Adam P. Butler

According to our database, Adam P. Butler authored at least 3 papers between 2007 and 2022.

Collaborative distances:

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

2022

Variant Library Annotation Tool (VaLiAnT): an oligonucleotide library design and annotation tool for saturation genome editing and other deep mutational scanning experiments.

Luca Barbon, Victoria Offord, Elizabeth J. Radford, Adam P. Butler, Sebastian S. Gerety, David J. Adams, Hong Kee Tan, Andrew J. Waters

Bioinform., 2022

2011

Data mining using the Catalogue of Somatic Mutations in Cancer BioMart.

Rebecca Shepherd, Simon A. Forbes, David Beare, Sally Bamford, Charlotte Cole, Sari Ward, Nidhi Bindal, Prasad Gunasekaran, Mingming Jia, Chai Yin Kok, Kenric Leung, Andrew Menzies, Adam P. Butler, Jon W. Teague, Peter J. Campbell, Michael R. Stratton, P. Andrew Futreal

Database J. Biol. Databases Curation, 2011

2007

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.

Ed Dicks, Jon W. Teague, Philip Stephens, Keiran Raine, Andrew D. Yates, C. Mattocks, P. Tarpey, Adam P. Butler, Andrew Menzies, David Richardson, Andrew M. Jenkinson, Helen Davies, Sarah Edkins, Simon A. Forbes, Kristian A. Gray, Christopher Greenman, Rebecca Shepherd, Michael R. Stratton, P. Andrew Futreal, Richard Wooster

Bioinform., 2007