August 23, 2017 article Open access Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data Molecular Cytogenetics DOI: 10.1186/s13039-017-0333-5 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 3 stored of 110 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses 2024 npj Genomic Medicine article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access 10 citations Technologies for Pharmacogenomics: A Review 2020 Genes article Pharmacology, Toxicology and Pharmaceutics Pharmacogenetics and Drug Metabolism Open access 83 citations The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research 2020 F1000Research article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access 7 citations 3 results References 0