Stanley F. Nelson - researchr alias

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Viewing Publication 1 - 7 from 7

2015

Rich annotation of DNA sequencing variants by leveraging the Ensembl Variant Effect Predictor with pluginsMichael Yourshaw, S. Paige Taylor, Aliz R. Rao, Martín G. Martín, Stanley F. Nelson. bib, 16(2):255-264, 2015. [doi]

2011

Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNVJarupon Fah Sathirapongsasuti, Hane Lee, Basil A. J. Horst, Georg Brunner, Alistair J. Cochran, Scott Binder, John Quackenbush, Stanley F. Nelson. bioinformatics, 27(19):2648-2654, 2011. [doi]

2010

2009

Local alignment of two-base encoded DNA sequenceNils Homer, Barry Merriman, Stanley F. Nelson. bmcbi, 10, 2009. [doi]

2008

Multimarker analysis and imputation of multiple platform pooling-based genome-wide association studiesNils Homer, Waibhav Tembe, Szabolcs Szelinger, Margot Redman, Dietrich A. Stephan, John V. Pearson, Stanley F. Nelson, David Craig. bioinformatics, 24(17):1896-1902, 2008. [doi]

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