Abstract
Detecting genomic structural variants from high-throughput sequencing data is a complex and unresolved challenge. We have developed a statistical learning approach, based on Random Forests, that integrates prior knowledge about the characteristics of structural variants and leads to improved discovery in high-throughput sequencing data. The implementation of this technique, forestSV, offers high sensitivity and specificity coupled with the flexibility of a data-driven approach. © 2012 Nature America, Inc. All rights reserved.
Cite
CITATION STYLE
Michaelson, J. J., & Sebat, J. (2012). ForestSV: Structural variant discovery through statistical learning. Nature Methods, 9(8), 819–821. https://doi.org/10.1038/nmeth.2085
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