= BAFsegmentation = BAFsegmentation is a method to identify regions of allelic imbalance from B allele frequencies obtained from SNP arrays described in ''Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays'' [[BR]] J. Staaf, D. Lindgren, J. Vallon-Christersson, A. Isaksson, H. Göransson, G. Juliusson, R. Rosenquist, M. Höglund, Å. Borg, M. Ringnér [[BR]] ''submitted'' [[BR]] === License === The BAFsegmentation software will be available as a stand-alone software package upon acceptance of the paper describing the method, and will become available as as a plug-in to BASE as the handling of SNP arrays in BASE is developed. Both versions are available under the [http://www.gnu.org/copyleft/gpl.html GNU General Public License]. === Download BAFsegmentation === The method will be downloadable as a stand-alone version upon acceptance of the submitted manuscript describing BAFsegmentation. === Supplemental Data === * The plots referred to in additional data file 4 in the manuscript are available [http://cbbp.thep.lu.se/~markus/publications/papers/BAFsegmentation_supplemental_data.zip here]. * The simulated data set will be available upon acceptance of the manuscript. === Contact === If you have comments please send an email to johan.staaf@med.lu.se