A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.
By Y. Nannya, M. Sanada, Kumi Nakazaki, N. Hosoya, Lili Wang, A. Hangaishi, M. Kurokawa, S. Chiba, D. Bailey, G. Kennedy and 1 more. Cancer Research, 2005
686 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/af2bea41b78fd485e05e3834f83595fd85bdb910
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In Genetics
- Stephen W. Scherer
- Brian Walenz
- Pauline Crystal Ng
- Vikas Bansal
- Granger G. Sutton
- Vineet Bafna
- Steven Henikoff
- Heng Li
In Molecular Biology
- Brian Walenz
- Stephen W. Scherer
- Pauline Crystal Ng
- Vikas Bansal
- Granger G. Sutton
- Vineet Bafna
- Steven Henikoff
- Burkhard Rost
In Plant Science
Citations in the corpus
- Diagnosis of human preimplantation embryo viability. (2015, background): “…that do not require extensive pre-amplification of DNA and instead were designed for large quantities of starting material [i.e. as in cancer (Nannya et al., 2005), genome-wide association studies (Glessner and Hakonarson, 2011) and prenatal diagnosis (Rajcan-Separovic, 2012; Shaffer et al.,…”
- The Diploid Genome Sequence of an Individual Human (2007, methodology): “jp), the copy number changes were inferred using a HMM built into CNAG [98].”
- Acquired mutations in TET2 are common in myelodysplastic syndromes (2009, methodology): “We used the Genotyping Analysis Software GTYPE (Affymetrix) for analysis of data and quality control, and the public domain CNAG software packag”
- Development of query strategies to identify a histologic lymphoma subtype in a large linked database system. (2006, neutral): “In addition to the application to BAC based microarrays, this approach has been employed in the context of the oligonucleotide platforms (Iafrate et al. 2004; Nannya et al. 2005; Zhao et al. 2004).”