摘要:
The audio coding method and system of lattice vector quantization is provided in the invention. The method comprises: dividing frequency domain coefficients of an audio signal for which a modified discrete cosine transform (MDCT) has been performed into a plurality of coding sub-bands, and quantizing and coding an amplitude envelope value of each coding sub-band to obtain coded bits of amplitude envelopes; performing bit allocation on each coding sub-band, and performing normalization, quantization and coding respectively on vectors in a low bit coding sub-band with pyramid lattice vector quantization and on vectors in a high bit coding sub-band with sphere lattice vector quantization to obtain coded bits of the frequency domain coefficients; multiplexing and packing the coded bits of the amplitude envelope and the coded bits of the frequency domain coefficients of each coding sub-band, then sending them to a decoding side.
摘要:
The invention provides a compensation method for audio frame loss in a MDCT domain, the method comprising: when a frame currently lost is a Pth frame, obtaining a set of frequencies to be predicted, and for each frequency in the set, using phases and amplitudes of a plurality of frames before a (P−1)th frame in a MDCT-MDST domain to predict a phase and an amplitude of the Pth frame, and using the predicted phase and amplitude to obtain a MDCT coefficient of the Pth frame at each corresponding frequency; for a frequency outside the set, using MDCT coefficients of a plurality of frames before the Pth frame to calculate a MDCT coefficient value of the Pth frame at the frequency; performing an IMDCT for the MDCT coefficients of the Pth frame to obtain a time domain signal of the Pth frame.
摘要:
The invention provides a compensation method for audio frame loss in a MDCT domain, the method comprising: when a frame currently lost is a Pth frame, obtaining a set of frequencies to be predicted, and for each frequency in the set, using phases and amplitudes of a plurality of frames before a (P−1)th frame in a MDCT-MDST domain to predict a phase and an amplitude of the Pth frame, and using the predicted phase and amplitude to obtain a MDCT coefficient of the Pth frame at each corresponding frequency; for a frequency outside the set, using MDCT coefficients of a plurality of frames before the Pth frame to calculate a MDCT coefficient value of the Pth frame at the frequency; performing an IMDCT for the MDCT coefficients of the Pth frame to obtain a time domain signal of the Pth frame.
摘要:
The invention features methods for evaluating the conformation of a polymer, for example, for determining the conformational distribution of a plurality of polymers and to detect binding or denaturation events. The methods employ a nanopore which the polymer, e.g., a nucleic acid, traverses. As the polymer traverses the nanopore, measurements of transport properties of the nanopore yield data on the conformation of the polymer.
摘要:
A solid state nanopore device including two or more materials and a method for fabricating the same. The device includes a solid state insulating membrane having an exposed surface, a conductive material disposed on at least a portion of the exposed surface of the solid state membrane, and a nanopore penetrating an area of the conductive material and at least a portion of the solid state membrane. During fabrication a conductive material is applied on a portion of a solid state membrane surface, and a nanopore of a first diameter is formed. When the surface is exposed to an ion beam, material from the membrane and conductive material flows to reduce the diameter of the nanopore. A method for evaluating a polymer molecule using the solid state nanopore device is also described. The device is contacted with the polymer molecule and the molecule is passed through the nanopore, allowing each monomer of the polymer molecule to be monitored.
摘要:
Provided is a cancer therapeutic agent comprising a cancer targeting molecule linked to a liver-expressed chemokine (LEC). In one embodiment, the cancer targeting molecule is an antibody that targets cancer cells or tumors in vivo. The cancer targeting molecule is associated non-covalently or covalently with LEC. The cancer therapeutic agents of the invention are useful for the treatment of cancer in an individual by reducing the size of a tumor or inhibiting the growth of cancer cells in an individual and/or by inhibiting the development of metastasis. The effectiveness of the therapy using the LEC cancer therapeutic agents can be increased by reducing the activity of immunoregulatory T cells and/or by adoptively transferring immune T cells.
摘要:
The invention features methods for evaluating the conformation of a polymer, for example, for determining the conformational distribution of a plurality of polymers and to detect binding or denaturation events. The methods employ a nanopore which the polymer, e.g., a nucleic acid, traverses. As the polymer traverses the nanopore, measurements of transport properties of the nanopore yield data on the conformation of the polymer.
摘要:
The invention features methods for evaluating the conformation of a polymer, for example, for determining the conformational distribution of a plurality of polymers and to detect binding or denaturation events. The methods employ a nanopore which the polymer, e.g., a nucleic acid, traverses. As the polymer traverses the nanopore, measurements of transport properties of the nanopore yield data on the conformation of the polymer.
摘要:
There is provided controlled fabrication of a solid state structural feature on a solid state structure by exposing the structure to a fabrication process environment the conditions of which are selected to produce a prespecified feature in the structure. A physical detection species is directed toward a designated structure location during process environment exposure of the structure, and the detection species is detected in a trajectory from traversal of the designated structure location, to indicate changing physical dimensions of the prespecified feature. The fabrication process environment is then controlled in response to the physical species detection to fabricate the structural feature. Also provided is a method for controlling a physical dimension of a structural feature or to form a feature by exposing the structure to a flux of ions at a selected structure temperature, the exposure conditions being controlled to cause formation of the feature or to cause at least one physical dimension of the feature to be changed, substantially by transport of material of the structure to the structural feature in response to the ion flux exposure.
摘要:
System and methods of managing reference frame adaptively for video communication under a network are provided. The system adaptively decides the interval between each I frame, the bitrate of the encoded bit steams, and the resolution of the encoded video to achieve quick connection. The system may set the appropriate reference frame(s) for the current frame, manage the reference frame(s) in the DPB to be long/short term reference frame(s) or mark them as unused for reference; mark the current frame to be a long term reference frame, a short term reference frame, unused for reference or skip encoding the current frame; adaptively change the ratio of long term reference frame(s) with respect to the short term reference frame(s) in the DPB; adaptively change the frequency ratio of marking the current frame as long term reference frame and marking the current frame as short term reference frame.