Please use this identifier to cite or link to this item:
https://doi.org/10.1038/ncomms11307
DC Field | Value | |
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dc.title | Fast and sensitive mapping of nanopore sequencing reads with GraphMap | |
dc.contributor.author | Sović, I | |
dc.contributor.author | Šikić, M | |
dc.contributor.author | Wilm, A | |
dc.contributor.author | Fenlon, S.N | |
dc.contributor.author | Chen, S | |
dc.contributor.author | Nagarajan, N | |
dc.date.accessioned | 2020-10-31T11:36:40Z | |
dc.date.available | 2020-10-31T11:36:40Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Sović, I, Šikić, M, Wilm, A, Fenlon, S.N, Chen, S, Nagarajan, N (2016). Fast and sensitive mapping of nanopore sequencing reads with GraphMap. Nature Communications 7 : 11307. ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms11307 | |
dc.identifier.issn | 2041-1723 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/182483 | |
dc.description.abstract | Realizing the democratic promise of nanopore sequencing requires the development of new bioinformatics approaches to deal with its specific error characteristics. Here we present GraphMap, a mapping algorithm designed to analyse nanopore sequencing reads, which progressively refines candidate alignments to robustly handle potentially high-error rates and a fast graph traversal to align long reads with speed and high precision (>95%). Evaluation on MinION sequencing data sets against short- and long-read mappers indicates that GraphMap increases mapping sensitivity by 10-80% and maps >95% of bases. GraphMap alignments enabled single-nucleotide variant calling on the human genome with increased sensitivity (15%) over the next best mapper, precise detection of structural variants from length 100 bp to 4 kbp, and species and strain-specific identification of pathogens using MinION reads. GraphMap is available open source under the MIT license at https://github.com/isovic/graphmap. | |
dc.publisher | Nature Publishing Group | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | algorithm | |
dc.subject | bioinformatics | |
dc.subject | genome | |
dc.subject | mapping method | |
dc.subject | nanotechnology | |
dc.subject | precision | |
dc.subject | World Wide Web | |
dc.subject | accuracy | |
dc.subject | Article | |
dc.subject | error | |
dc.subject | genetic algorithm | |
dc.subject | GraphMap algorithm | |
dc.subject | human | |
dc.subject | human genome | |
dc.subject | nanopore | |
dc.subject | sequence analysis | |
dc.subject | single nucleotide polymorphism | |
dc.subject | algorithm | |
dc.subject | biology | |
dc.subject | genetics | |
dc.subject | genomics | |
dc.subject | high throughput sequencing | |
dc.subject | nanopore | |
dc.subject | procedures | |
dc.subject | reproducibility | |
dc.subject | sequence alignment | |
dc.subject | Algorithms | |
dc.subject | Computational Biology | |
dc.subject | Genome, Human | |
dc.subject | Genomics | |
dc.subject | High-Throughput Nucleotide Sequencing | |
dc.subject | Humans | |
dc.subject | Nanopores | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.subject | Reproducibility of Results | |
dc.subject | Sequence Alignment | |
dc.type | Article | |
dc.contributor.department | MEDICINE | |
dc.description.doi | 10.1038/ncomms11307 | |
dc.description.sourcetitle | Nature Communications | |
dc.description.volume | 7 | |
dc.description.page | 11307 | |
dc.published.state | Published | |
Appears in Collections: | Elements Staff Publications |
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