Scientific Reports,
Journal Year:
2019,
Volume and Issue:
9(1)
Published: Jan. 10, 2019
Abstract
Potential
hybridization
between
wolves
and
dogs
has
fueled
the
sensitive
conservation
political
debate
underlying
recovery
of
grey
wolf
throughout
Europe.
Here
we
provide
first
genetic
analysis
wolf-dog
admixture
in
an
area
entirely
recolonized,
northwestern
Alps.
As
part
a
long-term
monitoring
program,
performed
screening
thousands
non-invasive
samples
collected
Switzerland
adjacent
territories
since
return
mid-1990s.
We
identified
total
115
individuals,
only
2
them
showing
significant
signs
stemming
from
past
interbreeding
with
dogs,
followed
by
backcrossing.
This
low
rate
introgression
(<2%
accounting
for
all
ever
detected
over
1998–2017)
parallels
those
other
European
populations,
especially
Western
Europe
(<7%).
Despite
potential
stray
few
founders
strong
anthropogenic
pressures,
integrity
Alpine
population
remained
intact
entire
recolonization
process.
In
context
widespread
misinformation,
this
finding
should
reduce
conflicts
among
different
actors
involved
facilitate
conservation.
Real-time
will
be
necessary
to
identify
hybrids
support
effective
management
emblematic
population.
American Journal of Primatology,
Journal Year:
2018,
Volume and Issue:
80(3)
Published: Feb. 19, 2018
Knowing
the
density
or
abundance
of
primate
populations
is
essential
for
their
conservation
management
and
contextualizing
socio‐demographic
behavioral
observations.
When
direct
counts
animals
are
not
possible,
genetic
analysis
non‐invasive
samples
collected
from
wildlife
allows
estimates
population
size
with
higher
accuracy
precision
than
possible
using
indirect
signs.
Furthermore,
in
contrast
to
traditional
survey
methods,
prolonged
periodic
sampling
across
months
years
enables
inference
group
membership,
movement,
dynamics,
some
kin
relationships.
Data
may
also
be
used
estimate
sex
ratios,
differences
dispersal
distances,
detect
gene
flow
among
locations.
Recent
advances
capture‐recapture
models
have
further
improved
derived
samples.
Simulations
these
methods
shown
that
confidence
interval
point
includes
true
when
assumptions
met,
therefore
this
range
minima
maxima
should
emphasized
monitoring
studies.
Innovations
such
as
use
sniffer
dogs
anti‐poaching
patrols
sample
collection
important
ensure
adequate
sampling,
expected
development
efficient
cost‐effective
genotyping
by
sequencing
DNAs
will
automate
speed
analyses.
PeerJ,
Journal Year:
2020,
Volume and Issue:
8, P. e9085 - e9085
Published: May 4, 2020
Application
of
high-throughput
sequencing
technologies
to
microsatellite
genotyping
(SSRseq)
has
been
shown
remove
many
the
limitations
electrophoresis-based
methods
and
refine
inference
population
genetic
diversity
structure.
We
present
here
a
streamlined
SSRseq
development
workflow
that
includes
development,
multiplexed
marker
amplification
sequencing,
automated
bioinformatics
data
analysis.
illustrate
its
application
five
groups
species
across
phyla
(fungi,
plant,
insect
fish)
with
different
levels
genomic
resource
availability.
found
relying
on
previously
developed
assay
is
not
optimal
leads
resulting
low
number
reliable
locus
being
genotyped.
In
contrast,
de
novo
ad
hoc
primer
designs
gives
highly
assays
can
be
sequenced
produce
high
quality
genotypes
for
20–40
loci.
highlight
critical
upfront
factors
consider
effective
setup
in
wide
range
situations.
Sequence
analysis
accounting
all
linked
polymorphisms
along
sequence
quickly
generates
powerful
multi-allelic
haplotype-based
genotypic
dataset,
calling
new
theoretical
analytical
frameworks
extract
more
information
from
multi-nucleotide
polymorphism
systems.
Molecular Ecology Resources,
Journal Year:
2024,
Volume and Issue:
24(3)
Published: Jan. 30, 2024
Abstract
Accurate
and
efficient
microsatellite
loci
genotyping
is
an
essential
process
in
population
genetics
that
also
used
various
demographic
analyses.
Protocols
for
next‐generation
sequencing
of
enable
high‐throughput
cross‐compatible
allele
scoring,
common
issues
are
not
addressed
by
conventional
capillary‐based
approaches.
To
improve
this
process,
we
have
developed
all‐in‐one
software,
called
Seq2Sat
(
seq
uence
to
micro
sat
ellite),
C++
support
automated
genotyping.
It
directly
takes
raw
reads
amplicons
conducts
read
quality
control
before
inferring
genotypes
based
on
depth‐of‐read,
ratio,
sequence
composition
length.
We
a
module
sex
identification
chromosome–specific
locus
amplicons.
allow
greater
user
access
complement
autoscoring,
SatAnalyzer
(micro
ellite
analyzer
),
user‐friendly
web‐based
platform
reads‐to‐report
analyses
calling
genotype
autoscoring
produces
interactive
graphs
manual
editing.
allows
users
troubleshoot
multiplex
optimization
analysing
distribution
across
samples
high‐quality
library
preparation.
evaluate
its
performance,
benchmarked
our
toolkit
Seq2Sat/SatAnalyzer
against
capillary
gel
method
existing
MEGASAT,
using
two
datasets.
Results
showed
can
achieve
>99.70%
accuracy
~5
times
faster
than
MEGASAT
despite
many
more
informative
tables
figures
being
generated.
freely
available
github
https://github.com/ecogenomicscanada/Seq2Sat
)
dockerhub
https://hub.docker.com/r/rocpengliu/satanalyzer
).
Ticks and Tick-borne Diseases,
Journal Year:
2024,
Volume and Issue:
15(4), P. 102344 - 102344
Published: April 21, 2024
The
brown
dog
tick,
Rhipicephalus
sanguineus
sensu
lato
(s.l.),
is
an
important
vector
for
Rickettsia
rickettsii,
causative
agent
of
Rocky
Mountain
spotted
fever.
Current
public
health
prevention
and
control
efforts
to
protect
people
involve
preventing
tick
infestations
on
domestic
animals
in
around
houses.
Primary
tools
rely
acaricides,
often
synthetic
pyrethroids
(SPs);
resistance
this
chemical
class
widespread
ticks
other
arthropods.
s.l.
a
complex
that
likely
contains
multiple
unique
species
although
the
distribution
global,
there
are
differences
morphology,
ecology,
perhaps
competence
among
these
major
lineages.
Two
lineages
within
Rh.
s.l.,
commonly
referred
as
temperate
tropical,
have
been
documented
from
locations
North
America,
but
thought
occupy
different
ecological
niches.
To
evaluate
potential
acaricide
better
define
distributions
tropical
throughout
US
northern
Mexico,
we
employed
highly
multiplexed
amplicon
sequencing
approach
characterize
sequence
diversity
at:
1)
three
loci
voltage-gated
sodium
channel
(VGSC)
gene,
which
numerous
genetic
mutations
associated
with
SPs;
2)
region
gamma-aminobutyric
acid-gated
chloride
gene
(GABA-Cl)
containing
several
dieldrin/fipronil
species;
3)
mitochondrial
genes
(COI,
12S,
16S).
We
utilized
geographically
diverse
set
Rh
collected
pets
2013
smaller
canines
Baja
California,
Mexico
2021.
determined
single
nucleotide
polymorphism
(T2134C)
domain
III
segment
6
VGSC,
has
previously
SP
was
abundant
lineage
(>50
%)
absent
lineage,
suggesting
SPs
may
be
common
lineage.
found
evidence
copies
GABA-Cl
both
lineages,
some
fipronil
species,
effects
patterns
currently
unknown.
widespread,
accounting
79
%
analyzed
present
at
13/14
collection
sites.
co-occurred
four
states,
far
north
New
York.
None
examined
were
positive
rickettsii
or
massiliae.
Conservation Genetics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 2, 2025
The
use
of
molecular
markers
to
assess
genetic
diversity
has
become
a
common
component
recovery
action
plans
for
threatened
and
endangered
species.
In
this
study,
we
an
unusually
large
number
microsatellite
(N
=
91)
characterize
the
variation
Chiricahua
Leopard
Frogs
(Lithobates
chiricahuensis)
across
their
range
in
order
understand
distribution
variation,
identify
bottlenecks,
measure
changes
over
time
single,
highly-managed
population.
Populations
were
best
divided
into
three
genetically
distinct
clusters,
with
southeastern
Arizona
New
Mexico
populations
forming
clusters.
While
there
is
moderate
distributed
sampled
populations,
each
population
on
its
own
shows
relatively
low
allelic
diversity.
Most
displayed
strong
signals
recent
bottlenecks
or
deficiency
heterozygous
genotypes
that
typically
associated
frequent
inbreeding.
have
history
no
management
through
translocations
harbored
greatest
unique
alleles
overall
richness,
especially
subset
Mexican
populations.
Finally,
long-term
cohort
sampling
at
one
specific
site
(the
Southwestern
Research
Station
Portal,
Arizona)
allowed
us
demonstrate
how
rapidly
can
decrease
matter
years
few
founders.
This
work
provide
important
context
conservation
agencies,
but
even
suite
beyond
what
typical
may
not
be
enough
are
extremely
bottlenecked
levels
standing
Baghdad Journal of Biochemistry and Applied Biological Sciences,
Journal Year:
2025,
Volume and Issue:
5(4)
Published: Jan. 20, 2025
Polymerase
Chain
Reaction
(PCR)
techniques
have
revolutionized
forensic
DNA
analysis,
enabling
the
precise
amplification
of
trace
samples.
This
abstract
provides
a
concise
overview
pivotal
role
PCR
in
science.
It
delves
into
principles
PCR,
emphasizing
its
ability
to
amplify
specific
sequences
with
remarkable
sensitivity
and
specificity.
Multiplex
variant
technique,
allows
for
simultaneous
multiple
genetic
loci,
enhancing
efficiency
investigations.
further
highlights
broad
applications
criminal
investigations,
paternity
testing,
disaster
victim
identification.
Recent
advancements,
such
as
MiniSTRs
Next-Generation
Sequencing
(NGS),
are
elucidated
their
crucial
contributions
addressing
challenging
scenarios.
Despite
instrumental
role,
PCR-based
analysis
is
not
without
challenges,
considerations
including
contamination
low-template
The
concludes
aforward-looking
perspective
on
emerging
field
epigenetics
metagenomic
offering
glimpse
promising
future
analysis.
stands
an
indispensable
tool
modern
science,
unraveling
identities
from
most
minute
traces.
PLoS ONE,
Journal Year:
2025,
Volume and Issue:
20(2), P. e0318806 - e0318806
Published: Feb. 20, 2025
Microsatellite
markers
analyzed
by
capillary
sequencing
remain
useful
tools
for
rapid
genotyping
and
low-cost
studies.
This
contrasts
with
the
lack
of
a
free
application
to
analyze
chromatograms
microsatellite
that
is
not
restricted
human
genotyping.
To
fill
this
gap,
I
have
developed
STRyper,
macOS
whose
source
code
published
under
General
Public
License.
STRyper
only
uses
libraries,
making
it
very
lightweight,
responsive,
behaving
like
modern
application.
Its
three-pane
window
enables
easy
management
viewing
imported
from
FSA
HID
files,
creation
size
standards
marker
panels
(including
bins).
features
powerful
search
capabilities
(with
smart
folders)
graphical
user
interface
allowing,
among
others,
manual
correction
DNA
ladders
individual
genotypes
drag-and-drop.
It
also
introduces
new
way
mitigate
effect
variations
in
electrophoretic
conditions
on
estimated
allele
sizes.
Ecology and Evolution,
Journal Year:
2025,
Volume and Issue:
15(4)
Published: April 1, 2025
The
management
and
conservation
of
large
mammals,
such
as
black
bears
(Ursus
americanus),
have
long
been
informed
by
genetic
estimates
population
size
individual
dispersal.
Amplicon
sequencing
methods,
also
known
'genotyping-in-thousands-by
sequencing'
(GT-seq),
now
enable
the
efficient
cost-effective
genotyping
hundreds
loci
individuals
in
same
run.
Here,
we
develop
a
GT-seq
panel
for
identification
kinship
inference
Alaska
bears.
Using
genomic
data
from
restriction
site-associated
DNA
hunter-harvested
Southcentral
(n
=
85),
identified
170
microhaplotype
single
nucleotide
polymorphism
(SNP)
that
were
highly
heterozygous
local
populations.
To
sexing
individuals,
included
previously
published
sex-linked
locus
panel.
We
empirically
validated
using
samples
collected
at
different
spatial
scales.
These
tissues
82)
obtained
within
small
geographic
area
Anchorage,
Alaska,
which
likely
to
be
relatives
well
geographically
widespread
locations
throughout
Alaska.
Empirical
validation
indicated
high
success
genotype
reproducibility
across
replicate
subsamples.
Computer
simulations
demonstrated
had
ample
statistical
power
distinguishing
distinct
first-order
(parent-offspring
full-sibling
pairs)
unrelated
individuals.
As
final
proof
concept,
was
used
identify
close
kin
sampled
urban
wild
habitats
anticipate
will
useful
resource
monitoring
bear