我们谨此致谢, 并感谢贝勒医学院的瑞王和华邱提供 cryoET 数据集和来自钻石光源的安德鲁 Bodey, 帮助 I13 beamtime。这项研究的部分得到了国家卫生研究院 (NIH) 赠款 No. (P41GM103832) 的支持, 我们承认钻石光源为 Imanol Luengo 在博士 STU0079 下共同出资。

注意: 对于每个处理步骤, 通常有用的参数范围以及此处显示的每个数据类型的特定参数都在 表 1 中提供. 
 1. 准备工作区和加载数据 <ol> <li> 启动 SuRVoS 工作台, 单击 "打开数据集" 按钮, 然后在结果弹出式菜单中选择要分段的数据文件。选择数据集的适当方向。接下来, 选择或创建一个将存储工作区和相关文件的文件夹。建议在开始新的分段时此文件夹为空。加载数据后, 工作台将在左侧的 "插件" 窗格、右侧的可视化窗格和两个窗格之间的一组工具快捷方式 ( 图 1 ) 中打开. </li>
</ol> 2。预处理和数据表示 <ol> <li> 在 "选择 ROI" 选项卡中, 输入感兴趣区域的 z、y 和 x 开始和结束坐标, 然后单击 "添加"。要选择合适的 y, x 坐标将鼠标悬停在图像上的某个点上。使用可视化窗格顶部的滑块选择 z 坐标。添加区域后, 请确保选中此复选框。将对所选区域执行所有下游计算。通常, 从一个小的、有代表性的感兴趣区域 (ROI) 开始, 优化参数, 然后应用这些参数到要分段的整个区域. </li>
	<li> 在 "功能通道" 选项卡中, 使用顶部的下拉菜单选择功能/筛选并将其添加到队列中 (有关功能通道的更多信息, 请参见讨论)。通过单击其名称来添加和选择功能/筛选器后, 修改特定于功能/筛选器的选项, 然后选择要在其上运行功能/筛选器的输入数据集。选择所有选项后, 单击功能/筛选器名称右侧的复选框以进行计算。
	<ol> <li> 为了优化新数据集的参数, 请添加多个筛选器/功能, 然后为它们选择参数, 然后再按顺序计算, 一个接着一个。为此, 请添加每个新的筛选器/功能并选择适当的参数, 选中每个要运行的筛选器/功能左侧的复选框, 然后单击窗格顶部的 "计算功能" 框。有关其他信息, 请参见讨论. </li>
	</ol> </li> </ol> 3。生成适当的超级区域 <ol> <li> 在 "超级区域" 选项卡的 "Supervoxels" 部分中, 使用 "源" 下拉菜单选择要从中创建 Supervoxels 的筛选数据集。然后指定 supervoxels 的形状、间距和紧凑性 (有关详细信息, 请参阅讨论和 图 2 )。最后, 单击 "应用" 按钮以生成 supervoxels。一旦创建了 supervoxels, 它们就可以在可视化窗格中查看、打开或关闭, 并在可视化选项卡和查看器窗口快捷方式中控制其透明度. </li>
	<li> 在 "超级区域" 选项卡的 "Megavoxels" 部分中, 使用 "源" 下拉菜单选择要从中创建 Megavoxels 的筛选数据集。接下来, 指定 megavoxels 的 lambda、numBins 和伽玛参数 (有关详细信息, 请参阅讨论)。一旦创建了 megavoxels, 它们就可以在可视化窗格中查看、打开或关闭, 并在可视化选项卡和查看器窗口快捷方式中控制其透明度. </li>
</ol> 4。注释的简介 <ol> <li> 在批注选项卡中使用 "添加级别" 按钮添加批注级别。添加了级别后, 请使用该级别的 "添加标签" 按钮为批注添加标签。添加后, 可以修改标签的名称和颜色, 以便于批注. </li>
	<li> 下一步, 为了开始注释, 请从工具快捷方式部分中选择钢笔图标。选中此选项时, 将在可视化窗格的顶部显示一组选择。这些选项控制钢笔宽度, 以及体、supervoxels 或 megavoxels 是否用于批注。
	<ol> <li> 为了进行模型训练, 通常应在 "注释级别" 下拉框中选择 "supervoxels", 并使用中等到大的钢笔宽度。在 "批注" 选项卡中, 通过选中标签信息的最右边框, 选择要批注的标签。接下来, 在可视化窗格中单击以批注单个 supervoxel, 或单击并拖动以注释许多. 
		注意: 可以在 "注释级别" 下拉框中选择体和 megavoxels, 并用相同的方式进行批注, 在 megavoxels 的情况下, 可以通过单击鼠标来使许多类似的体被分割. </li>
	</ol> </li> </ol> 5。使用 microCT 数据集演示的模型训练进行分割. 
 注意: 许多数据集的第一个分割是区分多个大区域。例如, 将细胞核从细胞质中分离出来, 或者从外部的冰层和支撑结构中剥离出细胞。对于这种类型的分割, 有明确划定的边界和大区域, 模型训练是有用的。为了证明这一点, 将使用草的 X 射线相衬层析数据. 
<ol> <li> 加载数据, 使用筛选器和功能套件进行预处理, 并根据上述各节中的说明, 使用 表 1 中的参数确定适当的 supervoxels 和/或 megavoxels 作为指南。继续使用 表 1 中的参数和4节中的说明, 大致注释了数据集的一些大区域, 如 图 3 所示. 
	注意: 此时不需要完全分割数据集. </li>
	<li> 在 "模型训练" 选项卡中, 将预测级别设置为包含手动培训批注的级别, 在描述符部分将该区域设置为 Supervoxels。接下来, 选择要用于区分数据区域的描述符, 方法是单击 "选择源" 下拉列表, 然后检查选项的功能和筛选器的框 (请参见 表 1 和讨论). </li>
	<li> 下一步, 单击预测按钮。计算完成后, 将用对所有 non-labeled 体的预测来更新可视化窗格, 以显示它们预计属于哪些注释类。通常, 每个分类器方法的默认参数都提供一个良好的起点, 用户只需在分类器之间切换, 就可以找到合适的。但是, 对于专家或有经验的用户, 每个分类器的选项都可用, 并且可以修改. </li>
	<li> 在评估培训方法的效果并选择一个后, 通过单击 "细化" 部分中的 "细化" 下拉列表, 应用其他细化。在 "模型训练" 选项卡的底部, 在 "#34" 中; 更新批注和 #34; 节中, 确保将可视化下拉菜单设置为 Predictions.使用 "可信度" 滑块将或多或少的 unannotated supervoxels 分配给所选的批注标签. </li>
	<li> 根据视觉检查选择了适当的置信级别后, 使用置信度工具底部的标签旁边的 save 按钮将预测保存到特定的标签中。可视化窗格将更新以显示更改。每个标签都可以单独保存, 实际上, 可以通过在 "从" 和 "z"、"y" 和 "x" 框中输入值并单击每个标签的 "保存" 按钮, 从较小的分区中保存标签. </li>
	<li> 通过提供4节所述的进一步培训数据来处理次要标签。在标签中添加适当的预测后, 在没有未标记的 supervoxels 的情况下, 重复进行模型训练和细化并添加高置信度预测的过程。这是有效的, 因为每次运行模型培训过程时, 都有更多的分配 supervoxels 来进行训练, 因此随着迭代的增加, 该过程变得更加健壮. </li>
</ol> 6。使用超级区域进行分割, 用 CryoET 数据集演示. 
 注意: 由于超级区域分割对较小的、离散的边界区域很有用, 因此这里的焦点将放在这个数据集内的细胞器和微管的分割上。模型训练用于快速地从背景冰和碳中分割血小板;这些参数不会进一步讨论, 但在 表 1 中介绍. 
<ol> <li> 加载数据, 使用筛选器和功能套件进行预处理, 并根据上述各节中的说明, 使用 表 1 中的参数确定适当的 supervoxels 和/或 megavoxels 作为参考. </li>
	<li> 将适当的级别和标签添加到 "批注" 选项卡中, 选择一个标签, 并使用 supervoxels 选定的中等钢笔宽度开始注释。注意需要为对象选择不同的标签, 以便避免将它们标记为单个对象. </li>
	<li> 为了进一步清理注释, 请使用形态学细化方法 (膨胀、侵蚀、打开、闭合和填充孔)。这些选项可以在 "批注" 选项卡的底部找到。要使用它们, 请选择分割标签和细化方法。输入半径值并选择如何应用细化。然后单击 "优化". </li>
</ol> 7。基于固有特征的数据对象的分类和分析, 用 CryoSXT 数据集演示 注意: 通常, 分段后的下一步是对数据进行分析。SuRVoS 中的标签拆分工具允许使用基于对象的固有特征 (如平均对象强度、方差、体积或位置) 的规则对分段对象进行分类。标签统计工具允许对每个新对象类的这些度量之间的关系进行可视化。这些是对复杂的3D 数据集进行分割后分析的强大的新工具. 
<ol> <li> 加载数据, 使用筛选器和功能套件进行预处理, 使用 表 1 中的参数确定适当的 supervoxels 和/或 megavoxels 和分段, 如上节所述. </li>
	<li> 分割后, 单击可视化窗格 (称为 "标签拆分器") 的第二个选项卡。这将在窗口的右侧添加一个新区域-规则创建窗格. </li>
	<li> 在该区域的顶部, 为标签拆分选择适当的级别和标签。然后选择要查询的数据集, 然后单击 "标签"。选定标签中的所有对象现在将以蓝色作为单独的对象在可视化窗格中进行分级, 并且显示对象的平均强度的图形将在 "规则创建" 窗格中出现。若要更改在绘图中显示的度量值, 请单击右侧顶部的下拉框. </li>
	<li> 若要开始将对象拆分为相关的类, 请单击 "规则创建" 窗格底部的 "添加新标签"。与此新标签关联的名称和颜色可以按照前面的说明进行更改。
	<ol> <li> 单击 "添加新规则", 并使用下拉式和 "任意多边形" 词条框定义要应用的规则。单击 "应用" 以查看 "可视化" 窗格中新规则的效果以及 "规则创建" 窗格中的绘图。可以将多个规则应用于单个标签, 并且可以在同一数据集中创建多个标签. 
		注意: 为了收集任何未标记的对象, 请创建一个新标签, 而不是向其添加规则, 单击 "选择其他". </li>
	</ol> </li> <li> 当感兴趣的对象被拆分为新标签时, 在 "批注" 选项卡中创建一个新的空级别。然后在 "规则创建" 选项卡中选择此级别, 然后单击 "保存标签"。这将将新标签保存到此空级别. </li>
	<li> 在可视化窗格的边缘上, 单击 "标签统计信息" 选项卡。这将打开一个新的可视化窗格, 可用于开始了解数据中的对象类之间的关系。在顶部, 选择适当的级别和标签, 以及要查询的数据集。
	<ol> <li> 通过选中它们旁边的框来选择一些感兴趣的度量值。然后单击 "标签"。这将为每个选定的度量值生成配对的比较图。若要更新绘图, 请选择或取消选中相应的度量值, 然后单击 "更新绘图". </li>
	</ol> </li> </ol> 8。导出数据和分割 <ol> <li> 在可视化窗格的 "标签统计" 选项卡中分别单击导出绘图和导出数据, 导出绘图和原始测量数据. </li>
	<li> 通过单击 "插件" 窗格中的 "导出" 选项卡导出图像数据和分割。首先, 单击以选择要保存数据的文件夹。接下来, 选择输出 (原始数据、原始注释、分割掩码或屏蔽数据) 和格式 (HDF5、湄公河和 TIFF)。最后, 选择要使用复选框导出的批注级别, 然后单击 "导出"。在必要时, 可以在导出之前缩放和反转数据。导出蒙版数据时, 可以使用下拉菜单选择掩码 (s) 将应用到的数据集. </li>
</ol>

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作者宣布, 他们没有竞争的金融利益。

SuRVoS 工作台不同于其他的分割程序, 参数的优化是在开始实际分割之前的一个必要的重要步骤。在一些手动或半的分段程序中, 用户开始在打开一个新项目的时候进行分段。与 SuRVoS, 因为大量的体积将被分割, 很少用户输入和边界由程序划定, 优化参数是关键的成功的分割。具体而言, 特色频道和 super-region 建设是两个值得注意的领域。
特征通道与模型训练
除了原始数据之外, SuRVoS 允许用户创建从现有数据集派生的其他数据集或通道。这些通道可以通过选择计算方法或特征提取器来创建。每个数据表示都是并行的, 可以单独显示, 以评估功能或筛选应用程序的结果。由于这些特性, 它们被称为 SuRVoS 中的特征通道。SuRVoS 中提供了许多功能频道选项。有关此处使用的选项和参数的信息, 请参见表 1, 以获取可用功能通道的完整列表和说明访问 https://diamondlightsource.github.io/SuRVoS/ 2。首先, 噪声数据集将受益于高斯或全变滤波器的去噪。建议使用这些噪数据源之一来执行进一步的功能通道和 supervoxel/megavoxel 计算。一般情况下, 噪数据集的总变体被用作特征信道和 supervoxel/megavoxel 计算的源数据。建议先使用默认值运行, 然后在3D 中评估结果, 最后对数据集的参数进行迭代优化。此外, 功能通道可以被构建成 "过滤器集", 专门隔离数据集的各个方面, 然后可以用作数据源来创建 supervoxels 和 megavoxels。虽然此策略高度依赖于数据集, 但它可能是有益的。
在模型训练中, 特征信道也被用作训练分类器的来源。在决定使用哪些功能通道时, 建议在处理少量注释时使用一些健壮的功能通道 (例如, 从 blob 检测、纹理和结构或健壮功能类别) 来训练分类.在处理大量培训数据时, 建议从任何类别中使用更多的功能通道, 只要它们向分类器提供不同的信息 (例如, 请从本地添加到上面的列表功能通道特征和高斯特征类别)。
模型训练有三主要部分: 提供描述数据的输入数据源, 使用这些投入来训练分类器, 最后精炼输出预测。通常, 数据的较小区域需要更多的用户注释才能准确地训练分类器, 而较大的数据区域则需要较少的用户注释。在没有选择细化的情况下进行模型训练, 可以用来找到最佳的预测。然后在需要时包括细化和优化 lambda 参数, 以修复预测的问题, 如孔或锯齿边缘。
Supervoxels 和 megavoxels
Supervoxels 是多个相邻的簇, 类似的体38,39。Supervoxels 开始作为一个标准的3D 网格覆盖的数据, 然后迭代变形, 以坚持的基础边界, 从而更好地代表数据。Supervoxel 的创建和变形由四用户输入控制: 数据源、superpixel 形状、间距和紧凑性。数据源提供在 supervoxel 创建过程中查询的数据输入。任何源都可以使用, 包括已筛选的数据源。superpixel 形状参数确定起始3D 网格和所得到的 supervoxels 的近似所需形状。改变这些参数可以在变形前增加或减小 supervoxels 的大小。间距参数定义了边界在每个方向上的重要性。更改这些参数可以在一个或两个方向上强调边界, 以牺牲其他的 (s) 为代价, 这意味着结果的 supervoxels 将变形, 以便更好地遵循给定方向的数据边界。最后一个参数, 紧凑, 控制多少 supervoxels 可以变形。低紧度数使 supervoxels 变形更多。这些参数应进行优化, 以提供表示感兴趣数据边界的 supervoxels。注意: 当前, supervoxel 形状参数在相乘时必须等于或小于1024。
在某些方面, supervoxel 参数可以互相补偿, 这意味着在决定参数时没有一个 "正确的答案"。例如, 一个大的起始网格 (例如superpixel 形状:10 x 10 x 10) 和一个低紧致数 (ex 20) 可以给 supervoxels 具有类似的边界粘度, 与一个小的起始网格 (例如superpixel 形状 5 x 5 x 5) 和更高的紧凑号 (例如50)。因为在第二个场景中有更多更小的 supervoxels, 所以它们不需要变形来表示边界。这两组参数都适用于数据集的分割。
在选择 supervoxel 参数时, 最大的考虑因素是 supervoxels 如何表示数据。如图 2D所示, 单独显示 supervoxels, 而不在它们下面的数据, 是评估 supervoxel 参数的好方法。当以这种方式显示时, 数据中发现的形状的边缘和轮廓在 supervoxels 中仍然可见。
Megavoxels 是多个相邻的、类似的 supervoxels38、39的企业集团。它们再次由四用户输入控制: 数据源、lambda、numbins 和伽玛。与 supervoxels 一样, 数据源提供在 megavoxel 创建期间查询的数据输入。lambda 和 numbins 都影响 megavoxels 的大小和边界粘附。随着 megavoxels 的增大 (高λ、低 numbins), 它们的边界粘着减小。反过来也是真的, 边界加入将增加与较小的 megavoxels (低λ, 高 numbins), 但随着 megavoxel 大小的减少, 所以它们的用处, 在分割大量的体迅速。可选的伽玛参数控制平滑系数与合并两个 supervoxels 的成本。伽玛的小值可以提高两个 supervoxels 之间的相似性, 以减少 megavoxels 总体的成本。
与 supervoxels 一样, 在选择和优化 megavoxel 参数时最大的考虑因素是 megavoxels 表示数据的程度。如 supervoxels 所述, 单独显示 megavoxels 可用于评估参数。但是, 因为 megavoxels 通常会大得多, 并且是三维的, 所以使用注释工具 to 选择单一 megavoxels, 以确保区域之间的利益是紧密的边界也建议。
注释策略
描述了两个一般的注释策略: 模型训练方法对于分离数据集的大区域很有用, 而 super-region 的分割方法对于较小的、更多样化的功能 (如单个的细胞器) 是有用的。注释可以按分层方式进行组织, 以便能够首先对大区域进行注释, 然后使用父子关系将它们细分为更具体的区域。可以通过单击标签颜色选择右侧的区域并从上一个级别选择适当的父标签来分配标签的父标签。在实践中, 大多数数据集都使用模型训练和 super-region 细分策略来细分特定区域/感兴趣的特性。
在这里的模型训练示例中, 一些培训输入 (以手动用户 supervoxel-based 注释的形式) 在数据的三个等距切片上使用。通过这种方式, SuRVoS 的模型训练方面大大提高了分割的速度, 特别是当处理大的, 区分的区域, 如在草子实体的区域之间的鸿沟, 如在图 3。
当模型训练时, 如果无法看到预测, 则可能需要转到 "可视化" 选项卡, 并确保预测层已打开并设置为适当的透明度。此外, 0 的信心将分配每个未标记的 supervoxel 到一个标签, 根据任何最接近的匹配。如果只有一个标签类别有任何比例匹配, 那么100的置信度只会分配一个标签。介于两者之间的一切都是这两个极端的权衡。在选择置信度时, 建议检查几个切片以直观地检查在将预测保存到标签之前没有错误预测的体。
使用 super-regions 进行注释的一个好策略是使用放大工具来放大数据, 在一个切片上同时使用 "快速、凌乱" 的方法 (图 4C) 对一些细胞器进行注释。接下来, 在 Z 中向上或向下移动几个切片, 然后重复此过程。因为 supervoxels 是三维的, 所以 "凌乱" 方法的许多错误都是由上面或下面切片中的注释来确定的。这样, 分割速度加快, 边界由 supervoxels 而不是手动提供。
为了清除标签, 提供了标准的细分细化选项。膨胀导致所选的分割标签在给定半径下增长, 侵蚀导致它收缩。开闭是第一次侵蚀的应用, 然后是扩张, 反之亦然。和填充孔正是这样。这些操作的顺序很重要。一般情况下, 执行填充孔, 然后打开, 然后膨胀工作很好。每个细化方法都可以应用于单个切片 ("此切片")、2D 中的所有切片 ("所有切片 (2D)") 或 3D ("整卷 (3D)")。建议所有切片 (2D)。
意义和未来方向
高效而准确的分割是处理3D 数据集的下一个瓶颈, 特别是在长期会话中自动收集数 tb 的图像数据。与手工分割相比, SuRVoS 工作台可以将分割过程的速度提高5倍。此外, 由于边界是由 supervoxels 划定的, 因此产生的分割的变异性应该提高。在未来, 我们希望探讨如何使用一个代表性的3D 区域的兴趣作为培训数据, 以适用于其余的卷, 甚至是一个单独的卷, 具有高度的信心。这一进步将进一步减少用户的时间和投入所需的数量, 即使是复杂的生物量, 帮助缓解图像处理和分割瓶颈。这反过来, 将允许定量比较的生物数据在不同的状态 (如病区, 疾病, 治疗) 与强大的实验数字。

SuRVoS 工作台是一款软件, 旨在让研究人员从各种样本的体积数据中获取科学的相关信息, 而不管感兴趣的结构、分辨率或成像模式1, 2。体积数据, 如这些通常是收集使用 X 射线或电子断层扫描系统, 常规的基础在大型实验室或集中设施, 由于其复杂性。这两种方法, 以及其他技术, 产生了大量的信息丰富的数据集, 这证明了用半自动方法或手工进行分段是有挑战性的。特别是, 近原生状态的低温固定化的数据集需要低剂量的成像条件, 导致较低的信噪比和较差的对比, 特别是在低温电子断层扫描 (cryoET)3,4,5.在一些3D 数据集中的一个附加因素是所涉及的具有挑战性的实验条件所引入的工件的存在, 例如, 由于数据收集在一个有限的倾斜范围, 导致缺少信息和延伸方向为光束3,4,5。即使低信噪比或缺少楔形工件是不成问题的 (如聚焦离子束 sem6或串行块面扫描电镜7), 样品的复杂性和三维性质, 以及大量的数据平均值分析仍然得益于自动化的数据分割过程。
目前, 在考虑细胞的生物体积, 有许多选择自动或半自动识别非常具体的细胞功能, 如肌动蛋白, 微管, 或特定的蛋白质复合物, 使用基于模板的搜索,或识别特定类型数据集的特征 (例如高对比度、着色、树脂嵌入样本)8、9、10、11、12。但是, 在这些情况下,先验信息或特定的示例准备协议是必需的, 这限制了这些细分策略的广泛适用性。还有一些工具可以在体素级别执行模型训练, 以便在给定用户输入13时了解各种感兴趣结构的外观。然而, 在这个层次上, 培训和测试模型的复杂性可能是容易出错和计算成本高昂的。鉴于具有挑战性的图像条件, 以及缺乏广泛适用, 半自动分割策略, 手工分割是常见的, 即使在使用复杂的生物材料14,15,16,17. 然而, 人们普遍认为, 手工分割的过程不仅耗时, 而且容易出错, 主观和可变的4,5,18,19 ,20。一些分割程序提供了一些工具来简化手工分割过程 (即插值, 套索, 或吹工具)21,22, 但是, 在嘈杂数据集的情况下, 它们很难成功应用,即使使用成功, 该过程仍然是主观的和可变的。
传统上, 分割的使用有两种截然不同的方式: 定性或定量。随着成像技术和分割策略的提高, 将分割作为一种定量的工具来回答生物问题和作为算法开发的 "基础真相" 变得更加普遍了8,12, 15、23、24、25。为了做到这一点, 需要进行详细的检查和平衡, 以便在整个过程26中减少可变性和主观性。然而, 这些预防措施进一步增加了分割的耗时性。因此, 提供更快、更少的变量分割策略至关重要。
SuRVoS 工作台开始解决这些问题, 为用户提供了一系列的机器学习和图像处理工具, 帮助用户进行分段处理, 同时还引导用户完成所需的步骤。为了实现这一目标, 在 SuRVoS 中共同实施了两个关键的创新。首先, 它使用 super-region 的层次结构, 根据其固有的属性对数据的相似的邻近区域进行分组。层次结构中的每个区域都使用较少的元素表示相同的卷, 同时仍然提供强大的边界粘附。因此, super-regions 降低了将一个卷分割成几个数量级的复杂性, 但仍然表示数据, 而没有明显的信息丢失27。其次, SuRVoS 提供了一种半自动的分割策略, 它使用最小的手工分割输入来训练分类器, 然后用于分段剩余的卷28,29。这种策略减少了手工分割, 大大减少了用户在分段上花费的时间, 并且, 在使用 super-regions 时, 删除了手工划定的边界, 有可能减少可变性和主观性。
SuRVoS 的另一个关键特性是标签拆分工具, 用户可以根据其固有的属性对一系列已经分段的对象进行分类。在对各种感兴趣对象进行分割后, 该工具可用于根据平均对象强度、方差、大小、位置、等度量值将集合划分为子类. 在将大型对象组分类时, 这很有用。高复杂性。例如, 一组细胞器可以分为线粒体, 空泡, 脂滴等;或一组材料的夹杂物可以根据大小或形状分开。一旦分割了单个标签, 就可以使用任意数量的分类器将其分割成组, 从而减少识别偏差。
SuRVoS 工作台已成功地用于从几种成像技术中分割数据。在这里, 植物的果体的同步辐射 X 射线相衬层析 (microCT) 被用来证明 segmentati在使用模型训练时, 人血小板的低温电子断层扫描 (cryoET) 用于演示使用 super-and megavoxels 的分割, 而哺乳动物细胞系的低温软 X 射线断层扫描 (cryoSXT) 则用于演示标签分裂工具

<table><tbody><tr><td>computer</td><td>n/a</td><td>n/a</td><td>Must be running Linux operating system and have an NVidia GPU with at least 4 GB of memory</td></tr></tbody></table>

volume segmentation and analysis of biological materials using survos (super-region volume segmentation) workbench

分割是将特定区域或对象隔离在一个成像的体积内, 以便对这些感兴趣的领域进行进一步研究。在考虑复杂生物系统的分析时, 三维图像数据的分割是一项费时费力的劳动密集型步骤。随着许多成像模式的可用性和自动化数据收集方案的增加, 这对现代实验生物学家从数据到知识的迁移提出了更大的挑战。本出版物描述了 SuRVoS 工作台的使用, 这是一个旨在解决这些问题的程序, 它为半自动段复杂的生物体积数据提供了方法。这里介绍了三不同放大率和成像方式的数据集, 每种方法都突出了与 SuRVoS 的分割策略。植物的子实体的相衬 X 射线断层扫描 (microCT) 用于演示使用模型训练的分割, 人血小板的低温电子断层扫描 (cryoET) 用于演示使用 super-and megavoxels 的分割, 以及低温软X 射线断层扫描 (cryoSXT) 的哺乳动物细胞线是用来证明的标签分裂工具。还介绍了每个数据类型的策略和参数。通过将选择的半自动过程混合成一个单一的交互式工具, SuRVoS 提供了一些好处。与手工分割相比, 在许多图像处理领域中, 总体时间段的体积数据减少了五倍。这是一个重要的节省, 当全手工分割可能需要数周的努力。此外, 主观性是通过使用计算确定的边界来解决的, 并通过它们的运算属性而不是逐例地分解复杂的对象集合。

Watch this Scientific Journal Video about Volume Segmentation and Analysis of Biological Materials Using SuRVoS Super-region Volume Segmentation Workbench at JoVE.com

Volume Segmentation and Analysis of Biological Materials Using SuRVoS Super-region Volume Segmentation Workbench

利用 SuRVoS (超区域体积分割) 工作台进行生物材料的体积分割与分析

从许多成像技术中分割三维数据是复杂生物系统分析的一个主要瓶颈。在这里, 我们描述了使用 SuRVoS 工作台, 以半自动段体积数据在不同长度尺度使用的例子数据集从低温电子断层扫描, 低温软 x 射线断层扫描, 和相衬 x 射线断层扫描技术。

Segmentation is the process of isolating specific regions or objects within an imaged volume, so that further study can be undertaken on these areas of ...

volume-segmentation-analysis-biological-materials-using-survos-super

Nanyang Technological University

Research

JoVE Journal

Biology

Volume Segmentation and Analysis of Biological Materials Using SuRVoS (Super-region Volume Segmentation) Workbench

9.7K 次观看.  Diamond Light Source. 从许多成像技术中分割三维数据是复杂生物系统分析的一个主要瓶颈。在这里, 我们描述了使用 SuRVoS 工作台, 以半自动段体积数据在不同长度尺度使用的例子数据集从低温电子断层扫描, 低温软 x 射线断层扫描, 和相衬 x 射线断层扫描技术。

视频: Volume Segmentation and Analysis of Biological Materials Using SuRVoS Super-region Volume Segmentation Workbench

From Voxels to Knowledge: A Practical Guide to the Segmentation of Complex Electron Microscopy 3D-Data

Modern 3D electron microscopy approaches have recently allowed unprecedented insight into the 3D ultrastructural organization of cells and tissues, enabling the visualization of large macromolecular machines, such as adhesion complexes, as well as higher-order structures, such as the cytoskeleton and cellular organelles in their respective cell and tissue context. Given the inherent complexity of cellular volumes, it is essential to first extract the features of interest in order to allow visualization, quantification, and therefore comprehension of their 3D organization. Each data set is defined by distinct characteristics, e.g., signal-to-noise ratio, crispness (sharpness) of the data, heterogeneity of its features, crowdedness of features, presence or absence of characteristic shapes that allow for easy identification, and the percentage of the entire volume that a specific region of interest occupies. All these characteristics need to be considered when deciding on which approach to take for segmentation.
The six different 3D ultrastructural data sets presented were obtained by three different imaging approaches: resin embedded stained electron tomography, focused ion beam- and serial block face- scanning electron microscopy (FIB-SEM, SBF-SEM) of mildly stained and heavily stained samples, respectively. For these data sets, four different segmentation approaches have been applied: (1) fully manual model building followed solely by visualization of the model, (2) manual tracing segmentation of the data followed by surface rendering, (3) semi-automated approaches followed by surface rendering, or (4) automated custom-designed segmentation algorithms followed by surface rendering and quantitative analysis. Depending on the combination of data set characteristics, it was found that typically one of these four categorical approaches outperforms the others, but depending on the exact sequence of criteria, more than one approach may be successful. Based on these data, we propose a triage scheme that categorizes both objective data set characteristics and subjective personal criteria for the analysis of the different data sets.

The bottleneck for cellular 3D electron microscopy is feature extraction (segmentation) in highly complex 3D density maps. We have developed a set of criteria, which provides guidance regarding which segmentation approach (manual, semi-automated, or automated) is best suited for different data types, thus providing a starting point for effective segmentation.

从体素知识:实用指南复电镜三维数据的分割

Modern 3D electron microscopy approaches have recently allowed unprecedented insight into the 3D ultrastructural organization of cells and tissues, ...

科研

生物工程

A Label-Free Segmentation Approach for Intravital Imaging of Mammary Tumor Microenvironment

The ability to visualize complex and dynamic physiological interactions between numerous cell types and the extracellular matrix (ECM) within a live tumor microenvironment is an important step toward understanding mechanisms that regulate tumor progression. While this can be accomplished through current intravital imaging techniques, it remains challenging due to the heterogeneous nature of tissues and the need for spatial context within the experimental observation. To this end, we have developed an intravital imaging workflow that pairs collagen second harmonic generation imaging, endogenous fluorescence from the metabolic co-factor NAD(P)H, and fluorescence lifetime imaging microscopy (FLIM) as a means to non-invasively compartmentalize the tumor microenvironment into basic domains of the tumor nest, the surrounding stroma or ECM, and the vasculature. This non-invasive protocol details the step-by-step process ranging from the acquisition of time-lapse images of mammary tumor models to post-processing analysis and image segmentation. The primary advantage of this workflow is that it exploits metabolic signatures to contextualize the dynamically changing live tumor microenvironment without the use of exogenous fluorescent labels, making it advantageous for human patient-derived xenograft (PDX) models and future clinical use where extrinsic fluorophores are not readily applicable.

The intravital imaging method described here utilizes collagen second harmonic generation and endogenous fluorescence from the metabolic co-factor NAD(P)H to non-invasively segment an unlabeled tumor microenvironment into tumor, stromal, and vascular compartments for in-depth analysis of 4D intravital images.

一种用于乳腺肿瘤微环境活体内成像的无标记分割方法

The ability to visualize complex and dynamic physiological interactions between numerous cell types and the extracellular matrix (ECM) within a live tumor ...

癌症研究

Three and Four-Dimensional Visualization and Analysis Approaches to Study Vertebrate Axial Elongation and Segmentation

Somitogenesis is a hallmark of vertebrate embryonic development. For years, researchers have been studying this process in a variety of organisms using a wide range of techniques encompassing ex vivo and in vitro approaches. However, most studies still rely on the analysis of two-dimensional (2D) imaging data, which limits proper evaluation of a developmental process like axial extension and somitogenesis involving highly dynamic interactions in a complex 3D space. Here we describe techniques that allow mouse live imaging acquisition, dataset processing, visualization and analysis in 3D and 4D to study the cells (e.g., neuromesodermal progenitors) involved in these developmental processes. We also provide a step-by-step protocol for optical projection tomography and whole-mount immunofluorescence microscopy in mouse embryos (from sample preparation to image acquisition) and show a pipeline that we developed to process and visualize 3D image data. We extend the use of some of these techniques and highlight specific features of different available software (e.g., Fiji/ImageJ, Drishti, Amira and Imaris) that can be used to improve our current understanding of axial extension and somite formation (e.g., 3D reconstructions). Altogether, the techniques here described emphasize the importance of 3D data visualization and analysis in developmental biology, and might help other researchers to better address 3D and 4D image data in the context of vertebrate axial extension and segmentation. Finally, the work also employs novel tools to facilitate teaching vertebrate embryonic development.

Here, we describe computational tools and methods that allow visualization and analysis of three and four-dimensional image data of mouse embryos in the context of axial elongation and segmentation, obtained by in toto optical projection tomography, and by live imaging and whole-mount immunofluorescence staining using multiphoton microscopy.

研究脊椎动物轴向伸长和分割的三维和四维可视化分析方法

Somitogenesis is a hallmark of vertebrate embryonic development. For years, researchers have been studying this process in a variety of organisms using a ...

发育生物学

Substructure Analyzer: A User-Friendly Workflow for Rapid Exploration and Accurate Analysis of Cellular Bodies in Fluorescence Microscopy Images

The last decade has been characterized by breakthroughs in fluorescence microscopy techniques illustrated by spatial resolution improvement but also in live-cell imaging and high-throughput microscopy techniques. This led to a constant increase in the amount and complexity of the microscopy data for a single experiment. Because manual analysis of microscopy data is very time consuming, subjective, and prohibits quantitative analyses, automation of bioimage analysis is becoming almost unavoidable. We built an informatics workflow called Substructure Analyzer to fully automate signal analysis in bioimages from fluorescent microscopy. This workflow is developed on the user-friendly open-source platform Icy and is completed by functionalities from ImageJ. It includes the pre-processing of images to improve the signal to noise ratio, the individual segmentation of cells (detection of cell boundaries) and the detection/quantification of cell bodies enriched in specific cell compartments. The main advantage of this workflow is to propose complex bio-imaging functionalities to users without image analysis expertise through a user-friendly interface. Moreover, it is highly modular and adapted to several issues from the characterization of nuclear/cytoplasmic translocation to the comparative analysis of different cell bodies in different cellular sub-structures. The functionality of this workflow is illustrated through the study of the Cajal (coiled) Bodies under oxidative stress (OS) conditions. Data from fluorescence microscopy show that their integrity in human cells is impacted a few hours after the induction of OS. This effect is characterized by a decrease of coilin nucleation into characteristic Cajal Bodies, associated with a nucleoplasmic redistribution of coilin into an increased number of smaller foci. The central role of coilin in the exchange between CB components and the surrounding nucleoplasm suggests that OS induced redistribution of coilin could affect the composition and the functionality of Cajal Bodies.

We present a freely available workflow built for rapid exploration and accurate analysis of cellular bodies in specific cell compartments in fluorescence microscopy images. This user-friendly workflow is designed on the open-source software Icy and also uses ImageJ functionalities. The pipeline is affordable without knowledge in image analysis.

子结构分析仪:用于荧光显微镜图像中细胞体快速探索和精确分析的用户友好型工作流程

The last decade has been characterized by breakthroughs in fluorescence microscopy techniques illustrated by spatial resolution improvement but also in ...

Whole-brain Segmentation and Change-point Analysis of Anatomical Brain MRI&#8212;Application in Premanifest Huntington's Disease

Recent advances in MRI offer a variety of useful markers to identify neurodegenerative diseases. In Huntington&#39;s disease (HD), regional brain atrophy begins many years prior to the motor onset (during the &#34;premanifest&#34; period), but the spatiotemporal pattern of regional atrophy across the brain has not been fully characterized. Here we demonstrate an online cloud-computing platform, &#34;MRICloud&#34;, which provides atlas-based whole-brain segmentation of T1-weighted images at multiple granularity levels, and thereby, enables us to access the regional features of brain anatomy. We then describe a regression model that detects statistically significant inflection points, at which regional brain atrophy starts to be noticeable, i.e. the &#34;change-point&#34;, with respect to a disease progression index. We used the CAG-age product (CAP) score to index the disease progression in HD patients. Change-point analysis of the volumetric measurements from the segmentation pipeline, therefore, provides important information of the order and pattern of structural atrophy across the brain. The paper illustrates the use of these techniques on T1-weighted MRI data of premanifest HD subjects from a large multicenter PREDICT-HD study. This design potentially has wide applications in a range of neurodegenerative diseases to investigate the dynamic changes of brain anatomy.

This paper describes a statistical model for volumetric MRI data analysis, which identifies the &#34;change-point&#34; when brain atrophy begins in premanifest Huntington&#39;s disease. Whole-brain mapping of the change-points is achieved based on brain volumes obtained using an atlas-based segmentation pipeline of T1-weighted images.

解剖性脑 MRI 的全脑分割及变化点分析--Premanifest 亨廷顿病的应用

Recent advances in MRI offer a variety of useful markers to identify neurodegenerative diseases. In Huntington&#39;s disease (HD), regional brain atrophy ...

医学

A Method for 3D Reconstruction and Virtual Reality Analysis of Glial and Neuronal Cells

Serial sectioning and subsequent high-resolution imaging of biological tissue using electron microscopy (EM) allow for the segmentation and reconstruction of high-resolution imaged stacks to reveal ultrastructural patterns that could not be resolved using 2D images. Indeed, the latter might lead to a misinterpretation of morphologies, like in the case of mitochondria; the use of 3D models is, therefore, more and more common and applied to the formulation of morphology-based functional hypotheses. To date, the use of 3D models generated from light or electron image stacks makes qualitative, visual assessments, as well as quantification, more convenient to be performed directly in 3D. As these models are often extremely complex, a virtual reality environment is also important to be set up to overcome occlusion and to take full advantage of the 3D structure. Here, a step-by-step guide from image segmentation to reconstruction and analysis is described in detail.

The described pipeline is designed for the segmentation of electron microscopy datasets larger than gigabytes, to extract whole-cell morphologies. Once the cells are reconstructed in 3D, customized software designed around individual needs can be used to perform a qualitative and quantitative analysis directly in 3D, also using virtual reality to overcome view occlusion.

胶质细胞和神经细胞的三维重建与虚拟现实分析方法

Serial sectioning and subsequent high-resolution imaging of biological tissue using electron microscopy (EM) allow for the segmentation and reconstruction ...

神经科学

Workflow for High-content, Individual Cell Quantification of Fluorescent Markers from Universal Microscope Data, Supported by Open Source Software

Advances in understanding the control mechanisms governing the behavior of cells in adherent mammalian tissue culture models are becoming increasingly dependent on modes of single-cell analysis. Methods which deliver composite data reflecting the mean values of biomarkers from cell populations risk losing subpopulation dynamics that reflect the heterogeneity of the studied biological system. In keeping with this, traditional approaches are being replaced by, or supported with, more sophisticated forms of cellular assay developed to allow assessment by high-content microscopy. These assays potentially generate large numbers of images of fluorescent biomarkers, which enabled by accompanying proprietary software packages, allows for multi-parametric measurements per cell. However, the relatively high capital costs and overspecialization of many of these devices have prevented their accessibility to many investigators.
Described here is a universally applicable workflow for the quantification of multiple fluorescent marker intensities from specific subcellular regions of individual cells suitable for use with images from most fluorescent microscopes. Key to this workflow is the implementation of the freely available Cell Profiler software1&#160;to distinguish individual cells in these images, segment them into defined subcellular regions and deliver fluorescence marker intensity values specific to these regions. The extraction of individual cell intensity values from image data is the central purpose of this workflow and will be illustrated with the analysis of control data from a siRNA screen for G1 checkpoint regulators in adherent human cells. However, the workflow presented here can be applied to analysis of data from other means of cell perturbation (e.g., compound screens) and other forms of fluorescence based cellular markers and thus should be useful for a wide range of laboratories.

Presented is a flexible informatics workflow enabling multiplexed image-based analysis of fluorescently labeled cells. The workflow quantifies nuclear and cytoplasmic markers and computes marker translocation between these compartments. Procedures are provided for perturbation of cells using siRNA and reliable methodology for marker detection by indirect immunofluorescence in 96-well formats.

工作流的高含量，荧光标记的万能工具显微镜数据，支持开源软件的单个细胞定量

Advances in understanding the control mechanisms governing the behavior of cells in adherent mammalian tissue culture models are becoming increasingly ...

生物学

Biological Sample Preparation by High-pressure Freezing, Microwave-assisted Contrast Enhancement, and Minimal Resin Embedding for Volume Imaging

The described sample preparation technique is designed to combine the best quality of ultrastructural preservation with the most suitable contrast for the imaging modality in a focused ion beam scanning electron microscope (FIB-SEM), which is used to obtain stacks of sequential images for 3D reconstruction and modelling. High-pressure freezing (HPF) allows close to native structural preservation, but the subsequent freeze substitution often does not provide sufficient contrast, especially for a bigger specimen, which is needed for high-quality imaging in the SEM required for 3D reconstruction. Therefore, in this protocol, after the freeze substitution, additional contrasting steps are carried out at room temperature. Although these steps are performed in a microwave, it is also possible to follow traditional bench processing, which requires longer incubation times.The subsequent embedding in minimal amounts of resin allows for faster and more precise targeting and preparation inside the FIB-SEM. This protocol is especially useful for samples that require preparation by high-pressure freezing for a reliable ultrastructural preservation but do not gain enough contrast during the freeze substitution for volume imaging using FIB-SEM. In combination with the minimal resin embedding, this protocol provides an efficient workflow for the acquisition of high-quality volume data.

Here we present a protocol for combining two sample processing techniques, high-pressure freezing and microwave-assisted sample processing, followed by minimal resin embedding for acquiring data with a focused ion beam scanning electron microscope (FIB-SEM). This is demonstrated using a mouse tibial nerve sample and Caenorhabditis elegans.

高压冷冻、微波辅助对比度增强和最小树脂嵌入在体积成像中的生物样品制备

The described sample preparation technique is designed to combine the best quality of ultrastructural preservation with the most suitable contrast for the ...

Serial Block-Face Scanning Electron Microscopy (SBF-SEM) of Biological Tissue Samples

Serial block-face scanning electron microscopy (SBF-SEM) allows for the collection of hundreds to thousands of serially-registered ultrastructural images, offering an unprecedented three-dimensional view of tissue microanatomy. While SBF-SEM has seen an exponential increase in use in recent years, technical aspects such as proper tissue preparation and imaging parameters are paramount for the success of this imaging modality. This imaging system benefits from the automated nature of the device, allowing one to leave the microscope unattended during the imaging process, with the automated collection of hundreds of images possible in a single day. However, without appropriate tissue preparation cellular ultrastructure can be altered in such a way that incorrect or misleading conclusions might be drawn. Additionally, images are generated by scanning the block-face of a resin-embedded biological sample and this often presents challenges and considerations that must be addressed. The accumulation of electrons within the block during imaging, known as "tissue charging," can lead to a loss of contrast and an inability to appreciate cellular structure. Moreover, while increasing electron beam intensity/voltage or decreasing beam-scanning speed can increase image resolution, this can also have the unfortunate side effect of damaging the resin block and distorting subsequent images in the imaging series. Here we present a routine protocol for the preparation of biological tissue samples that preserves cellular ultrastructure and diminishes tissue charging. We also provide imaging considerations for the rapid acquisition of high-quality serial-images with minimal damage to the tissue block.

Serial Block-Face Scanning Electron Microscopy SBF-SEM of Biological Tissue Samples

This protocol outlines a routine method for using serial block-face scanning electron microscopy (SBF-SEM), a powerful 3D imaging technique. Successful application of SBF-SEM hinges on proper fixation and tissue staining techniques, as well as careful consideration of imaging settings. This protocol contains practical considerations for the entirety of this process.

生物组织样本的串行块面扫描电子显微镜 （SBF-SEM）

Serial block-face scanning electron microscopy (SBF-SEM) allows for the collection of hundreds to thousands of serially-registered ultrastructural images, ...

Staining and High-Resolution Imaging of Three-Dimensional Organoid and Spheroid Models

In vitro three-dimensional (3D) cell culture models, such as organoids and spheroids, are valuable tools for many applications including development and disease modeling, drug discovery, and regenerative medicine. To fully exploit these models, it is crucial to study them at cellular and subcellular levels. However, characterizing such in vitro 3D cell culture models can be technically challenging and requires specific expertise to perform effective analyses. Here, this paper provides detailed, robust, and complementary protocols to perform staining and subcellular resolution imaging of fixed in vitro 3D cell culture models ranging from 100 &#181;m to several millimeters. These protocols are applicable to a wide variety of organoids and spheroids that differ in their cell-of-origin, morphology, and culture conditions. From 3D structure harvesting to image analysis, these protocols can be completed within 4-5 days. Briefly, 3D structures are collected, fixed, and can then be processed either through paraffin-embedding and histological/immunohistochemical staining, or directly immunolabeled and prepared for optical clearing and 3D reconstruction (200 &#181;m depth) by confocal microscopy.

Here, we provide detailed, robust, and complementary protocols to perform staining and subcellular resolution imaging of fixed three-dimensional cell culture models ranging from 100 &#181;m to several millimeters, thus enabling the visualization of their morphology, cell-type composition, and interactions.

三维类器官和球状体模型的染色和高分辨率成像

In vitro three-dimensional (3D) cell culture models, such as organoids and spheroids, are valuable tools for many applications including development and ...

利用 SuRVoS (超区域体积分割) 工作台进行生物材料的体积分割与分析

摘要

探索更多视频

此视频中的章节

从体素知识:实用指南复电镜三维数据的分割

一种用于乳腺肿瘤微环境活体内成像的无标记分割方法

研究脊椎动物轴向伸长和分割的三维和四维可视化分析方法

子结构分析仪:用于荧光显微镜图像中细胞体快速探索和精确分析的用户友好型工作流程

解剖性脑 MRI 的全脑分割及变化点分析--Premanifest 亨廷顿病的应用

胶质细胞和神经细胞的三维重建与虚拟现实分析方法

工作流的高含量，荧光标记的万能工具显微镜数据，支持开源软件的单个细胞定量

高压冷冻、微波辅助对比度增强和最小树脂嵌入在体积成像中的生物样品制备

生物组织样本的串行块面扫描电子显微镜（SBF-SEM）

三维类器官和球状体模型的染色和高分辨率成像

利用 SuRVoS (超区域体积分割) 工作台进行生物材料的体积分割与分析

摘要

探索更多视频

此视频中的章节

从体素知识:实用指南复电镜三维数据的分割

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