bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Июль 28, 2023
Abstract
Advances
in
Electron
Microscopy,
image
segmentation
and
computational
infrastructure
have
given
rise
to
large-scale
richly
annotated
connectomic
datasets
which
are
increasingly
shared
across
communities.
To
enable
collaboration,
users
need
be
able
concurrently
create
new
annotations
correct
errors
the
automated
by
proofreading.
In
large
datasets,
every
proofreading
edit
relabels
cell
identities
of
millions
voxels
thousands
like
synapses.
For
analysis,
require
immediate
reproducible
access
this
constantly
changing
expanding
data
landscape.
Here,
we
present
Connectome
Annotation
Versioning
Engine
(CAVE),
a
for
connectome
analysis
up-to
petascale
(∼1mm
3
)
while
annotating
is
ongoing.
segmentation,
CAVE
provides
distributed
continuous
versioning
reconstructions.
Annotations
defined
locations
such
that
they
can
quickly
assigned
underlying
segment
enables
fast
queries
CAVE’s
arbitrary
time
points.
supports
schematized,
extensible
annotations,
so
researchers
readily
design
novel
annotation
types.
already
used
many
connectomics
including
largest
available
date.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2021,
Номер
unknown
Опубликована: Июль 29, 2021
Abstract
To
understand
the
brain
we
must
relate
neurons’
functional
responses
to
circuit
architecture
that
shapes
them.
Here,
present
a
large
connectomics
dataset
with
dense
calcium
imaging
of
millimeter
scale
volume.
We
recorded
activity
from
approximately
75,000
neurons
in
primary
visual
cortex
(VISp)
and
three
higher
areas
(VISrl,
VISal
VISlm)
an
awake
mouse
viewing
natural
movies
synthetic
stimuli.
The
data
were
co-registered
volumetric
electron
microscopy
(EM)
reconstruction
containing
more
than
200,000
cells
0.5
billion
synapses.
Subsequent
proofreading
subset
this
volume
yielded
reconstructions
include
complete
dendritic
trees
as
well
local
inter-areal
axonal
projections
map
up
thousands
cell-to-cell
connections
per
neuron.
release
open-access
resource
scientific
community
including
set
tools
facilitate
retrieval
downstream
analysis.
In
accompanying
papers
describe
our
findings
using
provide
comprehensive
structural
characterization
cortical
cell
types
1–3
most
detailed
synaptic
level
connectivity
diagram
column
date
2
,
uncovering
unique
cell-type
specific
inhibitory
motifs
can
be
linked
gene
expression
4
.
Functionally,
identify
new
computational
principles
how
information
is
integrated
across
space
5
characterize
novel
neuronal
invariances
6
bring
structure
function
together
decipher
general
principle
wires
excitatory
within
7,
8
Frontiers in Neuroinformatics,
Год журнала:
2022,
Номер
16
Опубликована: Фев. 15, 2022
Technological
advances
in
imaging
and
data
acquisition
are
leading
to
the
development
of
petabyte-scale
neuroscience
image
datasets.
These
large-scale
volumetric
datasets
pose
unique
challenges
since
analyses
often
span
entire
volume,
requiring
a
unified
platform
access
it.
In
this
paper,
we
describe
Brain
Observatory
Storage
Service
Database
(BossDB),
cloud-based
solution
for
storing
accessing
petascale
BossDB
provides
support
ingest,
storage,
visualization,
sharing
through
RESTful
Application
Programming
Interface
(API).
A
key
feature
is
scalable
indexing
spatial
automatic
manual
annotations
facilitate
discovery.
Our
project
open
source
can
be
easily
cost
effectively
used
variety
modalities
applications,
has
worked
with
over
petabyte
size.
Frontiers in Cell and Developmental Biology,
Год журнала:
2022,
Номер
10
Опубликована: Апрель 5, 2022
Electron
microscopy
is
the
primary
approach
to
study
ultrastructural
features
of
cerebrovasculature.
However,
2D
snapshots
a
vascular
bed
capture
only
small
fraction
its
complexity.
Recent
efforts
synaptically
map
neuronal
circuitry
using
volume
electron
have
also
sampled
brain
microvasculature
in
3D.
Here,
we
perform
meta-analysis
7
data
sets
spanning
different
species
and
regions,
including
two
from
MICrONS
consortium
that
made
segment
vasculature
addition
all
parenchymal
cell
types
mouse
visual
cortex.
Exploration
these
revealed
rich
information
for
detailed
investigation
Neurovascular
unit
(including,
but
not
limited
to,
endothelial
cells,
mural
perivascular
fibroblasts,
microglia,
astrocytes)
could
be
discerned
across
broad
microvascular
zones.
Image
contrast
was
sufficient
identify
subcellular
details,
junctions,
caveolae,
peg-and-socket
interactions,
mitochondria,
Golgi
cisternae,
microvilli
other
cellular
protrusions
potential
significance
signaling.
Additionally,
non-cellular
structures
basement
membrane
spaces
were
visible
traced
between
arterio-venous
zones
along
wall.
These
explorations
structural
may
important
functions,
such
as
blood-brain
barrier
integrity,
blood
flow
control,
clearance,
bioenergetics.
They
identified
limitations
where
accuracy
consistency
segmentation
further
honed
by
future
efforts.
The
purpose
this
article
introduce
valuable
community
resources
within
framework
cerebrovascular
research.
We
do
so
providing
an
assessment
their
contents,
identifying
study,
discussing
next
step
ideas
refining
analysis.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Ноя. 1, 2023
A
primary
cilium
is
a
thin
membrane-bound
extension
off
cell
surface
that
contains
receptors
for
perceiving
and
transmitting
signals
modulate
state
activity.
While
many
types
have
cilium,
little
known
about
cilia
in
the
brain,
where
they
are
less
accessible
than
on
cultured
cells
or
epithelial
tissues
protrude
from
bodies
into
deep,
dense
network
of
glial
neuronal
processes.
Here,
we
investigated
frequency,
internal
structure,
shape,
position
large,
high-resolution
transmission
electron
microscopy
volumes
mouse
visual
cortex.
Cilia
extended
nearly
all
excitatory
inhibitory
neurons,
astrocytes,
oligodendrocyte
precursor
(OPCs),
but
were
absent
oligodendrocytes
microglia.
Structural
comparisons
revealed
membrane
structure
at
base
microtubule
organization
differed
between
neurons
glia.
OPC
distinct
shortest
contained
pervasive
vesicles
only
occasionally
observed
neuron
astrocyte
cilia.
Investigating
cilia-proximal
features
directly
adjacent
to
synapses,
suggesting
well
poised
encounter
locally
released
signaling
molecules.
proximity
synapses
was
random,
not
enriched,
synapse-rich
neuropil.
The
anatomy,
including
changes
centriole
location,
defined
key
structural
placement
shape.
Together,
anatomical
insights
both
within
around
glia
provide
new
formation
function
across
brain.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Июль 28, 2023
Abstract
Advances
in
Electron
Microscopy,
image
segmentation
and
computational
infrastructure
have
given
rise
to
large-scale
richly
annotated
connectomic
datasets
which
are
increasingly
shared
across
communities.
To
enable
collaboration,
users
need
be
able
concurrently
create
new
annotations
correct
errors
the
automated
by
proofreading.
In
large
datasets,
every
proofreading
edit
relabels
cell
identities
of
millions
voxels
thousands
like
synapses.
For
analysis,
require
immediate
reproducible
access
this
constantly
changing
expanding
data
landscape.
Here,
we
present
Connectome
Annotation
Versioning
Engine
(CAVE),
a
for
connectome
analysis
up-to
petascale
(∼1mm
3
)
while
annotating
is
ongoing.
segmentation,
CAVE
provides
distributed
continuous
versioning
reconstructions.
Annotations
defined
locations
such
that
they
can
quickly
assigned
underlying
segment
enables
fast
queries
CAVE’s
arbitrary
time
points.
supports
schematized,
extensible
annotations,
so
researchers
readily
design
novel
annotation
types.
already
used
many
connectomics
including
largest
available
date.