bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Dec. 16, 2023
We
introduce
PhyloJunction,
a
computational
framework
designed
to
facilitate
the
prototyping,
testing,
and
characterization
of
evolutionary
models.
PhyloJunction
is
distributed
as
an
open-source
Python
library
that
can
be
used
implement
variety
models,
through
its
flexible
graphical
modeling
architecture
dedicated
model
specification
language.
Model
design
use
are
exposed
users
via
command-line
interfaces,
which
integrate
steps
simulating,
summarizing,
visualizing
data.
This
paper
describes
features
-
include,
but
not
limited
to,
general
implementation
popular
family
phylogenetic
diversification
models
and,
moving
forward,
how
it
may
expanded
only
include
new
also
become
platform
for
conducting
teaching
statistical
learning.
Genetics Selection Evolution,
Journal Year:
2024,
Volume and Issue:
56(1)
Published: April 2, 2024
Abstract
Background
Chinese
indigenous
sheep
are
valuable
resources
with
unique
features
and
characteristics.
They
distributed
across
regions
different
climates
in
mainland
China;
however,
few
reports
have
analyzed
the
environmental
adaptability
of
based
on
their
genome.
We
examined
variants
signatures
selection
involved
adaptation
to
extreme
humidity,
altitude,
temperature
conditions
173
genomes
from
41
phenotypically
geographically
representative
breeds
characterize
genetic
basis
underlying
these
populations.
Results
Based
analysis
population
structure,
we
inferred
that
divided
into
four
groups:
Kazakh
(KAZ),
Mongolian
(MON),
Tibetan
(TIB),
Yunnan
(YUN).
also
detected
a
set
candidate
genes
relevant
conditions,
such
as
drought-prone
(
TBXT
,
TG
HOXA1
),
high-altitude
DYSF
EPAS1
JAZF1
PDGFD
NF1
)
warm-temperature
TSHR
ABCD4
TEX11
).
Among
all
genes,
eight
CNTN4
DOCK10
LOC105608545
LOC121816479
SEM3A
SVIL
overlap
between
conditions.
The
gene
shows
strong
signature
for
positive
group
harbors
single
nucleotide
polymorphism
(SNP)
missense
mutation
located
positions
90,600,001
90,650,001
chromosome
7,
which
leads
change
protein
structure
influences
its
stability.
Conclusions
Analysis
uncovered
likely
related
SNP
affects
It
provides
information
evolution
phylogeographic
These
results
provide
important
future
breeding
studies
new
perspectives
how
animals
can
adapt
climate
change.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Jan. 3, 2025
The
chloroplast
(cp)
genome
is
a
widely
used
tool
for
exploring
plant
evolutionary
relationships,
yet
its
effectiveness
in
fully
resolving
these
relationships
remains
uncertain.
Integrating
cp
data
with
nuclear
DNA
information
offers
more
comprehensive
view
but
often
requires
separate
datasets.
In
response,
we
employed
the
same
raw
read
sequencing
to
construct
genome-based
trees
and
phylogenetic
using
Read2Tree,
cost-efficient
method
extracting
conserved
gene
sequences
from
data,
focusing
on
Aurantioideae
subfamily,
which
includes
Citrus
relatives.
resulting
were
consistent
existing
derived
high-throughput
sequencing,
diverged
trees.
To
elucidate
underlying
complex
processes
causing
discordances,
implemented
an
integrative
workflow
that
utilized
multiple
alignments
of
each
generated
by
conjunction
other
phylogenomic
methods.
Our
analysis
revealed
incomplete
lineage
sorting
predominantly
drives
while
introgression
ancient
also
contribute
topological
discrepancies
within
certain
clades.
This
study
underscores
cost-effectiveness
both
analyses
understanding
relationships.
Genome Biology and Evolution,
Journal Year:
2023,
Volume and Issue:
15(12)
Published: Nov. 24, 2023
Abstract
Phylogenetic
comparative
methods
are
increasingly
used
to
test
hypotheses
about
the
evolutionary
processes
that
drive
divergence
in
gene
expression
among
species.
However,
it
is
unknown
whether
distributional
assumptions
of
phylogenetic
models
designed
for
quantitative
phenotypic
traits
realistic
data
and
importantly,
reliability
conclusions
studies
may
depend
on
well
described
by
chosen
model.
To
evaluate
this,
we
first
fit
several
trait
evolution
8
previously
published
datasets,
comprising
a
total
54,774
genes
with
145,927
unique
gene–tissue
combinations.
Using
developed
approach,
then
assessed
how
best
model
set
an
absolute
(not
just
relative)
sense.
First,
find
Ornstein–Uhlenbeck
models,
which
values
constrained
around
optimum,
were
preferred
66%
Second,
61%
combinations,
best-fit
was
found
perform
well;
rest
be
performing
poorly
at
least
one
statistics
examined.
Third,
when
simple
do
not
well,
this
appears
typically
consequence
failing
fully
account
heterogeneity
rate
evolution.
We
advocate
assessment
performance
should
become
routine
component
studies;
doing
so
can
improve
inferences
inspire
development
novel
models.
PLoS Biology,
Journal Year:
2024,
Volume and Issue:
22(10), P. e3002847 - e3002847
Published: Oct. 9, 2024
In
both
statistical
genetics
and
phylogenetics,
a
major
goal
is
to
identify
correlations
between
genetic
loci
or
other
aspects
of
the
phenotype
environment
focal
trait.
these
2
fields,
there
are
sophisticated
but
disparate
traditions
aimed
at
tasks.
The
disconnect
their
respective
approaches
becoming
untenable
as
questions
in
medicine,
conservation
biology,
evolutionary
biology
increasingly
rely
on
integrating
data
from
within
among
species,
once-clear
conceptual
divisions
blurred.
To
help
bridge
this
divide,
we
lay
out
general
model
describing
covariance
contributions
quantitative
phenotypes
different
individuals.
Taking
approach
shows
that
standard
models
(e.g.,
genome-wide
association
studies;
GWAS)
phylogenetic
comparative
regression)
can
be
interpreted
special
cases
more
quantitative-genetic
model.
fact
share
same
core
architecture
means
build
unified
understanding
strengths
limitations
methods
for
controlling
structure
when
testing
associations.
We
develop
intuition
why
spurious
may
occur
analytically
conduct
population-genetic
simulations
traits.
structural
similarity
problems
phylogenetics
enables
us
take
methodological
advances
one
field
apply
them
other.
demonstrate
by
showing
how
GWAS
technique-including
relatedness
matrix
(GRM)
well
its
leading
eigenvectors,
corresponding
principal
components
genotype
matrix,
regression
model-can
mitigate
analyses.
As
case
study,
re-examine
an
analysis
coevolution
expression
levels
genes
across
fungal
phylogeny
show
including
eigenvectors
covariates
decreases
false
positive
rate
while
simultaneously
increasing
true
rate.
More
generally,
work
provides
foundation
integrative
processes
shape
it.
Molecular Biology and Evolution,
Journal Year:
2024,
Volume and Issue:
41(11)
Published: Oct. 17, 2024
Abstract
As
phylogenomic
datasets
have
grown
in
size,
researchers
developed
new
ways
to
measure
biological
variation
and
assess
statistical
support
for
specific
branches.
Larger
more
sites
loci
therefore
less
sampling
variance.
While
we
can
accurately
the
mean
signal
these
datasets,
lower
variance
is
often
reflected
uniformly
high
measures
of
branch
support—such
as
bootstrap
posterior
probability—limiting
their
utility.
also
revealed
substantial
topologies
found
across
individual
loci,
such
that
single
species
tree
inferred
by
most
phylogenetic
methods
represents
a
limited
summary
data
many
purposes.
In
contrast
support,
degree
underlying
topological
among
should
be
approximately
constant
regardless
size
dataset.
“Concordance
factors”
(CFs)
similar
statistics
become
increasingly
important
tools
phylogenetics.
this
review,
explain
why
CFs
thought
descriptors
rather
than
argue
they
provide
information
about
predictive
power
not
contained
support.
We
review
growing
suite
measuring
concordance,
compare
them
common
framework
reveals
interrelationships,
demonstrate
how
calculate
using
an
example
from
birds.
discuss
might
change
future
move
beyond
estimating
“tree
life”
toward
myriad
evolutionary
histories
genomic
variation.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 7, 2025
A
bstract
The
variation
of
evolutionary
histories
along
the
genome
presents
a
challenge
for
phylogenomic
methods
to
identify
non-recombining
regions
and
reconstruct
phylogenetic
tree
each
region.
To
address
this
problem,
many
studies
used
non-overlapping
window
approach,
often
with
an
arbitrary
selection
fixed
sizes
that
potentially
include
intra-window
recombination
events.
In
study,
we
proposed
information
theoretic
approach
select
size
best
reflects
underlying
alignment.
First,
simulated
chromosome
alignments
reflected
key
characteristics
empirical
dataset
found
AIC
is
good
predictor
accuracy
in
correctly
recovering
topologies
Due
issue
missing
data
datasets,
then
designed
stepwise
applied
method
genomes
erato
-
sara
Heliconius
butterflies
great
apes.
We
butterflies’
chromosomes
ranged
from
<
125bp
250bp,
which
are
much
shorter
than
those
previous
study
even
though
difference
did
not
significantly
change
most
common
across
genome.
On
other
hand,
apes’
500bp
1kb
proportion
major
topology
(grouping
human
chimpanzee)
falling
between
60%
87%,
consistent
findings.
Additionally,
observed
notable
impact
stochastic
error
concatenation
when
using
small
large
windows,
respectively.
For
instance,
apes
was
50%
250bp
but
reached
almost
100%
64kb
windows.
conclusion,
our
highlights
challenges
associated
selecting
analyses
proposes
as
more
objective
way
optimal
whole
alignments.
Molecular Ecology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 10, 2025
ABSTRACT
Reconstructing
the
evolutionary
history
of
young
lineages
diverging
with
gene
flow
is
challenging
due
to
factors
like
incomplete
lineage
sorting,
introgression,
and
selection
causing
tree
discordance.
The
European
crow
hybrid
zone
between
all‐black
carrion
crows
grey‐coated
hooded
exemplifies
this
challenge.
Most
genome
in
Western
Central
populations
near‐identical
crows,
but
differs
substantially
from
their
Iberian
congeners.
A
notable
exception
a
single
major‐effect
colour‐locus
under
sexual
aligning
‘species’
tree.
To
understand
underlying
processes,
we
reconstructed
biogeographic
species
complex.
During
Pleistocene
took
refuge
Peninsula
Middle
East,
respectively.
Allele‐sharing
likewise
black
at
represents
last
trace
ancestry,
resisting
expanding
that
have
homogenised
most
genome.
model
introgression
an
ancestor
into
near
Pyrenées
was
significantly
less
supported.
We
found
no
positive
relationship
recombination
rate
consistent
absence
genome‐wide,
polygenic
barriers
Overall,
study
portrays
scenario
where
few
large‐effect
loci,
subject
divergent
selection,
resist
rampant
asymmetric
exchange.
This
underscores
importance
integrating
population
demography
biogeography
accurately
interpret
patterns
discordance
following
divergence.
The Plant Journal,
Journal Year:
2024,
Volume and Issue:
118(3), P. 753 - 765
Published: Jan. 13, 2024
SUMMARY
Specific
ecological
conditions
in
the
high
mountain
environment
exert
a
selective
pressure
that
often
leads
to
convergent
trait
evolution.
Reticulations
induced
by
incomplete
lineage
sorting
and
introgression
can
lead
discordant
patterns
among
gene
species
trees
(hemiplasy/xenoplasy),
providing
false
illusion
traits
under
study
are
homoplastic.
Using
phylogenetic
networks,
we
explored
effect
of
exchange
on
evolution
Soldanella
,
genus
profoundly
influenced
historical
introgression.
At
least
three
features
evolved
independently
multiple
times:
single‐flowered
dwarf
phenotype,
dysploid
cytotype,
generalism.
The
present
analyses
also
indicated
recurring
occurrence
stoloniferous
growth
might
have
been
prompted
an
event
between
ancestral
still
extant
species,
although
its
emergence
via
cannot
be
completely
ruled
out.
Phylogenetic
regression
suggested
independent
larger
genomes
snowbells
is
most
likely
result
interplay
hybridization
events
euploid
taxa
hostile
environments
at
range
margins
genus.
key
intrinsic
extrinsic
has
significantly
impacted
not
only
but
recent
events.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Feb. 20, 2024
A
bstract
Just
exactly
which
tree(s)
should
we
assume
when
testing
evolutionary
hypotheses?
This
question
has
plagued
comparative
biologists
for
decades.
Given
a
perfectly
estimated
tree
(if
this
is
even
possible
in
practice),
seldom
know
with
certainty
whether
such
truly
best
(or
adequate)
to
represent
the
history
of
our
studied
traits.
Regardless
certainty,
choosing
required
all
phylogenetic
methods.
Yet,
conflict
and
error
are
ubiquitous
modern
biology,
still
learning
about
their
dangers
hypotheses.
Here
investigated
consequences
gene
tree-species
mismatch
regression
presence
incomplete
lineage
sorting.
Our
simulation
experiments
reveal
excessively
high
false
positive
rates
mismatched
both
small
large
trees,
simple
complex
traits,
known
phylogenies.
In
some
cases,
find
evidence
directionality
error:
incorrectly
assuming
species
traits
that
evolved
according
sometimes
fares
worse
than
opposite.
To
explore
difficult
yet
realistic
scenarios,
also
used
rather
trees
conduct
case
studies,
as
well
an
expansive
expression
dataset
investigate
arguably
best-case
scenario
one
may
have
better
chance
match
trait.
Though
never
meant
be
panacea
ail
methods,
found
promise
application
robust
estimator
potential,
albeit
imperfect,
solution
issues
raised
by
mismatch,
perhaps
offering
path
forward.
Collectively,
results
emphasize
importance
careful
study
design
highlighting
need
fully
appreciate
role
adequate
modeling
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Nov. 5, 2023
Abstract
Reconciliation
algorithms
provide
an
accounting
of
the
evolutionary
history
individual
gene
trees
given
a
species
tree.
Many
reconciliation
consider
only
duplication
and
loss
events
(and
sometimes
horizontal
transfer),
ignoring
effects
coalescent
process,
including
incomplete
lineage
sorting
(ILS).
Here,
we
present
new
heuristic
algorithm
for
carrying
out
that
accurately
accounts
ILS
by
treating
it
as
series
nearest
neighbor
interchange
(NNI)
events.
For
discordant
branches
tree
identified
last
common
ancestor
(LCA)
mapping,
our
recursively
chooses
optimal
comparing
cost
to
NNI
loss.
We
demonstrate
accuracy
method,
which
call
reconcILS
,
using
simulation
engine
(
dupcoal
)
can
generate
produced
interaction
duplication,
loss,
ILS.
Despite
being
show
is
much
more
accurate
than
models
ignore
ILS,
at
least
or
better
leading
methods
model
while
also
able
handle
larger
datasets.
use
applying
dataset
23
primate
genomes,
highlighting
its
compared
standard
in
presence
large
amounts