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    • 1. 发明申请
    • Methods for Detecting and Measuring Specific Nucleic Acid Sequences
    • 检测和测量特定核酸序列的方法
    • US20140106983A1
    • 2014-04-17
    • US14105944
    • 2013-12-13
    • Suk-Wah Tam-ChangKenneth W HunterNelson G Publicover
    • Suk-Wah Tam-ChangKenneth W HunterNelson G Publicover
    • C12Q1/68
    • C12Q1/6876C12Q1/6816C12Q1/6818C12Q1/6837C12Q2525/185C12Q2525/301C12Q2565/107C12Q2565/101C12Q2525/101
    • The invention provides novel oligonucleotides and methods of using the same for detection or measurement of specific nucleic acid molecules. The invention also features nucleic acid arrays comprising the oligonucleotides of the invention. An oligonucleotide of the invention comprises (1) a reporter-binding sequence capable of hybridizing to a fluorrophore-labeled reporter sequence and (2) a hairpin-forming sequence capable of forming a stem-loop. Formation of the stem-loop modifies (e.g., quenching) the fluorescence signals of the reporter sequence when the reporter sequence is hybridized to the oligonucleotide. This can be achieved, for example, by bringing one or more guanine based in the oligonucleotide into close proximity to the fluorophore(s) of the reporter sequence by virtue of the formation of the stem-loop. Disruption of the stem-loop, such as by hybridization of a target sequence to at least part of the hairpin-forming sequence, produces a detectable change in the fluorescence signals.
    • 本发明提供新的寡核苷酸及其用于检测或测量特异性核酸分子的方法。 本发明还具有包含本发明寡核苷酸的核酸阵列。 本发明的寡核苷酸包含(1)能够与荧光标记的报道基因序列杂交的报告基因结合序列和(2)能够形成茎环的发夹形成序列。 当报告物序列与寡核苷酸杂交时,茎环的形成修饰(例如,淬灭)报告基因序列的荧光信号。 这可以通过例如通过使一个或多个基于寡核苷酸的鸟嘌呤通过茎 - 环的形成使报告物序列的荧光团靠近来实现。 茎环的破坏,例如通过目标序列与形成发夹的序列的至少部分的杂交产生荧光信号的可检测的变化。
    • 2. 发明申请
    • SYSTEMS AND METHODS FOR HIGH-RESOLUTION GAZE TRACKING
    • 高分辨率高程跟踪系统与方法
    • US20130114850A1
    • 2013-05-09
    • US13290948
    • 2011-11-07
    • Nelson G. PublicoverWilliam C. TorchChristopher N. Spitler
    • Nelson G. PublicoverWilliam C. TorchChristopher N. Spitler
    • G06K9/00
    • G06K9/00604A61B3/0025A61B3/024A61B3/113G02B27/0093G06F3/013G06K9/0061G06T7/74G06T2207/30201H04N5/2256H04N5/247
    • A system is mounted within eyewear or headwear to unobtrusively produce and track reference locations on the surface of one or both eyes of an observer. The system utilizes multiple illumination sources and/or multiple cameras to generate and observe glints from multiple directions. The use of multiple illumination sources and cameras can compensate for the complex, three-dimensional geometry of the head and anatomical variations of the head and eye region that occurs among individuals. The system continuously tracks the initial placement and any slippage of eyewear or headwear. In addition, the use of multiple illumination sources and cameras can maintain high-precision, dynamic eye tracking as an eye moves through its full physiological range. Furthermore, illumination sources placed in the normal line-of-sight of the device wearer increase the accuracy of gaze tracking by producing reference vectors that are close to the visual axis of the device wearer.
    • 将系统安装在眼镜或头饰内以便不引人注目地产生和跟踪观察者的一只眼睛或两只眼睛的表面上的参考位置。 该系统利用多个照明源和/或多个照相机来产生和观察来自多个方向的闪光。 使用多个照明源和照相机可以补偿头部的复杂的三维几何形状和在个体之间出现的头部和眼睛区域的解剖变化。 系统会持续跟踪初始位置和眼镜或头饰的任何滑动。 此外,随着眼睛在其完整的生理范围内移动,使用多个照明源和照相机可以保持高精度,动态的眼睛跟踪。 此外,放置在设备佩戴者的正常视线中的照明源通过产生靠近设备佩戴者的视轴的参考矢量增加了注视跟踪的精度。
    • 4. 发明授权
    • Systems and methods for high-resolution gaze tracking
    • 高分辨率注视跟踪的系统和方法
    • US08929589B2
    • 2015-01-06
    • US13290948
    • 2011-11-07
    • Nelson G. PublicoverWilliam C. TorchChristopher N. Spitler
    • Nelson G. PublicoverWilliam C. TorchChristopher N. Spitler
    • G06K9/00A61B3/113
    • G06K9/00604A61B3/0025A61B3/024A61B3/113G02B27/0093G06F3/013G06K9/0061G06T7/74G06T2207/30201H04N5/2256H04N5/247
    • A system is mounted within eyewear or headwear to unobtrusively produce and track reference locations on the surface of one or both eyes of an observer. The system utilizes multiple illumination sources and/or multiple cameras to generate and observe glints from multiple directions. The use of multiple illumination sources and cameras can compensate for the complex, three-dimensional geometry of the head and anatomical variations of the head and eye region that occurs among individuals. The system continuously tracks the initial placement and any slippage of eyewear or headwear. In addition, the use of multiple illumination sources and cameras can maintain high-precision, dynamic eye tracking as an eye moves through its full physiological range. Furthermore, illumination sources placed in the normal line-of-sight of the device wearer increase the accuracy of gaze tracking by producing reference vectors that are close to the visual axis of the device wearer.
    • 将系统安装在眼镜或头饰内以便不引人注目地产生和跟踪观察者的一只眼睛或两只眼睛的表面上的参考位置。 该系统利用多个照明源和/或多个照相机来产生和观察来自多个方向的闪光。 使用多个照明源和照相机可以补偿头部的复杂的三维几何形状和在个体之间出现的头部和眼睛区域的解剖变化。 系统会持续跟踪初始位置和眼镜或头饰的任何滑动。 此外,随着眼睛在其完整的生理范围内移动,使用多个照明源和照相机可以保持高精度,动态的眼睛跟踪。 此外,放置在设备佩戴者的正常视线中的照明源通过产生靠近设备佩戴者的视轴的参考矢量增加了注视跟踪的精度。
    • 5. 发明申请
    • PHOTON EVENT DISTRIBUTION SAMPLING APPARATUS AND METHOD
    • 光电事件分配采样设备和方法
    • US20110210239A1
    • 2011-09-01
    • US13103749
    • 2011-05-09
    • John L. SutkoNelson G. Publicover
    • John L. SutkoNelson G. Publicover
    • G01J1/02G01J1/58
    • G02B21/16G01N21/6456G01N21/6458
    • Locations of the origins of the photons are acquired from a scanned sample with reference to a scan frame. The location on the sample from which a photon was emitted is inferred from the location of the scan as commanded by a scan drive signal, a feedback signal related to the position of the scan device, or alternatively by the point in time during a scan at which the photon is detected. A position function, e.g., photon probability density, is associated with a photon position. Summing or other processing of photon probability density functions can require fewer photons to converge to an ideal density distribution associated with an image feature than are required using conventional pixel binning. Stored data can be mapped into pixels or voxels of a display or otherwise processed. Original data remains available in the digital storage for post-hoc analysis. Imprecision introduced by the display process need not adversely affect the precision of the collected data.
    • 参考扫描帧从扫描的样本获取光子的起源的位置。 根据扫描驱动信号所指示的扫描位置,与扫描装置的位置相关的反馈信号,或者在扫描期间的时间点,从扫描位置扫描发射光子的位置。 检测到光子。 位置函数,例如光子概率密度,与光子位置相关联。 光子概率密度函数的求和或其他处理可能需要更少的光子收敛到与图像特征相关联的理想密度分布,而不需要使用常规像素分档。 存储的数据可以映射到显示器的像素或体素或以其他方式处理。 原始数据在数字存储中仍然可用于事后分析。 由显示过程引入的不精确度不必对收集的数据的精度产生不利影响。
    • 6. 发明申请
    • Methods for Detecting and Measuring Specific Nucleic Acid Sequences
    • 检测和测量特定核酸序列的方法
    • US20140378675A1
    • 2014-12-25
    • US14479198
    • 2014-09-05
    • Suk-Wah Tam-ChangKenneth W. HunterNelson G. Publicover
    • Suk-Wah Tam-ChangKenneth W. HunterNelson G. Publicover
    • C12Q1/68
    • C12Q1/6876C12Q1/6816C12Q1/6818C12Q1/6837C12Q2525/185C12Q2525/301C12Q2565/107C12Q2565/101C12Q2525/101
    • The invention provides novel oligonucleotides and methods of using the same for detection or measurement of specific nucleic acid molecules. The invention also features nucleic acid arrays comprising the oligonucleotides of the invention. An oligonucleotide of the invention comprises (1) a reporter-binding sequence capable of hybridizing to a fluorophore-labeled reporter sequence and (2) a hairpin-forming sequence capable of forming a stem-loop. Formation of the stem-loop modifies (e.g., quenching) the fluorescence signals of the reporter sequence when the reporter sequence is hybridized to the oligonucleotide. This can be achieved, for example, by bringing one or more guanine based in the oligonucleotide into close proximity to the fluorophore(s) of the reporter sequence by virtue of the formation of the stem-loop. Disruption of the stem-loop, such as by hybridization of a target sequence to at least part of the hairpin-forming sequence, produces a detectable change in the fluorescence signals.
    • 本发明提供新的寡核苷酸及其用于检测或测量特异性核酸分子的方法。 本发明还具有包含本发明寡核苷酸的核酸阵列。 本发明的寡核苷酸包含(1)能够与荧光团标记的报告基因序列杂交的报告基因结合序列和(2)能够形成茎环的发夹形成序列。 当报告物序列与寡核苷酸杂交时,茎环的形成修饰(例如,淬灭)报告基因序列的荧光信号。 这可以通过例如通过使一个或多个基于寡核苷酸的鸟嘌呤通过茎 - 环的形成使报告物序列的荧光团靠近来实现。 茎环的破坏,例如通过目标序列与形成发夹的序列的至少部分的杂交产生荧光信号的可检测的变化。
    • 8. 发明申请
    • SYSTEMS AND METHODS FOR MEASURING REACTIONS OF HEAD, EYES, EYELIDS AND PUPILS
    • 用于测量头部,眼睛,眼睛和皮肤的反应的系统和方法
    • US20120293773A1
    • 2012-11-22
    • US13113006
    • 2011-05-20
    • Nelson G. PublicoverWilliam C. Torch
    • Nelson G. PublicoverWilliam C. Torch
    • A61B3/113
    • A61B5/162A61B3/0008A61B3/0025A61B3/112A61B3/113A61B3/14A61B5/1103A61B5/1114A61B5/6803A61B2560/0242A61B2562/0204
    • Systems and methods are provided to measure reaction times and/or responses for head, eye, eyelid movements, and/or changes in pupil geometry. The system includes eyewear or headwear including one or more eye-tracking cameras for monitoring the position and geometry of at least one eye and its components of the user, one or more scene cameras for monitoring the user's surroundings, and one or more processors to determine reaction times. Optionally, the system may include one or more of a multi-axis accelerometer to monitor head movements, light sources to trigger visual evoked responses, and/or electronic inputs that may be used to indicate the time of occurrence of external reference events. Measured reaction times and other measurements may be monitored for use in a range of applications. Responses and reaction times may be measured continuously over extended periods, even over a lifetime to measure consequences of the aging process.
    • 提供系统和方法以测量头部,眼睛,眼睑运动和/或瞳孔几何形状变化的反应时间和/或响应。 该系统包括眼镜或头饰,包括一个或多个眼睛跟踪摄像机,用于监视至少一只眼睛及其用户部件的位置和几何形状,一个或多个用于监测用户环境的场景摄像机,以及一个或多个处理器以确定 反应时间。 可选地,系统可以包括用于监测头部运动的多轴加速度计中的一个或多个,用于触发视觉诱发反应的光源和/或可用于指示外部参考事件发生的时间的电子输入。 可以监测测量的反应时间和其他测量值以用于一系列应用。 响应和反应时间可以在一段时间内连续测量,甚至在一生中测量老化过程的后果。
    • 9. 发明授权
    • Photon event distribution sampling apparatus and method
    • 光子事件分布采样设备及方法
    • US08168955B2
    • 2012-05-01
    • US13103749
    • 2011-05-09
    • John L. SutkoNelson G. Publicover
    • John L. SutkoNelson G. Publicover
    • G01J1/00G01B11/00
    • G02B21/16G01N21/6456G01N21/6458
    • Locations of the origins of the photons are acquired from a scanned sample with reference to a scan frame. The location on the sample from which a photon was emitted is inferred from the location of the scan as commanded by a scan drive signal, a feedback signal related to the position of the scan device, or alternatively by the point in time during a scan at which the photon is detected. A position function, e.g., photon probability density, is associated with a photon position. Summing or other processing of photon probability density functions can require fewer photons to converge to an ideal density distribution associated with an image feature than are required using conventional pixel binning. Stored data can be mapped into pixels or voxels of a display or otherwise processed. Original data remains available in the digital storage for post-hoc analysis. Imprecision introduced by the display process need not adversely affect the precision of the collected data.
    • 参考扫描帧从扫描的样本获取光子的起源的位置。 根据扫描驱动信号所指示的扫描位置,与扫描装置的位置相关的反馈信号,或者在扫描期间的时间点,从扫描位置扫描发射光子的位置。 检测到光子。 位置函数,例如光子概率密度,与光子位置相关联。 光子概率密度函数的求和或其他处理可能需要更少的光子收敛到与图像特征相关联的理想密度分布,而不需要使用常规像素分档。 存储的数据可以映射到显示器的像素或体素或以其他方式处理。 原始数据在数字存储中仍然可用于事后分析。 由显示过程引入的不精确度不必对收集的数据的精度产生不利影响。
    • 10. 发明授权
    • Photon event distribution sampling apparatus and method
    • 光子事件分布采样设备及方法
    • US07960702B2
    • 2011-06-14
    • US11597028
    • 2005-05-20
    • John L. SutkoNelson G. Publicover
    • John L. SutkoNelson G. Publicover
    • G01J1/00G01B11/00
    • G02B21/16G01N21/6456G01N21/6458
    • Locations of the origins of the photons are acquired from a scanned sample with reference to a scan frame. The location on the sample from which a photon was emitted is inferred from the location of the scan as commanded by a scan drive signal, a feedback signal related to the position of the scan device, or alternatively by the point in time during a scan at which the photon is detected. A position function, e.g., photon probability density, is associated with a photon position. Summing or other processing of photon probability density functions can require fewer photons to converge to an ideal density distribution associated with an image feature than are required using conventional pixel binning. Stored data can be mapped into pixels or voxels of a display or otherwise processed. Original data remains available in the digital storage for post-hoc analysis. Imprecision introduced by the display process need not adversely affect the precision of the collected data.
    • 参考扫描帧从扫描的样本获取光子的起源的位置。 根据扫描驱动信号所指示的扫描位置,与扫描装置的位置相关的反馈信号,或者在扫描期间的时间点,从扫描位置扫描发射光子的位置。 检测到光子。 位置函数,例如光子概率密度,与光子位置相关联。 光子概率密度函数的求和或其他处理可能需要更少的光子收敛到与图像特征相关联的理想密度分布,而不需要使用常规像素分档。 存储的数据可以映射到显示器的像素或体素或以其他方式处理。 原始数据在数字存储中仍然可用于事后分析。 由显示过程引入的不精确度不必对收集的数据的精度产生不利影响。