►
Description
DevoWorm meeting: March 23, 2020. Attendees: Richard Gordon, Devansh Batra, Ujjwal Singh, Bradly Alicea, Yash Patel, Susan Crawford-Young, Amrendra Pratap Singh, and Jesse Parent
A
A
All
right
would
always
start
the
meeting.
Welcome
to
the
meeting
this
week.
I
know
everyone's
kind
of
jumbled
around
because
of
the
coronavirus
I'm
out
of
my
meeting
space,
my
usual
meeting
space
currently,
but
it
seems
to
be
pretty
okay
with
right
now,
so
why
don't
we
go
over
a
couple
things
before
we
get
to
is?
Wall
was
gonna
present
his
proposal
or
well
he's
gonna,
give
us
an
update
on
and
what
he's
been
doing
recently
in
terms
of
3d
modeling.
He.
B
A
A
A
A
C
elegans,
the
group
is
called
evil
worm,
but
we've
been
interested
in
other
organisms
as
well,
and
so
we've
done
C
elegans
we've
done
some
work
with
your
Safa
and
there's
some
data
was
zebrafish.
Your
honor
Evos
oocyte
and
we've
also
worked
on
something
called
tunicates
or
sea
squirts,
and
it's
a
pretty
big
group
of
organisms
pretty
diverse,
but
it
has
a
really
interesting
developmental
period,
and
so
we've
done
a
little
bit
of
data
analysis
on
that
and
I
found
a
paper
that
it's
a
very
longest
paper
and
I
can
share
it
with
you.
A
It's
in
this
folder
and
it's
on
the
the
eventful
history
of
the
non-embryonic
development
in
tunicates.
So
tunicates
have
a
very
interesting
embryo
and
it's
actually
a
lot
like
C
elegans
and
that
you
can
take
the
individual
cells
and
trace
them
from
a
single
cell
into
an
embryo
of
a
couple
hundred
cells.
And
so
you
can.
They
have
the
lineage
tree
traced
out
and
from
there.
You
can
do
a
lot
of
things
in
terms
of
analysis
of
the
embryonic
development.
A
It's
also
interesting
because
it
has
a
very
small
connector.
So
in
C
elegans
we
talk
about
the
connectome
being
302
neurons
in
in
sea,
squirts
and
tourniquets.
They
have
177
neuron
nervous
system,
at
least
in
the
developmental
phase,
and
so
that's
a
that's
another
thing
that
I
don't
think
anyone's
really
quantified
it
the
way
they've
done
with
C
elegans.
They
know
the
number
of
neurons,
but
they
don't
have
them
catalogued.
A
If
you
know
anything
about
open
word,
the
more
general
Jerome
project,
you
know
that
there
have
been
a
couple
of
draft
connectomes
where
people
have
actually
really
characterized
each
cell
in
the
connect.
Oh,
they
don't
have
that
forestry
ticket,
but
they
do
know
that
it's
a
small
connector,
so
that's
another
advantage
to
working
with
it.
Achatz.
The
third
one
is
that
they
have
this
extensive
non
embryonic
development
phase
and
the
this
phase
ranges.
You
know
it
grows
from.
Maybe
a
couple
hundred
cells
to
over.
A
You
know
thousands
of
cells
and
it
changes
shape
significantly
during
this
non
embryonic
development
phase,
and
so
this
is
what
those
papers
about
and
they
kind
of
review
a
lot
of
this
part
of
the
rich
life
history.
Is
this
it's
a
pretty
diverse
group
of
organisms,
but
they
just
kind
of
do
a
general
review
of
it.
So
tunicates
encompass
a
large
group
of
marine
filter
feeding
animals.
More
than
half
of
them
are
able
to
reproduce
asexually
a
particularly
from
now.
A
A
So
even
that
is
within
this
order
is
quite
diverse,
and
so
I
mean
it
happens,
that
ways
and
different
species,
and
so
they
review
150
years
of
literature
in
this
review
to
provide
a
view
of
non
embryonic
development
which
they
deviate.
Anyd
diversity
and
we
present
a
comparative
picture
of
budding
tissues
across
tunicates.
So
this
is
mainly
having
to
do
with
that
budding
period
of
this
non
embryonic
phase
and
they're
just
kind
of
reviewing
a
lot
of
the
evidence
for
house
reverse.
It
is
and
basic
mechanisms
and
so
forth.
A
They
typically
have
a
biphasic
life
cycle,
with
a
photonic
planktonic
larvae
and
have
post
metamorphic
phase
that
is
benthic
in
the
city,
and
this
is
probably
did
a
non
specialist
doesn't
make
sense,
but
it
basically
says
that
there's
this
life
cycle,
where
they
have
different
stages,
they
have
a
larva
stage
and
a
post
metamorphic
stage.
So
it's
sort
of
like
is
in
butterflies.
You
know
they
come
from
larva
stage
and
then
they
transformed
that's
kind
of
what
happens
in
tunicates,
although
not
a
not
in
the
same
way.
A
A
A
A
So
yeah,
so
they
go
over
this
and
I
don't
want
to
get
too
deeply
into
the
paper,
because
you
can
read
it
on
your
own
and
so
putting
an
unbuttoned
species
or
scattered
amongst
forming
tourniquet
orders,
and
so
the
order.
An
order
is
a
group
of
working
group
of
species
that
are
related
loosely,
and
there
are
four
orders
where
this
is
where
you
get
both
of
these
types
of
reproduction.
And
it's
not
like
typical
of
like
one
group
of
organisms
of
the
common
ancestry
or
maybe
one
order
it
scattered
throughout.
A
Implication
there
is
that
it's
it's
not
something.
That's
occurred
in
one
ancestral
species
and
then
descended
in
it.
It's
the
sentiment
species,
it's
something
that
happens
Sarah,
what
they
call
polyfill
ethically
or
it
happens
just
kind
of
based
on
the
species
or
they
may
be
based
on
a
couple
of
species
in
their
conditions.
So
it
could
be
something
less
influenced
by
environment.
It
could
be
something
that
just
happens
as
a
strategy
that
they
have
that
dormant
and
other
species
in
that
order.
It's
you
know
it's.
It's
definitely
not
a.
A
A
That's
usually
species
actually
know
that
people
work
within
the
lab
say
where
that's
common
in
need
common
enough
in
nature
that
people
can
get
a
hand,
get
a
bunch
of
them
to
study
in
a
lab
setting
out
in
the
field,
and
but
that,
of
course
limits
our
ability
to
understand
diversity
of
these
processes,
because
a
model
species
like
C
elegans
represents
a
little
bit
of
biology
and,
like
you
know,
we
think
of
C
elegans
is
like
the
nematodes
right
now.
There
are
a
lot
of
needs
within
species.
A
They
range
very
broadly
in
terms
of
the
number
of
cells
they
have
in
terms
of
the
types
of
reproduction.
Some
are
sexually
reproducing
exclusively
summer
exclusively.
You
know,
hermaphrodites,
etc.
There's
a
lot
of
diversity
there,
but
we
usually
just
use
the
C
elegans
model
and
we
use
it
to
say
things
about
human
biology.
So
you
know
it's
not
just
that.
We
use
it
to
look
at
nematodes,
but
so
model
organisms
are,
you
know.
A
So
they
actually
don't
forget
if
a
phylogeny
in
this
part
may
be
a
little
over
the
head
of
a
lot
of
people
in
the
group
here,
but
I
hope.
Phylogenetics
is
kind
of
one
of
those
things
where
they
throw
around
a
lot
of
jargon
and
you
have
to
like
read
a
couple
papers
on
it
to
know
what
they're
doing
but
they're
doing,
but
basically
what
they
do
in
file
with
phylogenetic
says
they
study.
So
this
is
a
tree
of
a
bunch
of
tourniquet
species.
B
A
B
A
A
A
A
A
B
A
A
A
A
Trees
but
they
and
they
talk
about
it-
a
bit
in
this
paper.
So
definitely
they
don't
understand
this
part
of
the
paper.
That's
fine,
and
then
we
have
some
pictures
here
of
some
of
some
kind
of
gate,
development
and
somebody's
strategies.
We
have
a
couple
of
nice
color
photographs
of
different
tunicates,
as
you
can
see
there.
A
A
Here's
another
image,
another
set
of
images
that
show
some
more
examples
of
larvae.
Again,
you
have
this
tube,
so
the
tube
will
eventually
become
a
free,
moving
organism
of
the
ocean,
but
it's
just
a
tube
in
the
larval
phase,
and
then
you
have
these
different
strategies
for
budding
media.
They
show
that
at
the
cellular
level,
where
you
have
buds
that
are
forming
your
vesicles,
you
have
a
tip
a
primordial
tip
and
this
kind
of
shows
this
process.
A
So
there
are
a
lot
of
orders
like
I
said
before
the
model
organism
is
a
good
way
to
a
characterized
the
process,
but
not
a
very
good
way
to
characterize
the
diversity,
and
so
we
have
a
lot.
There
are
a
lot
of
orders
and
groups
of
this
phylogeny
from
which
budding
is
very
poorly
known,
and
so
there
is
a
lot
of
diversity
in
this
budding.
I
think
these
two
figures
two
and
three
show
the
differences.
What
they're
trying
to
get
in.
So
this
is
one
type
of
budding
here
and
then
figure.
A
A
A
A
And
so
then
they
get
a
density,
so
they
actually
talk
about
something
called
homology.
So
homology
is
when
you
have
species
that
are
related
and
they
share
trees.
The
common
ancestor
had
this
tree
and
then
it
exists
in
the
related
species
that
derived
from
this
common
ancestor,
and
so
you
can
call
something
homologous
if
it's
shared
within
dance
between
the
two
sister
species.
Now
homology
is
interesting
because
you
can
have
mutations
that
occur
along
the
way.
So
you
can
have
some
processor
trait
that
looks
similar
like
bird
wings
across
birds,
but
they're.
A
They
function
differently,
they
may
look
different,
but
they
have
basically
the
same
homologous
relationship,
and
so
this
is
one
thing
they
use
to
understand:
common
ancestry
and
infer
common
ancestry,
and
so
like
amongst
phylogenetic
system.
Ology
is
a
big
issue.
Is
something
homologous
and
you
know
it's
like.
So
you
would
have
like
a
homologue
would
be
like.
You
know,
a
certain
type
of
budding,
but
it's
maybe
a
little
bit
different
than
its
sister
species,
but
they're
both
common.
A
You
know
they
both
have
a
common
origin,
and
so
they
talk
about
this
non
embryonic
development
and
how
homologous
it
is
across
species,
and
so
then
they
have
a
table.
There
are
actually
six
budding
modes
in
tunicates.
They've
talked
about
the
first
two
here
are
those
felonio
on
the
Peregrine
keel,
which
are
the
main
ones,
and
then
there's
basal,
vascular,
epicardial,
epicardial
and
pharyngeal,
and
so
all
those
different
types
of
budding
were
identified.
The
literature
or
have
been
identified
in
the
literature
and
they
give
example
species
of
each.
A
So
this
is
and
then
of
course,
to
Nakata,
which
is
this
big
group
of
tunicates.
This
is
something
that,
if
you're
interested
in
the
evolution
of
development
is
a
great
model
system
for
this,
and
so
this
is,
if
you're
interested
in
the
theory
of
it
or
if
you're
interested
in
this
topic
of
evo-devo.
This
is
a
section
you
should
read
over
if
they're
proposing
that
abused
as
a
model
system
for
evo-devo-
and
certainly
you
know,
the
evolution
of
development
is
an
interesting
area.
A
A
A
So
the
first
step
is
to
get
the
presentations
down
and
into
this
place,
and
then
this
this
is
a
lecture
tab.
So
this
actual
just
has
a
list
of
the
lectures
with
the
abstracts,
and
so
this
is
a
know
a
great
now
it's
as
mirror
of
the
other
site.
Well,
what
maybe
we
can
do
with
this
is
like
turn
it
into
a
resource
for
education,
and
so
we
have
the
slides.
We
have
all
the
materials
here.
A
So
what
we
have
are,
like
you
know,
different
years,
I
think
it
goes
back
to
2009
yeah,
those
from
2009
up
to
2014
and
each
year
there
were
a
series
of
lectures
by
people
in
developmental
biology
and
biophysics,
and
they
have
a
talk.
You
know,
they'll
have
an
abstract
with
slides
and
you
know
they're,
but
there
are
a
lot
of
things
we
can
do
with
this.
You
know
just
have
to
have
this
list
of
slides
and
videos.
A
We
can
put
build,
maybe
tutorials
around
it
or
you
know,
kind
of
profile,
different
topics
or
things
like
that.
So
right
now
that
they
have
this
little
stub
and
we
have
the
presentations
but
I
mean
I'm
thinking
kind
of
like
back
to
the
evil.
Warm
open,
worm,
education
thing
that
we
talked
about
at
the
beginning
of
this
year.
That
was
done
last
last
year
for
Mozilla
open
leaders.
A
It's
something
like
that.
We
can
talk
about
it
later,
but
where
we
have
like
you
know
the
presentations
of
lectures
broken
out,
maybe
by
year,
and
then
maybe
some
tutorials
to
go
along
with
it
and
I
turn
it
into
a
sort
of
educational
experience.
Rather
than
like
a
list
of
lectures,
I'm
not
sure
how
to
how
that
was
this
be
approached,
I
mean
that
would
be
something
that
would
have
to
be
discussed
amongst
people.
What
what
they
think
would
be
interesting.
A
I
know
that
we
have
a
couple
people
here
who
were
involved
in
open
leaders
when
I
was
in
Devon
and
so
they'll
be
interested
in
maybe
giving
some
feedback
on
this
Jessi
is
also
interested
in
this
type
of
educational
online
educational
stages.
So
you
might
have
some
interesting
comments
to
make
on
that.
A
Why
don't
I
put
a
link
in
the
chat
and
you
can
look
it
over
yeah,
so
dick
says
the
other
site
is
temporary
and
that's
why
we
wanted
to
originally
mirror
over
to
this
one,
but
we
can
also
build
up
some
infrastructure
around
this.
This
set
of
lectures
because
we
already
have
a
lot
of
content
here.
We
have
presentations
and
a
lecture
series
type
thing.
You
know
their
topics
and
I
mean
there's
a
lot
of
information
in
here
for
the
casual
viewer
to
come
in
and
to
read
this.
A
B
So
today,
like
I,
am
going
to
talk
about
compa,
salinity,
computations,
so
basically,
compasses
theories
of
pair
is
a
kind
of
software
which
is
used
to
simulate,
build
test,
run
and
visualize
multi
scale,
multi
cell
GGH,
based
simulations
and
so
like.
We
can
start
with
introduction,
so
the
sample
theory
as
I
have
suggested
a
three
dimensional
sequence
for
software
program:
solving
environment
for
simulations
for
bio
complexity,
problems,
integrating
multiple
mathematical
models.
B
These
include
cellular
parts
models
which
can
model
cellquest,
Wingrove,
TV
cell
death
and
ashen
iron
volume
and
the
surface
area
constraints,
as
well
as
the
partial
differential
equation,
solvers
or
modelling
reaction
diffusion
of
the
chemicals
fields
and
cell
type
automata
for
differentiation.
Now
it
has
the
police
and
the
scripting
language.
B
Also,
it
does
not
require
key
combinations
again
and
again
like
once.
You
have
tried
the
food
you
can
change,
will
change
in
the
code
and
enter
it
simultaneously
without
recompiling,
again
and
again,
model
I
used
these.
The
best
part
of
this
compression
theory
is
like
these
model
described
using
XML
Python
scripts.
These
are
something
which
we
are
focusing
since
the
last
almost
like.
B
B
It
has
multi-platform
support
like
Linux,
UNIX
windows
and
mac
OS,
so
here
some
about
like
installation
guide,
so
in
the
middle
for
the
Windows
10
installation
is
statement
very
easy,
like
I
recommend
everyone
to
please
if
you
have
Windows
Start
to
do
it
on
windows,
because
in
Linux
it
is
very
much
like
very
much
difficult
to
install
it.
So
what
you
have
to
just
go
to
a
compass,
LCDs
website
main
page,
you
have
till
the
menu
in
the
left
side,
Vale
of
click
on
the
binaries
option.
B
You
can
see
the
different
download
options
for
digital
platforms
like
Mac,
OS,
Linux
and
Windows
or
Windows
click
on
the
download
button.
It
will
see
once
you
find
it
to
third-party
site,
which
we
try,
which
will
help
you
to
download
all
of
their
servers,
and
it
is
our
anxiety
or
something,
and
you
just
have
to
furnish
your
installed
just
have
to
execute
the
exe
files
like
if
I
want
to
show
like
this
is
the
composition,
theory,
XML
files
and
you
just
have
to
click
on
it.
B
B
By
the
way
the
process
is
same,
like
you
can
find
the
Linux
so
from
the
download
link,
then
you
have
to
unzip
it
and
follow
the
PDF,
so
I
have
downloaded
it
online
as
well,
and
I
have
found
out
the
problems
which
are
here
so
just
in
case
you
are
using
for
this.
I
would
like
to
make
sure
that
you
are
not
going
to
the
problems
so
in
this
command
in
this
command.
This
email
GUI,
which
is
down
to
the
using
sweet.
B
So
this
is
the
old,
outdated
version
of
CMH
UI,
which
is
not
going
to
work
today.
So
what
to
do
is
once
you
have
installed
all
these
files.
You
have
to
install
this
one
I
10
QT
graphs
for
simulations,
but
at
this
step
at
cmeg,
why?
You
know
that
very
much
comfortable
you
can
set
the
where
the?
Where
is
the
source
code
binary
files,
all
your
options,
but
once
you
can
configure
it
will
show
you
some
errors
like
see
me,
33
point
30
or
higher
is
required,
and
currently
it
is
install
its
limit
3.10.
B
So
you
have
to
install
the
voice
image
again
from
the
south
from
the
C
make
library
of
C
make
website.
It
will
give
you
some
3.17
version.
Then
you
are
again
going
to
encounter
a
problem
because
C
make
Gy
is
outdated.
Now
cmeg
is
itself
a
model
or
making
this
box,
so
you
have
to
update
the
simi
GI
as
well.
Once
you
have
done
that
as
well.
B
You
are
again
going
to
encounter
a
problem
that
is
the
outdated
version
of
Fatihah
library,
so
we
can
I
appeal
in
a
Python
version,
may
not
match
which
is
going
to
cause
some
surface
problem,
so
you
have
to
go
to
the
library
files
and,
if
you
have
to
edit,
like
I,
have
compiled
of
a
document
for
installation
with
all
these
collections
initiated
with
you
on
slack
that
for
something.
So
this
is
about
installation
and
problems
with
it.
B
So
reading
our
very
worst
simulation
subscriber,
we
have
to
familiarize
ourselves
with
the
environment,
so
change
done
how
the
main
screen
looks
like
it
has
some
options
that
I
use
visualization.
It
is
more
like
any
other
general
editor
and
going
to
so
higher
than
to
ask
for
simulations
you.
Can
they
have
some
timers
which
are
already
installed
through
when
you
are
installing
Confucian
3d?
So
you
can
check
out
these
models
if
you
want
to
run,
mica
has
loaded
one
of
the
tumor
models,
so
it
is
how
these
positions
are
being
seen.
B
W
added,
plus
plus,
is
a
custom
editor
for
the
computer
theory.
Basically,
composition.
Theory
is
not
something
that
you
can
build
model
by
track.
Provides
you
some
essential.
Some
prerequisites
features
of
the
mod
of
the
model
which
you
are
going
to
create,
and
then
you
have
just.
You
have
to
write
a
code
like
simple
C++
code.
To
make
things
happen.
It
is
easy
because
it
supports
Python,
with
C++
and
and
I
have
still
done
that
you
can
use
this
asila
to
write
your
anchors
further
than
your
simulations.
B
B
B
B
B
B
So
in
this
way,
like
you
can
open
the
folders
and
it
will
open
a
and
expenditure
file.
So
this
is
the
Phi
and
and
I'm
trying
to
show
you
XML
document,
mainly
yeah,
so
the
SVR
has
specified
to
print
medium.
Openness
is
in
our
contingency,
which
you
can
separate
out
here,
so
this
is
slices
finest
basically
generated,
as
you
have
specified
the
parameters
in
compasses
3d
environment
when
you
are
creating
a
new
project,
despite
trying
to
get
it
so.
B
Things
also,
the
passenger,
also
in
the
meeting
with
the
customer.
Take
it
easy
to
share
code
across
the
multiple
platforms,
use
the
standard,
lovely
to
increase
the
chances
that
research
to
be
accepted
and
further
refined
by
the
other
scientists
and
these
standards.
That
is,
efficiency
and
IP,
and
all
these
things
are
easy,
like
we
are
trying
to
do
simulations
for
basically
lines.
A
One
I
think
was:
he
said
something
about
his
program.
Handle
differentiation.
Waves,
I,
know
that,
like
what
I
actually
visited
the
group
a
couple
years
ago-
and
they
said
that
well
they
showed
me
some
of
the
models
like
what
it
can
do
and
it
says
to
handle
a
lot
of
dynamics.
So
do
you
do?
Is
you
build
these
lot
of
these
cells
and
you
can
model
the
cells?
You
know
form
different,
you
know
tissues
or
whatever
you
want
to
form,
and
then
you
can
animate
these
cells
themselves
so
specify
themselves.
A
You
know
information
about
which
their
content
is,
you
know
different
receptors,
and
then
you
can
model
things
that
go
on
in
the
cell.
All
sorts
of
processes
I
think
they
were
modeling
things
like
River
and
they
were
modeling
embryo.
There
are
some
embryo
models
of
people
published,
so
there
I
think
they
can
probably
handle
it.
It
would
be,
you
know
it
after
like
thinks
we
might
want
to
represent
it.
I
think
he
definitely
would
handle
that
there.
There
are
a
lot
of.
A
There
are
a
number
of
publications
that
you
go
to
the
website
for
copy,
so
3d
they
have
a
bunch
of
publications.
Listed
they've
done
a
range
of
different
types
of
studies
of
this
platform,
so
Susan
asks.
Does
your
program
include
forces
like
pressure
and
strain?
Yes,
it's
it's
physical.
You
know
there.
There
are
a
lot
of
physics
models,
so
it's
largely
there.
Are
you
interested
in
modeling
all
sorts
of
physics
going
on
in
different
tissues,
organs.
B
Monsters,
Susan
arms
is
basically
is
cross
off
the
neck.
You
can
every
respect
of
what
you
want
to
do
place
terror.
All
these
things,
using
sequence
for
all
you
have
to
do.
You
find
some
constraint
on
the
condition
that
you
can
do,
and
this
is
the
best
part
of
this
software,
because
it
is
not
something
which
you
have
to
do,
which
is
predefined,
like
you
can
do
this,
you
have
the
software.
You
have
to
find
parameters
like
if
you
actually
show
this.
B
A
B
With
the
chemical
feed,
you
can
also
fun
attention
forces
like
focal
point
plasticity.
It
has
explanation
like
what
will
go
to
included
or
they'll
ask
for
the
project.
I
have
left
included
a
Content
module
click
on
next
click.
On
finish,
and
here
you
can
see
all
your
files
like,
which
are
called
anyway,
you
can
add
as
many
as
parameters
that
you
have
in
this
section
and
you
can
get
so
yes
to
the
question
is
yes,
we
can
include
all
rather.
A
A
A
Yeah,
that's
very
good,
so
yeah
this.
This
is
based
on
something
called
the
stubble
Euler
pots
mop,
which
is
like
that's
like
a
cellular
automaton.
But
it's
not
quite
like
that.
But
it's
a
physics
it's
something
from
physics
and
they
use
it.
To
sort
of
you
know
you
have
these
cells
that
are
arrayed
in
different
locations.
You
know
for
building
like
a
tissue
or
an
organ,
and
then
you
specify
the
relationships
between
the
cells
and
they
have
all
these
built-in
functions.
A
So
that's
what
makes
it
attractive
as
opposed
to
using
something
like
MorphOS
oeq,
which
we
saw
in
past
meetings
where
we
have
a
cellular
automata.
We
can
build
like
something
neck.
You
know
is
able
to
generate
patterns
and
other
things
like
that,
but
it
can't
implement
physics
routines
that
we
might
want
to
do
it
with
the
model.
Things
like
you
know,
biological
processes.
A
So
you
know
each
that's
a
good
lesson
that
you
know
each
type
of
model
is
implemented
will
have
different
strengths
and
weaknesses.
Not
just
you
know
can't
just
throw
any
modeling
platform
you
want
at
a
problem.
I.
Think
three
like
I
said:
I
visited
the
group
that
made
this
software
a
couple
years
ago
and
they
you
know
they
were.
They
showed
me
a
lot
about
like
what
it
can
do,
but
I've
never
really
had
a
chance
to
develop
it
very
much.
I
think
it
would
be
a
good
opportunity,
for
you
know
someone.
A
A
B
B
A
A
So
this
is,
this
is
for
the
project
where
you're
sort
of
refactorings
Devo
zoo.
That's
what
your
proposal
or
refactoring
means
like
revising
it.
So
so
the
first
picture
actually
go
back
to
the
first
picture.
I
was
gonna,
make
some
comments
yeah.
So
this
is.
This
is
interesting,
it's
good,
except
that
it
was
wondering
if
we
could
replace
the
warm
full
worm
with
like
an
embryo
of
some
type,
because
it's
development-oriented
I
mean
open
less
projects,
I
prayed
the
evil
we
project.
So,
though,
I
think
we
don't
have.
B
B
A
Tutorials,
so
this
would
be
like
oh
tweets,
any
corrective
force
yeah.
This
would
be
the
two
tort
like
microscopy
tutorials,
so
this
would
be
like
yeah
there's
a
there's,
a
page
where
we
do
that.
I,
don't
like
to
have
the
Alex
kg
tutorials,
maybe
with
some
ice
Hans
for
the
links
yeah.
We
can
talk
about
that
and
then
number
five,
so
yeah
we
don't
have
like
slitter
account
for
diva
worm
per
se,
but
we
can
pull
an
open
worm.
Usually
that's
handled,
though,
like
in
a
little.
A
Like
we
go
like
a
plugin
app
like
on
the
front
page
like
I'm,
the
open
website,
there's
a
like
something
like
this.
This
might
be
except
better
to
handle
it.
Okay,
well,
yeah,
that's
good!
Why
don't
I
mock-up
some
of
those
in
drawing
is
and
I'll
get
back
with
you,
and
if
anyone
has
any
comments
you
can
have
them,
you
can
make
them.
So
let
me
go
through
these
Chad's
messages
before
we
go,
so
we
have
a
bunch
of
chat
messages
here.
A
We
have
people
say
they
want
to
try
copy,
sell,
3d
dick
is
getting
tired
out.
Well,
ok,
now
we're
at
the
top
of
the
hour,
so
Linux
installation
device
and
updates
on
pandemics.
So
this
is
a
link.
It's
shared
with
the
19
information.
Please
check
it
out,
and
this
is
images.
Look
good!
Thank
you,
okay!
A
Okay,
I
just
wanted
to
alert
you
that
next
week,
I'm
gonna
cancel
the
meeting.
I
have
another
engagement.
If
you
want
to
use
this
link
to
meet
on
your
own,
that's
you're
welcome
to
do
it
or
whatever
we
won't
have
a
formal
meeting
next
week
and
then
we'll
sit
up
the
following
week.
I,
don't
know
what
wasn't
yet
I
can
get
some.
You
know
feedback.
Maybe
someone
wants
to
present
something
yeah
dick
says:
keep
in
touch
or
a
copy,
so
3d
I
think
we'll
revisit
this.