摘要:
A coding apparatus which suppresses an extreme increase in a bit rate, includes: a downmixing and coding unit (301) that downmixes audio signals that have been provided, to reduce the number of channels to be fewer than the number of the provided audio signals, and to code the downmix signals; an object parameter extracting unit (304) that extracts parameters indicating correlation between the audio signals; and a multiplexing circuit (309) that multiplexes the extracted parameters with the generated downmix coded signals. The object parameter extracting unit (304) includes: an object classifying unit (305) that classifies each of the provided audio signals into a predetermined one of types based on audio characteristics; and an object parameter extracting circuit (308) that extracts parameters using a temporal granularity and a frequency granularity each of which is determined for a corresponding one of the types.
摘要:
To provide an audio signal processing apparatus which can perform, with low operation amount, audio signal processing that is either time stretch and/or compression processing or frequency modulation processing. The audio signal processing apparatus is intended to transform an input audio signal sequence using a predetermined adjustment factor. The audio signal processing apparatus includes a filter bank (2601) which transforms the input audio signal sequence into Quadrature Mirror Filter (QMF) coefficients using a filter for Quadrature Mirror Filter analysis (a QMF analysis filter) and an adjusting unit (2602) which adjusts the QMF coefficients based on a predetermined adjustment factor.
摘要:
An AC motor is provided. In the AC motor, there are M pieces (M is an integer of 3 or more) of stator pole groups SPG are arranged in a rotor axis direction, where each of the stator poles groups is composed of a plurality of stator poles which are for the same phase and arranged in a circumferential direction of the motor. Between the stator pole groups SPG, “M−1” pieces of annular windings WR are arranged which allow one-way current to flow therethrough. The windings WR are arranged such that the directions of current passing therethrough are reversed in turn in the rotor axis direction. The stator pole groups SPG are excited to generate magnetic fluxes φG directed in a one way. The excited directions of the magnetic fluxes φG are reversed in turn in the rotor axis direction.
摘要:
A liquid crystal display device includes a first substrate, a second substrate, liquid crystal disposed between the first substrate and the second substrate, an electrode formed over the first substrate, and an alignment film disposed between the electrode and the liquid crystal. The electrode has a pad portion that protrudes from at least part of a side of the electrode and electrically leads out onto the first substrate through a conductive material that is located between the second substrate and the first substrate, and a direction in which at least one side of the pad portion which protrudes from the electrode is set to angle of 15° or more and 35° or less relative to a side of the first substrate which crosses the extended line of the at least one side of the pad portion.
摘要:
The present invention discloses an oligonucleotide which comprises a part or the entire sequence of the nucleotide sequence depicted in SEQ ID NO: 1, 2, 3 or 4, or a part or the entire sequence of a nucleotide sequence complementary to the nucleotide sequence, wherein the oligonucleotide is capable of hybridizing with the nucleotide sequence of Mycobacterium kansasii; a primer and a probe for use in the detection of Mycobacterium kansasii comprising the oligonucleotide; and a method for detecting Mycobacterium kansasii using the primer and/or probe.The method for detecting Mycobacterium kansasii enables the detection of M. kansasii more rapidly and with higher accuracy compared with a conventional bacterium identification method performed by culture examination on a bacterium. Further, the method can exclude any false positive result for the diagnosis and can also detect and diagnose M. kansasii with higher accuracy compared with a diagnosis method performed by PCR using a conventional primer and/or probe. Still further, the method can quantify a M. kansasii cell.
摘要翻译:本发明公开了一种寡核苷酸,其包含SEQ ID NO:1,2,3或4所示核苷酸序列的一部分或全部序列,或与该核苷酸序列互补的核苷酸序列的一部分或全部序列,其中 寡核苷酸能够与堪萨斯分枝杆菌的核苷酸序列杂交; 用于检测包含寡核苷酸的堪萨斯分枝杆菌的引物和探针; 以及使用引物和/或探针检测堪萨斯分枝杆菌的方法。 与通过细菌培养检查进行的常规细菌鉴定方法相比,用于检测堪萨斯分枝杆菌的方法能够更快速地和更准确地检测堪萨斯州。 此外,与通过使用常规的引物和/或探针的PCR进行的诊断方法相比,该方法可以排除诊断中的任何假阳性结果,并且还可以以更高的精度检测和诊断堪萨斯堪萨斯州堪萨斯州。 此外,该方法可以量化堪萨斯统计学(Kansasii)细胞。
摘要:
The present invention discloses an oligonucleotide which comprises a part or the entire sequence of the nucleotide sequence shown in SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7 or SEQ ID NO: 8, or a part or the entire sequence of a sequence complementary to the nucleotide sequence shown in SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7 or SEQ ID NO: 8, wherein the oligonucleotide is capable of hybridizing with a nucleotide sequence of Mycobacterium intracellulare gene; a primer or a probe for the detection of M. intracellulare, which comprises the aforementioned oligonucleotide; and a method for detection of M. intracellulare using the aforementioned primer and/or the probe.According to the detection method of the present invention, any false-positive result in diagnosis can be eliminated and detection or diagnosis of M. intracellulare can be carried out with higher accuracy, more preciseness, and more specifically compared to a conventional diagnostic method employing a cell culture assay or a PCR assay. The method also enables to quantify a microbial cell.
摘要翻译:本发明公开了包含SEQ ID NO:1,SEQ ID NO:2,SEQ ID NO:3,SEQ ID NO:4,SEQ ID NO:5所示核苷酸序列的部分或全部序列的寡核苷酸, SEQ ID NO:6,SEQ ID NO:7或SEQ ID NO:8,或与SEQ ID NO:1,SEQ ID NO:2,SEQ ID NO所示的核苷酸序列互补的序列的部分或全部序列 3,SEQ ID NO:4,SEQ ID NO:5,SEQ ID NO:6,SEQ ID NO:7或SEQ ID NO:8,其中所述寡核苷酸能够与胞内分枝杆菌基因的核苷酸序列杂交; 用于检测胞内分枝杆菌的引物或探针,其包含上述寡核苷酸; 以及使用上述引物和/或探针检测胞内分枝杆菌的方法。 根据本发明的检测方法,可以消除诊断中的任何假阳性结果,并且可以以更高的精度,更精确的方式进行胞内分枝杆菌的检测或诊断,并且更具体地与使用 细胞培养测定或PCR测定。 该方法还能够定量微生物细胞。
摘要:
A plurality of audio object (AOB) files and a plurality of picture object (POB) files are stored. Default Playlist Information and sets of Playlist Information each show an order in which AOBs stored in the plurality of AOB files are to be reproduced. The DPLGI includes DPLI_POB_SRPs that specify at least one POB to be displayed during the playback period of AOBs indicated by the playback order given in the Default Playlist Information. The TKGI includes TKI_POB_SRPs that specify at least one POB to be displayed only during the playback period of a particular AOB out of the AOBs indicated by the playback order given in the Default Playlist Information.
摘要:
A semiconductor memory card stores a plurality of audio objects (AOBs) that compose a plurality of tracks and playlist information showing a reproduction order for the tracks. The semiconductor memory card also stores, as resume information (PLMG_RSM_PL), (1) a Playlist_Number showing which playlist information was used the last time playback was performed for the semiconductor memory card, (2) a Track_Number showing the last track to be played back, and (3) a Playback_Time showing a position at which where playback was stopped as a time expressed in relation to the start of the track.
摘要:
There was no method of positioning virtual sound sources of object signals obtained from received coded object information, in a listening space on a receiving site side. Provided are an object decoding unit (806) that receives a plurality of pieces of coded acoustic information coded on an object basis and decodes the received coded acoustic information on an object basis to generate object signals, and an a rendering unit (807) that positions, for each acoustic signal resulting from synthesizing the object signals, a virtual sound source of each of the object signals resulting from the object-based decoding, in a listening space, and priority information indicating a priority of the acoustic signal is multiplexed with the coded acoustic information, and the rendering unit (807) determines, with reference to the priority indicated in the priority information or the number of object signals included in the acoustic signal, a size of an area of the listening space which is allocated to the acoustic signal, and positions, within the area, the virtual sound source of each of the object signals included in the acoustic signal.
摘要:
The object of the present invention is to provide a novel primer for use in the detection of Mycobacterium avium (M. avium), and a method for detection of M. avium conveniently, rapidly and with high precision by using the primer. More specifically, disclosed are an oligonucleotide which comprises a part or an entire of the nucleotide sequence selected from SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:37, SEQ ID NO:38, SEQ ID NO:39, SEQ ID NO:40, SEQ ID NO:41, SEQ ID NO:42, SEQ ID NO:130, SEQ ID NO:131, SEQ ID NO:132, SEQ ID NO:133, SEQ ID NO:134, SEQ ID NO:135 and SEQ ID NO:136, or a part or an entire of the sequence complementary to the nucleotide sequence, and which is capable of hybridizing with the nucleotide sequence for a Mycobacterium avium gene; a primer and a probe for use in the detection of M. avium, which comprises the oligonucleotide; and a method for detection of M. avium using the primer and/or probe.
摘要翻译:本发明的目的是提供一种用于检测鸟分枝杆菌(鸟分枝杆菌)的新型引物,以及通过使用引物,快速且高精度地检测鸟分枝杆菌的方法。 更具体地,公开了包含选自SEQ ID NO:1,SEQ ID NO:2,SEQ ID NO:3,SEQ ID NO:4,SEQ ID NO:5, SEQ ID NO:37,SEQ ID NO:38,SEQ ID NO:39,SEQ ID NO:40,SEQ ID NO:41,SEQ ID NO:42,SEQ ID NO:130,SEQ ID NO:131, NO:132,SEQ ID NO:133,SEQ ID NO:134,SEQ ID NO:135和SEQ ID NO:136,或与核苷酸序列互补的部分或全部序列,并且能够与 鸟分枝杆菌基因的核苷酸序列; 用于检测鸟分枝杆菌的引物和探针,其包含寡核苷酸; 以及使用引物和/或探针检测鸟分枝杆菌的方法。