M
Masaru Sakamoto
Researcher at University of California
Publications - 5
Citations - 358
Masaru Sakamoto is an academic researcher from University of California. The author has contributed to research in topics: Nucleic acid & Comparative genomic hybridization. The author has an hindex of 5, co-authored 5 publications receiving 358 citations.
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Comparative genomic hybridization (cgh)
Daniel Pinkel,Joe W. Gray,Anne Kallioniemi,Olli-Pekka Kallioniemi,Frederick Waldman,Masaru Sakamoto +5 more
TL;DR: In this article, the authors used in situ hybridization to detect abnormal nucleic acid sequence copy numbers in one or more genomes wherein repetitive sequences that bind to multiple loci in a reference chromosome spread are either substantially removed and/or their hybridization signals suppressed.
Patent
Detection of chromosomal abnormalities associated with breast cancer
Daniel Pinkel,Joe W. Gray,Anne Kallioniemi,Ollie-Pekka Kallioniemi,Frederic Waldman,Masaru Sakamoto +5 more
TL;DR: In this paper, the authors used in situ hybridization to detect abnormal nucleic acid sequence copy numbers in one or more genomes wherein repetitive sequences that bind to multiple loci in a reference chromosome spread are either substantially removed and/or their hybridization signals suppressed.
Patent
Chromosome-specific staining to detect genetic rearrangements associated with chromosome 3 and/or chromosome 17
TL;DR: The nucleic acid probes are typically of a complexity greater than 50 kb, the complexity depending upon the cytogenetic application as discussed by the authors, and are used for in situ hybridization and stain both interphase and metaphase chromosomes with reliable signals.
Patent
Comparative genomic hyridization
Daniel Pinkel,Joe W. Gray,Anne Kallioniemi,Ollie-Pekka Kallioniemi,Frederic Waldman,Masaru Sakamoto +5 more
TL;DR: In this paper, the authors used in situ hybridization to detect abnormal nucleic macid sequence copy numbers in one or more genomes wherein repetitive sequences that bind to multiple loci in a reference chromosome spread are either substantially removed and/or their hybridization signals suppressed.
Patent
Methods of staining target chromosomal DNA employing high complexity nucleic acid probes
TL;DR: The nucleic acid probes are typically of a complexity greater than 50 kb, the complexity depending upon the cytogenetic application as discussed by the authors, and are used for in situ hybridization and stain both interphase and metaphase chromosomes with reliable signals.