Basics of Image and data analysis in 3D



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Basics of Image and data analysis in 3D outline Why image processing, and how? Image processing in 2D What is an ideal image? Histogram tells stories! Before taking the image: the right imaging conditions! Tools for 2D image analysis/processing 3D volume reconstruction by FIB/SEM Processing steps for 3D reconstruction Registration, Segmentation, Quantification Visualisation

Image processing basics the bible John C. Russ (2002) The Image Processing Handbook 5 th edition, CRC Press The (free) tools http://rsbweb.nih.gov/ij/ http://fiji.sc/wiki/index.php/fiji

What is a good image..? Histogram of 8 bit Tif image 8-bit= 256 grey levels 0= Black 255= White Number of pixels with a certain grey level different grey levels

A little too dark Adjusted contrast/brightness (after recording) missing grey levels! After resampling the image (inventing pixels)

BSE SE

dealing with noise noisy original median filter original smooth very noisy

Filters. Median Gaussian blur Mean reduce in general the resolution They take into account the neighbourhood of a pixel FFT (fast fourier transform) filter (bandpass) FFT bandpass filter High-pass, Small size details (high space frequency) Low-pass, Large size details (low space frequency)

Image processing in 2D Best: start with a good image: equalized histogram, use all 256 grey levels Reduce noise during acquisition Carefully use filters Filtering means mixing in of information from neighbouring pixels: loss of resolution try several to see which one works best do resampling only in the very end 3D imaging with a FIB/SEM FIB Nanotomography 3D Microscopy

Image processing in 3D 2D processing (shading correction) Image alignment (registration) Cropping (subvolume) Noise reduction (2D or 3D) Segmentation Visualization Shading correction background

Registration before after Registration before after

cropping Cutting of the border Post acquisition alignment (registration) banana < > cucumber problem

4800 images (5nm pixel size) at 1.7nm slice thickness Alignment marks 8kx8k image 20sec. For 2kx2k ROI 5nm pixel Alignment on notches raw StackReg on unprocessed images StackReg on binary enhanced images

StackReg Aligned on Notches

X-Z plane StackReg Aligned on Notches

Aligned with StackReg

Segmentation Identifying the different phases/volumes/objects Creating binary images/stacks of the different objects Pb free solder SnAgCu: one detector is not enough InLens: SE low energy M. Maleki, EPFL-LMAF EsB: Energy selective Backscattered ETD (SE classic)

EsB 10µm 10x10x10nm voxel size, 2048x1536x2000 2 images (2x3Mb) / slice! (DUAL Channel!) 1.6keV, EsB & InLens-SE detector 12Gb data InLens SE

Phase 1. Dark in EsB image, White in SE InLens 10x10x10nm voxel size, 2048x1536x2000 pixel/slices 2 images (3Mb) / slice 12Gb data Phase 2: White in SE InLens Dark in EsB image 10x10x10nm voxel size, 2048x1536x2000 pixel/slices 2 images (3Mb) / slice 12Gb data

3D FIB/SEM: volume reconstruction Nb 3 Sn multifilament superconducting cable 0.5 mm Nb 3 Sn superconductor multifilament cable: 14 000 Nb 3 Sn filaments (diameter ~5um) in Cu matrix 1.8kV EsB detector: Materials & orientation contrast

Es B Threshold SE Solid Oxide Fuel Cell cathode P. Tanasini, LENI

The right conditions 1.87kV, EsB detector Image: 2048x1536 10nm pixel size 2200 images 36hours

Segmentation and analysis Comparison with Transmission X ray Microscopy (TXM) Joy C. Andrews, Yijin Liu, and Piero Pianetta Stanford Synchrotron Radiation Lightsource Stanford Linear Accelerator Center Yong S. Chu National Synchrotron Light Source II Brookhaven National Laboratory beam stop capillary condenser pin hole tomography rotation axis sample objective ZP optically coupled CCD at image plane L C L C S L S ZP L ZP CCD George J. Nelson, William M. Harris, Jeffrey J. Lombardo, John R. Izzo, Jr., and Wilson K. S. Chiu *

YSZ LSM FIB data down-sampled to 25nm voxel size TXM Pore FIB The segmentation dilemma Median filter

thresholding

The gradient problem Erode (shrink 1 pixel) Dilate (grow 1 pixel)

Segmentation tools for life science Problem: Structure (shape) determines function of objects Single cell on substrate Image stack: 1024x786 pixel: (10nm image pixel size) 2kV, 60um Aperture, high current, EsB detector (grid 1.5kV) 600 slices, 20nm thickness, milling current 700pA

Segmentation based on grey levels Medical steel Ceramic coating: TiO 2 Cell outer membrane and more

A little bit more complex. brain tissue, resin embedded

Which detector? In chamber SE (Everhard Thornley) in Lens SE in Lens BSE (energy selective) Big volumes Voxel: 7.5x7.5x7.5nm Image 3096x2304 3300 slices (48hours) 23x17x24 um 9700um 3 ~7000 synapses 23Gb data

Reconstruction: Christel Genoud 2weeks of work Automated segmentation of neuronal structures Ilastik v0.5 Fred Hamprecht, University of Heidelberg

Synapse recognition Anna Kreshuk Automated segmentation of neuronal structures Ilastik v0.5 Fred Hamprecht, University of Heidelberg FIB Nanotomography in life science Specimen preparation (fixation, staining, dehydration, resin infiltration same as for BIO TEM) Image contrast and resolution TEM quality Stable and reliable automated acquisition (less artifacts than ultramicrotomy)

Image processing in 3D Start with a good image (low noise, equilibrated histogram, right detector) 2D processing (shading correction) Image alignment (registration) Cropping (subvolume) Noise reduction (2D or 3D) Segmentation (most important) Visualization (strong area for commercial software)