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Row decoder

Figure 16.3 shows a circuit diagram of an electronic artificial skin system. Integrated circuits are formed by organic transistors with a pentacene channel layer this has p-type conduction and consists of sensor matrix, column selector, and row decoder. The manufacturing process flow of the sensor matrix has been described above other circuits are processed similarly. [Pg.398]

Fig. 16.3. Circuit diagram of electronic artificial skin consisting of a 16 x 16 access transistor matrix, column selector, and row decoder. The manufactured transistor with pentacene channel layer has p-type conduction. R0-R3 are row addresses, C0-C1 are column... Fig. 16.3. Circuit diagram of electronic artificial skin consisting of a 16 x 16 access transistor matrix, column selector, and row decoder. The manufactured transistor with pentacene channel layer has p-type conduction. R0-R3 are row addresses, C0-C1 are column...
In order to realize the cut-and-paste feature, all the circuits of the system must be scalable in size. The access FET matrix is scalable because it is a simple repetition of senseis. The FET matrix can be cut to any required size. We have also developed row decoders and column selectors that are equally scalable. [Pg.534]

FIGURE 6.3.6 A measured waveform of electronic artificial skin. When pressure is applied to the sensor matrix, the pressnre-sensitive mhher becomes condnctive and bit line is pulled up to the supply voltage. (1) The input signals of column and row addresses. (11) The activation signal of the row decoder and column selector. (Ill) The measured waveform. The decoder output (word line) and bit output (bit line). [Pg.536]

Figure 8.34 The crystal structure decoding and deconstruction process for Cr(CO) 6 from (a) the full three-dimensional packing to (b) the enclosure shell of first neighbours to (c) a molecular layer and finally (d) a molecular row. (Reprinted with permission from Section Key Reference 1990 American Chemical Society). Figure 8.34 The crystal structure decoding and deconstruction process for Cr(CO) 6 from (a) the full three-dimensional packing to (b) the enclosure shell of first neighbours to (c) a molecular layer and finally (d) a molecular row. (Reprinted with permission from Section Key Reference 1990 American Chemical Society).
This algorithm takes min(m, n) stages. The total number of pivots accepted is the rank, r, of the equation system.The final array can be decoded by associating each coefficient column with the corresponding variable. Rearranging the array to place the pivotal rows and columns in the order of selection, one can write the results in the partitioned form... [Pg.183]

When searching for local similarities of two molecules, the decoded local shape matrices Ib(a,b,Mi) of molecule M) are compared to various diagonal blocks of the global shape matrix s(a,b,M2) of molecule M2. In the most general case, the local shape matrix Ib(a,b,Mi) is used as a template, and it is compared to k-dimensional blocks of s(a,b,M2) obtained by all possible simultaneous row and column permutations. If the size ordering is considered important then only those permutations are taken which preserve the monotonicity of size ordering in the permuted diagonal block that is compared to the template. A local similarity measure... [Pg.170]

Fig. 5.3.13 Hadamard encoding and decoding for simultaneous four-slice imaging. The encoding is based on four experiments, A-D. In each experiment, all four slices are excited by a multi-frequency selective pulse. Its phase composition is determined by the rows of the Hadamard matrix H2. The image response is the sum of responses for each individual, frequency selective part of the pulse. Thus, addition and subtraction of the responses to the four experiments separates the information for each slice. This operation is equivalent to Hadamard transformation of the set of image responses. Adapted from [Miil21 with permission from Wiley-Liss. Inc., a division of John-Wiley Sons, Inc. Fig. 5.3.13 Hadamard encoding and decoding for simultaneous four-slice imaging. The encoding is based on four experiments, A-D. In each experiment, all four slices are excited by a multi-frequency selective pulse. Its phase composition is determined by the rows of the Hadamard matrix H2. The image response is the sum of responses for each individual, frequency selective part of the pulse. Thus, addition and subtraction of the responses to the four experiments separates the information for each slice. This operation is equivalent to Hadamard transformation of the set of image responses. Adapted from [Miil21 with permission from Wiley-Liss. Inc., a division of John-Wiley Sons, Inc.
Diversity Sciences developed a library synthesis strategy that combines the simplicity of parallel synthesis and the power of resin-mixing techniques. The general format is four 96-well plates that give rise to 384 synthetic wells, as shown in Figure 8.9. The layout of the synthesis blocks enables 16 unique monomers in monomer position A (across rows) and 24 unique monomers in monomer position B (down the columns). All of the 384 wells are preloaded with off-the-shelf resin where each well has a unique binary code embedded in the analytical construct. The first two points of diversity (monomer A and monomer B) is added in all possible combinations by parallel synthesis. Each spatial location has a unique binary-mass code that encodes for a particular combination of monomer A and monomer B. For example, binary code number 8 represents monomer Al and monomer B8. After the addition of monomer B, the resin from all 384 wells is mixed together and split into 96 identical pools, to which monomer C is added. The third monomer, monomer C, is spatially encoded, since the 96 pools are not mixed after the last step and screened as pools. Upon decoding, the identification of the binary code reveals the combination of monomer A and monomer B on each bead. [Pg.243]

The genetic code. The table shows the possible codons found in mRNA. To read the universal biological language from this chart, find the first base in the column on the left, the second base from the row across the top, and the third base from the column to the right. This will direct you to one of the sixty-four squares in the matrix. Within that square you will find the codon and the amino acid that it specifies. In the cell this message is decoded by tRNA molecules like those shown to the right of the table. [Pg.732]

The sensor cells are addressed using the active matrix addressing technique, using two decoders one that acts as a colnmn driver and the other that acts as a row selector. These two decoders are synchronised using two binary counters one that iterates... [Pg.98]

Figure 53 DECODER spectra for (a) no orientation (b) some biaxiality (c) pronounced biaxiality. The top row shows the orientation distribution the middle row, the contour plot of the two-dimensional spectrum the bottom row, the stacked plot. (From Ref. 178, 1993 American Chemical Society.)... Figure 53 DECODER spectra for (a) no orientation (b) some biaxiality (c) pronounced biaxiality. The top row shows the orientation distribution the middle row, the contour plot of the two-dimensional spectrum the bottom row, the stacked plot. (From Ref. 178, 1993 American Chemical Society.)...
Smallest Hamming weight of the heaviest row of H the logic depth of each parity or syndrome bit generator circuit usually depends on the Hamming weight of the associated row. The heaviest row determines the speed of the encoder and the decoder circuits. [Pg.186]

As stated in Section 2.1, once calculated H, encoding and decoding formulas can be obtained easily from it. In this case, u is part of b, and the parity bits are located in the columns with only one 1. Each parity bit is calculated by XORing the bits with a 1 in its row. For example, bit bis of the codeword is a parity bit, because the corresponding column in H has only one 1, in the second row. Searching the other Is in the same row, they are in the columns corresponding to Ui, Us, ue, ug and ug. [Pg.186]


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See also in sourсe #XX -- [ Pg.398 ]




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