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      Genome sequence of the oyster mushroom Pleurotus ostreatus strain PC9

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          Abstract

          The oyster mushroom Pleurotus ostreatus is a basidiomycete commonly found in the rotten wood and it is one of the most cultivated edible mushrooms globally. Pleurotus ostreatus is also a carnivorous fungus, which can paralyze and kill nematodes within minutes. However, the molecular mechanisms of the predator–prey interactions between P. ostreatus and nematodes remain unclear. PC9 and PC15 are two model strains of P. ostreatus and the genomes of both strains have been sequenced and deposited at the Joint Genome Institute (JGI). These two monokaryotic strains exhibit dramatic differences in growth, but because PC9 grows more robustly in laboratory conditions, it has become the strain of choice for many studies. Despite the fact that PC9 is the common strain for investigation, its genome is fragmentary and incomplete relative to that of PC15. To overcome this problem, we used PacBio long reads and Illumina sequencing to assemble and polish a more integrated genome for PC9. Our PC9 genome assembly, distributed across 17 scaffolds, is highly contiguous and includes five telomere-to-telomere scaffolds, dramatically improving the genome quality. We believe that our PC9 genome resource will be useful to the fungal research community investigating various aspects of P. ostreatus biology.

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          Most cited references54

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          BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs.

          Genomics has revolutionized biological research, but quality assessment of the resulting assembled sequences is complicated and remains mostly limited to technical measures like N50.
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            Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement

            Advances in modern sequencing technologies allow us to generate sufficient data to analyze hundreds of bacterial genomes from a single machine in a single day. This potential for sequencing massive numbers of genomes calls for fully automated methods to produce high-quality assemblies and variant calls. We introduce Pilon, a fully automated, all-in-one tool for correcting draft assemblies and calling sequence variants of multiple sizes, including very large insertions and deletions. Pilon works with many types of sequence data, but is particularly strong when supplied with paired end data from two Illumina libraries with small e.g., 180 bp and large e.g., 3–5 Kb inserts. Pilon significantly improves draft genome assemblies by correcting bases, fixing mis-assemblies and filling gaps. For both haploid and diploid genomes, Pilon produces more contiguous genomes with fewer errors, enabling identification of more biologically relevant genes. Furthermore, Pilon identifies small variants with high accuracy as compared to state-of-the-art tools and is unique in its ability to accurately identify large sequence variants including duplications and resolve large insertions. Pilon is being used to improve the assemblies of thousands of new genomes and to identify variants from thousands of clinically relevant bacterial strains. Pilon is freely available as open source software.
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              Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation

              Long-read single-molecule sequencing has revolutionized de novo genome assembly and enabled the automated reconstruction of reference-quality genomes. However, given the relatively high error rates of such technologies, efficient and accurate assembly of large repeats and closely related haplotypes remains challenging. We address these issues with Canu, a successor of Celera Assembler that is specifically designed for noisy single-molecule sequences. Canu introduces support for nanopore sequencing, halves depth-of-coverage requirements, and improves assembly continuity while simultaneously reducing runtime by an order of magnitude on large genomes versus Celera Assembler 8.2. These advances result from new overlapping and assembly algorithms, including an adaptive overlapping strategy based on tf-idf weighted MinHash and a sparse assembly graph construction that avoids collapsing diverged repeats and haplotypes. We demonstrate that Canu can reliably assemble complete microbial genomes and near-complete eukaryotic chromosomes using either Pacific Biosciences (PacBio) or Oxford Nanopore technologies and achieves a contig NG50 of >21 Mbp on both human and Drosophila melanogaster PacBio data sets. For assembly structures that cannot be linearly represented, Canu provides graph-based assembly outputs in graphical fragment assembly (GFA) format for analysis or integration with complementary phasing and scaffolding techniques. The combination of such highly resolved assembly graphs with long-range scaffolding information promises the complete and automated assembly of complex genomes.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                G3 (Bethesda)
                Genetics
                g3journal
                G3: Genes|Genomes|Genetics
                Oxford University Press
                2160-1836
                February 2021
                22 December 2020
                22 December 2020
                : 11
                : 2
                : jkaa008
                Affiliations
                [1 ] Institute of Molecular Biology , Academia Sinica, Nangang, Taipei 115, Taiwan
                [2 ] Genome and Systems Biology Degree Program, National Taiwan University and Academic Sinica , Taipei, Taiwan
                [3 ] Department of Molecular Biology and Genetics, Cornell University , Ithaca, NY 14853-2703, USA
                [4 ] Department of Microbiology and Plant Pathology, University of California , Riverside, CA 92521, USA
                [5 ] Department of Biochemical Science and Technology, National Taiwan University , Taipei 106, Taiwan
                Author notes
                Corresponding author: Institute of Molecular Biology, Academia Sinica, 128 Academia Road, Section 2, Nangang, Taipei 115, Taiwan. pinghsueh@ 123456gate.sinica.edu.tw
                Author information
                https://orcid.org/0000-0003-3151-4381
                https://orcid.org/0000-0002-7591-0020
                https://orcid.org/0000-0002-9052-5411
                Article
                jkaa008
                10.1093/g3journal/jkaa008
                8022983
                33585864
                a77f7717-3920-4b73-9f80-73159ebc4bbc
                © The Author(s) 2020. Published by Oxford University Press on behalf of Genetics Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 03 September 2020
                : 01 October 2020
                : 01 October 2020
                Page count
                Pages: 7
                Funding
                Funded by: Academia Sinica Career Development;
                Award ID: AS-CDA-106-L03
                Funded by: Taiwan Ministry of Science and Technology;
                Award ID: 106-2311-B-001-039-MY3
                Categories
                Fungal Genetics and Genomics
                AcademicSubjects/SCI01180
                AcademicSubjects/SCI01140
                AcademicSubjects/SCI00010
                AcademicSubjects/SCI00960

                Genetics
                oyster mushroom,pleurotus ostreatus,whole-genome sequencing
                Genetics
                oyster mushroom, pleurotus ostreatus, whole-genome sequencing

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