Alignment-free genomic sequence comparison using FCGR and signal processing
Abstract Background Alignment-free methods of genomic comparison offer the possibility of scaling to large data sets of nucleotide sequences comprised of several thousand or more base pairs. Such methods can be used for purposes of deducing “nearby” species in a reference data set, or for constructi...
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| Aineistotyyppi: | Artikkeli |
| Kieli: | English |
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BMC
2019-12-01
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| Sarja: | BMC Bioinformatics |
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| Linkit: | https://doi.org/10.1186/s12859-019-3330-3 |