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:
2022,
Volume and Issue:
13(1)
Published: July 14, 2022
One
major
challenge
in
analyzing
spatial
transcriptomic
datasets
is
to
simultaneously
incorporate
the
cell
transcriptome
similarity
and
their
locations.
Here,
we
introduce
SpaceFlow,
which
generates
spatially-consistent
low-dimensional
embeddings
by
incorporating
both
expression
information
using
spatially
regularized
deep
graph
networks.
Based
on
embedding,
a
pseudo-Spatiotemporal
Map
that
integrates
pseudotime
concept
with
locations
of
cells
unravel
spatiotemporal
patterns
cells.
By
comparing
multiple
existing
methods
several
at
spot
single-cell
resolutions,
SpaceFlow
shown
produce
robust
domain
segmentation
identify
biologically
meaningful
patterns.
Applications
reveal
evolving
lineage
heart
developmental
data
tumor-immune
interactions
human
breast
cancer
data.
Our
study
provides
flexible
learning
framework
Clinical and Translational Medicine,
Journal Year:
2022,
Volume and Issue:
12(1)
Published: Jan. 1, 2022
Abstract
The
idea
that
tumour
microenvironment
(TME)
is
organised
in
a
spatial
manner
will
not
surprise
many
cancer
biologists;
however,
systematically
capturing
architecture
of
TME
still
possible
until
recent
decade.
past
five
years
have
witnessed
boom
the
research
high‐throughput
techniques
and
algorithms
to
delineate
at
an
unprecedented
level.
Here,
we
review
technological
progress
omics
how
advanced
computation
methods
boost
multi‐modal
data
analysis.
Then,
discussed
potential
clinical
translations
precision
oncology,
proposed
transfer
ecological
principles
biology
interpretation.
So
far,
placing
us
golden
age
research.
Further
development
application
may
lead
comprehensive
decoding
ecosystem
bring
current
spatiotemporal
molecular
medical
into
entirely
new
paradigm.
Genome biology,
Journal Year:
2022,
Volume and Issue:
23(1)
Published: Oct. 17, 2022
Abstract
Background
Cell-cell
interactions
are
important
for
information
exchange
between
different
cells,
which
the
fundamental
basis
of
many
biological
processes.
Recent
advances
in
single-cell
RNA
sequencing
(scRNA-seq)
enable
characterization
cell-cell
using
computational
methods.
However,
it
is
hard
to
evaluate
these
methods
since
no
ground
truth
provided.
Spatial
transcriptomics
(ST)
data
profiles
relative
position
cells.
We
propose
that
spatial
distance
suggests
interaction
tendency
cell
types,
thus
could
be
used
evaluating
tools.
Results
benchmark
16
by
integrating
scRNA-seq
with
ST
data.
characterize
into
short-range
and
long-range
distributions
ligands
receptors.
Based
on
this
classification,
we
define
enrichment
score
apply
an
evaluation
workflow
tools
15
simulated
5
real
datasets.
also
compare
consistency
results
from
single
commonly
identified
interactions.
Our
suggest
predicted
highly
dynamic,
statistical-based
show
overall
better
performance
than
network-based
ST-based
Conclusions
study
presents
a
comprehensive
scRNA-seq.
CellChat,
CellPhoneDB,
NicheNet,
ICELLNET
other
terms
software
scalability.
recommend
at
least
two
ensure
accuracy
have
packaged
detailed
documentation
GitHub
(
https://github.com/wanglabtongji/CCI
).
Computational and Structural Biotechnology Journal,
Journal Year:
2022,
Volume and Issue:
20, P. 4870 - 4884
Published: Jan. 1, 2022
Transcriptome
level
expression
data
connected
to
the
spatial
organization
of
cells
and
molecules
would
allow
a
comprehensive
understanding
how
gene
is
structure
function
in
biological
systems.
The
transcriptomics
platforms
may
soon
provide
such
information.
However,
current
still
lack
resolution,
capture
only
fraction
transcriptome
heterogeneity,
or
throughput
for
large
scale
studies.
strengths
weaknesses
ST
computational
solutions
need
be
taken
into
account
when
planning
basis
analysis
developed
single-cell
RNA-sequencing
data,
with
advancements
taking
connectedness
transcriptomes.
scRNA-seq
tools
are
modified
new
like
deep
learning-based
joint
expression,
spatial,
image
extract
information
spatially
resolved
can
reveal
remarkable
insights
patterns
cell
signaling,
type
variations
connection
type-specific
signaling
complex
tissues.
This
review
covers
topics
that
help
choosing
platform
research.
We
focus
on
currently
available
methods
their
limitations.
Of
solutions,
we
an
overview
steps
used
analysis.
compatibility
types
provided
by
frameworks
summarized.
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.