Construction and application of a full‐coverage, high‐resolution, human chromosome 8q genomic microarray for comparative genomic hybridization

Background Array‐based comparative genomic hybridization (aCGH) enables genome‐wide quantitative delineation of genomic imbalances. A high‐resolution contig array was developed specifically for chromosome 8q because this chromosome arm is frequently altered in many human cancers. Methods A minimal t...

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Veröffentlicht in:	Cytometry. Part A 2005-01, Vol.63A (1), p.10-19
Hauptverfasser:	van Duin, Mark, van Marion, Ronald, Watson, J. E. Vivienne, Paris, Pamela L., Lapuk, Anna, Brown, Nils, Oseroff, Vanessa V., Albertson, Donna G., Pinkel, Daniel, de Jong, Pieter, Nacheva, Elizabeth P., Dinjens, Winand, van Dekken, Herman, Collins, Colin
Format:	Artikel
Sprache:	eng
Schlagworte:	8q contig Adenocarcinoma - genetics amplification cancer Cardia chromosomal aberrations Chromosome Aberrations Chromosomes, Human, Pair 8 comparative genomic hybridization deletion Fixatives Formaldehyde gain Gene Dosage Genome, Human genomic array Humans In Situ Hybridization, Fluorescence Male Nucleic Acid Hybridization Oligonucleotide Array Sequence Analysis Prostatic Neoplasms - genetics Stomach Neoplasms - genetics Tumor Cells, Cultured
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