TGSGapCloser
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Description
A gap-closing software tool that uses error-prone long reads generated by third-generation-sequence techniques (Pacbio, Oxford Nanopore, etc.) or preassembled contigs to fill N-gap in the genome assembly.
Environment Modules
Run module spider tgsgapcloser
to find out what environment modules are available for this application.
System Variables
- HPC_TGSGAPCLOSER_DIR - installation directory
- HPC_TGSGAPCLOSER_BIN - executable directory
Citation
If you publish research that uses tgsgapcloser you have to cite it as follows: