forestSV: structural variant discovery through statistical learning.
Level V
Where this comes from
- Record sourced from PubMed, PMID 22751202.
- Also identified by DOI 10.1038/nmeth.2085 and PMC identifier 3427657.
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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.
Medical subject headings
- Genomic Structural Variation
- High-Throughput Nucleotide Sequencing