7 results about "Sequence ID" patented technology

The invention discloses an mRNA non-coding region sequence optimization method and system and electronic equipment, and the mRNA non-coding region sequence optimization method comprises the steps: constructing an initial candidate library according to a target protein; inputting the initial candidate library into a pre-trained mRNA sequence optimization model to obtain a prediction data set; performing multi-dimensional scoring and sequence optimization on the prediction data set to obtain a sequence recommendation group; performing biological verification on the sequence recommendation group to obtain an optimized mRNA sequence; wherein the prediction data set comprises a sequence ID, a sequence content, a prediction TE score and a confidence interval. According to the method, the translation efficiency of the mRNA sequence can be efficiently and accurately predicted, the candidate sequence with high expression potential is screened out, meanwhile, the consumption of computing resources is reduced, and the overall design cost is reduced.

A user equipment (UE) is described. The UE may comprise reception circuitry configured to monitor a first Sidelink positioning reference signal (SL-PRS). The UE may also comprise transmission circuitry configured to perform a transmission of a second SL-PRS. When the UE detects the SL-PRS, the UE may select a different SL-PRS sequence ID from a SL-PRS sequence ID which is used for the first SL-PRS. A sequence for the second SL-PRS may be generated by using the selected SL-PRS sequence ID.

Example embodiments of the present disclosure relate to sounding reference signal (SRS) resource coordination for low power high precision positioning (LPHAP) positioning. In one aspect, an apparatus determines at least one of a first list of SRS sequence IDs for LPHAP UEs and a second list of SRS sequence IDs for non-LPHAP UEs. The apparatus then transmits information indicating the first list or the second list to at least one base station. According to some embodiments of the present disclosure, the following advantages can be realized: by making each gNB use a different SRS sequence, the problem of interference between gNBs is effectively avoided; and the special SRS sequence ID list is allocated to the LPHAP UE, so that the problem of interference between the LPHAP UE and the common UE is effectively avoided.

RNA molecules containing a guide sequence portion having 17 to 50 consecutive nucleotides within any of the sequences shown in Sequence ID No. 1 to 24195, as well as compositions, methods, and uses thereof.

According to an embodiment of the present disclosure, there is provided a photovoltaic power generation method including an operation of setting a first maximum waiting time and transmitting a registration start signal and the first maximum waiting time to one or more module level power electronics (MLPEs), an operation of receiving unique information from a first MLPE among the one or more MLPEs, an operation of assigning a first sequence ID to the unique information of the first MLPE, and an operation of setting a second maximum waiting time and transmitting the registration start signal and the second maximum waiting time to the one or more MLPEs.

A computer-implemented method for generic tenant data replication for disaster recovery, includes regularly checking, by a primary replication agent on a primary site, for changes to a primary change log on the primary site. Based on an insert of a new change record in a secondary change log on a secondary site, triggering a stored procedure from secondary stored procedures on the secondary site, that extracts a change operation and data from the secondary change log and performs the changed operation on a secondary tenant table on the secondary site. By a secondary replication agent on the secondary site and from the primary replication agent, receiving a call not containing a sequence id for a change record marked as completed in the secondary change log, and deleting the change record. Using a replication agents control plane, providing central monitoring for the primary replication agent and the secondary replication agent.

This terminal comprises: a main radio (MR) reception unit that receives, from a network, a sequence ID of a low-power synchronization signal; an MR transmission unit that transmits the sequence ID of the low-power synchronization signal to a low-power wake-up receiver (LR); an LR reception unit that receives the low-power synchronization signal and a low-power wake-up signal; and an LR control unit that executes synchronization or measurement when the low-power synchronization signal is received, and activates the MR when the low-power wake-up signal is received. The LR reception unit receives the sequence ID of the low-power synchronization signal from the MR, and on the basis of the sequence ID of the low-power synchronization signal, receives the low-power synchronization signal addressed thereto that is transmitted from the network.