Briefings in Bioinformatics,
Год журнала:
2024,
Номер
26(1)
Опубликована: Ноя. 22, 2024
Abstract
The
assay
for
transposase-accessible
chromatin
with
sequencing
(ATAC-seq)
identifies
accessibility
across
the
genome,
crucial
gene
expression
regulating.
However,
bulk
ATAC-seq
obscures
cellular
heterogeneity,
while
single-cell
suffers
from
issues
such
as
sparsity
and
costliness.
To
this
end,
we
introduce
DECA,
a
sophisticated
deep
learning
model
based
on
vision
transformer
to
deconvolve
cell
type
information
profiles,
utilizing
datasets
reference
enhanced
precision
resolution.
Notably,
patch
attention
generated
by
DECA’s
multi-head
mechanism
aligns
interactions
detected
Hi-C.
Additionally,
DECA
predicted
lineage-specific
composition
changes
due
genetic
perturbation.
signatures
are
enriched
cell-type
specific
variations.
Ultimately,
applied
pan-cancer
demonstrated
its
capability
proportions
clinical
significance.
Taken
together,
deconvolves
predicts
their
profiles
data,
which
enable
exploring
regulatory
programs
in
development
diseases.
The
oviduct
is
the
site
of
fertilization
and
preimplantation
embryo
development
in
mammals.
Evidence
suggests
that
gametes
alter
oviductal
gene
expression.
To
delineate
adaptive
interactions
between
gamete/embryo,
we
performed
a
multi-omics
characterization
tissues
utilizing
bulk
RNA-sequencing
(RNA-seq),
single-cell
(scRNA-seq),
proteomics
collected
from
distal
proximal
at
various
stages
after
mating
mice.
We
observed
robust
region-specific
transcriptional
signatures.
Specifically,
presence
sperm
induces
genes
involved
pro-inflammatory
responses
region
0.5
days
post-coitus
(dpc).
Genes
inflammatory
were
produced
specifically
by
secretory
epithelial
cells
oviduct.
At
1.5
2.5
dpc,
pyruvate
glycolysis
enriched
region,
potentially
providing
metabolic
support
for
developing
embryos.
Abundant
proteins
fluid
differentially
naturally
fertilized
superovulated
samples.
RNA-seq
data
used
to
identify
transcription
factors
predicted
influence
protein
abundance
proteomic
via
novel
machine
learning
model
based
on
transformers
integrating
transcriptomics
data.
identified
influential
correlated
predictive
expressions
alignment
with
vivo
-derived
Lastly,
found
some
differences
sperm-exposed
mouse
oviducts
compared
hydrosalpinx
fallopian
tubes
patients.
In
conclusion,
our
subsequent
confirmation
proteins/RNAs
indicate
responsive
embryos
spatiotemporal
manner.
The Innovation Life,
Год журнала:
2024,
Номер
unknown, С. 100105 - 100105
Опубликована: Янв. 1, 2024
<p>Artificial
intelligence
has
had
a
profound
impact
on
life
sciences.
This
review
discusses
the
application,
challenges,
and
future
development
directions
of
artificial
in
various
branches
sciences,
including
zoology,
plant
science,
microbiology,
biochemistry,
molecular
biology,
cell
developmental
genetics,
neuroscience,
psychology,
pharmacology,
clinical
medicine,
biomaterials,
ecology,
environmental
science.
It
elaborates
important
roles
aspects
such
as
behavior
monitoring,
population
dynamic
prediction,
microorganism
identification,
disease
detection.
At
same
time,
it
points
out
challenges
faced
by
application
data
quality,
black-box
problems,
ethical
concerns.
The
are
prospected
from
technological
innovation
interdisciplinary
cooperation.
integration
Bio-Technologies
(BT)
Information-Technologies
(IT)
will
transform
biomedical
research
into
AI
for
Science
paradigm.</p>
Frontiers in Genetics,
Год журнала:
2025,
Номер
16
Опубликована: Фев. 17, 2025
Single-cell
RNA
sequencing
(scRNA-seq)
has
emerged
as
a
powerful
tool
for
understanding
cellular
heterogeneity,
providing
unprecedented
resolution
in
molecular
regulation
analysis.
Existing
supervised
learning
approaches
cell
type
annotation
primarily
utilize
gene
expression
profiles
from
scRNA-seq
data.
Although
some
methods
incorporated
interaction
network
information,
they
fail
to
use
cell-specific
association
networks.
This
limitation
overlooks
the
unique
patterns
within
individual
cells,
potentially
compromising
accuracy
of
classification.
We
introduce
WCSGNet,
graph
neural
network-based
algorithm
automatic
cell-type
that
leverages
Weighted
Cell-Specific
Networks
(WCSNs).
These
networks
are
constructed
based
on
highly
variable
genes
and
inherently
capture
both
structure
features.
Extensive
experimental
validation
demonstrates
WCSGNet
consistently
achieves
superior
classification
performance,
ranking
among
top-performing
while
maintaining
robust
stability
across
diverse
datasets.
Notably,
exhibits
distinct
advantage
handling
imbalanced
datasets,
outperforming
existing
these
challenging
scenarios.
All
datasets
codes
reproducing
this
work
were
deposited
GitHub
repository
(
https://github.com/Yi-ellen/WCSGNet
).
The
oviduct
is
the
site
of
fertilization
and
preimplantation
embryo
development
in
mammals.
Evidence
suggests
that
gametes
alter
oviductal
gene
expression.
To
delineate
adaptive
interactions
between
gamete/embryo,
we
performed
a
multi-omics
characterization
tissues
utilizing
bulk
RNA-sequencing
(RNA-seq),
single-cell
(scRNA-seq),
proteomics
collected
from
distal
proximal
at
various
stages
after
mating
mice.
We
observed
robust
region-specific
transcriptional
signatures.
Specifically,
presence
sperm
induces
genes
involved
pro-inflammatory
responses
region
0.5
days
post-coitus
(dpc).
Genes
inflammatory
were
produced
specifically
by
secretory
epithelial
cells
oviduct.
At
1.5
2.5
dpc,
pyruvate
glycolysis
enriched
region,
potentially
providing
metabolic
support
for
developing
embryos.
Abundant
proteins
fluid
differentially
naturally
fertilized
superovulated
samples.
RNA-seq
data
used
to
identify
transcription
factors
predicted
influence
protein
abundance
proteomic
via
novel
machine
learning
model
based
on
transformers
integrating
transcriptomics
data.
identified
influential
correlated
predictive
expressions
alignment
with
vivo-derived
Lastly,
found
some
differences
sperm-exposed
mouse
oviducts
compared
hydrosalpinx
Fallopian
tubes
patients.
In
conclusion,
our
subsequent
vivo
confirmation
proteins/RNAs
indicate
responsive
embryos
spatiotemporal
manner.
Briefings in Bioinformatics,
Год журнала:
2025,
Номер
26(2)
Опубликована: Март 1, 2025
Abstract
Rapid
advancement
of
sequencing
technologies
now
allows
for
the
utilization
precise
signals
at
single-cell
resolution
in
various
omics
studies.
However,
massive
volume,
ultra-high
dimensionality,
and
high
sparsity
nature
data
have
introduced
substantial
difficulties
to
traditional
computational
methods.
The
intricate
non-Euclidean
networks
intracellular
intercellular
signaling
molecules
within
datasets,
coupled
with
complex,
multimodal
structures
arising
from
multi-omics
joint
analysis,
pose
significant
challenges
conventional
deep
learning
operations
reliant
on
Euclidean
geometries.
Graph
neural
(GNNs)
extended
data,
allowing
cells
their
features
datasets
be
modeled
as
nodes
a
graph
structure.
GNNs
been
successfully
applied
across
broad
range
tasks
analysis.
In
this
survey,
we
systematically
review
107
successful
applications
six
variants
tasks.
We
begin
by
outlining
fundamental
principles
variants,
followed
systematic
GNN-based
models
epigenomics,
transcriptomics,
spatial
proteomics,
multi-omics.
each
section
dedicated
specific
type,
summarized
publicly
available
commonly
utilized
articles
reviewed
that
section,
totaling
77
datasets.
Finally,
summarize
potential
shortcomings
current
research
explore
directions
future
anticipate
will
serve
guiding
resource
researchers
deepen
application
omics.
Quantitative Biology,
Год журнала:
2025,
Номер
13(4)
Опубликована: Апрель 24, 2025
Abstract
Cellular
plasticity
enables
cells
to
dynamically
adapt
environmental
changes
by
altering
their
phenotype.
This
plays
a
crucial
role
in
tissue
repair
and
regeneration
contributes
pathological
processes
such
as
cancer
metastasis.
Advances
single‐cell
omics
have
significantly
advanced
the
study
of
cellular
states
provided
new
opportunities
for
accurate
cell
classification
uncovering
transitions.
In
this
perspective,
we
emphasize
integrating
chromatin
accessibility
data
extrinsic
factors,
microenvironmental
cues,
with
transcriptomic
develop
holistic
models
identifying
plastic
states.
Additionally,
coupling
artificial
intelligence
offers
transformative
potential
address
existing
challenges
fill
gaps
characterizing
cells.
We
envision
development
universal
metric,
standardized
metric
quantifying
plasticity.
would
enable
consistent
measurement
across
diverse
studies,
creating
unified
framework
that
bridges
fields
developmental
biology,
research,
regenerative
medicine.
Fostering
innovative
approaches
analyzing
promises
not
only
deepen
our
understanding
but
also
accelerate
therapeutic
advancements,
paving
way
novel
precision
medicine
strategies
treat
complex
diseases
cancer.
Brain Communications,
Год журнала:
2024,
Номер
6(4)
Опубликована: Янв. 1, 2024
Abstract
Treatments
that
can
completely
resolve
brain
diseases
have
yet
to
be
discovered.
Omics
is
a
novel
technology
allows
researchers
understand
the
molecular
pathways
underlying
diseases.
Multiple
omics,
including
genomics,
transcriptomics
and
proteomics,
imaging
technologies,
such
as
MRI,
PET
EEG,
contributed
disease-related
therapeutic
target
detection.
However,
new
treatment
discovery
remains
challenging.
We
focused
on
establishing
multi-molecular
maps
using
an
integrative
approach
of
omics
provide
insights
into
disease
diagnosis
treatment.
This
requires
precise
data
collection
processing
normalization.
Incorporating
map
with
advanced
technologies
through
artificial
intelligence
will
help
establish
system
for
regulation
at
level.
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Авг. 30, 2024
Single-cell
RNA
sequencing
(scRNA-seq)
technologies
have
become
essential
tools
for
characterizing
cellular
landscapes
within
complex
tissues.
Large-scale
single-cell
transcriptomics
holds
great
potential
identifying
rare
cell
types
critical
to
the
pathogenesis
of
diseases
and
biological
processes.
Existing
methods
often
rely
on
one-time
clustering
using
partial
or
global
gene
expression.
However,
these
may
be
overlooked
during
phase,
posing
challenges
their
accurate
identification.
In
this
paper,
we
propose
a
Cluster
decomposition-based
Anomaly
Detection
method
(scCAD),
which
iteratively
decomposes
clusters
based
most
differential
signals
in
each
cluster
effectively
separate
achieve
We
benchmark
scCAD
25
real-world
scRNA-seq
datasets,
demonstrating
its
superior
performance
compared
10
state-of-the-art
methods.
In-depth
case
studies
across
diverse
including
mouse
airway,
brain,
intestine,
human
pancreas,
immunology
data,
clear
renal
carcinoma,
showcase
scCAD's
efficiency
scenarios.
Furthermore,
can
correct
annotation
identify
immune
subtypes
associated
with
disease,
thereby
offering
valuable
insights
into
disease
progression.