Abstract:
A collapsible and assembled container for sterilization, including but not limited to UV sterilization that objected placed in the container. The container includes moveable panels (1, 2, 3, 4) with an electronic circuit board (100) including one or more actuating elements such as UV LEDs and switch elements (6A, 6B, 6C). The moveable panels further includes sensors (5A, 5B, 5C) that cooperate with switch elements (6A, 6B, 6C) to activate the actuating elements only when the collapsible container is fully and correctly deployed. The container prohibits the actuating elements from being activated unless the collapsible container is fully and correctly deployed, and prevents harmful exposure to the actuating elements that can lead to eye damage, skin cancer, etc. to the user.
Abstract:
This disclosure relates to systems and methods that identify, predict, and rank immunogenic T-cell epitopes. In particular, this disclosure identifies epitopes that arose from disease-associated mutations, wherein the epitopes are predicted to elicit immune response from T cells. Specifically, this disclosure simultaneously considers peptide-level information, including MHC Class I and II presentation, helper and cytotoxic T cell response and sample-level information, including mutation clonality and MHC allele dosage. In some embodiment, the systems and methods are used for personalized treatment of cancers.
Abstract:
This disclosure describes techniques for simplifying depth inter mode coding in a three-dimensional (3D) video coding process, such as 3D-HEVC. The techniques may include generating a motion parameter candidate list for a current depth prediction unit (PU) in a depth component of a current view of the multiview video data. The techniques may include deriving one or more candidates for the motion parameter candidate list based at least in part on accessing a reference texture block. The techniques may include deriving a derived depth coding (DDD) candidate for the motion parameter candidate list based only on the reference texture block that is already accessed for deriving the one or more candidates for the motion parameter candidate list. The described techniques include decoding or encoding motion information for the current depth PU based on the motion parameter candidate list for the current depth PU.
Abstract:
This disclosure describes techniques for constraining depth intra mode coding in a three-dimensional (3D) video coding process, such as 3D-High Efficiency Video Coding (3D-HEVC). In some examples, the techniques for constraining depth intra mode coding may prevent transform tree nodes from being split into sub-transform tree nodes when a depth prediction unit that corresponds to the transform tree node is predicted according to a depth modeling mode (DMM). In further examples, the techniques for constraining depth intra mode coding may prevent the DMM mode from being used when the maximum transform unit size that corresponds to a depth prediction unit is greater than the size of the depth prediction unit. The techniques for constraining depth intra mode coding may prevent characteristics of the DMM prediction modes used in 3D-HEVC and characteristics of the transform tree subdivision used in 3D-HEVC from interfering with each other.
Abstract:
This disclosure is related to depth Intra mode coding in a 3D video coding process, such as 3D-HEVC. The disclosure describes techniques for simplifying the derivation of an initialization value for determining an initialized probability state for CABAC coding a depth intra mode syntax element. In some examples, the techniques may reduce the number of context models and/or buffer size used for storing context information by an encoder or decoder for derivation of the initial probability state.
Abstract:
In general, this disclosure describes techniques for simplifying SDC coding of large intra-prediction blocks, such as 64x64 blocks, in a 3D video coding process, such as 3D-HEVC. In some examples, the techniques may include processing 64x64 intra-prediction blocks as four 32x32 intra-prediction blocks in intra SDC. Processing large intra-prediction blocks as multiple, smaller intra-prediction blocks in intra SDC may reduce maximum buffer size requirements in the intra SDC process.
Abstract:
Nutritive polypeptides are provided herein. Also provided are various other embodiments including nucleic acids encoding the polypeptides, recombinant microorganisms that make the polypeptides, vectors for expressing the polypeptides, methods of making the polypeptides using recombinant microorganisms, compositions and formulations that comprise the polypeptides, and methods of using the polypeptides, compositions and formulations.
Abstract:
A video coder may perform a simplified depth coding (SDC) mode, including simplified residual coding, to code a depth block according to any of a variety of, e.g., at least three, depth intra prediction modes. For example, the video coder may perform the SDC mode for coding a depth block according to depth modeling mode (DMM) 3, DMM 4, or a region boundary chain coding mode. In such examples, the video coder may partition the depth block, and code respective DC residual values for each partition. In some examples, the video coder may perform the SDC mode for coding a depth block according to an intra prediction mode, e.g., an HEVC base specification intra prediction mode, such as a DC intra prediction mode or one of the directional intra prediction modes. In such examples, the video coder may code a single DC residual value for the depth block.
Abstract:
In an example, a process for coding video data includes coding, with a variable length code, a syntax element indicating depth modeling mode (DMM) information for coding a depth block of video data. The process also includes coding the depth block based on the DMM information.