Briefings in Bioinformatics,
Journal Year:
2022,
Volume and Issue:
23(5)
Published: July 17, 2022
Abstract
The
rapid
development
of
spatial
transcriptomics
allows
the
measurement
RNA
abundance
at
a
high
resolution,
making
it
possible
to
simultaneously
profile
gene
expression,
locations
cells
or
spots,
and
corresponding
hematoxylin
eosin-stained
histology
images.
It
turns
promising
predict
expression
from
images
that
are
relatively
easy
cheap
obtain.
For
this
purpose,
several
methods
devised,
but
they
have
not
fully
captured
internal
relations
2D
vision
features
dependency
between
spots.
Here,
we
developed
Hist2ST,
deep
learning-based
model
RNA-seq
Around
each
sequenced
spot,
image
is
cropped
into
an
patch
fed
convolutional
module
extract
features.
Meanwhile,
with
whole
neighbored
patches
through
Transformer
graph
neural
network
modules,
respectively.
These
learned
then
used
by
following
zero-inflated
negative
binomial
distribution.
To
alleviate
impact
small
data,
self-distillation
mechanism
employed
for
efficient
learning
model.
By
comprehensive
tests
on
cancer
normal
datasets,
Hist2ST
was
shown
outperform
existing
in
terms
both
prediction
region
identification.
Further
pathway
analyses
indicated
our
could
reserve
biological
information.
Thus,
enables
generating
data
elucidating
molecular
signatures
tissues.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: March 1, 2023
Abstract
Spatial
transcriptomics
technologies
generate
gene
expression
profiles
with
spatial
context,
requiring
spatially
informed
analysis
tools
for
three
key
tasks,
clustering,
multisample
integration,
and
cell-type
deconvolution.
We
present
GraphST,
a
graph
self-supervised
contrastive
learning
method
that
fully
exploits
data
to
outperform
existing
methods.
It
combines
neural
networks
learn
informative
discriminative
spot
representations
by
minimizing
the
embedding
distance
between
adjacent
spots
vice
versa.
demonstrated
GraphST
on
multiple
tissue
types
technology
platforms.
achieved
10%
higher
clustering
accuracy
better
delineated
fine-grained
structures
in
brain
embryo
tissues.
is
also
only
can
jointly
analyze
slices
vertical
or
horizontal
integration
while
correcting
batch
effects.
Lastly,
superior
deconvolution
capture
niches
like
lymph
node
germinal
centers
exhausted
tumor
infiltrating
T
cells
breast
tissue.
Nature Methods,
Journal Year:
2023,
Volume and Issue:
20(2), P. 218 - 228
Published: Jan. 23, 2023
Abstract
Spatial
transcriptomic
technologies
and
spatially
annotated
single-cell
RNA
sequencing
datasets
provide
unprecedented
opportunities
to
dissect
cell–cell
communication
(CCC).
However,
incorporation
of
the
spatial
information
complex
biochemical
processes
required
in
reconstruction
CCC
remains
a
major
challenge.
Here,
we
present
COMMOT
(COMMunication
analysis
by
Optimal
Transport)
infer
transcriptomics,
which
accounts
for
competition
between
different
ligand
receptor
species
as
well
distances
cells.
A
collective
optimal
transport
method
is
developed
handle
molecular
interactions
constraints.
Furthermore,
introduce
downstream
tools
signaling
directionality
genes
regulated
using
machine
learning
models.
We
apply
simulation
data
eight
acquired
with
five
show
its
effectiveness
robustness
identifying
varying
resolutions
gene
coverages.
Finally,
identifies
new
CCCs
during
skin
morphogenesis
case
study
human
epidermal
development.
Genome Research,
Journal Year:
2021,
Volume and Issue:
31(10), P. 1706 - 1718
Published: Oct. 1, 2021
Spatial
transcriptomics
is
a
rapidly
growing
field
that
promises
to
comprehensively
characterize
tissue
organization
and
architecture
at
the
single-cell
or
subcellular
resolution.
Such
information
provides
solid
foundation
for
mechanistic
understanding
of
many
biological
processes
in
both
health
disease
cannot
be
obtained
by
using
traditional
technologies.
The
development
computational
methods
plays
important
roles
extracting
signals
from
raw
data.
Various
approaches
have
been
developed
overcome
technology-specific
limitations
such
as
spatial
resolution,
gene
coverage,
sensitivity,
technical
biases.
Downstream
analysis
tools
formulate
cell–cell
communications
quantifiable
properties,
provide
algorithms
derive
properties.
Integrative
pipelines
further
assemble
multiple
one
package,
allowing
biologists
conveniently
analyze
data
beginning
end.
In
this
review,
we
summarize
state
art
transcriptomic
pipelines,
discuss
how
they
operate
on
different
technological
platforms.
Current Opinion in Systems Biology,
Journal Year:
2021,
Volume and Issue:
26, P. 12 - 23
Published: March 26, 2021
Cell-cell
communication
is
a
fundamental
process
that
shapes
biological
tissue.
Historically,
studies
of
cell-cell
have
been
feasible
for
one
or
two
cell
types
and
few
genes.
With
the
emergence
single-cell
transcriptomics,
we
are
now
able
to
examine
genetic
profiles
individual
cells
at
unprecedented
scale
depth.
The
availability
such
data
presents
an
exciting
opportunity
construct
more
comprehensive
description
communication.
This
review
discusses
recent
explosion
methods
developed
infer
from
non-spatial
spatial
promising
technologies
which
complementary
strengths
limitations.
We
propose
several
avenues
propel
this
rapidly
expanding
field
forward
in
meaningful
ways.
Nucleic Acids Research,
Journal Year:
2022,
Volume and Issue:
50(22), P. e131 - e131
Published: Oct. 4, 2022
Recent
advances
in
spatial
transcriptomics
(ST)
have
brought
unprecedented
opportunities
to
understand
tissue
organization
and
function
context.
However,
it
is
still
challenging
precisely
dissect
domains
with
similar
gene
expression
histology
situ.
Here,
we
present
DeepST,
an
accurate
universal
deep
learning
framework
identify
domains,
which
performs
better
than
the
existing
state-of-the-art
methods
on
benchmarking
datasets
of
human
dorsolateral
prefrontal
cortex.
Further
testing
a
breast
cancer
ST
dataset,
showed
that
DeepST
can
at
finer
scale.
Moreover,
achieve
not
only
effective
batch
integration
data
generated
from
multiple
batches
or
different
technologies,
but
also
expandable
capabilities
for
processing
other
omics
data.
Together,
our
results
demonstrate
has
exceptional
capacity
identifying
making
desirable
tool
gain
novel
insights
studies.
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Nov. 23, 2022
Abstract
Spatial
transcriptomics
are
a
collection
of
genomic
technologies
that
have
enabled
transcriptomic
profiling
on
tissues
with
spatial
localization
information.
Analyzing
data
is
computationally
challenging,
as
the
collected
from
various
often
noisy
and
display
substantial
correlation
across
tissue
locations.
Here,
we
develop
spatially-aware
dimension
reduction
method,
SpatialPCA,
can
extract
low
dimensional
representation
biological
signal
preserved
structure,
thus
unlocking
many
existing
computational
tools
previously
developed
in
single-cell
RNAseq
studies
for
tailored
analysis
transcriptomics.
We
illustrate
benefits
SpatialPCA
domain
detection
explores
its
utility
trajectory
inference
high-resolution
map
construction.
In
real
applications,
identifies
key
molecular
immunological
signatures
detected
tumor
surrounding
microenvironment,
including
tertiary
lymphoid
structure
shapes
gradual
transition
during
tumorigenesis
metastasis.
addition,
detects
past
neuronal
developmental
history
underlies
current
landscape
locations
cortex.
Genome Medicine,
Journal Year:
2024,
Volume and Issue:
16(1)
Published: Jan. 12, 2024
Abstract
Optimal
integration
of
transcriptomics
data
and
associated
spatial
information
is
essential
towards
fully
exploiting
to
dissect
tissue
heterogeneity
map
out
inter-cellular
communications.
We
present
SEDR,
which
uses
a
deep
autoencoder
coupled
with
masked
self-supervised
learning
mechanism
construct
low-dimensional
latent
representation
gene
expression,
then
simultaneously
embedded
the
corresponding
through
variational
graph
autoencoder.
SEDR
achieved
higher
clustering
performance
on
manually
annotated
10
×
Visium
datasets
better
scalability
high-resolution
than
existing
methods.
Additionally,
we
show
SEDR’s
ability
impute
denoise
expression
(URL:
https://github.com/JinmiaoChenLab/SEDR/
).
Genome biology,
Journal Year:
2022,
Volume and Issue:
23(1)
Published: March 25, 2022
Abstract
The
recent
advancement
in
spatial
transcriptomics
technology
has
enabled
multiplexed
profiling
of
cellular
transcriptomes
and
locations.
As
the
capacity
efficiency
experimental
technologies
continue
to
improve,
there
is
an
emerging
need
for
development
analytical
approaches.
Furthermore,
with
continuous
evolution
sequencing
protocols,
underlying
assumptions
current
methods
be
re-evaluated
adjusted
harness
increasing
data
complexity.
To
motivate
aid
future
model
development,
we
herein
review
statistical
machine
learning
transcriptomics,
summarize
useful
resources,
highlight
challenges
opportunities
ahead.