dist.dna(x, model = "K80", variance = FALSE, gamma = FALSE, pairwise.deletion = FALSE, base.freq = NULL, as.matrix = FALSE)"DNAbin" (use as.DNAbin is they are
stored as character)."raw", "N", "TS",
"TV", "JC69", "K80" (the default),
"F81", "K81", "F84", "BH87",
"T92", "TN93", "GG95", "logdet",
"paralin", "indel", or "indelblock".FALSE so the variances are not
computed.model = "indel" or "indelblock").as.matrix = TRUE. If model = "BH87", a numeric
matrix is returned because the Barry--Hartigan distance is not
symmetric.If variance = TRUE an attribute called "variance" is
given to the returned object.
model have been extensively described in the literature. A
brief description is given below; more details can be found in the
references.raw, N: This is simply the proportion or the number of
sites that differ between each pair of sequences. This may be useful
to draw ``saturation plots''. The options variance and
gamma have no effect, but pairwise.deletion can.
TS, TV: These are the numbers of transitions and
transversions, respectively.
JC69: This model was developed by Jukes and Cantor (1969). It
assumes that all substitutions (i.e. a change of a base by another
one) have the same probability. This probability is the same for all
sites along the DNA sequence. This last assumption can be relaxed by
assuming that the substition rate varies among site following a
gamma distribution which parameter must be given by the user. By
default, no gamma correction is applied. Another assumption is that
the base frequencies are balanced and thus equal to 0.25.
K80: The distance derived by Kimura (1980), sometimes referred
to as ``Kimura's 2-parameters distance'', has the same underlying
assumptions than the Jukes--Cantor distance except that two kinds of
substitutions are considered: transitions (A <-> G, C <-> T), and
transversions (A <-> C, A <-> T, C <-> G, G <-> T). They are assumed
to have different probabilities. A transition is the substitution of
a purine (C, T) by another one, or the substitution of a pyrimidine
(A, G) by another one. A transversion is the substitution of a
purine by a pyrimidine, or vice-versa. Both transition and
transversion rates are the same for all sites along the DNA
sequence. Jin and Nei (1990) modified the Kimura model to allow for
variation among sites following a gamma distribution. Like for the
Jukes--Cantor model, the gamma parameter must be given by the
user. By default, no gamma correction is applied.
F81: Felsenstein (1981) generalized the Jukes--Cantor model
by relaxing the assumption of equal base frequencies. The formulae
used in this function were taken from McGuire et al. (1999).
K81: Kimura (1981) generalized his model (Kimura 1980) by
assuming different rates for two kinds of transversions: A <-> C and
G <-> T on one side, and A <-> T and C <-> G on the other. This is
what Kimura called his ``three substitution types model'' (3ST), and
is sometimes referred to as ``Kimura's 3-parameters distance''.
F84: This model generalizes K80 by relaxing the assumption
of equal base frequencies. It was first introduced by Felsenstein in
1984 in Phylip, and is fully described by Felsenstein and Churchill
(1996). The formulae used in this function were taken from McGuire
et al. (1999).
BH87: Barry and Hartigan (1987) developed a distance based
on the observed proportions of changes among the four bases. This
distance is not symmetric.
T92: Tamura (1992) generalized the Kimura model by relaxing
the assumption of equal base frequencies. This is done by taking
into account the bias in G+C content in the sequences. The
substitution rates are assumed to be the same for all sites along
the DNA sequence.
TN93: Tamura and Nei (1993) developed a model which assumes
distinct rates for both kinds of transition (A <-> G versus C <->
T), and transversions. The base frequencies are not assumed to be
equal and are estimated from the data. A gamma correction of the
inter-site variation in substitution rates is possible.
GG95: Galtier and Gouy (1995) introduced a model where the
G+C content may change through time. Different rates are assumed for
transitons and transversions.
logdet: The Log-Det distance, developed by Lockhart et
al. (1994), is related to BH87. However, this distance is
symmetric. Formulae from Gu and Li (1996) are used.
dist.logdet in phangorn uses a different
implementation that gives substantially different distances for
low-diverging sequences.
paralin: Lake (1994) developed the paralinear distance which
can be viewed as another variant of the Barry--Hartigan distance.
indel: this counts the number of sites where there is an
insertion/deletion gap in one sequence and not in the other.
indelblock: same than before but contiguous gaps are
counted as a single unit. Note that the distance between -A- and
A-- is 3 because there are three different blocks of gaps, whereas
the ``indel'' distance will be 2.
Felsenstein, J. (1981) Evolutionary trees from DNA sequences: a maximum likelihood approach. Journal of Molecular Evolution, 17, 368--376.
Felsenstein, J. and Churchill, G. A. (1996) A Hidden Markov model approach to variation among sites in rate of evolution. Molecular Biology and Evolution, 13, 93--104.
Galtier, N. and Gouy, M. (1995) Inferring phylogenies from DNA sequences of unequal base compositions. Proceedings of the National Academy of Sciences USA, 92, 11317--11321.
Gu, X. and Li, W.-H. (1996) Bias-corrected paralinear and LogDet distances and tests of molecular clocks and phylogenies under nonstationary nucleotide frequencies. Molecular Biology and Evolution, 13, 1375--1383.
Jukes, T. H. and Cantor, C. R. (1969) Evolution of protein molecules. in Mammalian Protein Metabolism, ed. Munro, H. N., pp. 21--132, New York: Academic Press.
Kimura, M. (1980) A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. Journal of Molecular Evolution, 16, 111--120.
Kimura, M. (1981) Estimation of evolutionary distances between homologous nucleotide sequences. Proceedings of the National Academy of Sciences USA, 78, 454--458.
Jin, L. and Nei, M. (1990) Limitations of the evolutionary parsimony method of phylogenetic analysis. Molecular Biology and Evolution, 7, 82--102.
Lake, J. A. (1994) Reconstructing evolutionary trees from DNA and protein sequences: paralinear distances. Proceedings of the National Academy of Sciences USA, 91, 1455--1459.
Lockhart, P. J., Steel, M. A., Hendy, M. D. and Penny, D. (1994) Recovering evolutionary trees under a more realistic model of sequence evolution. Molecular Biology and Evolution, 11, 605--602.
McGuire, G., Prentice, M. J. and Wright, F. (1999). Improved error bounds for genetic distances from DNA sequences. Biometrics, 55, 1064--1070.
Tamura, K. (1992) Estimation of the number of nucleotide substitutions when there are strong transition-transversion and G + C-content biases. Molecular Biology and Evolution, 9, 678--687.
Tamura, K. and Nei, M. (1993) Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Molecular Biology and Evolution, 10, 512--526.
read.GenBank, read.dna,
write.dna, DNAbin,
dist.gene, cophenetic.phylo,
dist