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10.1093/molbev/msaa314

http://scihub22266oqcxt.onion/10.1093/molbev/msaa314
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33316067!7798910!33316067
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suck abstract from ncbi

pmid33316067      Mol+Biol+Evol 2021 ; 38 (5): 1777-1791
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  • Phylogenetic Analysis of SARS-CoV-2 Data Is Difficult #MMPMID33316067
  • Morel B; Barbera P; Czech L; Bettisworth B; Hubner L; Lutteropp S; Serdari D; Kostaki EG; Mamais I; Kozlov AM; Pavlidis P; Paraskevis D; Stamatakis A
  • Mol Biol Evol 2021[May]; 38 (5): 1777-1791 PMID33316067show ga
  • Numerous studies covering some aspects of SARS-CoV-2 data analyses are being published on a daily basis, including a regularly updated phylogeny on nextstrain.org. Here, we review the difficulties of inferring reliable phylogenies by example of a data snapshot comprising a quality-filtered subset of 8,736 out of all 16,453 virus sequences available on May 5, 2020 from gisaid.org. We find that it is difficult to infer a reliable phylogeny on these data due to the large number of sequences in conjunction with the low number of mutations. We further find that rooting the inferred phylogeny with some degree of confidence either via the bat and pangolin outgroups or by applying novel computational methods on the ingroup phylogeny does not appear to be credible. Finally, an automatic classification of the current sequences into subclasses using the mPTP tool for molecular species delimitation is also, as might be expected, not possible, as the sequences are too closely related. We conclude that, although the application of phylogenetic methods to disentangle the evolution and spread of COVID-19 provides some insight, results of phylogenetic analyses, in particular those conducted under the default settings of current phylogenetic inference tools, as well as downstream analyses on the inferred phylogenies, should be considered and interpreted with extreme caution.
  • |*Evolution, Molecular[MESH]
  • |*Genome, Viral[MESH]
  • |*Mutation[MESH]
  • |*Phylogeny[MESH]
  • |COVID-19/*genetics[MESH]
  • |Humans[MESH]


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