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Alignment-free genomic sequence comparison using FCGR and signal processing
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 constructing phylo...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937637/ https://www.ncbi.nlm.nih.gov/pubmed/31888438 http://dx.doi.org/10.1186/s12859-019-3330-3 |