会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明授权
    • SMS shortcode allocation
    • 短信短码分配
    • US08467814B2
    • 2013-06-18
    • US11853618
    • 2007-09-11
    • Jiuhe GanTong ZhuKenneth Tsz HoZhaowei Charlie JiangVenkata Narasimha Rao Yerubandi
    • Jiuhe GanTong ZhuKenneth Tsz HoZhaowei Charlie JiangVenkata Narasimha Rao Yerubandi
    • H04W4/00
    • H04W4/12H04L51/38
    • A system, apparatus, and method are directed towards managing short code allocation policies across a plurality of different carriers for multiple applications. Each carrier provides to a centralized routing service a short code policy that includes an extension allocation policy. The extension allocation policy may specify whether the extensions are allocated based on a dynamical recycle allocation, a range recycle allocation, a pass-through allocation, or a re-usekey based allocation policy, or other mechanism. When a message is sent from an application, a carrier is determined to send the message to a destination mobile device. The carrier's short code policy, including the extension allocation policy, is then used to select how to allocate and/or re-allocate a short code and extension for use with the message. The message may then be modified to include the selected short code and extension, and is then sent using the determined network carrier.
    • 系统,装置和方法旨在管理用于多个应用的​​多个不同载波的短代码分配策略。 每个运营商向集中式路由服务提供包括扩展分配策略的短代码策略。 扩展分配策略可以基于动态循环分配,范围回收分配,直通分配或基于重用键分配策略或其他机制来指定分机是否被分配。 当从应用发送消息时,确定运营商将消息发送到目的地移动设备。 然后,运营商的短代码策略(包括分机分配策略)用于选择如何分配和/或重新分配用于消息的短代码和分机。 然后可以修改消息以包括所选择的短代码和扩展,然后使用所确定的网络载体进行发送。
    • 8. 发明授权
    • Probe correction for gene expression level detection
    • 基因表达水平检测的探针校正
    • US07715990B2
    • 2010-05-11
    • US10500587
    • 2003-01-17
    • Guangzhou ZouHur-Song ChangYiping FanFan LongXun WangTong Zhu
    • Guangzhou ZouHur-Song ChangYiping FanFan LongXun WangTong Zhu
    • G01N33/483
    • G06F19/20C12Q1/6837C12Q2600/158
    • Individual probes on micro-arrays are re-scaled and corrected with a set of probe dependent coefficients derived from genomic-DNA hybridization signals. A dynamic range for gDNA binding is determined by measuring a concentration signal curve. Signals for each probe are measured during multiple hybridizations within a linear range. Concentration insensitive probes are then found for two sets of experiments. Probes are discarded based on a threshold compared to their standard deviation divided by their average in each set. The correction coefficients are used to calculate a corrected intensity for each probe. Probes having high uncertainty (0.5 in one embodiment) are discarded. A weighting factor for each probe is determined along with an uncertainty factor. Finally, a call for each gene is made, such as absent, marginal or present.
    • 使用从基因组DNA杂交信号衍生的一组探针依赖系数对微阵列上的单个探针进行重新定标和校正。 通过测量浓度信号曲线确定gDNA结合的动态范围。 在线性范围内的多次杂交期间测量每个探针的信号。 然后发现两组实验的浓度不敏感探针。 探针根据其标准偏差除以每组中的平均值的阈值进行丢弃。 校正系数用于计算每个探针的校正强度。 具有高不确定度的探针(在一个实施例中为0.5)被丢弃。 确定每个探头的加权系数以及不确定因素。 最后,调用每个基因,如缺席,边缘或存在。