Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: March 28, 2024
Abstract
Spatial
proteomics
elucidates
cellular
biochemical
changes
with
unprecedented
topological
level.
Imaging
mass
cytometry
(IMC)
is
a
high-dimensional
single-cell
resolution
platform
for
targeted
spatial
proteomics.
However,
the
precision
of
subsequent
clinical
analysis
constrained
by
imaging
noise
and
resolution.
Here,
we
propose
SpiDe-Sr,
super-resolution
network
embedded
denoising
module
IMC
enhancement.
SpiDe-Sr
effectively
resists
improves
4
times.
We
demonstrate
respectively
cells,
mouse
human
tissues,
resulting
18.95%/27.27%/21.16%
increase
in
peak
signal-to-noise
ratio
15.95%/31.63%/15.52%
cell
extraction
accuracy.
further
apply
to
study
tumor
microenvironment
20-patient
breast
cancer
cohort
269,556
single
discover
invasion
Gram-negative
bacteria
positively
correlated
carcinogenesis
markers
negatively
immunological
markers.
Additionally,
also
compatible
fluorescence
microscopy
imaging,
suggesting
an
alternative
tool
image
super-resolution.
Small Methods,
Journal Year:
2023,
Volume and Issue:
7(10)
Published: June 29, 2023
Abstract
Operando
wide‐field
optical
microscopy
imaging
yields
a
wealth
of
information
about
the
reactivity
metal
interfaces,
yet
data
are
often
unstructured
and
challenging
to
process.
In
this
study,
power
unsupervised
machine
learning
(ML)
algorithms
is
harnessed
analyze
chemical
images
obtained
dynamically
by
reflectivity
in
combination
with
ex
situ
scanning
electron
identify
cluster
particles
Al
alloy.
The
ML
analysis
uncovers
three
distinct
clusters
from
unlabeled
datasets.
A
detailed
examination
representative
patterns
confirms
communication
generated
OH
−
fluxes
within
particles,
as
supported
statistical
size
distribution
finite
element
modelling
(FEM).
procedures
also
reveal
statistically
significant
under
dynamic
conditions,
such
pH
acidification.
results
align
well
numerical
model
communication,
underscoring
synergy
between
data‐driven
physics‐driven
FEM
approaches.
Frontiers in Bioinformatics,
Journal Year:
2023,
Volume and Issue:
3
Published: July 26, 2023
Since
its
introduction
into
the
field
of
oncology,
deep
learning
(DL)
has
impacted
clinical
discoveries
and
biomarker
predictions.
DL-driven
predictions
in
oncology
are
based
on
a
variety
biological
data
such
as
genomics,
proteomics,
imaging
data.
DL-based
computational
frameworks
can
predict
genetic
variant
effects
gene
expression,
well
protein
structures
amino
acid
sequences.
Furthermore,
DL
algorithms
capture
valuable
mechanistic
information
from
several
spatial
“omics”
technologies,
transcriptomics
proteomics.
Here,
we
review
impact
that
combination
artificial
intelligence
(AI)
with
omics
technologies
had
focusing
applications
biomedical
image
analysis,
encompassing
cell
segmentation,
phenotype
identification,
cancer
prognostication,
therapy
prediction.
We
highlight
advantages
using
highly
multiplexed
images
(spatial
proteomics
data)
compared
to
single-stained,
conventional
histopathological
(“simple”)
images,
former
provide
insights
cannot
be
obtained
by
latter,
even
aid
explainable
AI.
reader
advantages/disadvantages
pipelines
used
preprocessing
(cell
type
annotation).
Therefore,
this
also
guides
choose
pipeline
best
fits
their
In
conclusion,
continues
established
an
essential
tool
discovering
novel
mechanisms
when
combined
tissue
balance
medical
data,
role
routine
will
become
more
important,
supporting
diagnosis
prognosis
enhancing
decision-making,
improving
quality
care
for
patients.
npj Precision Oncology,
Journal Year:
2025,
Volume and Issue:
9(1)
Published: March 11, 2025
The
tumor
microenvironment
(TME)
plays
a
crucial
role
in
orchestrating
cell
behavior
and
cancer
progression.
Recent
advances
spatial
profiling
technologies
have
uncovered
novel
signatures,
including
univariate
distribution
patterns,
bivariate
relationships,
higher-order
structures.
These
signatures
the
potential
to
revolutionize
mechanism
treatment.
In
this
review,
we
summarize
current
state
of
signature
research,
highlighting
computational
methods
uncover
spatially
relevant
biological
significance.
We
discuss
impact
these
on
fundamental
biology
translational
address
challenges
future
research
directions.
Nature Genetics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 1, 2025
The
spatial
organization
of
cells
in
tissues
underlies
biological
function,
and
recent
advances
profiling
technologies
have
enhanced
our
ability
to
analyze
such
arrangements
study
processes
disease
progression.
We
propose
MESA
(multiomics
ecological
analysis),
a
framework
drawing
inspiration
from
concepts
delineate
functional
shifts
across
tissue
states.
introduces
metrics
systematically
quantify
diversity
identify
hot
spots,
linking
patterns
phenotypic
outcomes,
including
Furthermore,
integrates
single-cell
multiomics
data
facilitate
an
in-depth,
molecular
understanding
cellular
neighborhoods
their
interactions
within
microenvironments.
Applying
diverse
datasets
demonstrates
additional
insights
it
brings
over
prior
methods,
newly
identified
structures
key
cell
populations
linked
Available
as
Python
package,
offers
versatile
for
quantitative
decoding
architectures
omics
health
disease.
Multiomics
analysis
(MESA)
calculates
ecodiversity-inspired
spatially
resolved
integrated
with
data,
enabling
the
comparison
states
range
conditions.
American Journal of Transplantation,
Journal Year:
2023,
Volume and Issue:
24(4), P. 549 - 563
Published: Nov. 17, 2023
Kidney
allograft
inflammation,
mostly
attributed
to
rejection
and
infection,
is
an
important
cause
of
graft
injury
loss.
Standard
histopathological
assessment
inflammation
provides
limited
insights
into
biological
processes
the
immune
landscape.
Here,
using
imaging
mass
cytometry
with
a
panel
28
validated
biomarkers,
we
explored
single-cell
landscape
kidney
in
32
transplant
biopsies
247
high-dimensional
histopathology
images
various
phenotypes
(antibody-mediated
rejection,
T
cell-mediated
BK
nephropathy,
chronic
pyelonephritis).
Using
novel
analytical
tools,
for
cell
segmentation,
segmented
over
900
000
cells
developed
tissue-based
classifier
3000
manually
annotated
microstructures
(glomeruli,
tubules,
interstitium,
arteries).
PhenoGraph,
identified
11
9
nonimmune
clusters
found
high
prevalence
memory
macrophage-enriched
populations
across
phenotypes.
Additionally,
trained
machine
learning
identify
spatial
biomarkers
that
could
discriminate
between
different
inflammatory
Further
validation
larger
cohorts
more
will
likely
help
interrogate
depth
than
has
been
possible
date.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: May 8, 2024
Abstract
Cell
states
are
regulated
by
the
response
of
signaling
pathways
to
receptor
ligand-binding
and
intercellular
interactions.
High-resolution
imaging
has
been
attempted
explore
dynamics
these
processes
and,
recently,
multiplexed
profiled
cell
achieving
a
comprehensive
acquisition
spatial
protein
information
from
cells.
However,
specificity
antibodies
is
still
compromised
when
visualizing
activated
signals.
Here,
we
develop
Precise
Emission
Canceling
Antibodies
(PECAbs)
that
have
cleavable
fluorescent
labeling.
PECAbs
enable
high-specificity
sequential
using
hundreds
antibodies,
allowing
for
reconstruction
spatiotemporal
pathways.
Additionally,
combining
this
approach
with
seq-smFISH
can
effectively
classify
cells
identify
their
signal
activation
in
human
tissue.
Overall,
PECAb
system
serve
as
platform
analyzing
complex
processes.
Journal of Materials Chemistry B,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 3, 2024
A
comprehensive
overview
of
recent
advancements
in
fluorescence
imaging
techniques
for
situ
sensing
various
biomarkers,
emphasizing
the
transformative
potential
artificial
intelligence
shaping
future
bioimaging.
Proceedings of the National Academy of Sciences,
Journal Year:
2025,
Volume and Issue:
122(6)
Published: Feb. 4, 2025
Spatial
patterns
of
cells
and
other
biological
elements
drive
physiologic
pathologic
processes
within
tissues.
While
many
imaging
transcriptomic
methods
document
tissue
organization,
discerning
these
is
challenging,
especially
when
they
involve
multiple
in
complex
arrangements.
To
address
this
challenge,
we
present
Patterning
Analysis
Cellular
Ensembles
(SPACE),
an
R
package
for
analysis
high-plex
spatial
data.
SPACE
compatible
with
any
data
collection
modality
that
records
values
(i.e.,
categorical
cell/structure
types
or
quantitative
expression
levels)
at
fixed
coordinates
2d
pixels
3d
voxels).
detects
not
only
broad
co-occurrence
but
also
context-dependent
associations,
gradients
orientations,
organizational
complexities.
Via
a
robust
information
theoretic
framework,
explores
all
possible
ensembles
elements—single
elements,
pairs,
triplets,
so
on—and
ranks
the
most
strongly
patterned
ensembles.
For
single
images,
rankings
reflect
differences
from
random
assortment.
sets
across
sample
groups
(e.g.,
genotypes,
treatments,
timepoints,
etc.).
Further
tools
then
characterize
nature
each
pattern
intuitive
interpretation.
We
validate
demonstrate
its
advantages
using
murine
lymph
node
images
which
ground
truth
has
been
defined.
detect
new
varied
datasets,
including
tumors
tuberculosis
granulomas.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 8, 2025
Abstract
As
spatial
molecular
data
grow
in
scope
and
resolution,
there
is
a
pressing
need
to
identify
key
structures
associated
with
disease.
Current
approaches
often
rely
on
hand-crafted
features
such
as
local
abundances
of
manually
annotated,
discrete
cell
types,
which
may
overlook
important
signals.
Here
we
introduce
variational
inference-based
microniche
analysis
(VIMA),
method
that
combines
deep
learning
principled
statistics
discover
greater
flexibility
precision.
VIMA
uses
autoencoder
extract
numerical
“fingerprints”
from
small
tissue
patches
capture
their
biological
content.
It
these
fingerprints
define
large
number
“microniches”
–
small,
potentially
overlapping
groups
highly
similar
biology
span
multiple
samples.
then
rigorous
microniches
whose
abundance
correlates
case-control
status.
We
show
simulations
well
calibrated
more
powerful
accurate
than
other
approaches.
apply
140-gene
transcriptomics
dataset
Alzheimer’s
dementia,
54-marker
CO-Detection
by
indEXing
(CODEX)
ulcerative
colitis
(UC),
7-marker
immunohistochemistry
rheumatoid
arthritis
(RA),
each
case
recapitulating
known
identifying
novel