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Multiple samples aCGH analysis for rare CNVs detection

Journal of Clinical Bioinformatics

Jun 11, 2013

Maciej SykulskiAnna Gambin

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Abstract

DNA copy number variations (CNV) constitute an important source of genetic variability. The standard method used for CNV detection is array comparative genomic hybridization (aCGH). We propose a novel multiple sample aCGH analysis methodology aiming in rare CNVs detection. In contrast t...read more

Mentioned in this Paper

Mental Retardation
DNA Copy Number Variations
Developmental Disabilities
Epilepsy
Genome
Biologic Segmentation
Array-Based Comparative Genomic Hybridization
Exons
Autistic Disorder
Pathogenic Organism
Paper Details
References
    • References24
    • Citations2
    • References24
    • Citations2
  • Multiple samples aCGH analysis for rare CNVs detection

    Journal of Clinical Bioinformatics

    Jun 11, 2013

    Maciej SykulskiAnna Gambin

    PMID: 23758813

    DOI: 10.1186/2043-9113-3-12

    Abstract

    DNA copy number variations (CNV) constitute an important source of genetic variability. The standard method used for CNV detection is array comparative genomic hybridization (aCGH). We propose a novel multiple sample aCGH analysis methodology aiming in rare CNVs detection. In contrast t...read more

    Mentioned in this Paper

    Mental Retardation
    DNA Copy Number Variations
    Developmental Disabilities
    Epilepsy
    Genome
    Paper Details
    References
    • References24
    • Citations2
    • References24
    • Citations2
  • Get paper from

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