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This phase of the life cycle is when the network is actually built. The time to install and commission each piece of equipment is always short, so testing for correct equipment implementation must be carried out efficiently. Automated testing is essential to reducing the time taken to install and commission a base station. Because implementations vary from vendor to vendor, the tests required also will vary. To ensure efficient installation and commissioning, the automated testing must be tailored to each vendor s implementation. Specialized test equipment is available to meet these needs. The HP 8921 series of test sets provide base station site test solutions for a number of wireless systems, including AMPS, CDMA, and TDMA. The base station testing carried out in this phase typically is a subset of the testing carried out in the manufacturing test (see 19) of the equipment. The tests carried out at installation and commissioning are specific to the type of wireless system being installed. Typical tests for a CDMA base station include waveform quality, frequency error, time offset, and code domain power. (The code domain power measurement calculates the power in each Walshcoded signal to ensure that all of the codes can be used to carry calls.) Base stations typically are connected to the test set for testing; if this goes well, some tests are run with the BS connected to the live network. These tests typically are various call scenarios, such as mobile-originated calls, mobile-terminated calls, and handovers. At this point some network- and vendor-specific features come in to play. Some base station implementations allow for the BS to be connected to the network, but with only specialized mobiles allowed access. This is particularly useful for
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Strictly speaking, IP is a routing protocol for the passing of data packets. Other protocols invoke IP for the purposes of getting those data packets from origination to destination. Thus, IP must work with the cooperation of
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The using directive has a second form that creates another name, called an alias, for a type or a namespace. This form is shown here: using alias = name; Here, alias becomes another name for the type (such as a class type) or namespace specified by name. Once the alias has been created, it can be used in place of the original name. Here the example from the preceding section has been reworked so that an alias for Counter.CountDown called MyCounter is created:
The rst tool in writing for response is knowing exactly what you want your readers to do as a result of reading your material. Determining an action objective makes writing easier and more straightforward. Keeping the end result in your mind as you write enables you to aim for it. When you know where you re heading, you re more likely to get there. Let s say, for example, that your boss has asked you to organize the summer picnic. You ve selected the venue and need to announce it. You
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Voice signals are rich in information content, but also tend to be redundant. Depending on the implementation, the size of voice templates is about 70 or 80 bytes for each second recorded. Storage requirements for voiceprints are large when compared to other biometrics, but are quite manageable for small applications that use short, single-word passwords. Template size is an issue for applications with a large population of users or for collection and analysis of long, text-independent samples and associated reference data. Voice samples are a waveform with time on the horizontal dimension and loudness on the vertical, as shown in Figure 4-3. The frequency of the wave refers to the number of complete cycles per second that the wave oscillates back and forth. Conventional analog phones transmit electromagnetic waves that cycle about 3,000 times per second. This frequency is normally expressed as 3,000 Hertz (Hz), or 3 kHz. When sound or voice waveforms are converted into digital representations, the signals are sampled over many small time intervals (T). This allows the original signal to be represented at multiples of the sampling period, as x(nT). Digital signals are technically superior to analog because they operate at higher speeds, have clearer voice quality, and fewer errors. Digital telephone lines operate at 8 kHz; however, most nontelephony applications of voice verification prefer voice signals sampled at 12 kHz or 16 kHz. For comparison, standard digital audio for compact discs (CDs) is sampled at a rate of 44.1 kHz.13 Voice verification considers the quality, duration, pitch, and loudness of the signal and compares these characteristics to the previously enrolled utterance. Although the phonetic content or meaning of the utterance is not directly relevant for verification, phonetic features or segments can be used as additional features for comparison. Phonetic units of the language, such as vowels and consonants, are typically of short duration (measured in milliseconds); however, there are methods for marking and extracting this information from speech. Although they are accomplished in a variety of different ways, there are four basic steps to speaker recognition. The first step is the digital acquisition of speech data. The second step is feature selection and extraction. The third step
All of the forces that affect conformation in biomolecules are electrical in nature, meaning they result from attractions or repulsions between charges. However, the specifics of how these attractions or repulsions manifest themselves can vary quite a bit depending on the situation. It is convenient and helpful to classify the various situations and give each a name as if they are actually separate forces. Just keep in mind that each force that we are about to describe is just a particular case or manifestation of the electromagnetic force generated by protons and electrons in the atoms making up biological molecules. We have already described covalent and ionic bonds. Covalent bonds play a major role in determining the primary structure of biomolecules. In Chap. 9 we will see covalent bonds also contribute to secondary and tertiary structure of some molecules via cross-linking, which is the covalent connecting of otherwise distance parts of a molecule. Ionic bonds, as we mentioned, specifically refer to the arrays of bonds between ions in a crystalline solid. Generally these will not concern us since the natural state of biomolecules is not a crystal. (One exception where we might be interested in ionic bonds in biomolecules is in the context of the biophysical technique of X-ray diffraction which requires crystallized samples of biomolecules.) On the other hand there are two cases where we are very interested in the forces between ions because they play a significant role in influencing the conformation of biomolecules. One is the attraction and repulsion of ions in solution (both individual ions and ionized portions of biomolecules) which we mentioned is most aptly treated as a case of ligand binding. The other is the formation of salt bridges, which can be thought of as single ionic bonds (as opposed to the arrays of ionic bonds found in crystals) that hold together otherwise distant parts of a biomolecule. All of the forces we are about to describe exert themselves both between molecules and between different parts of the same molecule. The general term for molecular forces other than covalent and ionic bonds is van der Waals forces, named for Dutch physicist Johannes van der Waals. You should be aware that textbooks vary somewhat in how they use the term van der Waals force. Some use the term very generally as meaning all noncovalent intermolecular forces, including ionic bonds. Others may limit its use to a subset of the forces described in the following sections. We will consider
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