Patent application number | Description | Published |
20100199315 | Method, system and apparatus for hiding programs - The present invention discloses a method, a system and an apparatus for hiding programs. With the technology solution, which involves obtaining a sub-EPG identifier, receiving a total EPG, which contains sub-EPG identifiers and sub-EPGs each of which corresponds to one of the sub-EPG identifiers and which is transmitted by a central front end, searching the received total EPG for a sub-EPG corresponding to the obtained sub-EPG identifier and hiding programs based on the found sub-EPG. With technology solution, the program hiding is realized, and the regional program hiding and the programs hiding from particular subscribers may be realized. | 08-05-2010 |
20110117905 | LTE RRC connection re-establishment requesting method, cause value setting method and terminal - The present invention discloses a method for requesting LTE RRC connection re-establishment and setting cause values as well as a terminal, and the connection re-establishment request method includes: an LTE terminal determines, according to the occurred scenario, which one of the following four types is the failure reason: radio resource failure, handoff failure, bottom layer error or UE-related error; and the LTE terminal initiates an RRC connection re-establishment request to the network side, wherein the RRC connection re-establishment request includes the failure cause value indicating the failure reason. The present invention can make the network side obtain the reason why the UE initiates the RRC re-establishment from RRC connection re-establishment request message, so as to take different subsequent operations with respect to these different failure reasons. | 05-19-2011 |
20110286416 | USER EQUIPMENT AND METHOD OF USER EQUIPMENT FOR RECEIVING DOWNLINK DATA - The present invention discloses a UE (User Equipment) and a method of the UE for receiving downlink data to avoid the occurrence of mistakes when the UE receives the downlink data. The method comprises the following steps: during the reestablishment, in the process of transmitting Service Data Units (SDU) to a Packet Data Convergence Protocol (PDCP) layer entity from a Radio Link Control (RLC) layer entity in the UE, if the PDCP entity judges that the PDCP Sequence Number (SN) of the received PDCP Protocol Data Unit (PDU) which includes the SDU satisfies the report condition, the PDCP PDU is received and the SDU included in the PDCP PDU is submitted to the upper layer entity, wherein the report condition is: PDCP SN=(Last_Submitted_PDCP_RX_SN+1)%(Maximum_PDCP_SN+1). | 11-24-2011 |
20110288845 | CONSTRUCTION METHOD AND SYSTEM OF FRAGMENTS ASSEMBLING SCAFFOLD, AND GENOME SEQUENCING DEVICE - The present invention relates to gene engineering filed, and provides a genome sequencing device, construction method of fragments assembling scaffold and system thereof. The method comprises the following steps: mapping the double-barreled data obtained through sequencing to contigs; calculating the mean length between contigs based on multiple pairs of double-barreled data mapped to contigs, which is taken as the gap size between contigs; constructing scaffold based on gap size between contigs and the double-barreled relation between contigs; and obtaining complete scaffold graph. Since the mean length between contigs is calculated from multiple pairs of double-barreled data and is taken as the gap size between contigs, the estimation precision of gap size between contigs is improved greatly. It can be used for genome sequencing including short sequencing read length to finish task of assembling sequencing fragments. | 11-24-2011 |
20110295784 | ERROR CORRECTING METHOD OF TEST SEQUENCE, CORRESPONDING SYSTEM AND GENE ASSEMBLY EQUIPMENT - The present invention provides an error correcting method of test sequence, which involves receiving test sequences, configuring high frequency short string list based on a preset high frequency threshold value, traversing each received test sequence, searching an area with the largest number of continuous high frequency short strings on each test sequence in combination with high frequency short string list, configuring whole left sequence and/or right sequence of high frequency short strings at left side and/or right side of searched area according to corresponding received test sequence and high frequency short string list, and constituting corresponding test sequence according to configured left and/or right sequence and searched area. The present invention also provides corresponding error correcting system of test sequence and gene assembly equipment. | 12-01-2011 |
20120224525 | Method for Acquiring Packet Data Convergence Protocol Status Report and Packet Data Convergence Protocol Entity - The present invention discloses a method for acquiring a Packet Data Convergence Protocol (PDCP) status report and a packet data convergence protocol entity. The method comprises the steps of: a PDCP entity transmitting to an opposite PDCP entity a PDCP Protocol Data Unit (PDU) used to request the transmission of a PDCP status report; and the PDCP entity receiving the PDCP status report which is transmitted from the opposite PDCP entity according to the PDCP PDU. By the present invention, the quality of service and the performance of the wireless communication system are improved. | 09-06-2012 |
20130095876 | Quick Positioning Method And Device For Multiple Cycles And Multiple Users - The disclosure provides a quick positioning method and device for multiple cycles and multiple users, and the method includes: a processing index is created for each attribute of a user in a base station, wherein same attributes with the same transmission cycles and the same transmission offsets share one processing index; when a user accesses the base station, the user is mounted into a corresponding processing index according to an attribute of the user, a transmission cycle of the attribute, and a transmission offset of the attribute; and by inquiring a processing index corresponding to the current time point, the base station demodulates the attribute of the user mounted in said processing index. With the disclosure, a target can be hit promptly, processing time is saved, processing efficiency is improved, and the processing time delay of the whole link is reduced. | 04-18-2013 |
20130162358 | REFERENCE CURRENT GENERATOR CIRCUIT - One aspect of the present invention includes a reference current generator circuit. The circuit includes a bias circuit configured to generate a reference current along a first current path and a second current along a second current path. The reference current and the second current can be proportional. The circuit also includes a first pair of transistors connected in series and configured to conduct the reference current in the first current path. The circuit further includes a second pair of transistors connected in series and configured to conduct the second current in the second current path. The second pair of transistors can be coupled to the first pair of transistors to provide a collective resistance value of the second pair of transistors that is proportional to temperature. | 06-27-2013 |
20140166374 | Tank weighing transducer - A tank weighing transducer, comprises: a supporting ring, a cover, a gasket, a locking screw, a weighing sensor, a circuit board, a battery, a base, a supporter nut, a supporter screw, and a detachable supporter, wherein the supporting ring and the cover are connected via the locking screw and the gasket; the weighing sensor and the circuit board are fixed on the base via the locking screw; the battery is put in the battery container on the base; the cover and the base are connected via the locking screw; and the detachable supporter is fixed on the base via the supporter nut and the supporter screw. The tank weighing transducer in the present invention is able to withstand load for a long period, and has a good impact resistance. | 06-19-2014 |
20140249038 | Method of detecting a pre-determined event in a nucleic acid sample and system thereof - Disclosed are a method of detecting a pre-determined event in a nucleic acid sample and a system thereof. The method of detecting the pre-determined event in the nucleic acid sample comprises the following steps: constructing a sequencing-library for the nucleic acid sample; sequencing the sequencing-library to obtain a sequencing result consisting of a plurality of sequencing data; determining the sequencing data from a pre-determined region; and determining an occurrence of the pre-determined event in the nucleic acid sample based on a composition of the sequencing data from the pre-determined region. | 09-04-2014 |
20140323320 | METHOD OF DETECTING FUSED TRANSCRIPTS AND SYSTEM THEREOF - Provided is a method of detecting method of detecting fusion transcripts in a sample to be analyzed. The method may comprises: subjecting the sample to be analyzed containing a RNA transcriptome to paired-end sequencing, to obtain paired-end RNA-Seq data of the sample to be analyzed; aligning the paired-end RNA-Seq data to a human reference genome sequence, to obtain first paired-end mapped reads, first single-end mapped reads, and first unmapped reads; evaluating an insertsize between two ends of the paired-end mapped reads by means of the first paired-end mapped reads, to obtain a proportion of paired-end mapped reads with overlapped 3′-ends; aligning the first unmapped reads to annotated transcripts, to obtain second single-end mapped reads and second unmapped reads; aligning the second unmapped reads to the annotated transcripts, to filter out unmapped reads caused by indel and obtain third unmapped reads; merging all single-end mapped reads, to obtain a set of single-end mapped reads; obtaining a gene pair linked by a cross-read as a primary set of candidate gene pairs based on the set of single-end mapped reads and combining with a relationship of the mapped paired-end reads; subjecting the primary set of candidate gene pairs to a filtration, to obtain a candidate set of fused gene pairs; bisecting the third unmapped read, to obtain a half-unmapped read; aligning the half-unmapped read to a gene-junction sequence in the candidate set of fused gene pairs, to obtain a potent region of a fused junction site in the gene in which the half-unmap read locates; outputting original reads of mapped half-unmapped reads, to obtain useful unmapped reads; subjecting the candidate set of fused gene pairs to a fusion simulation; aligning the useful unmapped reads to a junction library, to obtain a fused gene supported by the useful unmapped reads; calculating and gathering the fused sequence supported by the useful unmapped reads, to obtain information of the fused gene. And a system for detecting fusion transcripts is also provided. | 10-30-2014 |
20140336075 | METHOD AND SYSTEM FOR DETERMININING WHETHER GENOME IS ABNORMAL - The present invention provides a method and system for determining whether a genomic abnormality exists. The method for determining whether a genomic abnormality exists includes the steps of: separating fetal nucleated red blood cells from a sample from a pregnant woman; sequencing at least a part of the genome of the nucleated red blood cells, so as to obtain a sequencing result; and on the basis of the sequencing result, determining whether a genomic abnormality exists in the nucleated red blood cells. | 11-13-2014 |
20140350866 | Method of Gap Closing in Nucleotide Sequence and Apparatus Thereof - Provided is a method of gap closing in nucleotide sequence. The nucleic acid sequence comprises a first contig at one end of a gap in an unassembled region, and a second contig at the other end of the gap in the unassembled region. The method comprises: selecting reads having an overlap with one end of the first contig close to the gap as a set of reads for gap closing; selecting reads having a shortest overlap with the first contig in the set of reads for gap closing as a candidate read; determining whether reads having an overlapping length with the first contig shorter than an overlapping length between the candidate read and the first contig present in the set of reads for gap closing, and determining whether reads having no overlapping relationship with the candidate read present in the set of reads for gap closing; obtaining a result of presenting an extension conflict, and determining an unconfident candidate read, if reads having an overlapping length with the first contig shorter than an overlapping length between the candidate read and the first contig present in the set of reads for gap closing, reads having no overlapping relationship with the candidate read present in the set of reads for gap closing, or both reads having an overlapping length with the first contig shorter than an overlapping length between the candidate read and the first contig, and reads having no overlapping relationship with the candidate read present in the set of reads for gap closing; reselecting the candidate read until obtaining a confident candidate read, if the candidate read is unconfident; connecting the confident candidate read to the first contig, to form a new first contig; determining whether one end of the new first contig close to the gap has an overlap with one end of the second contig close to the gap; performing the step of selecting the set of reads for gap closing on the basis of the new first contig, if the one end of the new first contig close to the gap has no overlap with the one end of the second contig close to the gap, wherein the first contig in the step of selecting the set of reads for gap closing is replaced with the new first contig; connecting the new first contig to the second contig to complete gap closing, if one end of the new first contig close to the gap has an overlap with one end of the second contig close to the gap. | 11-27-2014 |
20140364321 | Method for analyzing DNA methylation based on MspJI cleavage - Provided is a method for detecting DNA methylation based on MspJI cleavage and performing bioinformatics analysis of genomic methylation. | 12-11-2014 |
20140370504 | METHOD FOR DETECTING GENETIC VARIATION - The present invention relates to a method for detecting genetic variation, comprising the following steps: acquiring reads from a test sample; aligning said reads with a reference genome sequence; dividing said reference genome sequence into windows, calculating the number of said reads which are aligned to each window, and acquiring the statistic for each window on the basis of the number of said reads; and for a fragment of the reference genome sequence, acquiring the genetic variation sites on the basis of the change in the statistics of all the windows thereon in the fragment of the reference genome sequence. | 12-18-2014 |
20140372547 | Method and Device for Implementing end-to-end Hardware Message Passing - A method and device for implementing end-to-end Hardware Message Passing (HMP) are disclosed. The device includes: a message memory, a controller, a message input interface and a message output interface. The message memory is configured to temporarily store a message. The controller is configured to perform management on a message in the form of hardware, store a message obtained from the message input interface into the message memory, and read a message from the message memory and transmit the message to a message user via the message output interface. The message input interface is directly connected with a message creator and is configured to obtain a message created by the message creator under the control of the controller. The message output interface is directly connected to the message and is configured to provide a message to the message user under the control of the controller. The disclosure can improve the efficiency of message passing and reduce software management overhead. | 12-18-2014 |
20150032930 | Hardware abstract data structure, data processing method and system - A Hardware Abstract Data Structure (HADS) includes a General Interface (GI), a Coherence Interface (CI), a Control and Configuration Logic (CCL), an Intelligence Logic (IL) and a Memory Pool (MP), wherein the GI is arranged to implement intercommunion between the HADS and a processor; the CI is arranged to implement coherence storage between multiple processors; the CCL is arranged to, in response to a command received by the GI, configure a hardware data structure for the MP; the IL is arranged to complete a large amount of simple and frequent data processing; and the MP is arranged to store data. Correspondingly, a method and data processing system are also disclosed. Through the disclosure, the HADS which is dynamically configurable, flexible, efficient, universal in interface and good in interconnectivity can be implemented to improve the data processing efficiency. | 01-29-2015 |
20150037286 | USE OF ROSEBURIA IN THE PREVENTION AND TREATMENT FOR OBESITY RELATED DISEASES - The present invention provides use of | 02-05-2015 |