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    • 2. 发明申请
    • Method and Device for the Reconstruction of the Shape of an Object from a Sequence of Sectional Images of Said Object
    • 用于根据所述对象的截面图像的序列重建对象的形状的方法和装置
    • US20100309304A1
    • 2010-12-09
    • US12739006
    • 2008-10-22
    • Bernard ChalmondAlain TrouveYong YuJiaping WangOlivier RenaudSpencer Shorte
    • Bernard ChalmondAlain TrouveYong YuJiaping WangOlivier RenaudSpencer Shorte
    • H04N7/18G06K9/00
    • G02B21/008G06T7/571G06T7/70G06T15/00G06T2200/04G06T2207/10056G06T2207/30024
    • A method of reconstructing the volume of an object from a sequence of section images, the images corresponding to different positions and/or orientations of an acquisition plane and being subject to uncertainties, the method comprising: a) selecting a finite base of functions on which the volume for reconstruction can be decomposed; b) selecting a first quantification function for quantizing the difference between the real position and/or orientation of each section relative to said object and its nominal position and/or orientation; c) selecting a second quantification function for quantizing the spatial coherence of the reconstructed volume; d) selecting a third quantification function for quantizing the difference between the section images of the object and the corresponding sections of the reconstructed volume; e) selecting an overall cost function, of value that depends on the values of said first, second, and third quantizing functions; and f) jointly estimating the real positions and/or orientations of the section, together with the coefficient for decomposing the image of the object on said function base, by minimizing said overall cost function.
    • 一种从部分图像序列重建物体的体积的方法,所述图像对应于采集平面的不同位置和/或取向并且受到不确定性的影响,所述方法包括:a)选择有限基础的函数, 重建体积可以分解; b)选择用于量化每个部分相对于所述物体的实际位置和/或取向与其标称位置和/或取向之间的差的第一量化功能; c)选择量化所述重建体积的空间相干性的第二量化函数; d)选择用于量化对象的截面图像和重构体积的相应部分之间的差的第三量化功能; e)选择取决于所述第一,第二和第三量化函数的值的总成本函数; 以及f)通过使所述总体成本函数最小化来共同估计所述部分的实际位置和/或取向以及用于分解所述功能基础上的对象的图像的系数。
    • 3. 发明申请
    • Method to Increase the Number of Detectable Photons During the Imaging of a Biological Marker
    • 在生物标记成像期间增加可检测光子数量的方法
    • US20130115647A1
    • 2013-05-09
    • US13637551
    • 2011-03-25
    • Kelly RogersSpencer ShorteJoseph DragavonSamantha Blazquez
    • Kelly RogersSpencer ShorteJoseph DragavonSamantha Blazquez
    • G01N21/64
    • G01N21/6486B82Y15/00G01N21/6428G01N2201/06193
    • The present invention relates a method to determine the presence of a photon producing biological marker in a cell, tissue or organism of interest. The method is based on Fluorescence by Unbound Excitation from Luminescence (FUEL) and comprises the steps of a) providing conditions suitable for the biological marker to produce at least one first photon by luminescence; b) providing a FUEL probe pair-upper (FPP-U) disposed in proximity to the cell, tissue or organism, wherein the at least one first photon of step a) excites the FPP-U, which emits at least one second photon. The FPP-U may be selected from the group of quantum dots, carbon nanotubes, fluorescent proteins, diamond nanocrystals and metalloporphyrins. This method is charcterized in that said biological marker and said FPP-U are not bound and in that each of the at least one second photon(s) are of a longer wavelength than each of the at least one first photon(s).
    • 本发明涉及确定感兴趣的细胞,组织或生物体中产生光子的生物标志物的存在的方法。 该方法基于通过未发光发光(FUEL)的荧光,并且包括以下步骤:a)提供适于生物标记物的条件以通过发光产生至少一个第一光子; b)提供设置在细胞,组织或生物体附近的FUEL探针对上(FPP-U),其中步骤a)的至少一个第一光子激发FPP-U,其发射至少一个第二光子。 FPP-U可以选自量子点,碳纳米管,荧光蛋白,金刚石纳米晶体和金属卟啉。 该方法的特征在于所述生物标记和所述FPP-U不结合,并且所述至少一个第二光子中的每一个具有比所述至少一个第一光子中的每一个更长的波长。
    • 5. 发明授权
    • Method to increase the number of detectable photons during the imaging of a biological marker
    • 在生物标记成像过程中增加可检测光子数量的方法
    • US09329132B2
    • 2016-05-03
    • US13637551
    • 2011-03-25
    • Kelly RogersSpencer ShorteJoseph DragavonSamantha Blazquez
    • Kelly RogersSpencer ShorteJoseph DragavonSamantha Blazquez
    • G01N21/64B82Y15/00
    • G01N21/6486B82Y15/00G01N21/6428G01N2201/06193
    • The present invention relates a method to determine the presence of a photon producing biological marker in a cell, tissue or organism of interest. The method is based on Fluorescence by Unbound Excitation from Luminescence (FUEL) and comprises the steps of a) providing conditions suitable for the biological marker to produce at least one first photon by luminescence; b) providing a FUEL probe pair-upper (FPP-U) disposed in proximity to the cell, tissue or organism, wherein the at least one first photon of step a) excites the FPP-U, which emits at least one second photon. The FPP-U may be selected from the group of quantum dots, carbon nanotubes, fluorescent proteins, diamond nanocrystals and metalloporphyrins. This method is characterized in that said biological marker and said FPP-U are not bound and in that each of the at least one second photon(s) are of a longer wavelength than each of the at least one first photon(s).
    • 本发明涉及确定感兴趣的细胞,组织或生物体中产生光子的生物标志物的存在的方法。 该方法基于通过未发光发光(FUEL)的荧光,并且包括以下步骤:a)提供适于生物标记物的条件以通过发光产生至少一个第一光子; b)提供设置在细胞,组织或生物体附近的FUEL探针对上(FPP-U),其中步骤a)的至少一个第一光子激发FPP-U,其发射至少一个第二光子。 FPP-U可以选自量子点,碳纳米管,荧光蛋白,金刚石纳米晶体和金属卟啉。 该方法的特征在于所述生物学标记和所述FPP-U不是结合的,并且所述至少一个第二光子中的每一个具有比所述至少一个第一光子中的每一个更长的波长。