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LOCLA is a novel genome assembly optimization tool, LOCLA, that iteratively enhances the quality of an assembly by locating sequencing reads on partially assembled scaffolds and thus enable gap filling and further scaffolding. LOCLA utilizes reads of diverse sequencing techniques, e.g., 10x Genomics (10xG) Linked-Reads, PacBio HiFi Reads and Oxford Nanopore Technologies. In our own experiments, we assembled 10x Genomics (10xG) Linked-Reads via Supernova assembler and TGS reads via Canu. Additional tools incorporated in our pipeline include Hybrid Scaffold developed by Bionano Genomics and RagTag.
The docker image of LOCLA is freely accessible at https://hub.docker.com/r/lsbnb/locla . Usage and technical notes are provided at our Githib website: https://github.com/lsbnb/locla .
ngs sequencing, genome assembly, tgs sequencing
ngs sequencing, genome assembly, tgs sequencing
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