BAUM: improving genome assembly by adaptive unique mapping and local overlap‐layout‐consensus approach

Motivation: It is highly desirable to assemble genomes of high continuity and consistency at low cost. The current bottleneck of draft genome continuity using the second generation sequencing (SGS) reads is primarily caused by uncertainty among repetitive sequences. Even though the single‐molecule real‐time sequencing technology is very promising to overcome the uncertainty issue, its relatively high cost and error rate add burden on budget or computation. Many long‐read assemblers take the overlap‐layout‐consensus (OLC) paradigm, which is less sensitive to sequencing errors, heterozygosity and variability of coverage. However, current assemblers of SGS data do not sufficiently take advantage of the OLC approach. Results: Aiming at minimizing uncertainty, the proposed method BAUM, breaks the whole genome into regions by adaptive unique mapping; then the local OLC is used to assemble each region in parallel. BAUM can (i) perform reference‐assisted assembly based on the genome of a close species (ii) or improve the results of existing assemblies that are obtained based on short or long sequencing reads. The tests on two eukaryote genomes, a wild rice Oryza longistaminata and a parrot Melopsittacus undulatus, show that BAUM achieved substantial improvement on genome size and continuity. Besides, BAUM reconstructed a considerable amount of repetitive regions that failed to be assembled by existing short read assemblers. We also propose statistical approaches to control the uncertainty in different steps of BAUM. Availability and implementation: http://www.zhanyuwang.xin/wordpress/index.php/2017/07/21/baum Supplementary information: Supplementary data are available at Bioinformatics online.

[1]  René L. Warren,et al.  Assembling millions of short DNA sequences using SSAKE , 2006, Bioinform..

[2]  Yang Dong,et al.  Genome and Comparative Transcriptomics of African Wild Rice Oryza longistaminata Provide Insights into Molecular Mechanism of Rhizomatousness and Self-Incompatibility. , 2015, Molecular plant.

[3]  A. Gnirke,et al.  High-quality draft assemblies of mammalian genomes from massively parallel sequence data , 2010, Proceedings of the National Academy of Sciences.

[4]  Thomas D. Otto,et al.  RATT: Rapid Annotation Transfer Tool , 2011, Nucleic acids research.

[5]  Sergey I. Nikolenko,et al.  SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing , 2012, J. Comput. Biol..

[6]  Tao Li,et al.  A new pheromone trail-based genetic algorithm for comparative genome assembly , 2008, Nucleic acids research.

[7]  Matthew Berriman,et al.  Iterative Correction of Reference Nucleotides (iCORN) using second generation sequencing technology , 2010, Bioinform..

[8]  Evgeny M. Zdobnov,et al.  BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs , 2015, Bioinform..

[9]  M. Berriman,et al.  Improving draft assemblies by iterative mapping and assembly of short reads to eliminate gaps , 2010, Genome Biology.

[10]  Siu-Ming Yiu,et al.  IDBA - A Practical Iterative de Bruijn Graph De Novo Assembler , 2010, RECOMB.

[11]  Steven J. M. Jones,et al.  Abyss: a Parallel Assembler for Short Read Sequence Data Material Supplemental Open Access , 2022 .

[12]  W. Pirovano,et al.  Toward almost closed genomes with GapFiller , 2012, Genome Biology.

[13]  Walter Pirovano,et al.  BIOINFORMATICS APPLICATIONS , 2022 .

[14]  Alexey Gurevich,et al.  QUAST: quality assessment tool for genome assembles , 2013 .

[15]  J. Landolin,et al.  Assembling Large Genomes with Single-Molecule Sequencing and Locality Sensitive Hashing , 2014 .

[16]  Eugene W. Myers,et al.  A whole-genome assembly of Drosophila. , 2000, Science.

[17]  F. Balloux,et al.  Transient structural variations have strong effects on quantitative traits and reproductive isolation in fission yeast , 2016, Nature Communications.

[18]  S. Turner,et al.  Real-Time DNA Sequencing from Single Polymerase Molecules , 2009, Science.

[19]  Ryan R. Wick,et al.  Unicycler: Resolving bacterial genome assemblies from short and long sequencing reads , 2016, bioRxiv.

[20]  N. W. Davis,et al.  The complete genome sequence of Escherichia coli K-12. , 1997, Science.

[21]  E. Birney,et al.  Velvet: algorithms for de novo short read assembly using de Bruijn graphs. , 2008, Genome research.

[22]  S. Salzberg,et al.  Repetitive DNA and next-generation sequencing: computational challenges and solutions , 2012, Nature Reviews Genetics.

[23]  O. Kohany,et al.  Repbase Update, a database of repetitive elements in eukaryotic genomes , 2015, Mobile DNA.

[24]  M. Schatz,et al.  Assembly of large genomes using second-generation sequencing. , 2010, Genome research.

[25]  Wing-Kin Sung,et al.  Opera: Reconstructing Optimal Genomic Scaffolds with High-Throughput Paired-End Sequences , 2011, J. Comput. Biol..

[26]  Peifeng Ji,et al.  The combination of direct and paired link graphs can boost repetitive genome assembly , 2016, Nucleic acids research.

[27]  Inanç Birol,et al.  Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate species , 2013, GigaScience.

[28]  Aaron A. Klammer,et al.  Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data , 2013, Nature Methods.

[29]  C. Nusbaum,et al.  ALLPATHS: de novo assembly of whole-genome shotgun microreads. , 2008, Genome research.

[30]  Sergey Koren,et al.  Hybrid assembly of the large and highly repetitive genome of Aegilops tauschii , a progenitor of bread wheat , with the mega-reads algorithm , 2016 .

[31]  S. Koren,et al.  Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation , 2016, bioRxiv.

[32]  Adam M Phillippy,et al.  New advances in sequence assembly , 2017, Genome research.

[33]  Mauricio O. Carneiro,et al.  The advantages of SMRT sequencing , 2013, Genome Biology.

[34]  Leping Li,et al.  ART: a next-generation sequencing read simulator , 2012, Bioinform..

[35]  Jian Wang,et al.  SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler , 2012, GigaScience.

[36]  James G. Baldwin-Brown,et al.  Contiguous and accurate de novo assembly of metazoan genomes with modest long read coverage , 2016, bioRxiv.

[37]  Karolj Skala,et al.  Evaluation of hybrid and non-hybrid methods for de novo assembly of nanopore reads , 2015, bioRxiv.

[38]  P. Pevzner,et al.  An Eulerian path approach to DNA fragment assembly , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[39]  M. Metzker Sequencing technologies — the next generation , 2010, Nature Reviews Genetics.

[40]  Eugene W. Myers,et al.  Toward Simplifying and Accurately Formulating Fragment Assembly , 1995, J. Comput. Biol..

[41]  M S Waterman,et al.  Identification of common molecular subsequences. , 1981, Journal of molecular biology.

[42]  Michael S. Waterman,et al.  A New Algorithm for DNA Sequence Assembly , 1995, J. Comput. Biol..

[43]  A. Gnirke,et al.  ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads , 2009, Genome Biology.

[44]  B. Berger,et al.  ARACHNE: a whole-genome shotgun assembler. , 2002, Genome research.

[45]  Lei M. Li,et al.  An algorithm for computing exact least-trimmed squares estimate of simple linear regression with constraints , 2004, Comput. Stat. Data Anal..

[46]  Ning Ma,et al.  BLAST+: architecture and applications , 2009, BMC Bioinformatics.

[47]  Anqi Wang,et al.  SEME: A Fast Mapper of Illumina Sequencing Reads with Statistical Evaluation , 2013, RECOMB.

[48]  Richard Durbin,et al.  Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .

[49]  Samuel A. Assefa,et al.  A post-assembly genome-improvement toolkit (PAGIT) to obtain annotated genomes from contigs , 2012, Nature Protocols.

[50]  Thomas M. Keane,et al.  ABACAS: algorithm-based automatic contiguation of assembled sequences , 2009, Bioinform..

[51]  Feng Luo,et al.  MECAT: fast mapping, error correction, and de novo assembly for single-molecule sequencing reads , 2017, Nature Methods.

[52]  Steven L Salzberg,et al.  Fast gapped-read alignment with Bowtie 2 , 2012, Nature Methods.