| Literature DB >> 23024907 |
Hector R A Basevi1, Kenneth M Tichauer, Frederic Leblond, Hamid Dehghani, James A Guggenheim, Robert W Holt, Iain B Styles.
Abstract
Bioluminescence Tomography attempts to quantify 3-dimensional luminophore distributions from surface measurements of the light distribution. The reconstruction problem is typically severely under-determined due to the number and location of measurements, but in certain cases the molecules or cells of interest form localised clusters, resulting in a distribution of luminophores that is spatially sparse. A Conjugate Gradient-based reconstruction algorithm using Compressive Sensing was designed to take advantage of this sparsity, using a multistage sparsity reduction approach to remove the need to choose sparsity weighting a priori. Numerical simulations were used to examine the effect of noise on reconstruction accuracy. Tomographic bioluminescence measurements of a Caliper XPM-2 Phantom Mouse were acquired and reconstructions from simulation and this experimental data show that Compressive Sensing-based reconstruction is superior to standard reconstruction techniques, particularly in the presence of noise.Entities:
Keywords: (170.3010) Image reconstruction techniques; (170.6280) Spectroscopy, fluorescence and luminescence; (170.6960) Tomography
Year: 2012 PMID: 23024907 PMCID: PMC3447555 DOI: 10.1364/BOE.3.002131
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732
Fig. 1(a) CSCG algorithm pseudocode. ϕ(x, λ) is the objective function (see Eq. (2)). f is a vector function that generates a new search direction using the gradient of ϕ(x, λ) and the previous search direction. α was chosen in this work to be 105. β was chosen in this work to be 10−20 of the initial value of λ. η was chosen in this work to be 2−1/2. (b) Flowchart of CSCG algorithm.
Fig. 2Caliper XPM-2 Phantom Mouse and the torso region used in reconstructions. The XPM-2 is shown in light blue, and the torso region used is overlaid in dark blue. The positions of the measurements acquired are shown as red spheres.
Fig. 3Reconstructions of two bioluminescent sources using simulated measurements in the absence of measurement noise. (a)Target (b)GN (c)NNLS (d)CSCG
Fig. 4Reconstructions of two bioluminescent sources using simulated measurements, as Fig. 3, in the presence of 1% normally distributed noise.
Fig. 5Reconstructions of two bioluminescent sources using simulated measurements, as Fig. 3, in the presence of 5% normally distributed noise.
Simulation localisation error (mm) of mean reconstructed source centre. Source locations were calculated by taking the centres of fitted Gaussian distributions. Source A is the left-most source, and source B is the right-most source, as displayed in Fig. 3, Fig. 4, and Fig. 5. At each noise level, 30 samples of noisy measurements were generated. The location of each source was taken to be the location of the maximum value in a region (a sphere of radius 8mm) around the true source centre.
| Noise | Source A
| Source B
| ||||
|---|---|---|---|---|---|---|
| GN | NNLS | CSCG | GN | NNLS | CSCG | |
| 0% | 1.8 | 0.6 | 0.6 | 3.6 | 1.6 | 0.9 |
| 1% | 4.0 | 1.0 | 0.5 | 2.9 | 0.9 | 0.7 |
| 5% | 5.3 | 1.7 | 1.7 | 2.8 | 1.7 | 1.1 |
Simulation mean volume (mm3) (see Table 1) as a percentage of the true volume. The volume of each source was taken to be the connected volume enclosed by half the maximum value in the region, containing the location of the maximum value.
| Noise | Source A
| Source B
| ||||
|---|---|---|---|---|---|---|
| GN | NNLS | CSCG | GN | NNLS | CSCG | |
| 0% | 43% | 340% | 74% | 86% | 740% | 96% |
| 1% | 36% | 290% | 110% | 72% | 660% | 150% |
| 5% | 26% | 82% | 57% | 58% | 330% | 230% |
Fig. 6Reconstructions of experimental measurements of an XPM-2 Phantom Mouse (Caliper Life Sciences, Hopkinton, MA, USA). (a)GN (b)NNLS (c)CSCG