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Article

Exon Array CGH: Detection of Copy-Number Changes at the Resolution of Individual Exons in the Human Genome

15 Apr 2005

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15756638
DOI: 10.1086/429588

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Exon Array CGH: Detection of Copy-Number Changes at the Resolution of Individual Exons in the Human GenomePMID 15756638Read ↗

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Exon-level array CGH in a large clinical cohort demonstrates increased sensitivity of diagnostic testing for Mendelian disorders.Semantic proximity Read ↗

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Progress in the detection of human genome structural variations.Semantic proximity Read ↗

Copy-number variations add a new layer of complexity in the human genome.Semantic proximity Read ↗

Characterizing the allele- and haplotype-specific copy number landscape of cancer genomes at single-cell resolution with CHISELSemantic proximity Read ↗

Sensitive detection of copy number alterations in samples with low circulating tumor DNA fractionSemantic proximity Read ↗

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Large-scale copy number polymorphism in the human genome.Semantic proximity Read ↗

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