Stanley F. Nelson

According to our database, Stanley F. Nelson authored at least 7 papers between 2008 and 2015.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of four.

2015

Rich annotation of DNA sequencing variants by leveraging the Ensembl Variant Effect Predictor with plugins.

Michael Yourshaw, S. Paige Taylor, Aliz R. Rao, Martín G. Martín, Stanley F. Nelson

Briefings Bioinform., 2015

2011

Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV.

Jarupon Fah Sathirapongsasuti, Hane Lee, Basil A. J. Horst, Georg Brunner, Alistair J. Cochran, Scott Binder, John Quackenbush, Stanley F. Nelson

Bioinform., 2011

2010

High-throughput sequencing of the DBA/2J mouse genome.

Xusheng Wang, Richa Agarwala, John A. Capra, Zugen Chen, Deanna M. Church, Daniel C. Ciobanu, Zhengsheng Li, Lu Lu, Khyobeni Mozhui, Megan K. Mulligan, Stanley F. Nelson, Katherine S. Pollard, William Taylor, Donald B. Thomason, Robert W. Williams

BMC Bioinform., 2010

SeqWare Query Engine: storing and searching sequence data in the cloud.

Brian D. O'Connor, Barry Merriman, Stanley F. Nelson

BMC Bioinform., 2010

Local alignment of generalized k-base encoded DNA sequence.

Nils Homer, Stanley F. Nelson, Barry Merriman

BMC Bioinform., 2010

2009

Local alignment of two-base encoded DNA sequence.

Nils Homer, Barry Merriman, Stanley F. Nelson

BMC Bioinform., 2009

2008

Multimarker analysis and imputation of multiple platform pooling-based genome-wide association studies.

Nils Homer, Waibhav Tembe, Szabolcs Szelinger, Margot Redman, Dietrich A. Stephan, John V. Pearson, Stanley F. Nelson, David W. Craig

Bioinform., 2008