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About: The following software represents a robust framework for the identification of structural variants using clone-end sequencing. Unlike previous methods, our approach does not rely on an a priori determined mapping of all reads to the reference. Instead, we build a framework for finding the most probable assignment of sequenced clones to potential structural variants based on the other clones. Please see the paper for more details. |
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News: August 9, 2008 - Dataset is available (MySQL tables for Trace and BLAT hits) April 14, 2008 - New version of the paper uploaded to the website January 18, 2008 - Website created and version 1.0 of source and results were uploaded to the website. |