4.6 Article

LongStitch: high-quality genome assembly correction and scaffolding using long reads

期刊

BMC BIOINFORMATICS
卷 22, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12859-021-04451-7

关键词

Long reads; De novo genome assembly; Genome scaffolding; Minimizers; Misassembly correction

资金

  1. Genome BC
  2. Genome Canada [243FOR, 281ANV]
  3. National Institutes of Health [2R01HG007182-04A1]

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LongStitch is a scalable pipeline that corrects and scaffolds draft genome assemblies exclusively using long reads. It incorporates multiple tools developed by the group and runs in up to three stages, including initial assembly correction (Tigmint-long), followed by two incremental scaffolding stages (ntLink and ARKS-long). Tested on various organisms and consistently improving assembly contiguity compared to other tools, LongStitch is expected to benefit a wide variety of de novo genome assembly projects.
Background Generating high-quality de novo genome assemblies is foundational to the genomics study of model and non-model organisms. In recent years, long-read sequencing has greatly benefited genome assembly and scaffolding, a process by which assembled sequences are ordered and oriented through the use of long-range information. Long reads are better able to span repetitive genomic regions compared to short reads, and thus have tremendous utility for resolving problematic regions and helping generate more complete draft assemblies. Here, we present LongStitch, a scalable pipeline that corrects and scaffolds draft genome assemblies exclusively using long reads. Results LongStitch incorporates multiple tools developed by our group and runs in up to three stages, which includes initial assembly correction (Tigmint-long), followed by two incremental scaffolding stages (ntLink and ARKS-long). Tigmint-long and ARKS-long are misassembly correction and scaffolding utilities, respectively, previously developed for linked reads, that we adapted for long reads. Here, we describe the LongStitch pipeline and introduce our new long-read scaffolder, ntLink, which utilizes lightweight minimizer mappings to join contigs. LongStitch was tested on short and long-read assemblies of Caenorhabditis elegans, Oryza sativa, and three different human individuals using corresponding nanopore long-read data, and improves the contiguity of each assembly from 1.2-fold up to 304.6-fold (as measured by NGA50 length). Furthermore, LongStitch generates more contiguous and correct assemblies compared to state-of-the-art long-read scaffolder LRScaf in most tests, and consistently improves upon human assemblies in under five hours using less than 23 GB of RAM. Conclusions Due to its effectiveness and efficiency in improving draft assemblies using long reads, we expect LongStitch to benefit a wide variety of de novo genome assembly projects. The LongStitch pipeline is freely available at .

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