Mathematical Biosciences & Engineering,
Год журнала:
2023,
Номер
20(9), С. 16648 - 16662
Опубликована: Янв. 1, 2023
Alzheimer's
disease
(AD)
is
an
irreversible
neurodegenerative
disease,
and
its
incidence
increases
yearly.
Because
AD
patients
will
have
cognitive
impairment
personality
changes,
it
has
caused
a
heavy
burden
on
the
family
society.
Image
genetics
takes
structure
function
of
brain
as
phenotype
studies
influence
genetic
variation
brain.
Based
structural
magnetic
resonance
imaging
data
transcriptome
healthy
control
samples
in
Disease
Neuroimaging
database,
this
paper
proposed
use
orthogonal
structured
sparse
canonical
correlation
analysis
for
diagnostic
information
fusion
algorithm.
The
algorithm
added
constraints
to
region
interest
(ROI)
Integrating
can
improve
performance
between
samples.
results
showed
that
could
extract
two
modal
discovered
regions
most
affected
by
multiple
risk
genes
their
biological
significance.
In
addition,
we
also
verified
significance
ROIs
AD.
code
available
at
https://github.com/Wanguangyu111/OSSCCA-DIF.
Diagnostics,
Год журнала:
2023,
Номер
13(6), С. 1026 - 1026
Опубликована: Март 8, 2023
Acute
lymphoblastic
leukemia
(ALL)
is
one
of
the
deadliest
forms
due
to
bone
marrow
producing
many
white
blood
cells
(WBC).
ALL
most
common
types
cancer
in
children
and
adults.
Doctors
determine
treatment
according
its
stages
spread
body.
rely
on
analyzing
samples
under
a
microscope.
Pathologists
face
challenges,
such
as
similarity
between
infected
normal
WBC
early
stages.
Manual
diagnosis
prone
errors,
differences
opinion,
lack
experienced
pathologists
compared
number
patients.
Thus,
computer-assisted
systems
play
an
essential
role
assisting
detection
ALL.
In
this
study,
with
high
efficiency
accuracy
were
developed
analyze
images
C-NMC
2019
ALL-IDB2
datasets.
all
proposed
systems,
micrographs
improved
then
fed
active
contour
method
extract
WBC-only
regions
for
further
analysis
by
three
CNN
models
(DenseNet121,
ResNet50,
MobileNet).
The
first
strategy
two
datasets
hybrid
technique
CNN-RF
CNN-XGBoost.
DenseNet121,
MobileNet
deep
feature
maps.
produce
features
redundant
non-significant
features.
So,
maps
Principal
Component
Analysis
(PCA)
select
highly
representative
sent
RF
XGBoost
classifiers
classification
using
serially
fused
models.
DenseNet121-ResNet50,
ResNet50-MobileNet,
DenseNet121-MobileNet,
DenseNet121-ResNet50-MobileNet
merged
classified
XGBoost.
classifier
reached
AUC
99.1%,
98.8%,
sensitivity
98.45%,
precision
98.7%,
specificity
98.85%
dataset.
With
dataset,
achieved
100%
results
AUC,
accuracy,
sensitivity,
precision,
specificity.
Briefings in Bioinformatics,
Год журнала:
2023,
Номер
24(5)
Опубликована: Авг. 1, 2023
Identifying
the
relationships
among
long
non-coding
RNAs
(lncRNAs),
microRNAs
(miRNAs)
and
diseases
is
highly
valuable
for
diagnosing,
preventing,
treating
prognosing
diseases.
The
development
of
effective
computational
prediction
methods
can
reduce
experimental
costs.
While
numerous
have
been
proposed,
they
often
to
treat
lncRNA-disease
associations
(LDAs),
miRNA-disease
(MDAs)
lncRNA-miRNA
interactions
(LMIs)
as
separate
task.
Models
capable
predicting
all
three
simultaneously
remain
relatively
scarce.
Our
aim
perform
multi-task
predictions,
which
not
only
construct
a
unified
framework,
but
also
facilitate
mutual
complementarity
information
lncRNAs,
miRNAs
diseases.In
this
work,
we
propose
novel
unsupervised
embedding
method
called
graph
contrastive
learning
(GCLMTP).
approach
aims
predict
LDAs,
MDAs
LMIs
by
extracting
representations
To
achieve
this,
first
triple-layer
lncRNA-miRNA-disease
heterogeneous
(LMDHG)
that
integrates
complex
between
these
entities
based
on
their
similarities
correlations.
Next,
employ
an
model
extract
potential
topological
feature
from
LMDHG.
leverages
convolutional
network
architectures
maximize
patch
corresponding
high-level
summaries
Subsequently,
tasks,
multiple
classifiers
are
explored
LDA,
MDA
LMI
scores.
Comprehensive
experiments
conducted
two
datasets
(from
older
newer
versions
database,
respectively).
results
show
GCLMTP
outperforms
other
state-of-the-art
disease-related
lncRNA
miRNA
tasks.
Additionally,
case
studies
further
demonstrate
ability
accurately
discover
new
associations.
ensure
reproducibility
made
source
code
publicly
available
at
https://github.com/sheng-n/GCLMTP.
Biomedicines,
Год журнала:
2025,
Номер
13(1), С. 136 - 136
Опубликована: Янв. 8, 2025
Background:
Over
the
past
few
decades,
micro
ribonucleic
acids
(miRNAs)
have
been
shown
to
play
significant
roles
in
various
biological
processes,
including
disease
incidence.
Therefore,
much
effort
has
devoted
discovering
pivotal
of
miRNAs
incidence
understand
underlying
pathogenesis
human
diseases.
However,
identifying
miRNA-disease
associations
using
experiments
is
inefficient
terms
cost
and
time.
Methods:
Here,
we
discuss
a
novel
machine-learning
model
that
effectively
predicts
disease-related
graph
convolutional
neural
network
with
collaborative
filtering
(GCNCF).
By
applying
network,
could
capture
important
feature
vectors
present
while
preserving
structure.
exploiting
filtering,
were
learned
through
matrix
factorization
deep
learning,
identified.
Results:
Extensive
experimental
results
based
on
area
under
curve
(AUC)
scores
(0.9216
0.9018)
demonstrated
superiority
our
over
previous
models.
Conclusions:
We
anticipate
not
only
serve
as
an
effective
tool
for
predicting
but
be
employed
universal
computational
framework
inferring
relationships
across
entities.
BMC Bioinformatics,
Год журнала:
2025,
Номер
26(1)
Опубликована: Янв. 17, 2025
Drug
response
prediction
is
critical
in
precision
medicine
to
determine
the
most
effective
and
safe
treatments
for
individual
patients.
Traditional
methods
relying
on
demographic
genetic
data
often
fall
short
accuracy
robustness.
Recent
graph-based
models,
while
promising,
frequently
neglect
role
of
atomic
interactions
fail
integrate
drug
fingerprints
with
SMILES
comprehensive
molecular
graph
construction.
We
introduce
multimodal
multi-channel
attention
network
adaptive
fusion
(MGATAF),
a
framework
designed
enhance
predictions
by
capturing
both
local
global
among
nodes.
MGATAF
improves
representation
integrating
fingerprints,
resulting
more
precise
effects.
The
methodology
involves
constructing
graphs,
employing
networks
capture
diverse
interactions,
using
these
at
multiple
abstraction
levels.
Empirical
results
demonstrate
MGATAF's
superior
performance
compared
traditional
other
techniques.
For
example,
GDSC
dataset,
achieved
5.12%
improvement
Pearson
correlation
coefficient
(PCC),
reaching
0.9312
an
RMSE
0.0225.
Similarly,
new
cell-line
tests,
outperformed
baselines
PCC
0.8536
0.0321
0.7364
0.0531
CCLE
dataset.
significantly
advances
effectively
types
complex
interactions.
This
enhances
offers
robust
tool
personalized
medicine,
potentially
leading
safer
Future
research
can
expand
this
work
exploring
additional
modalities
refining
mechanisms.
Computer Methods in Biomechanics & Biomedical Engineering,
Год журнала:
2025,
Номер
unknown, С. 1 - 16
Опубликована: Март 20, 2025
In
this
paper,
we
propose
a
novel
lncRNA-disease
association
prediction
algorithm
based
on
optimizing
measures
of
multi-graph
regularized
matrix
factorization
(OM-MGRMF).
The
method
first
calculates
the
semantic
similarity
diseases,
functional
lncRNAs,
and
Gaussian
both.
It
then
constructs
new
by
using
K-nearest-neighbor
(KNN)
algorithm.
Finally,
objective
function
is
constructed
through
utilization
ranking
regularization
constraints.
This
iteratively
optimized
an
adaptive
gradient
descent
experimental
results
OM-MGRMF
outperform
those
classical
methods
in
both
K-fold
cross-validation.
Briefings in Bioinformatics,
Год журнала:
2024,
Номер
25(3)
Опубликована: Март 27, 2024
Abstract
MicroRNAs
(miRNAs)
synergize
with
various
biomolecules
in
human
cells
resulting
diverse
functions
regulating
a
wide
range
of
biological
processes.
Predicting
potential
disease-associated
miRNAs
as
valuable
biomarkers
contributes
to
the
treatment
diseases.
However,
few
previous
methods
take
holistic
perspective
and
only
concentrate
on
isolated
miRNA
disease
objects,
thereby
ignoring
that
are
responsible
for
multiple
relationships.
In
this
work,
we
first
constructed
multi-view
graph
based
relationships
between
biomolecules,
then
utilized
attention
neural
network
learn
topology
features
diseases
each
view.
Next,
added
an
mechanism
again,
developed
multi-scale
feature
fusion
module,
aiming
determine
optimal
results
addition,
prior
attribute
knowledge
was
simultaneously
achieve
better
prediction
solve
cold
start
problem.
Finally,
learned
representations
were
concatenated
fed
into
multi-layer
perceptron
end-to-end
training
predicting
miRNA–disease
associations.
To
assess
efficacy
our
model
(called
MUSCLE),
performed
5-
10-fold
cross-validation
(CV),
which
got
average
Area
under
ROC
curves
0.966${\pm
}$0.0102
0.973${\pm
}$0.0135,
respectively,
outperforming
most
current
state-of-the-art
models.
We
examined
impact
crucial
parameters
performance
ablation
experiments
combination
architecture.
Furthermore,
case
studies
about
colon
cancer,
lung
cancer
breast
also
fully
demonstrate
good
inductive
capability
MUSCLE.
Our
data
code
free
available
at
public
GitHub
repository:
https://github.com/zht-code/MUSCLE.git.
miRNAs
(microRNAs)
are
endogenous
RNAs
with
lengths
of
18
to
24
nucleotides
and
play
critical
roles
in
gene
regulation
disease
progression.
Although
traditional
wet-lab
experiments
provide
direct
evidence
for
miRNA-disease
associations,
they
often
time-consuming
complicated
analyze
by
current
bioinformatics
tools.
In
recent
years,
machine
learning
(ML)
deep
(DL)
techniques
powerful
tools
large-scale
biological
data.
Hence,
developing
a
model
predict,
identify,
rank
connections
diseases
can
significantly
enhance
the
precision
efficiency
investigating
relationships
between
diseases.
this
study,
we
utilized
association
data
obtained
biotechnological
develop
DL
associations.
To
improve
accuracy
prediction
model,
introduced
two
labeling
strategies,
weight-based
majority-based
definitions,
classify
After
preprocessing,
was
trained
novel
combining
gated
recurrent
units
(GRU)
graph
convolutional
network
(GCN)
predict
level
The
datasets
were
from
HMDD
(the
Human
miRNA
Disease
Database)
categorized
distinct
approaches,
definitions
definitions.
We
classified
associations
into
three
groups,
"upregulated",
"downregulated"
"nonspecific",
regression
analysis
multiclass
classification.
This
GRU-GCN
coordinated
achieved
robust
area
under
curve
(AUC)
score
0.8
all
datasets,
demonstrating
efficacy
predicting
potential
relationships.
By
introducing
innovative
label-preprocessing
methods,
study
addressed
diseases,
improved
ambiguity
results
different
experiments.
Based
on
these
refined
label
developed
DL-based
refine
offers
valuable
tool
complementing
experimental
methods
enhancing
our
understanding
miRNA-related
mechanisms.
Biomedicines,
Год журнала:
2025,
Номер
13(3), С. 536 - 536
Опубликована: Фев. 20, 2025
Background:
In
recent
years,
micro
ribonucleic
acids
(miRNAs)
have
been
recognized
as
key
regulators
in
numerous
biological
processes,
particularly
the
development
and
progression
of
diseases.
As
a
result,
extensive
research
has
focused
on
uncovering
critical
involvement
miRNAs
disease
mechanisms
to
better
comprehend
underlying
causes
human
Despite
these
efforts,
relying
solely
experiments
identify
miRNA-disease
associations
is
both
time-consuming
costly,
making
it
an
impractical
approach
for
large-scale
studies.
Methods:
this
paper,
we
propose
novel
DeepWalk-based
graph
embedding
method
predicting
miRNA–disease
association
(DWMDA).
Using
DeepWalk,
extracted
meaningful
low-dimensional
vectors
from
miRNA
networks.
Then,
applied
deep
neural
network
using
diseases
via
DeepWalk.
Results:
An
ablation
study
was
conducted
assess
proposed
modules.
Furthermore,
DWMDA
demonstrates
exceptional
performance
two
major
cancer
case
studies
(breast
lung),
with
results
based
statistically
robust
measures,
further
emphasizing
its
reliability
identifying
between
Conclusions:
We
expect
that
our
model
will
not
only
facilitate
accurate
prediction
disease-associated
but
also
serve
generalizable
framework
exploring
interactions
among
various
entities.
Scientific Reports,
Год журнала:
2025,
Номер
15(1)
Опубликована: Фев. 22, 2025
Alzheimer's
disease
(AD)
is
the
most
common
cause
of
dementia,
emphasizing
critical
need
for
development
biomarkers
that
facilitate
accurate
and
objective
assessment
progression
early
detection
intervention
to
delay
its
onset.
In
our
study,
three
AD
datasets
from
Gene
Expression
Omnibus
(GEO)
database
were
integrated
differential
expression
analysis,
followed
by
a
weighted
gene
co-expression
network
analysis
(WGCNA),
potential
screened.
Our
study
identified
UBE2N
as
promising
biomarker
AD.
Functional
enrichment
revealed
associated
with
synaptic
vesicle
cycling
T
cell/B
cell
receptor
signaling
pathways.
Notably,
levels
found
be
significantly
reduced
in
cortex
hippocampus
TauP301S
mice.
Furthermore,
single-cell
data
patients
demonstrated
association
function.
These
findings
underscore
valuable
AD,
offering
important
insights
diagnosis
targeted
therapeutic
strategies.