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Improvement of the banana "Musa acuminata" reference sequence using NGS data and semi-automated bioinformatics methods
G. Martin, FC. Baurens, G. Droc, M. Rouard, A. Cenci, A. Kilian, A. Hastie, J. Doležel, JM. Aury, A. Alberti, F. Carreel, A. D'Hont,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
BioMedCentral
from 2000-12-01
BioMedCentral Open Access
from 2000
Directory of Open Access Journals
from 2000
Free Medical Journals
from 2000
PubMed Central
from 2000
Europe PubMed Central
from 2000 to 2020
ProQuest Central
from 2009-01-01
Open Access Digital Library
from 2000-07-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2000-01-01
Medline Complete (EBSCOhost)
from 2000-01-01
Health & Medicine (ProQuest)
from 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
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Springer Nature OA/Free Journals
from 2000-12-01
- MeSH
- Molecular Sequence Annotation MeSH
- Musa genetics MeSH
- Genetic Markers MeSH
- Genome, Plant * MeSH
- Contig Mapping MeSH
- Sequence Analysis, DNA MeSH
- Computational Biology methods MeSH
- High-Throughput Nucleotide Sequencing MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND: Recent advances in genomics indicate functional significance of a majority of genome sequences and their long range interactions. As a detailed examination of genome organization and function requires very high quality genome sequence, the objective of this study was to improve reference genome assembly of banana (Musa acuminata). RESULTS: We have developed a modular bioinformatics pipeline to improve genome sequence assemblies, which can handle various types of data. The pipeline comprises several semi-automated tools. However, unlike classical automated tools that are based on global parameters, the semi-automated tools proposed an expert mode for a user who can decide on suggested improvements through local compromises. The pipeline was used to improve the draft genome sequence of Musa acuminata. Genotyping by sequencing (GBS) of a segregating population and paired-end sequencing were used to detect and correct scaffold misassemblies. Long insert size paired-end reads identified scaffold junctions and fusions missed by automated assembly methods. GBS markers were used to anchor scaffolds to pseudo-molecules with a new bioinformatics approach that avoids the tedious step of marker ordering during genetic map construction. Furthermore, a genome map was constructed and used to assemble scaffolds into super scaffolds. Finally, a consensus gene annotation was projected on the new assembly from two pre-existing annotations. This approach reduced the total Musa scaffold number from 7513 to 1532 (i.e. by 80%), with an N50 that increased from 1.3 Mb (65 scaffolds) to 3.0 Mb (26 scaffolds). 89.5% of the assembly was anchored to the 11 Musa chromosomes compared to the previous 70%. Unknown sites (N) were reduced from 17.3 to 10.0%. CONCLUSION: The release of the Musa acuminata reference genome version 2 provides a platform for detailed analysis of banana genome variation, function and evolution. Bioinformatics tools developed in this work can be used to improve genome sequence assemblies in other species.
BioNano Genomics 9640 Towne Centre Drive San Diego CA 92121 USA
Bioversity International Parc Scientifique Agropolis 2 34397 Montpellier Cedex 5 France
CIRAD UMR AGAP TA A 108 03 Avenue Agropolis F 34398 Montpellier cedex 5 France
Commissariat à l'Energie Atomique Genoscope 2 rue Gaston Cremieux BP5706 91057 Evry France
Diversity Arrays Technology Yarralumla Australian Capital Territory 2600 Australia
References provided by Crossref.org
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