Implications of Error-Prone Long-Read Whole-Genome Shotgun Sequencing on Characterizing Reference Microbiomes

被引:12
|
作者
Hu, Yu [1 ]
Fang, Li [1 ]
Nicholson, Christopher [1 ,2 ]
Wang, Kai [1 ,3 ]
机构
[1] Childrens Hosp Philadelphia, Raymond G Perelman Ctr Cellular & Mol Therapeut, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Biol, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
关键词
GUT MICROBIOME; METAGENOMICS; IDENTIFICATION;
D O I
10.1016/j.isci.2020.101223
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Long-read sequencing techniques, such as the Oxford Nanopore Technology, can generate reads that are tens of kilobases in length and are therefore particularly relevant for microbiome studies. However, owing to the higher per-base error rates than typical short-read sequencing, the application of long-read sequencing on microbiomes remains largely unexplored. Here we deeply sequenced two human microbiotamock community samples (HM-276D and HM-277D) from the Human Microbiome Project. We showed that assembly programs consistently achieved high accuracy (similar to 99%) and completeness (similar to 99%) for bacterial strains with adequate coverage. We also found that long-read sequencing provides accurate estimates of species-level abundance (R = 0.94 for 20 bacteria with abundance ranging from 0.005% to 64%). Our results not only demonstrate the feasibility of characterizing complete microbial genomes and populations from error-prone Nanopore sequencing data but also highlight necessary bioinformatics improvements for future metagenomics tool development.
引用
收藏
页数:33
相关论文
共 50 条
  • [31] New genomic features of the polled intersex syndrome variant in goats unraveled by long-read whole-genome sequencing
    Simon, R.
    Lischer, H. E. L.
    Pienkowska-Schelling, A.
    Keller, I.
    Hafliger, I. M.
    Letko, A.
    Schelling, C.
    Luehken, G.
    Drogemuller, C.
    ANIMAL GENETICS, 2020, 51 (03) : 439 - 448
  • [32] Genome-wide detection of structural variation in some sheep breeds using whole-genome long-read sequencing data
    Qiao, Guoyan
    Xu, Pan
    Guo, Tingting
    He, Xue
    Yue, Yaojing
    Yang, Bohui
    JOURNAL OF ANIMAL BREEDING AND GENETICS, 2024, 141 (04) : 403 - 414
  • [33] Novel Partial Exon 51 Deletion in the Duchenne Muscular Dystrophy Gene Identified via Whole Exome Sequencing and Long-Read Whole-Genome Sequencing
    Li, Qianqian
    Chen, Zhanni
    Xiong, Hui
    Li, Ranran
    Yu, Chenguang
    Meng, Jingjing
    Shi, Panlai
    Kong, Xiangdong
    FRONTIERS IN GENETICS, 2021, 12
  • [34] Predictive Power of Long-Read Whole-Genome Sequencing for Rapid Diagnostics of Multidrug-Resistant Brachyspira hyodysenteriae Strains
    Vereecke, Nick
    Botteldoorn, Nadine
    Brosse, Charlotte
    Bonckaert, Caroline
    Nauwynck, Hans
    Haesebrouck, Freddy
    Boyen, Filip
    Maes, Dominiek
    Theuns, Sebastiaan
    MICROBIOLOGY SPECTRUM, 2023, 11 (01):
  • [35] A 12-kb structural variation in progressive myoclonic epilepsy was newly identified by long-read whole-genome sequencing
    Takeshi Mizuguchi
    Takeshi Suzuki
    Chihiro Abe
    Ayako Umemura
    Katsushi Tokunaga
    Yosuke Kawai
    Minoru Nakamura
    Masao Nagasaki
    Kengo Kinoshita
    Yasunobu Okamura
    Satoko Miyatake
    Noriko Miyake
    Naomichi Matsumoto
    Journal of Human Genetics, 2019, 64 : 359 - 368
  • [36] A 12-kb structural variation in progressive myoclonic epilepsy was newly identified by long-read whole-genome sequencing
    Mizuguchi, Takeshi
    Suzuki, Takeshi
    Abe, Chihiro
    Umemura, Ayako
    Tokunaga, Katsushi
    Kawai, Yosuke
    Nakamura, Minoru
    Nagasaki, Masao
    Kinoshita, Kengo
    Okamura, Yasunobu
    Miyatake, Satoko
    Miyake, Noriko
    Matsumoto, Naomichi
    JOURNAL OF HUMAN GENETICS, 2019, 64 (05) : 359 - 368
  • [37] Exploration of whole genome amplification generated chimeric sequences in long-read sequencing data
    Lu, Na
    Qiao, Yi
    An, Pengfei
    Luo, Jiajian
    Bi, Changwei
    Li, Musheng
    Lu, Zuhong
    Tu, Jing
    BRIEFINGS IN BIOINFORMATICS, 2023, 24 (05)
  • [38] Long-read whole genome sequencing reveals HOXD13 alterations in synpolydactyly
    Melas, Marilena
    Kautto, Esko A.
    Franklin, Samuel J.
    Mori, Mari
    McBride, Kim L.
    Mosher, Theresa Mihalic
    Pfau, Ruthann B.
    Hernandez-Gonzalez, Maria Elena
    McGrath, Sean D.
    Magrini, Vincent J.
    White, Peter
    Samora, Julie Balch
    Koboldt, Daniel C.
    Wilson, Richard K.
    HUMAN MUTATION, 2022, 43 (02) : 189 - 199
  • [39] Whole-genome long-read TAPS deciphers DNA methylation patterns at base resolution using PacBio SMRT sequencing technology
    Chen, Jinfeng
    Cheng, Jingfei
    Chen, Xiufei
    Inoue, Masato
    Liu, Yibin
    Song, Chun-Xiao
    NUCLEIC ACIDS RESEARCH, 2022, 50 (18) : E104
  • [40] ESPRESSO: Robust discovery and quantification of transcript isoforms from error-prone long-read RNA-seq data
    Gao, Yuan
    Wang, Feng
    Wang, Robert
    Kutschera, Eric
    Xu, Yang
    Xie, Stephan
    Wang, Yuanyuan
    Kadash-Edmondson, Kathryn E.
    Lin, Lan
    Xing, Yi
    SCIENCE ADVANCES, 2023, 9 (03)