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Nucleic Acids Research, ISSN 0305-1048, 2016, Volume 44, Issue 20, pp. e154 - e154
Copy Number Variants (CNVs) are structural rearrangements contributing to phenotypic variation that have been proved to be associated with many disease states.... 
ARRAY-CGH DATA | HUMAN GENOME | GENETICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | VARIATION MAP | IDENTIFICATION | ABERRATIONS | STRUCTURAL VARIATION | CANCER | DEPTH | Exome | Computational Biology - methods | Reproducibility of Results | Algorithms | Humans | High-Throughput Nucleotide Sequencing | Software | Genomics - methods | Web Browser | DNA Copy Number Variations | Index Medicus | Methods Online
Journal Article
Biostatistics, ISSN 1465-4644, 10/2004, Volume 5, Issue 4, pp. 557 - 572
Journal Article
Fertility and Sterility, ISSN 0015-0282, 2017, Volume 107, Issue 5, pp. 1122 - 1129
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 12/2011, Volume 48, Issue 12, pp. 831 - 839
Journal Article
Bioinformatics, ISSN 1367-4803, 06/2014, Volume 30, Issue 12, pp. 1759 - 1761
Motivation: Studies of genomic DNA copy number alteration can deal with datasets with several million probes and thousands of subjects. Analyzing these data... 
SEGMENTATION | ARRAY CGH DATA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | Software | Algorithms | Genomics - methods | DNA Copy Number Variations | Index Medicus
Journal Article
Genomics, ISSN 0888-7543, 11/2015, Volume 106, Issue 5, pp. 257 - 264
This paper presents a new method for analyzing array comparative genomic hybridization (aCGH) data based on Correntropy. A new formulation based on low-rank... 
Half-Quadratic programming | Correntropy | DNA copy number | aCGH | Cancer | ACGH | SIGNAL | RECOVERY | ARRAY CGH DATA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | THRESHOLDING ALGORITHM | Algorithms | Animals | Comparative Genomic Hybridization - methods | Genomics - methods | Humans | DNA Copy Number Variations | Index Medicus
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 01/2014, Volume 42, Issue 1, pp. D993 - D1000
The DECIPHER database (https://decipher.sanger.ac.uk/) is an accessible online repository of genetic variation with associated phenotypes that facilitates the... 
DYSMORPHOLOGY | VARIANTS | ARRAY-CGH | BIOCHEMISTRY & MOLECULAR BIOLOGY | MICRODELETION SYNDROME | DEVELOPMENTAL DELAY | DELETIONS | Rare Diseases - genetics | Phenotype | Humans | Genotype | Internet | Genome, Human | Databases, Nucleic Acid | DNA Copy Number Variations | Index Medicus | VI. Genomic variation, diseases and drugs
Journal Article
BMC Bioinformatics, ISSN 1471-2105, 04/2018, Volume 19, Issue 1, pp. 131 - 131
Journal Article