The assembly generated from SSPACE‐LR was gap filled with GAPCloser (Illumina Data) and PBJelly2 (PacBio long reads). PBJelly2 software is used to fill gaps in the assembly using PacBio long reads. The program is designed to handle PacBio data taking its error model into consideration. It uses a PacBio read data‐specific aligner called BLASR (Chaisson and Tesler,
Pbjelly2
PBJelly2 is a software tool designed for gap filling in genome assemblies. It utilizes long-read sequencing data, such as PacBio or Nanopore, to close gaps and improve the contiguity of genome assemblies. PBJelly2 is a core bioinformatics tool for genome finishing and assembly optimization.
Lab products found in correlation
1 protocol using pbjelly2
Scaffolding and Gap Filling for Genome Assembly
The assembly generated from SSPACE‐LR was gap filled with GAPCloser (Illumina Data) and PBJelly2 (PacBio long reads). PBJelly2 software is used to fill gaps in the assembly using PacBio long reads. The program is designed to handle PacBio data taking its error model into consideration. It uses a PacBio read data‐specific aligner called BLASR (Chaisson and Tesler,
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