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  3. Genome annotation
  4. Repetitive DNA
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An improved approach for accurate and efficient calling of structural variations with low-coverage sequence data.

Specifications

Software type:
Package
Interface:
Command line interface
Restrictions to use:
None
Operating system:
Unix/Linux
Computer skills:
Advanced
Stability:
Stable
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Publications

  • (Zhang and Wu, 2011) SVseq: an approach for detecting exact breakpoints of deletions with low-coverage sequence data. Bioinformatics.
    PMID: 21994222

Classification

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