<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JBM</journal-id><journal-title-group><journal-title>Journal of Biosciences and Medicines</journal-title></journal-title-group><issn pub-type="epub">2327-5081</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jbm.2022.1011015</article-id><article-id pub-id-type="publisher-id">JBM-121376</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Comparative Study of Segmentation Methods of Rat Sinusoidal Network to Evaluate Nonalcoholic Steatohepatitis for Small Number of Medical Samples
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Masaki</surname><given-names>Murakishi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hiroto</surname><given-names>Shoji</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Science and Technology, Kwansei Gakuin University, Hyogo, Japan</addr-line></aff><pub-date pub-type="epub"><day>01</day><month>11</month><year>2022</year></pub-date><volume>10</volume><issue>11</issue><fpage>192</fpage><lpage>202</lpage><history><date date-type="received"><day>18,</day>	<month>October</month>	<year>2022</year></date><date date-type="rev-recd"><day>19,</day>	<month>November</month>	<year>2022</year>	</date><date date-type="accepted"><day>22,</day>	<month>November</month>	<year>2022</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Extracting portions of pathology images to determine disease states is a challenging task, and several segmentation approaches have been developed. This study evaluated four well-known methods to classify changes in rat hepatic sinusoidal network morphology in nonalcoholic stetohepatitis were evaluated. The classical methods of morphological transformation (MT), convex hull (CH), and counter extraction (CE), and a machine learning method, U-net, were compared using fractal dimensions as feature quantities. The findings show that MT and CH are more effective than U-net when the number of samples is small, as is usually the case with pathology images. U-net required a large number of images and was the best method in terms of extracting the morphology. When the number of samples is small, such as the case with pathological images, it may be advantageous to use a combination of basic segmentation methods rather than advanced machine learning techniques, such as U-net. The segmentation methods must be carefully chosen depending on the diseases to be discriminated and on the number of samples.
 
</p></abstract><kwd-group><kwd>Segmentation</kwd><kwd> Deep Learning</kwd><kwd> Fractal Dimensions</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The liver is one of the most important organs of the body, performing multiple vital functions including metabolism, producing bile, converting nutrients into forms the body can use, and storing the nutrients [<xref ref-type="bibr" rid="scirp.121376-ref1">1</xref>]. The liver sinusoid, a group of small blood vessels with the fenestrated endothelium that permits blood plasma to touch with hepatocytes, maintains these multiple unique functions [<xref ref-type="bibr" rid="scirp.121376-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref2">2</xref>]. However, in diseases such as abnormal hepatocyte function, fibrosis, and cirrhosis, the sinusoid changes and does not function properly. Capturing the morphological changes in the hepatic sinusoidal network is essential [<xref ref-type="bibr" rid="scirp.121376-ref1">1</xref>].</p><p>Hematoxylin and eosin (HE) stained liver specimens are among the most commonly used methods for the differential diagnosis of liver diseases. Hepatics sinusoids have been extracted to facilitate the structural analysis of HE images of hepatic tissue using prepared filters for image analysis [<xref ref-type="bibr" rid="scirp.121376-ref3">3</xref>]. Fluorescent images have also been used for pathology section analysis [<xref ref-type="bibr" rid="scirp.121376-ref4">4</xref>]. Fluorescence imaging is a technique to determine the existence of a target component around a bright image spot [<xref ref-type="bibr" rid="scirp.121376-ref4">4</xref>].</p><p>For pathology, it is necessary to identify the sinusoidal morphology accurately. To properly extract the sinusoidal morphology, a segmentation that fills in the cavities must be conducted as liver sinusoids are cavities tubes covered by sinusoidal epidermal cells [<xref ref-type="bibr" rid="scirp.121376-ref1">1</xref>]. Numerous processes have been proposed for segmentation over the years, including thresholding binarization, a method based on edge extraction [<xref ref-type="bibr" rid="scirp.121376-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref7">7</xref>]. Ascertaining the segmentation method most appropriate for image determination is crucial.</p><p>Many studies have proposed computational methods for image analysis in liver disease detection [<xref ref-type="bibr" rid="scirp.121376-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref7">7</xref>]. The most widely used image recognition is based on supervised learning using heuristically designed models, including convolution neural networks (CNN) [<xref ref-type="bibr" rid="scirp.121376-ref8">8</xref>]. In those methods, features are automatically extracted from multi-layered neural networks, which are then used to perform classification. However, these methods are still limited by being black box models; the chosen features and reasons for these classifications are unclear [<xref ref-type="bibr" rid="scirp.121376-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref6">6</xref>]. Moreover, for medical images, preparing a large number of samples, particularly for rare diseases, is not possible [<xref ref-type="bibr" rid="scirp.121376-ref5">5</xref>]. This makes it necessary to extract and characterize features as well.</p><p>This study aimed to find the appropriate segmentation methods and their combination with feature values for properly determining disease. The hepatic sinusoidal network pattern morphology was evaluated in the context of nonalcoholic steatohepatitis (NASH), which is related to metabolic syndrome. Rats were fed a high-fat/high-cholesterol (HFC) diet, causing pathological features similar to those of human patients with NASH [<xref ref-type="bibr" rid="scirp.121376-ref9">9</xref>]. These were used to evaluate the vascular pattern using fluorescent images. Not all the target area’s pixels are bright spots, and the bright area must be colored and stored for accuracy in sorting morphology [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>]. Hence, we explored four typical methods of segmentation: morphological transformations (MT) [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref11">11</xref>], convex hull (CH) [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref12">12</xref>], contour extraction (CE) [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref13">13</xref>], and U-net [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref14">14</xref>]. These methods add color to unpainted areas.</p><p>For the feature values for image classification, we compared the fractal dimension (FD) [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref15">15</xref>] for quantity values, though the feature values are automatically determined for disease identification in deep machine learning. This is because FDs have been applied to quantify many life phenomena, such as patterns of plant morphology structure [<xref ref-type="bibr" rid="scirp.121376-ref15">15</xref>], and coastline geometry [<xref ref-type="bibr" rid="scirp.121376-ref16">16</xref>]. Under such assumption, we performed segmentations of the obtained fluorescent images using the aforementioned four methods and calculated the FDs. The four segmentation methods were compared in terms of discriminative performance. CNN network, a deep machine-learning networks [<xref ref-type="bibr" rid="scirp.121376-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref17">17</xref>], was used to do the comparison of the obtained results.</p></sec><sec id="s2"><title>2. Material &amp; Methods</title><sec id="s2_1"><title>2.1. Animals</title><p>Six-week-old male Wister rats were purchased from the Shimizu Laboratory Supplies Co, Kyoto, Japan. The experiment was performed following the National Research Council’s guidelines for the care and use of mammals and with the approval of the Committee for Animal Research at Kwansei Gakuin University.</p><p>The rats were housed in two groups in standard breeding cages (27 &#215; 22 &#215; 12 cm) with freely available food and water under a 12-h light/12-h dark cycle (light in at 08:00). The rats were randomly divided into two groups of three rats each. Control groups (Cont) and HFC groups (HFC) were fed the control and HFC diets for 12 weeks, respectively. This is because why fibrosis begins to occur at 12 weeks, and the morphology changes [<xref ref-type="bibr" rid="scirp.121376-ref9">9</xref>]. For the diets, stroke-prone control chow diet (20.8% crud protein, 4.8% crude liquid, 3.2% crud fiber, 5.0% ash, 8.0%, moisture, and 58.2% carbohydrate) was used as a control diet, and the HFC diet was a mixture of 68% control diet, 25% palm oil, 5% cholesterol, and 2% cholic acid. Both diets were obtained from Funabashi Form (Chiba, Japan).</p><p>After 18 - 20 h of removal of food, the rats were sacrificed under pentobarbital (70mg/kg)-induced anesthesia, and the livers were removed. A part of each liver was fixed in 4% buffered paraformaldehyde for histological analysis.</p></sec><sec id="s2_2"><title>2.2. Immunofluorescent Staining and Observations by Confocal Microscopy</title><p>An immunofluorescence technique was applied to 30-μm thick frozen sections of the liver using a monoclonal antibody specific for hepatic sinusoidal endothelial cells (Anti-Rat Hepatic Sinusoidal Endothelial Cells; Immuno-Biological Laboratories Co. Ltd., Japan) [<xref ref-type="bibr" rid="scirp.121376-ref18">18</xref>]. Secondary antibodies were applied for Alexa 488-conjugated rabbit purchased from Molecular Probes (Eugene, OR, USA) were applied. The procedures for immunohistochemical staining followed the method used by Ref [<xref ref-type="bibr" rid="scirp.121376-ref19">19</xref>]. Confocal images were obtained using an Olympus FV 1000 confocal microscope running FluoView version 2.0c software (Olympus, Tokyo, Japan). The images were converted to 200 &#215; 200 pixels in size to apply the image analysis using the Python Pillow library [<xref ref-type="bibr" rid="scirp.121376-ref20">20</xref>].</p></sec><sec id="s2_3"><title>2.3. Segmentation</title><p><xref ref-type="fig" rid="fig1">Figure 1</xref> shows the schematic of the experimental procedure. Four different segmentation methods were used to delineate the images’ cross-sectional portions of hepatic sinusoids to determine the most effective method to differentiate between HFC and Cont. Each procedure is explained in this section.</p><sec id="s2_3_1"><title>2.3.1. Morphological Transformation (MT)</title><p>MT demarcates the contour or area of a subject in a binary image. Convolution layers perform convolutions such as erosion and dilation [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref11">11</xref>]. In this experiment, we applied a method that performs one erosion followed by one dilation as MT processing. A combined erosion and dilation opening transformation was used to reduce the high noise in the image, as shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>(b) and <xref ref-type="fig" rid="fig2">Figure 2</xref>(g).</p></sec><sec id="s2_3_2"><title>2.3.2. Convex Hull (CH)</title><p>CH is the smallest convex polygon encompassing everything in a point set [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref12">12</xref>]. This method is capable of examining and correcting defects in the curve. The convexity of the cross-sectional portion of a blood vessel in the image can be examined and segmented from surrounding points, as shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>(c) and <xref ref-type="fig" rid="fig2">Figure 2</xref>(h).</p></sec><sec id="s2_3_3"><title>2.3.3. Contour Extraction (CE)</title><p>CE is segmentation by connecting all points of object boundaries in the image [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref13">13</xref>]. Object boundary is a connection of pixels of the same color in an image. When the target image is binarized, it is possible to extract contours by thresholding to demarcate the object’s contours, as shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>(d) and <xref ref-type="fig" rid="fig2">Figure 2</xref>(i).</p></sec><sec id="s2_3_4"><title>2.3.4. U-Net</title><p>The U-net is one of the segmentation convolutional neural networks proposed initially for medical image segmentation by Ronneberger et al. [<xref ref-type="bibr" rid="scirp.121376-ref21">21</xref>]. U-net consists of a contracting path and an expansive path [<xref ref-type="bibr" rid="scirp.121376-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref21">21</xref>]. The contracting path follows the typical architecture of a convolutional network. The repeated application of two 3 &#215; 3 convolutions followed by a rectified linear unit (ReLU) and a 2 &#215; 2 max-pooling operation with stride 2 for down sampling. We set the first layer filter count as 64. At each downsampling step, we doubled the number of feature channels. Every step in the expansive path consists of an upsampling of the feature map followed by a 2 &#215; 2 convolution that halves the number of feature channels, a concatenation with the correspondingly cropped feature map from the contracting path, and two 3 &#215; 3 convolutions, each followed by a ReLU. The cropping is necessary due to the loss of border pixels in every convolution. At the final layer, a 1 &#215; 1 convolution is used to map each 64-component feature vector to the desired number of classes. In total the network has 23 convolutional layers. Segmentation utilizing U-net was performed using the library obtained from Github [<xref ref-type="bibr" rid="scirp.121376-ref22">22</xref>]. The epoch number was set as 100, enough to reduce the training error sufficiently when comparing dice coefficient explained in the next section.</p><p>We trained U-net on images with hand-drawn segmentation of cross-sections of hepatic sinusoids on binarized images as training data. Each of the 50 images was segmented using 50 training data samples each, as shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>(e) and <xref ref-type="fig" rid="fig2">Figure 2</xref>(j).</p></sec></sec><sec id="s2_4"><title>2.4. Dice Coefficients</title><p>The Dice coefficient is a statistical quantity measuring the similarity between two data sets. This index is arguably the most broadly used measure in image segmentation validation [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref23">23</xref>]. We applied the dice coefficient to compare the similarity between the four types of segmentation images and the extract segmentation images.</p><p>The handwritten segmentation images used as training data for the U-net were compared for similarity using the Dice coefficient for the four different segmentation images. The Dice coefficient is calculated using Equation (1).</p><p>D S C ( A , B ) = 2 | A ∩ B | / ( | A | + | B | ) , (1)</p><p>where A is the segmented area sets of hepatic sinusoid and B is the handwritten segmented area sets of hepatic sinusoid. The number of elements in that set, e.g. |X| means the number of elements in set X. “ ∩ ” represents the intersection of two sets.</p></sec><sec id="s2_5"><title>2.5. Fractal Analysis</title><p>FDs helps measure roughness and self-similarity in objects [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref16">16</xref>]. Fractal analysis, introduced to the world of research in 1982 by Mandelbrot, has been widely used in image processing [<xref ref-type="bibr" rid="scirp.121376-ref24">24</xref>]. The FD of processed images is calculated using the basic FD equation</p><p>D = − lim ε → 0 log N ( ε ) / log ε , (2)</p><p>where N(ε) is the least number of distinct copies of the images in the scale ε. The union of N(ε) distinct copies must cover the images altogether. We applied the box-counting method, a frequently used techniques, to estimate the FD of the image. In the method, the images are delimited into square boxes. Further, the number of boxes in which the feature is to be searched is included. The sizes of these delimited boxes are varied, and the number of boxes is counted each time. Each box containing an image is then plotted on a double-logarithmic graph. The absolute value of the slope is nearly equal to the number representing the FD, D [<xref ref-type="bibr" rid="scirp.121376-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref16">16</xref>]. The box-counting method was performed using ImageJ in Windows [<xref ref-type="bibr" rid="scirp.121376-ref25">25</xref>].</p></sec><sec id="s2_6"><title>2.6. Statistical Analysis</title><p>The obtained FDs were compared using a two-tailed Mann-Whitney U-test (MW test) between Cont and HFC groups. The statistical analyses were performed using the python library [<xref ref-type="bibr" rid="scirp.121376-ref26">26</xref>].</p><p>Boxplots are also used when information about distributions is important (see Figures 3-5). Data were plotted as mean &#177;95% confidence intervals using R software. A boxplot summarizes data using the smallest observation, lower quartile (base of rectangle), median (line in the rectangle), upper quartile (summit of rectangle), and largest observation. Data points considered outliers are marked by isolated points (circles).</p></sec><sec id="s2_7"><title>2.7. Classification Using CNN</title><p>To compare the obtained results, a classification technique, CNN, manly used for image recognition applications, was applied. CNNs are a kind of artificial neural networks that use convolution operations in at least one of their layers [<xref ref-type="bibr" rid="scirp.121376-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref17">17</xref>]. The CNN architecture consists of multiple stages or blocks composed of four main components: a filter bank called kernels, a convolution layer, a non-linearity activation function, and a pooling layer [<xref ref-type="bibr" rid="scirp.121376-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref17">17</xref>]. Each stage aims to represent features as sets of arrays called feature maps. We applied a typical CNN architecture comprising a stack of three 3 &#215; 3 convolutional stages followed with 2 &#215; 2 max-pooling stages and two fully connected layers, giving the final output as a classification module.</p><p>In this study, 50, 100, and 200 pieces of supervised image data samples of each group (HFC and Cont) were prepared, and the network was trained. Tests were conducted on ten pieces of the four types of segmented images. To enhance the training data, image rotation of π/2, π, and 2π/3 was prepared following [<xref ref-type="bibr" rid="scirp.121376-ref20">20</xref>].</p></sec></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Dice Coefficients</title><p><xref ref-type="fig" rid="fig2">Figure 2</xref> shows the fluorescent images of Cont and HFC and their segmentation results using each segmentation method, including MT, CH, CE and U-net. The Dice coefficient of 50 pieces of segmentation images by the four methods was calculated. <xref ref-type="fig" rid="fig3">Figure 3</xref> shows the Dice coefficients obtained by the four methods. U-net showed the most similarity, with an average parameter of 0.819. Conversely, the morphology treatment showed the lowest parameter, with an average of 0.2142.</p></sec><sec id="s3_2"><title>3.2. Fractal Dimensions</title><p><xref ref-type="fig" rid="fig4">Figure 4</xref> shows the boxplots of FDs of the images segmented using the four methods. The FD differs depending on the segmentation technique. Significant difference between Cont and HFC were identified in MT and CH methods.</p><p>The FDs of HFC exhibited lower parameters than Cont. It is also known that the numbers of medical image samples is generally limited. Therefore, we investigated the effects of the numbers of image data samples on MT and CH methods. <xref ref-type="fig" rid="fig5">Figure 5</xref> shows the boxplots of the obtained FDs of 10, 25, and 50 samples. The P-values were found to decrease with the sample size in both methods. A significant difference was observed in even ten samples. P-values for the CH method were smaller than those for the MT method for every sample size.</p></sec><sec id="s3_3"><title>3.3. Comparison of the Classifications Using Convolutional Neural Network</title><p>In the previous section, we demonstrated that the MT and CH methods could differentiate between Cont and HFC, even in 10 segmentation samples. To evaluate the methods, we used CNN, a widely used and powerful differentiation method. The most accurate classification was the one that trained and classified images with MT. <xref ref-type="fig" rid="fig6">Figure 6</xref> shows that, as the number of samples increased, the correct responses increased, and when 200 samples of supervised image data were used, the probability of correct classification was 79%.</p></sec></sec><sec id="s4"><title>4. Discussions</title><p>In this study, we examined the accuracy of the segmentation methods in differentiating between Cont and HFC. Although the U-net, a machine learning method, had the best results regarding morphological reproducibility, the statistical results suggested that FDs of the Cont and HFC images segmented using MT and CH method could be differentiated.</p><p>The other advantage of these methods was that significant difference might be observed even in a small number of samples. Although CNNs are known to have outstanding performance in classifications, they need many samples for effective classification, as shown in <xref ref-type="fig" rid="fig6">Figure 6</xref>. Therefore, when the number of samples is small, it is better to use biogenic features to classify patterns.</p><p>In the present study, we have chosen parameters in networks of U-net and CNN such that the effective detection or classification was performed as in [<xref ref-type="bibr" rid="scirp.121376-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref22">22</xref>]. We have noticed that several conditions often play a crucial role in the classification of segmented images [<xref ref-type="bibr" rid="scirp.121376-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref14">14</xref>]. Therefore, we have partly verified the classification by changing the CNN parameters. For example, we tried CNNs with different activation functions. However, the qualitative results obtained were the same.</p><p>One of the most important conclusions of the present study is that it is better to choose a method that extracts more features rather than similarities in the case of a small number of samples. If we assume that U-net performs accurate segmentation and detailed classification is performed by CNN, pattern classification can be performed based on the features accurately found in many images. However, in this study, we selected FDs as the feature quantity, which is an excellent indicator to quantify the natural products [<xref ref-type="bibr" rid="scirp.121376-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.121376-ref24">24</xref>]. Although less accurate, patterns segmented by MT and CH may have been an excellent indicator to extract more of the inherent fractal nature.</p><p>CNN-based pathology testing devices are being developed. However, it seems that with little supervised data, there will inevitably be individual differences [<xref ref-type="bibr" rid="scirp.121376-ref27">27</xref>]. This mechanism may be useful when using a small number of data.</p><p>In the future, by increasing the number of samples to analyze, we would like to investigate the bifurcation point when a skillful combination of machine learning is more advantageous for classification than applying prepared features, as we have investigated in this study. We believe this would provide a more detailed glimpse into machine learning’s superiority limitation.</p></sec><sec id="s5"><title>Acknowledgements</title><p>We thank to Prof. K. Osaki and Prof. T. Morimoto for their helpful comments.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Murakishi, M. and Shoji, H. (2022) Comparative Study of Segmentation Methods of Rat Sinusoidal Network to Evaluate Nonalcoholic Steatohepatitis for Small Number of Medical Samples. Journal of Biosciences and Medicines, 10, 192-202. https://doi.org/10.4236/jbm.2022.1011015</p></sec></body><back><ref-list><title>References</title><ref id="scirp.121376-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Dooley, J.S., Lok, A.S.F., Burroughs, A.K. and Heathcote, E.J. (2002) Sherlock’s Diseases of the Liver and Biliary System. 7th Edition, Wiley-Blackwell, Hoboken.</mixed-citation></ref><ref id="scirp.121376-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Oda, M., Yokomori, H. and Han, J.Y. 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