Environmental DNA,
Journal Year:
2023,
Volume and Issue:
unknown
Published: Nov. 29, 2023
The
sequencing
revolution
requires
accurate
taxonomic
classification
of
DNA
sequences.
Key
to
making
assignments
are
curated,
comprehensive
reference
barcode
databases.
However,
the
generation
and
curation
such
databases
has
remained
challenging
given
large
continuously
growing
volumes
both
sequence
data
novel
targets.
Monitoring
research
applications
require
a
greater
diversity
specialized
gene
regions
targeted
taxa
then
currently
curated
by
professional
staff.
Thus
there
is
need
for
an
easy
implement
computational
tool
that
can
generate
metabarcoding
libraries
any
bespoke
locus.
We
address
this
reimagining
CRUX
from
Anacapa
Toolkit
present
rCRUX
package
in
R
which,
like
it's
predecessor,
relies
on
homology
PCR
primer
compatibility
instead
keyword-searches
avoid
limitations
user-defined
metadata.
typical
workflow
involves
searching
plausible
seed
amplicons
(
PeerJ,
Journal Year:
2024,
Volume and Issue:
12, P. e18016 - e18016
Published: Oct. 24, 2024
Environmental
DNA
(eDNA)
metabarcoding
has
emerged
as
a
promising
approach
to
assess
biodiversity
and
derive
ecological
status
classes
from
water
samples.
However,
limitation
of
eDNA
surveys
is
that
detected
molecules
may
originate
other
places
or
even
dead
organisms,
distorting
local
assessments.
RNA
(eRNA)
recently
been
proposed
complementary
tool
for
more
localized
assessments
the
biological
community.
In
this
study,
we
evaluated
effectiveness
eRNA
inferring
richness
species
distribution
patterns
vertebrates
invertebrates
in
Central
European
lowland
river.
We
collected
samples
analyzed
them
using
12S
marker
COI
invertebrates.
31
fish,
16
mammal,
10
bird
one
lamprey
vertebrate
dataset.
While
results
were
largely
consistent,
higher
number
when
analysing
(mean
=
30.89)
than
26.16).
Also,
detections
had
stronger
signature
compared
against
traditional
fish
monitoring
data.
For
invertebrates,
109
arthropod,
22
annelid,
12
rotiferan,
eight
molluscan
four
cnidarian
species.
contrast
pattern
richness,
41.37)
22.42).
Our
findings
primarily
show
eRNA-based
are
comparable
invertebrate
taxa.
Biological
replication
was
important
both
template
studied.
Signal
eDNA.
Overall,
advantages
extra
steps
needed
analyses
depend
on
study
question
but
methods
provide
data
research.
Environmental DNA,
Journal Year:
2023,
Volume and Issue:
5(5), P. 1016 - 1031
Published: June 6, 2023
Abstract
Molecular
tools
of
species
identification
based
on
eNAs
(environmental
nucleic
acids;
environmental
DNA
[eDNA]
and
RNA
[eRNA])
have
the
potential
to
greatly
transform
biodiversity
science.
However,
ability
obtain
“real‐time”
estimates
may
be
complicated
by
differential
persistence
degradation
dynamics
molecular
template
(eDNA
or
eRNA)
barcode
marker
used.
Here,
we
collected
water
samples
over
a
28‐day
period
comparatively
assess
detection
using
eDNA
eRNA
metabarcoding
two
distinct
markers—a
mitochondrial
mRNA
(COI)
nuclear
rRNA
(18S)—following
complete
removal
Arthropoda
taxa
in
semi‐natural
freshwater
system.
Our
findings
demonstrate
that
community
composition
was
largely
influenced
choice,
rather
than
template,
individual
microcosm,
sampling
time
point.
Furthermore,
although
capture
similar
diversity
as
established
method,
this
finding
marker‐dependent.
Although
found
little
no
difference
decay
rates
observed
among
sample
groups
(COI
eDNA,
COI
eRNA,
18S
eRNA),
result
is
likely
due
limitations
eNA‐based
provide
strong
correlation
between
true
eNA
copy
numbers
present
environment
final
read
counts
obtained
(following
workflow).
Collectively,
our
further
support
for
use
multi‐marker
assessments
surveys
unravel
broadest
taxonomic
possible,
highlight
methods
providing
accurate
rate
estimates,
well
establish
need
comparative
studies
both
single‐species
diverse
range
taxa.
Fishes,
Journal Year:
2023,
Volume and Issue:
8(11), P. 550 - 550
Published: Nov. 15, 2023
Fishes
are
ecologically
important
organisms
that
have
long
lifespans,
high
mobilities,
and
diverse
trophic
levels.
Due
to
their
importance,
fishes
used
as
bioindicators
for
monitoring
aquatic
environments.
One
method
is
based
on
environmental
DNA
(eDNA),
which
the
deoxynucleic
acids
released
by
into
environment.
However,
there
has
been
a
problem
with
false
positives
because
eDNA
relatively
stable
in
environment
could
even
likely
represent
dead
or
non-inhabiting
organisms.
To
address
this
weakness,
RNA
(eRNA),
degrades
more
rapidly
than
environment,
can
be
utilized
complement
eDNA.
But,
date,
few
studies
eRNA
freshwater
fish
monitoring.
In
study,
determine
relative
usefulness
of
metabarcoding
fishes,
we
performed
12S
rRNA
targeting
using
water
samples
were
collected
from
three
locations
Han
River.
We
then
calculated
sensitivity
positive
predictivity
approach
comparing
our
data
previous
specimen
capture
survey
(PSCS)
last
six
years.
The
results
showed
42
species
detected
19
at
locations.
At
all
locations,
compared
PSCS
data,
average
was
higher
(46.1%)
(34.6%),
(31.7%)
(20.7%).
This
confirmed
advantage
broadly
determining
presence
absence
(including
those
no
longer
present
dead),
but
it
also
generates
positives;
meanwhile,
reports
living
species,
detects
fewer
Combining
therefore
emphasizes
advantages
compensates
disadvantages,
conducting
may
useful
identifying
actually
technique
future
provide
insights
fisheries.
Environmental DNA,
Journal Year:
2023,
Volume and Issue:
unknown
Published: Nov. 29, 2023
The
sequencing
revolution
requires
accurate
taxonomic
classification
of
DNA
sequences.
Key
to
making
assignments
are
curated,
comprehensive
reference
barcode
databases.
However,
the
generation
and
curation
such
databases
has
remained
challenging
given
large
continuously
growing
volumes
both
sequence
data
novel
targets.
Monitoring
research
applications
require
a
greater
diversity
specialized
gene
regions
targeted
taxa
then
currently
curated
by
professional
staff.
Thus
there
is
need
for
an
easy
implement
computational
tool
that
can
generate
metabarcoding
libraries
any
bespoke
locus.
We
address
this
reimagining
CRUX
from
Anacapa
Toolkit
present
rCRUX
package
in
R
which,
like
it's
predecessor,
relies
on
homology
PCR
primer
compatibility
instead
keyword-searches
avoid
limitations
user-defined
metadata.
typical
workflow
involves
searching
plausible
seed
amplicons
(