Abstract: A clock data recovery circuit and a clock data recovery method are provided. The clock data recovery circuit includes a time delay loop (100), a frequency locking loop (200) and a deserializer (300). The time delay loop (100) is configured to delay input data according to a phase of a clock signal to realize phase alignment; the frequency locking loop (200) is connected to the time delay loop (100), and is configured to adjust a frequency of the clock signal according to the delayed input data to make the frequency of the clock signal be consistent with a frequency of the input data; and the deserializer (300) is respectively connected to the time delay loop (100) and the frequency locking loop (200), and is configured to deserialize the input data according to the clock signal.

Abstract: The present disclosure relates to a decoding method, apparatus and computer-readable storage medium, which relates to the field of computer technology. The method of the present disclosure includes buffering one or more stream segments of a data stream which are received, wherein the data stream comprises an audio stream; parsing the one or more stream segments buffered until header information is obtained through the parsing; storing the header information; and decoding stream segments of the audio stream among various stream segments received according to the header information until the audio stream is completely decoded.

Abstract: Methods, systems, and devices for wireless communications are described. A user equipment (UE) may transmit, to a base station, a UE capability to receive a first portion of a tracking reference signal (TRS) and a second portion of the TRS, the first portion and the second portion associated with a TRS pattern. The UE may receive, from the base station, an indication of the TRS pattern, where the TRS pattern includes the first portion of the TRS pattern and the second portion of the TRS pattern. The UE may receive one or more TRSs according to the first portion of the TRS pattern and the second portion of the TRS pattern.

Abstract: A sample scraping method and a sample scraping device capable of efficiently scraping and collecting a biological tissue section without waste while suppressing contamination is provided. In a sample scraping method for scraping and collecting a biological tissue section held on a slide, the FFPE section held on the slide is heated, and the heated FFPE section is scraped by a blade such that the FFPE section that has been scraped off and remains on the blade is collected in a container.

Abstract: A method of wireless communication, by a first sidelink user equipment (UE), includes periodically receiving a set of sidelink beam failure detection reference signals (RSs) from a second sidelink UE. The method includes incrementing a beam failure detection (BFD) counter in response to one or more reference signals of the set of sidelink beam failure detection RSs having a received signal strength below a threshold. The first sidelink UE starts a beam failure detection timer in response to the reference signal(s) of the set of sidelink beam failure detection reference signals having the received signal strength below the threshold. Another method by a sidelink UE may periodically transmit a set of sidelink BFD RSs to another sidelink UE. The set of sidelink BFD RSs comprise one or more sidelink receive RSs. The sidelink UE configures the other sidelink UE with the sidelink receive BFD RSs.

Abstract: Example implementations include a method, apparatus and computer-readable medium of wireless communication over a sidelink between a first user equipment (UE) and a second UE. The first UE may receive, from a base station, a sidelink resource configuration indicating physical sidelink control channel (PSCCH)/physical sidelink shared channel (PSSCH) occasions on which to monitor a PSCCH for a grant from a second UE. The first UE may determine an active time for monitoring the PSCCH based on a discontinuous reception (DRX) mode for a link with the base station, the DRX mode including an active state in which a physical downlink control channel (PDCCH) is monitored and an inactive state in which the PDCCH is not monitored. The first UE may monitor the PSCCH during one or more of the PSCCH/PSSCH occasions that coincide with the active time.

Abstract: A method of wireless communication by a first sidelink user equipment (UE) transmits a sidelink (SL) beam failure recovery (BFR) message to a communications node, indicating a new candidate beam and an identifier (ID) of a second sidelink UE. The method also receives an acknowledgment of the SL BFR message. A communications node receives a sidelink beam failure recovery message from a first sidelink user equipment, indicating a new candidate beam and an ID of a second sidelink UE. The method also transmits information identifying the new candidate beam and the ID to the second sidelink UE. Another method by a first sidelink user equipment receives a sidelink beam failure recovery message from a base station, indicating a new candidate beam and an ID of a second sidelink UE. The method changes a beam used to communicate with the second sidelink UE in response to receiving the BFR message.

Abstract: Various aspects of the present disclosure generally relate to wireless communication. In some aspects, a user equipment (UE) may perform a physical layer measurement on a non-serving cell of the UE. The UE may report a measurement value of the physical layer measurement to a serving cell of the UE based at least in part on the physical layer measurement satisfying a threshold. The UE may receive, based at least in part on reporting the physical layer measurement, a physical layer reference signal measurement configuration for the non-serving cell. The UE may transmit a measurement report based at least in part on the physical layer reference signal measurement configuration. Numerous other aspects are provided.

Abstract: A sample scraping method and a sample scraping device capable of efficiently scraping and collecting a biological tissue section without waste while suppressing contamination is provided. In a sample scraping method for scraping and collecting a biological tissue section held on a slide, the FFPE section held on the slide is heated, and the heated FFPE section is scraped by a blade such that the FFPE section that has been scraped off and remains on the blade is collected in a container.

Abstract: Provided is a double-faced PSA sheet having excellent detergent resistance. The PSA sheet according to this invention comprises a PSA layer and is adhesive on both faces. The PSA sheet shows a push-peel strength of 30 N/cm2 or greater after a detergent immersion test involving immersion in a standard detergent at 40° C. for 24 hours. It also has an adhesive strength retention rate of 50% or higher, determined as the ratio of push-peel strength P2 after the detergent immersion test to push-peel strength P1 before the detergent immersion test.

Abstract: A cell processing apparatus includes a storage container that contains liquid L including a biological sample; a filter that prevents a first cell C1 in the biological sample from passing and allows a second cell C2 having a smaller diameter than that of the first cell C1 to pass; and a filtration cylinder for separating, in the storage container and via the filter, the liquid L into a first liquid L1 mainly including the first cell C1 and a second liquid L2 mainly including the second cell C2. A measurement target cell filtered by the filter among other cells can be easily collected.

Abstract: A cell processing apparatus includes a storage container that contains liquid L including a biological sample; a filter that prevents a first cell C1 in the biological sample from passing and allows a second cell C2 having a smaller diameter than that of the first cell C1 to pass; and a filtration cylinder for separating, in the storage container and via the filter, the liquid L into a first liquid L1 mainly including the first cell C1 and a second liquid L2 mainly including the second cell C2. A measurement target cell filtered by the filter among other cells can be easily collected.

Abstract: A cell processing apparatus 29 of the present invention includes a storage container 57 that can contain liquid L including a biological sample; a filter 60 that prevents a first cell C1 in the biological sample from passing therethrough and that allows a second cell C2 having a smaller diameter than that of the first cell C1 to pass therethrough; and a filtration cylinder 58 for separating, in the storage container 57 and via the filter 60, the liquid L into a first liquid L1 mainly including the first cell C1 and a second liquid L2 mainly including the second cell C2. A measurement target cell discriminated by the filter from the other cells can be easily collected.

Abstract: A cell processing apparatus 29 of the present invention includes a storage container 57 that can contain liquid L including a biological sample; a filter 60 that prevents a first cell C1 in the biological sample from passing therethrough and that allows a second cell C2 having a smaller diameter than that of the first cell C1 to pass therethrough; and a filtration cylinder 58 for separating, in the storage container 57 and via the filter 60, the liquid L into a first liquid L1 mainly including the first cell C1 and a second liquid L2 mainly including the second cell C2. A measurement target cell discriminated by the filter from the other cells can be easily collected.

Abstract: A method of activating an antigen is herein described. The method comprises providing an antigen activation solution and contacting the cell with the solution to activate the antigen. A method of detecting a cell fixed by a nonbridging fixation solution is also described. The method comprises providing an antigen activation solution, contacting the cell with the solution, immunostaining the cell, and detecting the stained cell. The solution used for these methods comprises an agent for breaking a hydrogen bond, and is also described herein.

Abstract: A method of activating an antigen is herein described. The method comprises providing an antigen activation solution and contacting the cell with the solution to activate the antigen. A method of detecting a cell fixed by a nonbridging fixation solution is also described. The method comprises providing an antigen activation solution, contacting the cell with the solution, immunostaining the cell, and detecting the stained cell. The solution used for these methods comprises an agent for breaking a hydrogen bond, and is also described herein.