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Assembling Long Gene Copies from Short Read Data
Assembles two or more gene copies from short-read Next-Generation Sequencing data. Works best when there are only two gene copies and read length >=250 base pairs. High and relatively even coverage are important.
- Version1.2.0
- R version≥ 3.5.0
- LicenseGPL-2
- Needs compilation?No
- Last release11/25/2022
Documentation
Team
Lei Yang
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- Depends1 package
- Imports11 packages
- Suggests3 packages