LOW-POWER METHOD AND DEVICE FOR COOLING PROSTHETIC LIMB SOCKET BASED ON PHASE CHANGE
    2.
    发明申请
    LOW-POWER METHOD AND DEVICE FOR COOLING PROSTHETIC LIMB SOCKET BASED ON PHASE CHANGE 有权
    基于相位变化的低功率方法和冷却前置式插座的装置

    公开(公告)号:US20160081822A1

    公开(公告)日:2016-03-24

    申请号:US14889162

    申请日:2014-05-07

    发明人: Jiang Zhe Yu Han

    IPC分类号: A61F2/80 A61F7/10

    摘要: A prosthesis includes a socket for receiving a residual limb, the socket having a socket wall defining a limb-receiving surface; a heat pipe including a working fluid and a wicking structure, the heat pipe having a socket section and a heat sink section, the heat pipe extending along its length through the socket wall proximate to or exposed at the limb-receiving surface, wherein the working fluid has a boiling point of from about 0° C. to 90° C. such that the working fluid is adapted to evaporate to form vapor under the influence of the heat of a residual limb in the socket thus drawing heat from and cooling the residual limb. A heat sink section of the heat pipe passes through the heat sink, the heat sink reducing the temperature of the working fluid.

    摘要翻译: 假体包括用于接收残肢的插座,所述插座具有限定肢体接收表面的插座壁; 所述热管包括工作流体和芯吸结构,所述热管具有插座部分和散热部分,所述热管沿着其长度通过所述插座壁延伸接近或暴露在所述肢体接收表面处,其中所述工作 流体具有约0℃至90℃的沸点,使得工作流体适于蒸发以在插座中残留肢体的热量的影响下形成蒸气,从而从残留物中吸收热量并冷却残余物 肢。 热管的散热片通过散热片,散热片降低了工作流体的温度。

    BIOMARKER ASSAY USING MICROPARTICLE AGGREGATION
    3.
    发明申请
    BIOMARKER ASSAY USING MICROPARTICLE AGGREGATION 审中-公开
    使用微生物聚集的生物标记测定

    公开(公告)号:US20160334396A1

    公开(公告)日:2016-11-17

    申请号:US14855870

    申请日:2015-09-16

    摘要: In various aspects and embodiments, the present invention is directed to versatile, label-free method for the quantitative and qualitative detection of biomarkers and/or other compounds in a fluid sample using functionalized microparticle aggregates. In these methods, micron-scale particles are functionalized to specifically interact with the biomarker being measured and added to the sample to form aggregates, the size and number of which are counted to find a volume fraction and/or number fraction of aggregates in the sample. There is a direct correlation between the volume fraction and number fraction of these aggregates and the concentration of the corresponding biomarker. By comparing the measured volume fraction and/or number fraction of aggregates in the sample to a calibration curve, the concentration of that biomarker may be determined even for biomarkers or other target compounds in samples at very low concentrations, without the need for fluorescence and enzyme labelling of antibodies.

    摘要翻译: 在各个方面和实施方案中,本发明涉及用于使用官能化的微粒聚集体定量和定性检测流体样品中的生物标志物和/或其它化合物的通用的,无标记的方法。 在这些方法中,微米级颗粒被官能化以与被测量的生物标志物特异性相互作用并加入到样品中以形成聚集体,其尺寸和数量被计数以找到样品中的聚集体的体积分数和/或数量分数 。 这些聚集体的体积分数和数量分数与相应生物标志物的浓度之间存在直接相关性。 通过将样品中聚集体的测量体积分数和/或数量分数与校准曲线进行比较,即使对于生物标志物或其它目标化合物,也可以以非常低的浓度测定该生物标志物的浓度,而不需要荧光和酶 标记抗体。

    ENHANCED REFERENCE REGION UTILIZATION FOR SCALABLE VIDEO CODING
    7.
    发明申请
    ENHANCED REFERENCE REGION UTILIZATION FOR SCALABLE VIDEO CODING 有权
    用于可扩展视频编码的增强参考区域利用

    公开(公告)号:US20140286409A1

    公开(公告)日:2014-09-25

    申请号:US13997935

    申请日:2012-12-28

    IPC分类号: H04N19/61 H04N19/91 H04N19/82

    摘要: Techniques to identify one or more candidate reference blocks used to generate a prediction block to encode a current coding block. The candidate reference blocks can be in the same layer as the current coding block or a different layer. In addition, the candidate reference blocks do not have to be co-located with the current coding block. Motion vectors and shift vectors can be used to identify the one or more candidate reference blocks. In addition, uniform and non-uniform weighting can be applied to the one or more candidate reference blocks to generate the prediction block. Accordingly, an encoder can determine and identify reference blocks to a decoder that can provide desirable rate-distortion cost.

    摘要翻译: 用于识别用于生成预测块以编码当前编码块的一个或多个候选参考块的技术。 候选参考块可以与当前编码块或不同层位于相同的层中。 此外,候选参考块不必与当前编码块共同定位。 运动矢量和移位矢量可用于识别一个或多个候选参考块。 此外,可以对一个或多个候选参考块应用均匀和不均匀的加权以生成预测块。 因此,编码器可以确定并识别能够提供所需速率失真成本的解码器的参考块。

    SYSTEMS, METHODS, AND COMPUTER PROGRAM PRODUCTS FOR SCALABLE VIDEO CODING BASED ON COEFFICIENT SAMPLING
    9.
    发明申请
    SYSTEMS, METHODS, AND COMPUTER PROGRAM PRODUCTS FOR SCALABLE VIDEO CODING BASED ON COEFFICIENT SAMPLING 有权
    基于系数采样的可扩展视频编码的系统,方法和计算机程序产品

    公开(公告)号:US20140140410A1

    公开(公告)日:2014-05-22

    申请号:US13995182

    申请日:2012-06-29

    IPC分类号: H04N19/30

    CPC分类号: H04N19/63 H04N19/30

    摘要: Methods, systems, and computer program products for the generation of multiple layers of scaled encoded video data compatible with the HEVC standard. Residue from prediction processing may be transformed into coefficients in the frequency domain. The coefficients may then be sampled to create a layer of encoded data. The coefficients may be sampled in different ways to create multiple respective layers. The layers may then be multiplexed and sent to a decoder. There, one or more of the layers may be chosen. The choice of certain layer(s) may be dependent on the desired attributes of the resulting video. A certain level of video quality, frame rate, resolution, and/or bit depth may be desired, for example. The coefficients in the chosen layers may then be assembled to create a version of the residue to be used in video decoding.

    摘要翻译: 用于生成与HEVC标准兼容的多层缩放编码视频数据的方法,系统和计算机程序产品。 可以将来自预测处理的残差变换为频域中的系数。 然后可以对系数进行采样以创建编码数据层。 可以以不同的方式对系数进行采样以创建多个相应的层。 然后可以将这些层复用并发送到解码器。 在那里,可以选择一个或多个层。 某些层的选择可以取决于所得到的视频的期望属性。 例如,可能需要某种级别的视频质量,帧速率,分辨率和/或比特深度。 然后可以组合所选择的层中的系数以创建要在视频解码中使用的残余的版本。