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R.F. Laine1-2, K.L. Tosheva1, R.D.M. Gray1, P. Almada1, D. Albrecht1, J. Mercer1, C. Leterrier3, P.M. Pereira1-2, S. Culley1-2 and R. Henriques1-2 Equal Contribution

This document summarizes an open-source image analysis software framework called NanoJ that was developed for super-resolution microscopy. NanoJ was built to combine high performance with ease of use. It includes tools for spatio-temporal alignment of raw data, super-resolution image reconstruction, image quality assessment, structural modeling, and control of the sample environment. The document highlights NanoJ's current capabilities for essential processing steps and expects future expansion through new tool development.
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© © All Rights Reserved
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Download as PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
18 views

R.F. Laine1-2, K.L. Tosheva1, R.D.M. Gray1, P. Almada1, D. Albrecht1, J. Mercer1, C. Leterrier3, P.M. Pereira1-2, S. Culley1-2 and R. Henriques1-2 Equal Contribution

This document summarizes an open-source image analysis software framework called NanoJ that was developed for super-resolution microscopy. NanoJ was built to combine high performance with ease of use. It includes tools for spatio-temporal alignment of raw data, super-resolution image reconstruction, image quality assessment, structural modeling, and control of the sample environment. The document highlights NanoJ's current capabilities for essential processing steps and expects future expansion through new tool development.
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
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figures/

NanoJ: High-Performance Open-Source


Super-Resolution Microscopy in ImageJ
R.F. Laine1-2 *, K.L. Tosheva1 *, R.D.M. Gray1, P. Almada1, D. Albrecht1, J. Mercer1, C. Leterrier3,
P.M. Pereira1-2 , S. Culley1-2 and R. Henriques1-2 ; *equal contribution
1University College London, UK; 2The Francis Crick Institute, UK; 3Aix-Marseille Univ, CNRS, INP, France
Correspondence to: [email protected], [email protected], [email protected]
Poster DOI: 10.6084/m9.figshare.7963556 [width=10cm]c1
‡ github.com/HenriquesLab — 7 @HenriquesLab [width=16cm]c1

Our team has built an open-source image analysis framework for super- Drift Multi-
resolution microscopy designed to combine high performance and ease cor- colour
of use. We named it NanoJ - a reference to the popular ImageJ soft- rec- chan-
tion nel
ware it was developed for. Here we highlight the current capabilities with reg-
of NanoJ for several essential processing steps: spatio-temporal align- NanoJ- is-
ment of raw data (NanoJ-Core), super-resolution image reconstruction Core. tra-
(NanoJ-SRRF), image quality assessment (NanoJ-SQUIRREL), struc- a) tion
tural modelling (NanoJ-VirusMapper) and control of the sample environ- Com- with
pos- NanoJ-
ment (NanoJ-Fluidics). We expect to expand NanoJ in the future through ite Core.
the development of new tools designed to improve quantitative data anal- im- a)
ysis and measure the reliability of fluorescent microscopy studies. age Com-
of pos-
two ite
frames im-
from age
a of
time- multi-
lapse colour
dataset beads,
of prior
the to
same (left)
field- and
of- af-
view. ter
b) (right)
Cross- chan-
correlation nel
map reg-
[width=0.8]c1 (CCM) is-
be- tra-
tween tion
the us-
two ing
frames NanoJ-
shown Core.
in Scale
a). bars:
The 25
vec- m,
tor in-
po- sets:
si- 0.5
tion m.
of b)
the Vec-
max- to-
i- rial
mum rep-
in- re-
di- sen-
cates ta-
the tion
lin- of
ear the
shift shift
be- be-
tween tween
the the
two two
frames. chan-
c) nels
Over- (left,
lay dis-
of place-
the ment
two vec-
frames tor
af- length
ter 50
drift times
cor- larger
rec- for
NanoJ-Core: Drift Correction tion
us-
rep-
re-
ing sen-
NanoJ- ta-
Core. tion
d) pur-
Ver- poses),
ti- hor-
cal i-
and zon-
hor- tal
i- (mid-
zon- dle)
tal and
Drift estimation is achieved by directly analysing a raw sequence of time-
drift ver-
points. Frames can then be directly translated to correct drift or a table curves ti-
with drift coordinates can be generated and used in other algorithms (e.g. ob- cal
SRRF). tained (right)
us- shift
ing maps
NanoJ- ob-
Core tained
from and
the ap-
100- plied
frame to
raw the
data. data
shown
in
NanoJ-Core: Channel Registration a).
Scale
bars:
Channel registration is able to calculate and apply an elastic transform to 25
realign different captured wavelengths. m.

[width=0.8]c1 [width=0.8]c1
NanoJ-SRRF: Live-Cell Super-Resolution Qual-
ity
NanoJ-VirusMapper: Structural Mapping and
and Modelling
res-
o-
lu-
tion
Super-Resolution Radial Fluctuations (SRRF) is able to generate a super- as-
resolution reconstruction by analysing fluctuations in the emission of flu- sess-
ment
orophores captured in a short image sequence. with
NanoJ-
VirusMapper features a single-particle analysis (SPA) algorithm, capable
SQUIRREL.
a) of generating structural models of conserved structures imaged by Super-
A Resolution Microscopy
super-
resolution
ren-
der-
[width=0.85]c1 ing
and
Live- ac-
cell quired
super- wide-
resolution field
mi- im-
croscopy age
with of
fixed [width=0.7]c1
NanoJ-
SRRF. Alexa647
Quan-
a) la-
ti-
Com- belled
ta-
par- mi-
tive
i- cro-
SPA-
son tubules.
based
of b)
mod-
wide- Left:
elling.
field SQUIR-
Mul-
and REL
ti-
SRRF er-
com-
re- ror
po-
con- map
nent
struc- high-
model
tion light-
of
from ing
the
UtrCH- dis-
Vac-
GFP crep-
cinia
actin an-
virus
la- cies
by
belling. be-
imag-
Scale tween
ing
bar: the
in
5 super-
super-
m. resolution
resolution
b) and
hun-
Time- diffraction-
dreds
course limited
of
of im-
flu-
the ages
o-
in- in
res-
set (a).
cently
shown Right:
la-
in Mag-
belled
a), ni-
viruses
ob- fied
and
tained in-
mod-
at sets
elling
33.3 at
their
Hz in-
struc-
and di-
ture
dis- cated
through
played po-
VirusMap-
ev- si-
per
ery tions
30 on
s. er-
Scale ror
bar: map.
1 c)
m. Left:
c) SQUIR-
Colour- REL
coded res-
time o-
course. lu-
Scale tion
bar: map
1 of
m. the
super-
resolution
im-
age
in
(a).
Right:
Mag-
ni-
fied
in-
sets
for
in-
di- NanoJ-Fluidics: Liquid Exchange
cated
res-
o-
lu-
tion
NanoJ-SQUIRREL: Estimating Image Quality blocks.
Whole
& Resolution im-
age NanoJ-Fluidics (Pumpy McPumpface) entails the control of a simple in-
scale
bars expensive LEGO-based syringe pump array that automates live-to-fixed
= imaging and sequential labelling of the sample. Protocols can be run au-
5 tomatically in parallel to the acquisition.
m,
SQUIRREL quantitatively calculates local quality and resolution in in-
super-resolution images. It highlights limitations on the data collected set
and a reference point to help researchers improve imaging fidelity. scale
bars
=
1
m.

[width=0.85]c1 [width=1]c1
Schemat-
ics
Author representation
of
the
NanoJ-
Fluidics
sys-
tem.
a)
3D
side
view
of
a
sin- I recognise a gender inequality in the author list (2F/8M). I am
gle [width=0.8]c1
committed to achieve a better balanced representation of gender
sy- and minorities in our future work.
ringe
pump.
b)
2D
top
view
of
a
sy-
ringe
pump
ar-
ray
(rep-
re-
sent-
ing
4
pumps
out
of
128
max-
i-
mum)
and
a
fluid
ex-
trac-
tion
peri-
staltic
pump,
both
con-
trolled
by
an
Ar- Funded by
duino
UNO.
c)
Ex-
am-
ple
of
pos-
si-
ble
work-
flows [width=0.95]c1

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