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. |
hg clone https://toolshed.g2.bx.psu.edu/repos/bgruening/tgsgapcloser
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
fills the N-gap of error-prone long reads | 1.0.3+galaxy0 | 20.01 |