►
Description
DevoWorm meeting: February 3, 2020. Attendees: Richard Gordon, Vinay Varma, Devansh Batra, Yash Agarwal, Bradly Alicea, and Jesse Parent
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You
more
the
first
step
in
the
creating
our
effort
to
fill
opportunities
of,
failing
and
isolating
the
DNA.
This
DNA
can
be
obtained
from
almost
any
cell
or
tissue
of
the
human
body.
We
do
not
need
a
large
amount
of
tissue
or
blood
to
provide
enough
DNA
for
analysis.
Dna
is
then
extracted
from
the
plur
or
the
tissue
sample
from
here.
We
carry
out
the
second
step
in
the
process
which
is
cutting
sizing,
assorted,
DNA
samples,
DNA
is
cut
using
this
cryptic
enzymes,
which
cut
the
DNA
time
at
a
specific
place,
is
restricted.
B
B
A
B
B
The
pan
pattern
that
Deanna
creates
in
agarose
gel
is
then
transferred
to
align
in
sheets
to
complete
this
transfer,
a
lavishly
displaced
on
the
jail
and
left
to
soak
overnight
in
the
high
salt
solution
after
Saudi
Voyager
is
completed.
The
nylon
membrane
contains
the
same
pattern
of
DNA
as
occurred
in.
B
B
So
this
is
how
our
F
and
Eastern
the
second
most
reused
procedure
comes,
is
the
ltr'
there.
Even
the
idea
stands
for
variable
number
tandem
repeats.
It
will
possess
specific
this
one
on
the
chromosome,
in
which
tandem
repeats
of
90
to
80
or
more
bases.
It
makes
a
different
number
of
times
between
individuals.
B
The
Hierophant
peer
nodes
and
the
probe
specifies
of
the
NPR
lucas.
The
fragments
are
little
shorter
than
RFLP,
but
they
created
the
exact
same
process
since
RFLP
and
VLT
are
accurate
in
the
same
fashion.
The
exhibits
advantages.
Some
everyone
it
is
of
PNM's
are
their
most
stable
reproducible,
which
is
a
valuable
trait
to
have
when
you
are
trying
to
determine
the
exact
match
of
the
person's
DNA,
which
must
exclude
of
the
certainty
of
confidence.
B
They
are
also
easy
to
prevent
contamination.
Since
DNA
sample
is
large,
then
the
types
of
DNA
and
small
amounts
of
DNA
contamination
does
not
alter
the
analysis.
Now,
if
you
want
to
talk
about
some
disadvantages
auspices
in
India,
they
are
very
time-consuming,
especially
the
hydrolysis
step
through
violations
at
which
they
are
discussed
earlier.
They
require
that
any
large
amount
of
DNA
must
be
used
off
in
adequate
samples.
Too
many
polymorphism
may
be
present
a
short
route
and
cost
is
very
high
due
to
labor
and
requirements.
B
This
is
a
big
step
forward
in
forensic
sciences,
since
the
length
of
DNA,
fragment
being
analyzed
is
short
enough
to
be
identified
by
polymerase
chain
reaction,
which
is
PCR.
So
now
we
are
able
to
analyze
very
small
sample
of
data
that
is
spherical
and
he
say
then
previously
known
vector
and
match
it
to
the
person's
identity.
Pci
develop
in
male
again
in
red
large
piece
and
use
the
same
sum.
In
the
sequence.
Are
cells
used
to
dedicate
DNA
to
amplify
the
specified.
A
B
B
Of
DNA
structure,
double
helix
is
the
form
with
the
DNA's
in
which
the
DNA
stored
as
we
recessed
earlier.
The
solution
is
cooled
to
55
degree
to
allow
the
primers
to
bind
to
the
ends
of
DNA.
As
you
can
see
here,
10
K
primers.
The
solution
is
then
heated
to
75
degree,
which
is
optimal
temperature
further
that
polymerase
to
create
a
new
copies
of
each
ta
listener.
B
So
one
PCR
cycle
takes
approximately
two
minutes
to
complete.
Each
cycle
doubles
the
amount
of
business
amount
of
targeted
sequence
in
the
test
tube,
and
it
only
takes
months.
50
cycles
reduce
hundreds
of
thousands
of
DNA
copies
so
long
as
primers
are
chosen
to
flank
and
stsi.
The
pan
amplified
will
be
present.
The
STR
Lucas
and
a
simple,
gel
or
column
will
determine
the
brand
name.
Thus
this
procedure
avoids
the
energy
flow
of
high
transition
steps
to
membrane
of
TR
approaches.
So
this
is
one
of
them.
B
And
since
of
one
piece,
a
process
takes
only
few
hours
compared
to
our
affinity
of
hydration
and
Flynn
exclusive,
which
can
take
several
days.
Str
can
use
much
smaller
samples
of
DNA
and
can
even
use
partially
degraded
DNA
to
create
a
fingerprint
first.
The
purity
and
quality
of
DNA
sample
is
not
as
great
a
factor
with
STR.
Then
the
traditional
methods
of
DNA
fingerprint
the
current
standard
forces
protocols,
analyzes
total
core
STR
loci,
which
has
been
carefully
chosen
for
the
uniqueness,
only
disadvantage
of
STR
approach
is
it
is
sensitive
to
contamination
de
contaminate
in
DNA.
B
Use
currently,
and
now
let
us
see
like
what
are
some
applications
of
DNA,
fingerprint
and
DNA
fingerprint
is-
is
widely
used
all
over
the
world.
They
can
use
to
solve
criminal
cases
used
to
conduct
paternity
tests
and
even
to
determine
the
authenticity
of
Reyes
boots.
Whatever
the
case
it
is,
it
is
evident
that
DNA
fingerprinting
has
I,
would
utilize
the
one
identifies
biological
matches.
B
We
can
discuss
some
examples
here.
So
one
of
the
exam
another
way
in
which
it
is
used
is
for
the
paternity
test,
the
identity
test
or
another
application
of
DNA
fingerprinting
that
has
very
complicated
around
the
world
in
any
test
potential.
Are
those
of
the
child
have
their
DNA
analyzed
with
the
child
and
the
mother's
DNA?
In
order
to
see
which
potential
father
has
some
mostly
em
in
common
with
the
child
in
question,
so
another
application
of
the
DNA
fingerprinting,
which
is
well
the
most
recent
matter,
is
molecule
a
cartilage.
This
methodology.
B
The
place
of
bloodline
of
Elliman
or
human
remains
recently,
or
the
skeleton
of
Neolithic
man
was
founded
in
1981,
and
nuclear
biologicals
used
understand
it
and
file
digesters
of
that
particular
scanner.
So
other
examples
are
specimens
from
these
type
of
crime.
Our
direly
nice
mail,
which
was
found
in
lives
as.
A
B
The
mummies
in
Egypt
found
entire
desert.
The
Iceland
was
found
around
fifty
three
hundred
years
old
and
the
DNA
was
extracted
from
the
remains
of
his
curve,
which
found
small
traces
of
food
that
he
eat.
This
was
one
of
the
most
historical
archaeological
discoveries
in
the
last
century.
The
inner
fingerprinting
is
an
important
tool
in
saw
our
images
to
piece
together
that
information
that
needs
to
pass
virtually
the
elephant
affinities
are
also
used
in
the
world
of
sports,
as
I
have
mentioned.
B
B
This
can
be
traded
with
the
synthetic
DNA
sphere
in
which
the
item
is
secret.
Dna
sequence,
where
the
original
batch
of
TNA's
destroyed
the
collectible
can
then
be
auctioned
off,
giving
the
buyer
assurance
the
dot
product
is
indeed
authentic.
This
is
just
another
instance
at
how
the
DNA
fingerprint
is
being
used
in
today's.
B
B
Some
machine
learning
applications
which
are
being
used
in
DNA
fingerprinting.
To
give
our
overall
view
machine
Bernie
is
used,
is
in
the
DNA
fingerprinting
latest
methods,
as
they
can
find
patterns,
much
easier
in
the
smaller
smallest
and
some
to
then.
The
traditional
humans
have
been
the
traditional
addition.
Today,
you
must
have
to
move
with
the
ice,
then
another
microscope,
so
it
is
where
the
machine
learning
is
contributing
in
the
air,
some
other
factors
as
well,
which
I
would
like
to
discuss
in
the
next.
A
A
There
was
a
paper
I
can't
remember
right
now
what
the
citation
is,
but
we've
reviewed
a
paper
a
while
back
in
the
group
about
this,
where
they
would
take
different
cell
types
and
then
they
would
look,
they
would
find
I,
don't
know
if
they
would
inserted
barcodes
through
some
technique
or
if
they
identified
barcodes,
but
they
were
able
to
trace
cells
through
lineage
trees.
Do
you
remember
that
paper
dick.
A
A
So
you
know
you
can
look
at
common
descent
and
look
at
you
know
you
have
these
they're,
basically
short
repeats
of
DNA,
so
you
get
a
sense
of
like
you
know
the
the
sort
of
uniqueness
of
that
stretch
of
DNA,
and
then
they
use
it
to
trace
a
lineage,
so
it
might
mutate
over
time
and
they
can
find
the
common
ancestor
or
just
use
that
as
a
way
to
identify
common
ancestry.
So
I
like
this
I
think
that
was
a
pretty
interesting
presentation
as
well.
A
B
B
B
Also
like
it
helps
thought
machine
only
helps
not
this
particular
neuron
DNA
from
them,
but
they
also
recognize
that
protein
would
be
structures
to
predict
the
protein
such
just
like
in
medicines
when
the
medicine
selecting
on
our
body
machine
learning,
applications
are
being
torn
out
like
we
do
in
a
lab,
something
like
that.
They
are
applications
so
that
you
can
actually
predict.
A
A
A
A
Yeah
that
sounds
good,
yeah
I
can
send
them
out.
You
know
in
a
separate
email,
so
no
one
has
any
other
questions.
I,
don't
really
have
anything
else
planned
for
the
rest
of
the
meeting.
I
do
have
some
big
some
people
expressed
interest
in
presenting
in
future
meetings,
so
we've
gone
through
a
couple
of
presentations
already
and
they've,
been
pretty
good.
I
mean
just
I
want
to
get
have
a
pretty
broad
meeting.
You
know
a
variety
of
things
for
people
to
experience
and
maybe
build
off
of
a
little
bit.
A
I
mean
it
doesn't
have
to
be
every
topic,
but
I
want
to
get
some
ideas
flowing
here.
So
is
anyone
interested
in
presenting
in
the
next
couple
weeks,
yeah
there's
a
schedule.
I
can
send
you
a
link
to
the
schedule,
but
basically
it's
more
or
less
open,
I
know.
Jesse
said
it
was
interested
in
presenting
and
so
we're
having
a
little
bit
of
trouble.
Finding
a
time
to
present
is
that
something
you
could
do
in
this
meeting
Jesse
or
is
that
something
we'd
have
to
do
offline.
A
Okay,
yeah
pre-record.
We
could
do
that
yeah.
So
what
do
we
try
to
plan
on
doing
that
in
the
next
two
weeks?
I,
don't
know
what
you're
yeah
so
I
mean
we've.
You
know
we
we've
kind
of
talked
about
this
a
couple
times
and
that's
kind
of
gotten
pushed
back,
but
I
guess
we
can
like
plan
to
do
it.
If
we
plan
to
do
it
to
a
deadline,
then
we
can
maybe
do
it
a
little
bit.
You
know
we
can
actually
get
it
out.
Now
you
sent
me
a
paper.
A
A
A
Right
now,
let
me
get
it.
I
just
wanted
to
refresh
my
memory
on
it,
but
I
think
that
would
be
an
interesting
topic
for
the
group.
Definitely
a
good
experience
for
you
to
go
through
the
paper,
so
well.
I
think
we
could
just
do
the
frist
in
paper
that
would
pray
BRE
and
it's
just
like
you
know,
to
get
some
practice
in
prison
and
you
know
maybe
come
up
with
a
topic
that
we
don't
usually
think
about
so
yeah.
It
was
the
topic.
A
Of
interest,
yeah
natural
selection
finds
the
natural
radiance
and
yeah
so
that
first
and
stuff
on
free
of
the
free
energy
principles
is
basically
the
it
so
Carl
Freston
is
he's
a
neuroimaging
big
name
in
neuroimaging,
and
he
does
a
lot
of
different
types
of
research
in
that
area.
But
he
also
has
this
thing
called
the
free
energy
principle
and
it's
very
similar
to
if
people
are
familiar
with
a
lot
of
the
complex
systems
work
in
the
past,
the
dissipative
structures
work
that
was
like
years
and
years
ago.
That's
basically
what
it
is.
A
A
A
Yeah,
that
would
be
a
good
topic,
I
think
to
talk
about
a
bit.
We
don't
really
yeah
I
mean
it's
it's.
We,
the
the
paper
that
I
was
involved
with
with
Rob
stone.
The
one
on
origins
of
the
embryo,
George
wrote
a
section
on
that,
and
that
was
it's
basically
the
similar
thing
that
he
duck
talks
about
this
paper,
his
new
paper.
So
we
can
talk
about
that.
Some
tea
one
meeting,
otherwise
I
think
we're.
A
A
A
A
Well,
I
guess
the
docker
thing
is
open,
so
the
doctor
issue
was
so
open.
Worm
has
created
this,
what
they
call
a
docker
file
and
that's
like
a
it's,
a
it's
a
package
that
or
a
container
that
you
can
run
a
bunch
of
programs
in
it's
kind
of
like
a
virtual
machine.
So
you
set
it
up
on
your
machine
and
it
replicates
everything.
A
You
know
you
don't
have
to
worry
about
compatibility.
You
can
run
all
these
programs
within
that
container
and
the
programs
and
there
are
different
open
worm,
demos,
and
so
they
have
different
demos
for,
like
you,
know,
electrical
activity
for
cell
type,
but
they
don't
have
anything
for
development,
and
so
the
idea
was
to
create
a
simulation
or
some
application
that
shows
development
in
some
way
and
so
Jesse
the
the
sort
of
the
goal
there
is
to
come
up
with
an
idea.
A
Maybe
for
a
simulation
or
something
I
had
mentioned
like
a
3d
simulation,
but
there
might
be
a
better
idea
out
there,
and
so
you
know,
we've
really
been
stuck
thinking
about
that.
How
we
might
we
contribute
to
that,
and
so,
if
any
of
you
have
any
idea
about
what
we
might
do
for
that,
that
would
have
to
be
something
that
would
be
relatively
easy
to
implement
and
then
it
would
just
be
implemented
in
that
container
and
it
would
be
included
in
the
new
version.
A
It
would
be.
You
know
something
along
the
lines
of
a
C
elegans
developmental
application.
You
know,
could
be
a
simulation
of
cells
dividing
it
could
be.
You
know
something
else.
I
mean
there
are
different
options
to
that.
So
so,
if
you
wanna
keep
thinking
about
that
Jessie,
that's
great.
If
anyone
else
has
any
ideas,
let
me
know
Siobhan
says
I
think
it
would
be
great
if
we
could
have
a
shortlist.
A
I
think
it
would
be
great
if
we
could
have
a
short
list
of
major
tasks
remaining.
Yes,
I
think
that
would
be
good
or
maybe
just
like
we
could
set
up.
Like
a
you
know,
some
sort
of
thing
on
github,
where
we
you
know
people
can
join
in
different
milestones
or
tasks,
and
then
we
can
follow
up
in
the
meetings.
A
I
didn't
really
put
that
together
yet,
but
we
can
so
the
doctor
simulation
blog
posts
are
pre
tree
models,
yeah
and
then
it
would
leave
easy
for
all
collaborators
to
read
them
and
then
take
up
or
discuss
yeah.
So
we
had
something
like
that:
I
haven't
updated
it
in
a
while,
but
I'll
probably
just
reorganize
it.
We
have
a.
A
A
B
A
A
A
A
A
B
B
A
That
would
be
the
idea,
so
the
idea
is,
you
can
build
a
simulation
to
you
know,
first
of
all,
I
think
the
easiest
way
to
do
it
would
be
some
sort
of
like
so
cell
division
model,
where
you
have
like
go
from
a
single
cell,
the
multiple
cells
and
then
it
would
just
create
this
embryo.
That
would
be
there.
We
could,
then
each
cell
could
be
specified
and
I
think
that
in
copy
cell
you
know
what
you
do.
A
A
A
So
the
idea
of
having
like
different
types
of
cells-
or
you
know,
different
classes
of
cells
is
definitely
something
that
exists
in
that
platform.
And
then
you
can
attach
data,
so
you
can
attach
information
about
the
cell
identity,
gene
expression.
So
in
open
one
right
now
we
have
models
that
have
each
cell
in
the
C
elegans
and
this
they're,
the
terminally
differentiated
adult
cells
and
each
one
of
those
cells.
We
have
attached
a
lot
of
information
to
so
you
know
you
can
go
into.
A
We
have
a
3d
model
of
the
adult
where
you
can
go
in
and
look
at
the
each
cell
and
the
actually
each
neuron
in
the
adult
and
highlight
it
and
then
there's
you
know
like
this
animation
of
the
neuron
with
its
processes,
and
then
it
tells
you
about
that
neuron
a
little
bit.
It
gives
it
a
identity,
and
then
it
gives
it
some
data
that's
attached
to,
and
you
know
that
and
then
you
know
we
can
work
from
there,
but
the
the
the
first
step
would
just
to
be
to
get
like
an
empty
model.
B
A
B
A
Don't
be
afraid
to
play
around
with
it,
I
mean
you
know
it's
just
like
to
see
what
I
can
do
and
like
there's
a
I,
don't
exactly
know
the
best
way
to
do
it,
but
that's
how
we
we
figure
that
out
is
by
you
know
kind
of
doing,
like
you
know,
a
smaller
demo
that
can
be
scaled
up.
So
you
just
like
start
with
something
really
simple,
maybe
just
like
just
showing
a
couple
of
rounds
of
cell
division
and
then
showing
how
to
you
know
can
be
done
and
then
maybe
scale
it
up
from
there.
A
B
B
A
A
vessel
area,
psychology
and
excellent
montaging,
so,
yes,
we
have
the
axolotl
data
which
I
haven't
gotten
that
yet
it
will,
when
I
get
the
data,
we'll
talk
about
that,
a
bit
more
but
again
like.
If
you
guys
remember
back
a
couple
of
sessions
ago,
we
had
a
talk
by
Susan
on
the
axolotl
embryos,
the
the
type
of
imaging
data
that
they've
collected
and
we're
trying
to
figure
out
a
way
to
visualize
that
in
a
way,
that's
that
can
be
navigable.
A
You
know
like
it's,
you
know,
maybe
some
sort
of
something
like
maybe
Google
Maps
or
something
where
you
know
you
can
put
the
data
together
and
visualize
it.
So
you
can
explore
it
as
a
user
and
you
know
I
mean
I,
don't
know
what
the
best
way
to
do.
That
is
necessarily
but
I.
You
know,
take
a
look
at
what
the
data
look
like
and
see
if
there's
something
that
is
suitable,
more
or
less
suitable.
A
So
there's
some
deformation,
but
there
are
government
deformation,
algorithms,
you
can
use
to
smooth
everything
out,
and
so
then
you
could
analyze
the
pattern
in
two
dimensions
to
see.
If
you
know
there's
something
that
we
don't
know
about,
because
we
typically
look
at
these
things
on
a
curve
and
there
might
be
some
process
going
on,
it
could
be
morphogenesis.
It
could
be
something
about
the
pattern
itself,
but
to
be
able
to
analyze
it.
A
A
A
So
I,
you
know
be
interesting
to
see
what
we
can
do
with
that
and
then
also
we
have
okay.
Devon
says:
okay:
I
was
asking
about
the
seashells,
we'll
try
to
find
if
there's
any,
and
this
is
something
they
think
that
was
going
to
be
acquired,
but
never
quite
got
to
the
stage
of
getting
it
collected.
Cone
shells
are
cheap
to
buy,
just
need
to
rotate
and
photograph,
so
ya,
dick
actually
in
the
summer
sea
goes
or
in
the
winters.
A
He
goes
to
generally
speaking,
not
this
year,
but
he
goes
down
to
Florida
and
he
collects
he
was
collecting
seashells
one
year
and
he
wanted
to
see
if
you
could
put
them
on
a
rotate
rotate
in
table
which
is
basically
like.
You
know
a
compass
in
a
something
you
can
someth
attach
the
seashell
to
and
just
rotate
it
by
hand
or
by
machine,
but
something
you
can
tell
what
the
rotational
angle
is
and
that
just
move
it
around.
A
Cone
shells
are
cheap
to
buy
patterns
are
presumably
be
generated,
some
Wolfram
patterns.
This
idea
has
never
been
tested
against
real
shells,
so
I
dick
means
by
Wolfram
patterns.
There
is
that
a
Stephen
Wolfram
wrote
a
book
on
cellular
automata
called
a
new
kind
of
science,
and
maybe
some
of
you
were
aware
of
this
book,
maybe
not
it's
about
20
years
old.
A
He
spent
like
10
years
writing
this
book
and
exploring
Celera
automata,
which
are
a
model
of
you
know
it's
a
simulation
model
where
you
have
cells
and
they
interact
with
each
other
over
space
and
over
time
and
they
produce
these
patterns
and
they
they're
they.
Basically,
each
cell
has
an
interaction
role
with
its
neighbor
and
the
interaction
rules
add
up
to
these
patterns,
so
you
can
implement
different
rules
for
the
entirety
of
the
automata
surface
cells
will
implement
this
pattern
time
after
time
and
end
up
with
these.
A
With
these
patterns,
they're,
usually,
like
you
know
what
triangles
with
a
lot
of
triangles
nested
in
them
or,
like
maybe
stripes,
you
know,
those
sorts
of
things
are
generated,
not
by
some
master
plan,
but
just
by
local
rules
being
amplified
across
the
surface
and
I.
Think
Jessie
would
find
that
really
interesting.
A
Looking
at
that
book-
or
maybe
it's
to
some
of
the
ideas
of
Wolfram's
rules
for
solar
automata,
he
generated
about
200
rules
in
this
book.
It's
you
know
it's
quite
extraordinary
and
then
the
idea
is
that
these
cellular
automata
represent
things
in
nature,
so
that
they're
equivalent
to
natural
processes
like
morphogenesis
or,
like
you
know,
traffic
patterns
in
a
city,
or
you
know
a
whole
host
of
things
in
nature
that
you
can
link
to
these
models.
A
It's
not
just
like
in
their
universal,
so
you
know
you
might
have
like
one
set
of
rules
that
will
model
many
different
things
in
nature.
That's
the
assumption.
This
is
the
citation
for
the
book.
I
new
kind
of
science,
yeah
I,
don't
know,
reading
the
whole
book,
it's
kind
of
like
reading
yeah,
it's
huge,
so
yeah
I
wouldn't
but
yeah
they
do
yeah.
This
is.
This
is
also
connects
to
something
we're
talking
about
with,
in
my
other
group,
with
Brayton
burg
vehicles
and
like
how
friedenberg
vehicles
aren't
really
like.
A
They
don't
have
a
lot
of
representation
in
them
and
I
don't
want
to
get
in
too
much
about
that
conversation.
But
we
can
talk
about
it
offline
if
you're
interested,
but
that
Braden
burg
vehicles
themselves,
don't
have
a
lot
of
representation,
but
you
know
there.
We
don't
really
know
how
much
representation
they
have.
You
can
add
representation,
maybe
into
a
vehicle
and
it
might
generate
much
richer,
behaviors,
so
yeah
yeah
I
think
that's
an
interesting
thing
to
follow
up
on
Jesse.
If
you
you
know
and
then
just
matter
I
think
the
book
is
mostly
online.
A
A
But
the
idea
is
that
we
have
the
basal
area
and
analysis
where
we've
looked
at
these
organisms,
these
colonies
of
cells
and
they
move
around
in
their
space
in
the
water
and
they
generate
a
lot
of
movement
patterns.
You
know
oscillations
and
things
like
that,
and
so
then
the
question
is:
is:
is
there
some
sort
of
information,
processing
or
behavior?
That's
going
on
that
we
can
analyze
or
you
know,
make
a
connection.
I,
don't
know
what
psychology,
but
it's
like
you
know
they
don't
have
brains,
but
they
generate
behavior.
A
So
is
there
some
sort
of
like
brain
like
thing
going
on
in
their
morphology?
Are
they
generating
intentional
behavior
things
like
that,
and
so
that's
going
to
be
an
interesting
topic
to
revisit
I'm
going
to
try
to
put
a
outline
together.
For
that
I
mean
that's
gonna,
be
something
that
we
probably
have
to
take.
A
couple
of
stabs
at
I
talked
a
little
bit
about
this
to
Thomas
who's,
doing
a
lot
of
data
generation
generating
movies,
Abascal
area.
And,
let's
see
you
know,
maybe
he
has
we
already
up
some
movies.
A
Maybe
he
can
generate
more
movies
and
we
can
get
those
data.
You
know
at
least
get
them
to
a
point
where
we
can
play
with
the
analysis
a
little
bit
so
I,
don't
I,
don't
have
a
timeline
for
that,
but
I'll
add
it
to
the
list
of
major
tasks
and
potential
papers.
That'll
work
is
that
should
drive
it
forward
a
little
bit
more.
A
A
So
it
says,
asked
Thomas
to
give
a
talk:
okay,
yeah
I'll,
probably
put
him
on
the
lineup
I'll,
ask
him
and
see
if
he
can
give
a
talk
on
some
of
his
he's,
cultured
a
lot
of
Basso
area
already.
So
maybe
you
could
talk
a
little
bit
about
that.
Give
you
an
idea
of
what
these
organisms
are,
what
they
do,
and
you
know
some
or
cell
culture
and
organism
culture
is
always
fun
to
find
out
about.
Is
it's
an
interesting
area
in
and
of
itself,
so,
okay,
so
yeah?