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NextDenovo: an efficient error correction and accurate assembly tool for noisy long reads

Hu, Jiang, Wang, Zhuo, Sun, Zongyi, Hu, Benxia, Ayoola, Adeola Oluwakemi, Liang, Fan, Li, Jingjing, Sandoval, José R., Cooper, David N., Ye, Kai, Ruan, Jue, Xiao, Chuan-Le, Wang, Depeng, Wu, Dong-Dong, Wang, Sheng·2024·Genome Biology

Abstract

Long-read sequencing data, particularly those derived from the Oxford Nanopore sequencing platform, tend to exhibit high error rates. Here, we present NextDenovo, an efficient error correction and assembly tool for noisy long reads, which achieves a high level of accuracy in genome assembly. We apply NextDenovo to assemble 35 diverse human genomes from around the world using Nanopore long-read data. These genomes allow us to identify the landscape of segmental duplication and gene copy number variation in modern human populations. The use of NextDenovo should pave the way for population-scale long-read assembly using Nanopore long-read data.

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Research works printed but not linked: 47

  1. Eid J, Fehr A, Gray J, Luong K, Lyle J, Otto G, Peluso P, Rank D, Baybayan P, Bettman B, et al. Real-time DNA sequencing from single polymerase molecules. Science. 2009;323:133–8. · DOI · Paper page
  2. Branton D, Deamer DW, Marziali A, Bayley H, Benner SA, Butler T, Di Ventra M, Garaj S, Hibbs A, Huang X, et al. The potential and challenges of nanopore sequencing. Nat Biotechnol. 2008;26:1146–53. · DOI
  3. Cheng H, Concepcion GT, Feng X, Zhang H, Li H. Haplotype-resolved de novo assembly using phased assembly graphs with hifiasm. Nat Methods. 2021;18:170–5. · DOI · Paper page
  4. Nurk S, Walenz BP, Rhie A, Vollger MR, Logsdon GA, Grothe R, Miga KH, Eichler EE, Phillippy AM, Koren S. HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads. Genome Res. 2020;30:1291–305. · DOI
  5. Lerat E. Identifying repeats and transposable elements in sequenced genomes: how to find your way through the dense forest of programs. Heredity. 2010;104:520–33. · DOI
  6. Jain M, Koren S, Miga KH, Quick J, Rand AC, Sasani TA, Tyson JR, Beggs AD, Dilthey AT, Fiddes IT, et al. Nanopore sequencing and assembly of a human genome with ultra-long reads. Nat Biotechnol. 2018;36:338 (-+). · DOI · Paper page
  7. Jain M, Olsen HE, Turner DJ, Stoddart D, Bulazel KV, Paten B, Haussler D, Willard HF, Akeson M, Miga KH. Linear assembly of a human centromere on the Y chromosome. Nat Biotechnol. 2018;36:321–3. · DOI
  8. Altemose N, Logsdon GA, Bzikadze AV, Sidhwani P, Langley SA, Caldas GV, Hoyt SJ, Uralsky L, Ryabov FD, Shew CJ, et al. Complete genomic and epigenetic maps of human centromeres. Science. 2022;376:eab14178. · DOI · Paper page
  9. Shang L, Li X, He H, Yuan Q, Song Y, Wei Z, Lin H, Hu M, Zhao F, Zhang C, et al. A super pan-genomic landscape of rice. Cell Res. 2022;32:878–96. · DOI
  10. Tong X, Han M-J, Lu K, Tai S, Liang S, Liu Y, Hu H, Shen J, Long A, Zhan C, et al. High-resolution silkworm pan-genome provides genetic insights into artificial selection and ecological adaptation. Nat Commun. 2022;13:5619. · DOI
  11. Wang T, Antonacci-Fulton L, Howe K, Lawson HA, Lucas JK, Phillippy AM, Popejoy AB, Asri M, Carson C, Chaisson MJP, et al. The Human Pangenome Project: a global resource to map genomic diversity. Nature. 2022;604:437–46. · DOI · Paper page
  12. Chen Y, Nie F, Xie S-Q, Zheng Y-F, Dai Q, Bray T, Wang Y-X, Xing J-F, Huang Z-J, Wang D-P, et al. Efficient assembly of nanopore reads via highly accurate and intact error correction. Nat Commun. 2021;12:60. · DOI · Paper page
  13. Koren S, Walenz BP, Berlin K, Miller JR, Bergman NH, Phillippy AM. Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation. Genome Res. 2017;27:722–36. · DOI
  14. Ruan J, Li H. Fast and accurate long-read assembly with wtdbg2. Nat Methods. 2020;17:155–8. · DOI
  15. Kolmogorov M, Yuan J, Lin Y, Pevzner PA. Assembly of long, error-prone reads using repeat graphs. Nat Biotechnol. 2019;37:540–6. · DOI · Paper page
  16. Jayakumar V, Sakakibara Y. Comprehensive evaluation of non-hybrid genome assembly tools for third-generation PacBio long-read sequence data. Brief Bioinform. 2017;20:866–76. · DOI
  17. Hu J, Fan J, Sun Z, Liu S. NextPolish: a fast and efficient genome polishing tool for long-read assembly. Bioinformatics. 2019;36:2253–5. · DOI
  18. Lee C, Grasso C, Sharlow MF. Multiple sequence alignment using partial order graphs. Bioinformatics. 2002;18:452–64. · DOI
  19. Morisse P, Marchet C, Limasset A, Lecroq T, Lefebvre A. Scalable long read self-correction and assembly polishing with multiple sequence alignment. Sci Rep. 2021;11:761. · DOI
  20. Mikheenko A, Prjibelski A, Saveliev V, Antipov D, Gurevich A. Versatile genome assembly evaluation with QUAST-LG. Bioinformatics. 2018;34:i142–50. · DOI
  21. Bailey JA, Eichler EE. Primate segmental duplications: crucibles of evolution, diversity and disease. Nat Rev Genet. 2006;7:552–64. · DOI
  22. Vollger MR, Dishuck PC, Sorensen M, Welch AE, Dang V, Dougherty ML, Graves-Lindsay TA, Wilson RK, Chaisson MJP, Eichler EE. Long-read sequence and assembly of segmental duplications. Nat Methods. 2019;16:88–94. · DOI
  23. Išerić H, Alkan C, Hach F, Numanagić I. Fast characterization of segmental duplication structure in multiple genome assemblies. Algorithms Mol Biol. 2022;17:1–15. · DOI
  24. Perry GH, Dominy NJ, Claw KG, Lee AS, Fiegler H, Redon R, Werner J, Villanea FA, Mountain JL, Misra R, et al. Diet and the evolution of human amylase gene copy number variation. Nat Genet. 2007;39:1256–60. · DOI
  25. Liu Y, Wang S, Li L, Yang T, Dong S, Wei T, Wu S, Liu Y, Gong Y, Feng X, et al. The Cycas genome and the early evolution of seed plants. Nature Plants. 2022;8:389–401. · DOI
  26. Peng Y, Yan H, Guo L, Deng C, Wang C, Wang Y, Kang L, Zhou P, Yu K, Dong X, et al. Reference genome assemblies reveal the origin and evolution of allohexaploid oat. Nat Genet. 2022;54:1248–58. · DOI
  27. Wang K, Wang J, Zhu C, Yang L, Ren Y, Ruan J, Fan G, Hu J, Xu W, Bi X, et al. African lungfish genome sheds light on the vertebrate water-to-land transition. Cell. 2021;184(1362–1376):e1318.
  28. Shao C, Sun S, Liu K, Wang J, Li S, Liu Q, Deagle BE, Seim I, Biscontin A, Wang Q, et al. The enormous repetitive Antarctic krill genome reveals environmental adaptations and population insights. Cell. 2023;186(6):1279–94. · DOI
  29. Yang X, Gao S, Guo L, Wang B, Jia Y, Zhou J, Che Y, Jia P, Lin J, Xu T, et al. Three chromosome-scale Papaver genomes reveal punctuated patchwork evolution of the morphinan and noscapine biosynthesis pathway. Nat Commun. 2021;12:6030. · DOI
  30. Deng Y, Liu S, Zhang Y, Tan J, Li X, Chu X, Xu B, Tian Y, Sun Y, Li B, et al. A telomere-to-telomere gap-free reference genome of watermelon and its mutation library provide important resources for gene discovery and breeding. Mol Plant. 2022;15:1268–84. · DOI
  31. Li H. Minimap2: pairwise alignment for nucleotide sequences. Bioinformatics. 2018;34:3094–100. · DOI · Paper page
  32. Chin C-S, Peluso P, Sedlazeck FJ, Nattestad M, Concepcion GT, Clum A, Dunn C, O’Malley R, Figueroa-Balderas R, Morales-Cruz A, et al. Phased diploid genome assembly with single-molecule real-time sequencing. Nat Methods. 2016;13:1050–4. · DOI
  33. Yang C, Chu J, Warren RL, Birol I. NanoSim: nanopore sequence read simulator based on statistical characterization. GigaScience. 2017;6:1–6. · DOI
  34. Li H. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arXiv e-prints 2013.
  35. McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, Garimella K, Altshuler D, Gabriel S, Daly M, DePristo MA. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 2010;20:1297–303. · DOI · Paper page
  36. Harrow J, Frankish A, Gonzalez JM, Tapanari E, Diekhans M, Kokocinski F, Aken BL, Barrell D, Zadissa A, Searle S, et al. GENCODE: the reference human genome annotation for The ENCODE Project. Genome Res. 2012;22:1760–74. · DOI · Paper page
  37. Shumate A, Salzberg SL. Liftoff: accurate mapping of gene annotations. Bioinformatics. 2021;37:1639–43. · DOI
  38. Jiang Z, Hubley R, Smit A, Eichler EE. DupMasker: a tool for annotating primate segmental duplications. Genome Res. 2008;18:1362–8. · DOI
  39. Telomere-to-Telomere consortium. Homo sapiens genome assembly T2T-CHM13v2.0. Datasets. National Center for Biotechnology Information. 2023. https://ftp.ncbi.nlm.nih.gov/genomes/all/GCF/009/914/755/GCF_009914755.1_T2T-CHM13v2.0/GCF_009914755.1_T2T-CHM13v2.0_genomic.fna.gz.
  40. Lawrence M, Gentleman R, Carey V. rtracklayer: an R package for interfacing with genome browsers. Bioinformatics. 2009;25:1841–2. · DOI
  41. Lee S, Cook D, Lawrence M. plyranges: a grammar of genomic data transformation. Genome Biol. 2019;20:4. · DOI
  42. Gel B, Serra E. karyoploteR: an R/Bioconductor package to plot customizable genomes displaying arbitrary data. Bioinformatics. 2017;33:3088–90. · DOI
  43. Solares EA, Chakraborty M, Miller DE, Kalsow S, Hall K, Perera AG, Emerson JJ, Hawley RS. Nanopore sequencing data for ISO-1. Datasets. National Center for Biotechnology Information. 2023. https://www.ncbi.nlm.nih.gov/bioproject/PRJNA433573.
  44. Lang D, Zhang S, Ren P, Liang F, Sun Z, Meng G, Tan Y, Li X, Lai Q, Han L, et al. The Oryza sativa genome data. Datasets. National Center for Biotechnology Information. 2023. https://www.ncbi.nlm.nih.gov/bioproject/PRJNA635654.
  45. Lin G, He C, Zheng J, Koo D-H, Le H, Zheng H, Tamang TM, Lin J, Liu Y, Zhao M, et al. The Zea mays genome data. Datasets. National Center for Biotechnology Information. 2023. https://www.ncbi.nlm.nih.gov/bioproject/PRJNA635654.
  46. The FlyBase Consortium. Genome assembly Release 6 plus ISO1 MT. Datasets. National Center for Biotechnology Information. 2023. https://www.ncbi.nlm.nih.gov/datasets/genome/GCF_000001215.4/.
  47. Hu J, Wang Z, Sun Z, Hu B, Ayoola AO, Liang F, Li J, Sandoval JR, Cooper DN, Ye K, et al. NextDenovo: an efficient error correction and accurate assembly tool for noisy long reads. Zenodo. 2023. https://zenodo.org/record/8418409. · DOI

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Metadata

Authors
Hu, J., Wang, Z., Sun, Z., Hu, B., Ayoola, A. O., Liang, F., Li, J., Sandoval, J. R., Cooper, D. N., Ye, K., Ruan, J., Xiao, C.-L., Wang, D., Wu, D.-D., & Wang, S.
Venue
Genome Biology
Published
2024-04-26
Volume
25
Issue
1
ISSN
1474-760X
Cited by
431
References
8
Language
en

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