex genetic disorders

Aditya Addepalli, Sakhare Kalyani, [ ... ], K. Naga Mohan

HeLa-CCL2 cell heterogeneity studied by single-cell DNA and RNA sequencing

Wan-er Hu, Xin Zhang, [ ... ], Xiao-dong Su

Clade II Candida auris possess genomic structural variations related to an ancestral strain

Tsuyoshi Sekizuka, Shigekazu Iguchi, [ ... ], Ken Kikuchi

DNA copy number variations in children with vesicoureteral reflux and urinary tract infections

Dong Liang, Kirk M. McHugh, [ ... ], David S. Hains

Association between polymorphisms in the SOX9 region and canine disorder of sex development (78,XX; SRY-negative) revisited in a multibreed case-control study

Joanna Nowacka-Woszuk, Izabela Szczerbal, [ ... ], Marek Switonski

Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease

Svetlana Frenkel, Charles N. Bernstein, [ ... ], Pingzhao Hu

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