Improving genome assemblies using multi-platform sequence data
dc.citation.epage | 232 | en_US |
dc.citation.spage | 220 | en_US |
dc.contributor.author | Kavak, P. | en_US |
dc.contributor.author | Ergüner, B. | en_US |
dc.contributor.author | Üstek, D. | en_US |
dc.contributor.author | Yüksel, B. | en_US |
dc.contributor.author | Saǧıroǧlu, M. Ş. | en_US |
dc.contributor.author | Güngör, T. | en_US |
dc.contributor.author | Alkan, Can | en_US |
dc.coverage.spatial | Naples, Italy | |
dc.date.accessioned | 2018-04-12T11:42:13Z | |
dc.date.available | 2018-04-12T11:42:13Z | |
dc.date.issued | 2015-09 | en_US |
dc.department | Department of Computer Engineering | en_US |
dc.description | Date of Conference: 10-12 September, 2015 | |
dc.description | Conference name: CIBB: International Meeting on Computational Intelligence Methods for Bioinformatics and Biostatistics - 12th International Meeting, CIBB 2015 | |
dc.description.abstract | Accurate de novo assembly using short reads generated by next generation sequencing technologies is still an open problem. Although there are several assembly algorithms developed for data generated with different sequencing technologies, and some that can make use of hybrid data, the assemblies are still far from being perfect. There is still a need for computational approaches to improve draft assemblies. Here we propose a new method to correct assembly mistakes when there are multiple types of data generated using different sequencing technologies that have different strengths and biases. We exploit the assembly of highly accurate short reads to correct the contigs obtained from less accurate long reads. We apply our method to Illumina, 454, and Ion Torrent data, and also compare our results with existing hybrid assemblers, Celera and Masurca. © Springer International Publishing Switzerland 2016. | en_US |
dc.description.provenance | Made available in DSpace on 2018-04-12T11:42:13Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 179475 bytes, checksum: ea0bedeb05ac9ccfb983c327e155f0c2 (MD5) Previous issue date: 2016 | en |
dc.identifier.doi | 10.1007/978-3-319-44332-4_17 | en_US |
dc.identifier.issn | 0302-9743 | en_US |
dc.identifier.uri | http://hdl.handle.net/11693/37501 | en_US |
dc.language.iso | English | en_US |
dc.publisher | Springer | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1007/978-3-319-44332-4_17 | en_US |
dc.source.title | Computational Intelligence Methods for Bioinformatics and Biostatistics - 12th International Meeting, CIBB 2015 | en_US |
dc.subject | Assembly improvement | en_US |
dc.subject | De novo assembly | en_US |
dc.subject | Next generation multi-platform sequencing | en_US |
dc.subject | Artificial intelligence | en_US |
dc.subject | Assembly algorithm | en_US |
dc.subject | Computational approach | en_US |
dc.subject | Genome assembly | en_US |
dc.subject | Highly accurate | en_US |
dc.subject | Multi-platform | en_US |
dc.subject | Next-generation sequencing | en_US |
dc.subject | Sequence data | en_US |
dc.subject | Bioinformatics | en_US |
dc.title | Improving genome assemblies using multi-platform sequence data | en_US |
dc.type | Conference Paper | en_US |
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