Figures
Abstract
Positron emission tomography (PET) is an important imaging modality for clincial use. Conventionally, the PET scanner is generally built to provide a roomy enough transverse field-of-view (FOV) for imaging most adults’ torsos. However, in many cases, the region-of-interest (ROI) for imaging is usually a small area inside the human body. Therefore, to fulfill a PET system which provides an FOV comparable in size to the target ROI seems appealing and more cost effective. Meanwhile, such a PET system has the potential for portable or bedside application with the reduced system size. In this work, we have investigated the feasibility of using dual-headed panel-detectors to build an ROI-focused PET scanner. A novel windowed list-mode ordered subset expectation maximization method was developed to perform the ROI image reconstruction. With this method, the ROI of the object can be reconstructed from the coincidences whose position determined by time-of-flight (TOF) measurements was inside the ROI. Monte Carlo simulation demonstrates the feasibility of detecting lesions not less than 1 cm in diameter, with a 300 ps full width at half maximum timing resolution. As a critical system performance, the impact of TOF information on image quality has been studied and the required TOF capability was assessed. With enhanced timing resolution, the distortions and artifacts were reduced effectively. The further improved TOF capability also shows a noticeable improvement of detection performance for low uptake lesions, as well as the recovery speed of lesion contrast, which is of practical significance in the lesion detection task.
Citation: Xie Q, Wan L, Cao X, Xiao P (2013) Conceptual Design and Simulation Study of an ROI-Focused Panel-PET Scanner. PLoS ONE 8(8): e72109. https://doi.org/10.1371/journal.pone.0072109
Editor: Ge Wang, Virginia Tech, United States of America
Received: March 6, 2013; Accepted: July 7, 2013; Published: August 20, 2013
Copyright: © 2013 Xie et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work is partially supported by Natural Science Foundation of China (NSFC, http://www.nsfc.gov.cn/) Grants #61027006 and #61210003, the Ministry of Science and Technology of China (MOST, http://www.most.gov.cn/) Grant #2012DFG31970, the Ministry of Education of China (MOE, http://www.most.gov.cn/) Grant #313023, and the Wuhan Programs for Science and Technology Development (http://www.whst.gov.cn/) Grant #201231234461. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
The clinical positron emission tomography (PET) scanner is generally built with hundreds of detection modules and tens of thousands of electronic channels to provide a transverse field-of-view (FOV) which is roomy enough for most adults’ torsos. Nowadays, the PET scanner’s patient bore often has a diameter of about 70 cm [1]–[3]. It is capable of accommodating a patient weighting up to 200 kg although most of patients are much slimmer. Meanwhile, the region-of-interest (ROI) for imaging is usually a small area inside human body, sometimes a specific organ or an even smaller subregion. It seems wasteful that PET scanner’s FOV must be sufficiently spacious but is rarely made full use of. Furthermore, a large FOV not only results in high manufacture complexity and cost, but also causes performance degradation. The spatial resolution will be affected due to photon alinearity as the ring diameter increases and the sensitivity reduced by the decrease of solid angle coverage. Consequently, it is natural to conceive a PET scanner with an FOV which is comparable in size to the target ROI. Such a design may provide several benefits. Firstly, the FOV will be much smaller but fully utilized, making the system more cost effective. Secondly, upgrading the system for higher performance becomes more affordable, as much less number of detection modules are involved. The last but not least, the system’s size is significantly reduced and make it possible for portable or bedside PET imaging.
Motivated by above observations, we come to the idea of fulfilling such an ROI-focused PET system by two parallel panel detectors. The detectors can be moved according to the ROI’s position, that is a feature of ultrasound or planar X-ray imaging. The panel’s distance can also be adjusted to suit the object’s size, just like in positron emission mammography [4]–[7]. Altogether, the panel configuration allows a PET FOV to be adaptive to the target ROI. Meanwhile, panel PET’s concise structure will greatly reduce the manufacture complexity and make it convenient in applications like real-time PET guided biopsy, intra-operative guidance and monitoring, portable or bedside imaging, and simultaneously multi-modality imaging.
There are two issues to be considered in the image reconstruction of this system design. Firstly, the dual-panel scanner configuration has the inherit limited-view problem, causing severe artifacts in reconstructed images [8]. For this problem, Karp et al have found 200–600 ps time-of-flight (TOF) information effective in reducing artifacts and distortions in reconstructed images of partial-ring PET scanners [9], [10]. However, Karp’s work is dealing with whole-object imaging, while the proposed system is aiming for ROI imaging. Therefore, it is natural and appealing to realize ROI reconstruction here, which has the potential of excluding the influence of high activity structures adjacent to the ROI [11] and accelerating reconstruction speed for real-time imaging applications [12]. ROI reconstruction, as the second issue to be concerned, has been a hot topic in biomedical imaging for a long time. Solid progress has been made in different kinds of imaging modalities, such as the interior reconstruction in computed tomography (CT) [13]–[17], single photon emission computed tomography (SPECT) [18], [19] and omni-tomography [20]. These works have proven that ROI imaging can be achieved via truncated Hilbert transformation (THT) or total variation (TV) minimization, as long as certain additional information is available. Similarly, ROI reconstruction for PET also requires some supplementary data, which is generally the TOF information. Wang has proposed an ROI ordered subset expectation maximization (OSEM) method for TOF-PET using exclusively the line-of-response (LOR) passing the ROI [21]. Kao has utilized the redundancy of TOF-PET data and developed analytic algorithms to perform windowed ROI reconstructions [11]. Although Wang and Kao’s methods are based on full-view data, it is still obvious that TOF capability is crucial in the proposed panel PET design for ROI reconstruction with limited-view problem.
In this work, we investigated the use of dual-head configuration for building an ROI-focused panel-PET scanner. A novel windowed list-mode OSEM algorithm was developed to perform ROI reconstruction, using events originated inside the ROI only. With the proposed scanner design and reconstruction method, we evaluated the impact of TOF on image quality to assess the required system timing resolution (TR).
Methods
Scanner Design
The proposed PET scanner consists of a pair of panel detectors, one is above the human torso and the other beneath. The two parallel panels can move in both the horizontal and vertical directions to fit the target ROI, while keep being directly opposite to each other. Figure 1 shows the transverse view of the proposed design. For simplicity, we only considered the 2D imaging mode in transverse plane, in which the flight of any gamma photon is restricted. Thus, the scanner’s FOV is defined by the length of and the distance between two panels. The design’s objective is a system so compact that its FOV is barely big enough for imaging the liver – the largest internal organ. For applications with organs or their subregions as imaging objects, such an FOV size will be adequate. Because the liver’s transverse diameter is in the range of 20 to 25 cm, we set the panel detector’s length to 28 cm. Meanwhile, the panel distance is adaptive to patients. It is preferred to deploy the detectors as close to the patient as possible to maximize the solid angle coverage. A large solid angle coverage will not only alleviate the limited-view problem, but also increase the system’s sensitivity. For the case study in this article, the distance between two panels was set as 30 cm according to the average normal adult torso depth. Each panel detector consists of LSO crystal elements in size of
mm
. Narrow crystal elements were used to achieve good spatial resolution and then improve the detectability of small lesions.
The scanner can adjust its position according to different target ROIs.
Windowed List-mode OSEM
The transverse diameter of an adult’s torso usually ranges from 30 to 60 cm, while the panel detector’s length is 28 cm. The proposed system’s FOV cannot entirely cover the patient’s torso and it never means to. Furthermore, the system is aiming for imaging only the target ROI, which is just a patch of the FOV. Thus, it is natural to use an ROI reconstruction method for the proposed panel PET. Utilizing the TOF information, we developed a windowed list-mode OSEM algorithm, which is capable of ROI reconstruction with panel PET’s inherent limited angular coverage.
The conventional list-mode based EM with TOF information [22] can be formulated as(1)
is the image intensity of pixel
after the
iteration.
is the complete data set containing all coincidences. For each coincidence, the difference between the two singles’ arrival moments is defined as
. All the measurable time differences are presumed to be discretized into
time bins.
is the probability of an emission from pixel
being detected by crystal pair
with a certain time difference
. The term
stands for the total probability of an event from pixel
being detected by all possible crystal pairs and with all measurable time differences, which is in fact the pixel’s sensitivity intensity.
is the index of the crystal pair which detected the
event. Besides,
can be factorized into a product of two independent components, which are the
representing the system’s detector and geometric efficiency and the
reflecting the TOF probability. The
can be obtained by GATE simulation [23], [24]. The TOF probability
is computed from a timing spread function along the LOR
, which is modeled as a Gaussian function with full width at half maximum (FWHM) determined by the system timing resolution (TR).
For ROI imaging, we modified the data acquisition procedure to filter the arriving events. Once a coincidence event is obtained, we calculate its annihilation position along the LOR based on the arrival time difference of the two gamma photons. The event is accepted only if the resulting position is inside the ROI, which is denoted as . Otherwise, the event is just ignored. The set of all acquired events is defined as
. This process is illustrated in Figure 2. Afterwards, the ROI is reconstructed from
by the ROI version of list-mode EM algorithm, which is expressed as follows:
(2)
indicates the arrival time difference of two photons,
is the speed of light,
is the distance between the annihilation position and the midpoint of line-of-response.
In a conventional TOF-PET system, while a large enough coincidence window is used, all possible time differences are measurable, as shown in Figure 3(a). Thus, there are and
. As to the scenario in ROI imaging as shown in Figure 3(b), the ROI based event filtering truncates the range of measurable time differences. Only time bins associated with locations inside ROI will be measured and included into the sensitivity summation, resulting in a truncated-version of sensitivity intensity
.
The distribution was assumed as a Gaussian function with full width at half maximum determined by the system timing resolution.
To speed up the convergence rate, ordered subsets (OS) were used in this work. The events in were chronologically divided into 16 subsets and one iteration of the windowed list-mode EM is split into 16 sub-iterations. In each sub-iteration, just one subset of events was selected to update the image. The initial intensity of each pixels in the FOV was set as a uniform positive value. One iteration is accomplished after all the subsets are processed.
Simulation Setup
In simulation study, NEMA NU 2-2001 image quality (NEMA-IQ) phantom [25] and Zubal abdomen phantom [26] were used as imaging objects. NEMA-IQ phantom was employed to evaluate the lesion detectability. As shown in Figure 4(a), it contains four hot and two cold lesions with different diameters, all of which are enclosed in the imaging ROI. The phantom’s background activity is 5.3 kBq/cc and the uptake ratio of hot lesion to background was set as 4∶1. The abdomen phantom in Figure 4(b) is derived from a 2D section of the original Zubal phantom. It was used to simulate a more realistic clinical situation. The image intensities of anatomical regions were arbitrarily assigned. The target ROI contains the entire liver. If the system is capable of imaging the liver with its compact form factor, it should have less difficult in handling other smaller organs. The thicknesses of both phantoms are 2 mm, matching the axial size of the panel detector in simulation.
(a) The NEMA-IQ phantom is about cm
in size, including four hot lesions (10 mm, 13 mm, 17 mm and 22 mm in diameter) and two cold lesions (28 mm and 37 mm in diameter). The region-of-interest size is
cm
. (b) The Zubal abdomen phantom is about
cm
in size. The region-of-interest size is
cm
.
We employed the Monte Carlo simulation tool GATE (Geant4 application for tomographic emission) package [27] to model the scanner. To reduce the computation cost, we generated list-mode data containing single events with perfect energy resolution and TR at first. These data were blurred afterwards with selected energy resolution and TR to obtain more realistic data [28]. The energy resolution was fixed at 0.13@511 keV, while different TRs were adopted to study the impact of TOF on image quality. An energy window of 400 to 600 keV and a coincidence window of 6 ns was applied to the re-sampled singles for sorting coincidences. In this preliminary study, the main objective is to validate the imaging ability of the system design and hence factors like positron range, photon alinearity, subject attenuation and Raleigh scattering were disabled in the simulation. For image reconstruction, the pixel size was chosen as mm
, which is half of the 2-mm crystal pitch size.
Results
Imaging Feasibility Validation
The imaging feasibility of the proposed system is demonstrated by the reconstructed NEMA-IQ phantom image in Figure 5, which is obtained by windowed list-mode OSEM with 300-ps FWHM TR. Figure 5(a) is the initial outcome of the reconstruction. The ROI is surrounded by high intensity artifacts, including a rectangle matching the ROI’s edge. Since it is the image inside ROI that matters, only this region is to be displayed. The resulted ROI image is shown in Figure 5(b). All the six lesions can be clearly identified, including the smallest one with diameter of 10 mm. However, all lesions are stretched in various degrees along the direction vertical to the panel detectors, while no obvious distortion is observed in the direction parallel to the detector panel. Besides, X shaped diagonal streak artifacts with rather uniform included angles were observed around each lesion. It seems that both the distortions and artifacts are related to the limited angular coverage.
(a) The initial reconstructed image of the NEMA-IQ phantom. (b) The reconstructed image after the region-of-interest is cropped out. (c) The reconstructed image obtained by conventional list-mode OSEM method. Note that only the structures inside the ROI are displayed.
The intensity profiles were plotted for further quantitative analysis in Figure 6. The profiles are mainly consistent with the true value. There is no obvious mis-localization of lesions. Meanwhile, the lesion boundary of profile I in Figure 6(b) seems to be more accurate than that of profile II in Figure 6(c) and profile III in Figure 6(d). That agrees with the observations that there are more distortions in the vertical direction than in the horizontal direction. The varying degrees of distortions are also the cause of anisotropic visual representation of structures of interest, such as the shape and size of lesions. Such anisotropism, as well as the pattern of X shaped artifacts, should be put into consideration when the image is further interpreted for lesion characterization.
The sample lines in (a) show the locations of the profiles.
For comparison, we also included the reconstruction results of the conventional OSEM in Figures 5 and 6. Only trivial differences were observed in the resulted images and profiles. Meanwhile, 4.2 million coincidence counts were used for traditional OSEM and 3 million used for the windowed version. There was a 30 reduction in the data required for the proposed method.
Impact of TOF on Image Quality
To evaluate the impact of TOF on image quality, we reconstructed images for NEMA-IQ phantom from TOF-PET data with different TRs, ranging from 100 ps to 1 ns FWHM. For comparison, a conventional full-ring PET scanner was modeled as well. The Siemens Biograph mCT PET scanner was taken as the prototype while its parameters like crystal size, energy resolution, energy window and etc. were configured to be the same as those of the panel-PET. The results are compared in Figure 7. For image with the 1-ns FWHM TR, all lesions are suffering from obvious artifacts and distortions. There are degradations in image resolution and contrast, as well as loss of structural details. As mentioned above, these problems appear mainly in the direction vertical to the detector panel. Such image quality deteriorations are gradually alleviated by the improvement on TOF capability. With a 100-ps FWHM TR, the artifacts and degradations were almost eliminated, especially the vertical distortions of lesions. Those conclusions were also supported by the numerical evaluation on intensity profiles for different TRs in Figure 8.
Note that only the structures inside the ROI are displayed.
The profiles were obtained from the reconstructed images shown in Figure 7.
The reconstructed images for Zubal phantom with different TRs were compared in Figure 9. Once again, the distortions in the vertical direction resulted in degradation of resolution and loss of structural details. It was observed that liver was stretched along the vertical direction. The counts from high-uptake liver region were mis-located into the surrounding low-uptake muscle region, thus the structure information of liver/muscle boundary was difficult to recognize. With enhanced TR, the visual detectability of the boundary was gradually recovered. Furthermore, the better TR also improved the visual detection performance of the low-uptake lesion, which is inside the liver and has a 1.5 lesion-to-background uptake ratio.
The circle shows the low uptake lesion inside the liver. Note that only the structures inside the ROI are displayed.
We also analyzed the contrast recovery coefficients (CRCs) for different lesions to characterize the lesion detectability. Circular region at the center of NEMA-IQ phantom with a diameter of 6 cm was chosen to estimate the background counts. The CRC of hot lesion was calculated as(3)and the cold lesion as
(4)
,
and
are the average intensities of hot lesion, cold lesion and background regions, respectively.
and
are the true values of the hot lesion and background regions, respectively. Figure 10 shows the CRCs versus iteration number for different lesions. For all lesions, the improved TR leads to a higher CRC value. Furthermore, for most lesions, it seems that a better TR also provides a faster contrast recovery speed. This is more obvious for the results from the TOF data with 100 ps TR, while its corresponding CRC curves usually converge after 2–3 iterations.
To avoid misleading impacts introduced by artifacts and distortions on contrast recovery coefficient values, only image results for 100–400 ps full width at half maximum TOF-PET data were analyzed here.
Apparently, TOF capability is vital for the imaging feasibility of the proposed ROI-focused panel-PET system. Nowadays, the state-of-the-art TR can reach ∼220 ps for an LSO-based detector module [29] and ∼520 ps for commercial systems [1], [30]. A 300–400 ps TOF capability seems to be achievable in the foreseeable future. Equipped with such a TOF capability, the proposed system can clearly detect lesions as small as 1 cm in diameter, without any mis-localization. Although the artifacts and distortions persisted, their patterns are predictable in certain degree.
Discussion and Conclusion
In this work, we proposed a panel PET system design for ROI-focused scanning on human torso. The conceptual scanner has a concise geometry and adjustable FOV, which may generate novel applications like portable or bedside PET imaging. To fulfill the ROI imaging, we developed a windowed list-mode OSEM reconstruction algorithm. This algorithm will perform a data discrimination based on the TOF measurements to obtain events whose annihilation positions are inside the ROI. We have used the simulated TOF-PET data to validated the developed algorithm. The ROI-tailored data-discrimination procedure has the potential to reduce the scatter and random events originating from the structures outside the ROI. Furthermore, event counts used in reconstruction will be reduced, depending on the ROI size, activity distribution and local detection efficiency. Since the time of list-mode based reconstruction is almost proportional to the number of events [12], the proposed algorithm would be valuable for certain real-time imaging applications, such as intra-operative guidance and monitoring. The benefits and properties of the windowed list-mode OSEM algorithm are worthy of further investigation.
We also investigated the impact of TOF capability on the resulting image quality of the proposed system. The results indicate that the system with a 300 ps FWHM TR can clearly detect and localize lesions as small as 1 cm in diameter. Meanwhile, the remaining artifacts and distortions have predictable patterns. If the patterns can be used as a prior knowledge, those errors’ influence on the image analysis may not be as severe as expected. Furthermore, a further analysis and modeling of those patterns may enable us to develop post-processing techniques to eliminate such errors in the resulting images.
Acknowledgments
We wish to express our gratitude to Ms. Luyao Wang, Mr. Daoming Xi, Mr. Yanzhao Li for all the inspiring discussions. Monte Carlo simulations presented in this paper were carried out using the High Performance Computing Center experimental testbed in SCTS/CGCL (see http://grid.hust.edu.cn/hpcc) and the High Performance Computing platform provided by Computer Technology Application Key Lab of Yunnan Province in Kunming University of Science and Technology.
Author Contributions
Conceived and designed the experiments: QGX PX. Performed the experiments: QGX LW XQC PX. Analyzed the data: QGX LW XQC PX. Contributed reagents/materials/analysis tools: QGX PX. Wrote the paper: QGX LW PX.
References
- 1. Jakoby BW, Bercier Y, Conti M, Casey ME, Bendriem B, et al. (2011) Physical and clinical performance of the mCT time-of-flight PET/CT scanner. Physics in Medicine and Biology 56: 2375–2389.
- 2. Surti S, Kuhn A, Werner ME, Perkins AE, Kolthammer J, et al. (2007) Performance of Philips Gemini TF PET/CT scanner with special consideration for its time-of-flight imaging capabilities. Journal of Nuclear Medicine 48: 471–480.
- 3. Teräs M, Tolvanen T, Johansson J, Williams J, Knuuti J (2007) Performance of the new generation of whole-body PET/CT scanners: Discovery STE and Discovery VCT. European Journal of Nuclear Medicine and Molecular Imaging 34: 1683–1692.
- 4. Thompson CJ, Murthy K, Weinberg IN, Mako F (1994) Feasibility study for positron emission mammography. Medical Physics 21: 529–538.
- 5. Abreu MC, Almeida P, Balau F, Ferreira NC, Fetal S, et al. (2005) Clear-PEM: A dedicated PET camera for improved breast cancer detection. Radiation Protection Dosimetry 116: 208–210.
- 6. Camarda M, Belcari N, Guerra AD, Galeotti S, Morsani F, et al. (2006) Development of the YAP-PEM scanner for breast cancer imaging. Physica Medica 21 Supplement 1114–116.
- 7. Peng H, Levin CS (2010) Design study of a high-resolution breast-dedicated PET system built from cadmium zinc telluride detectors. Physics in Medicine and Biology 55: 2761–2788.
- 8. Townsend D, Schorr B, Jeavons A (1980) Three-dimensional image reconstruction for a positron camera with limited angular acceptance. Nuclear Science, IEEE Transactions on 27: 463–470.
- 9. Surti S, Karp JS (2008) Design considerations for a limited angle, dedicated breast, TOF PET scanner. Physics in Medicine and Biology 53: 2911–2921.
- 10.
Lee E, Werner M, Karp J, Surti S (2011) Design optimization of a dedicated breast PET scanner using TOF imaging in a partial ring geometry. In: Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC), 2011 IEEE. 4276–4280.
- 11. Kao CM (2008) Windowed image reconstruction for time-of-flight positron emission tomography. Physics in Medicine and Biology 53: 3431–3445.
- 12. Tashima H, Yoshida E, Kinouchi S, Nishikido F, Inadama N, et al. (2012) Real-time imaging system for the OpenPET. Nuclear Science, IEEE Transactions on 59: 40–46.
- 13. Defrise M, Noo F, Clackdoyle R, Kudo H (2006) Truncated Hilbert transform and image reconstruction from limited tomographic data. Inverse Problems 22: 1037–1053.
- 14. Ye Y, Yu H, Wei Y, Wang G (2007) A general local reconstruction approach based on a truncated Hilbert transform. International Journal of Biomedical Imaging 2007: 1–8.
- 15. Yu H, Ye Y, Wang G (2008) Interior reconstruction using the truncated Hilbert transform via singular value decomposition. Journal of X-ray science and technology 16: 243–251.
- 16. Yu H, Wang G (2009) Compressed sensing based interior tomography. Physics in Medicine and Biology 54: 2791–2805.
- 17. Xu Q, Mou X, Wang G, Sieren J, Hoffman E, et al. (2011) Statistical interior tomography. Medical Imaging, IEEE Transactions on 30: 1116–1128.
- 18. Zeng GL, Gullberg GT (2010) SPECT region of interest reconstruction with truncated transmission and emission data. Medical physics 37: 4627–4633.
- 19. Yang J, Yu H, Jiang M, Wang G (2012) High-order total variation minimization for interior SPECT. Inverse Problems 28: 1–24.
- 20. Wang G, Zhang J, Gao H, Weir V, Yu H, et al. (2012) Towards omni-tomography–grand fusion of multiple modalities for simultaneous interior tomography. PLoS ONE 7: e39700.
- 21.
Wang W (2007) Investigation of local tomography property for TOF-PET OS-EM reconstruction. In: 9th International Meeting on Fully Three-Dimensional Image Reconstruction in Radiology and Nuclear Medicine. 100–103.
- 22.
Groiselle C, Glick S (2004) 3D PET list-mode iterative reconstruction using time-of-flight information. In: Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC), 2004 IEEE. volume 4, 2633–2638.
- 23.
Kao CM, Dong Y, Xie Q (2007) Evaluation of 3D image reconstruction methods for a dual-head small-animal PET scanner. In: Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC), 2007 IEEE. volume 4, 3046–3050.
- 24.
Kao CM, Dong Y, Xie Q, Chen CT (2007) Image reconstruction of a dual-head small-animal PET system by using Monte-Carlo computed system response matrix. In: 9th International Meeting on Fully Three-Dimensional Image Reconstruction in Radiology and Nuclear Medicine. 398–401.
- 25.
Association NEM (2001) NEMA Standards Publication NU-2 2001: Performance Measurements of Positron Emission Tomographs. Rosslyn, VA: National Electrical Manufacturers Association.
- 26. Zubal I, Harrell C, Smith E, Rattner Z, Gindi G, et al. (1994) Computerized three-dimensional segmented human anatomy. Medical Physics 21: 299–302.
- 27. Jan S, Santin G, Strul D, Staelens S, Assié K, et al. (2004) GATE: a simulation toolkit for PET and SPECT. Physics in Medicine and Biology 49: 4543–4561.
- 28.
Kao CM, Dong Y, Xie Q, Chen CT (2006) An investigation of the potential benefits in trading energy resolution for timing resolution in time-of-flight positron emission tomography. In: Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC), 2006 IEEE. volume 4, 2564–2569.
- 29. Moses W, Janecek M, Spurrier M, Szupryczynski P, Choong WS, et al. (2010) Optimization of a LSO-based detector module for time-of-flight PET. Nuclear Science, IEEE Transactions on 57: 1570–1576.
- 30. Zaidi H, Ojha N, Morich M, Griesmer J, Hu Z, et al. (2011) Design and performance evaluation of a whole-body ingenuity TF PET-MRI system. Physics in Medicine and Biology 56: 3091–3106.