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prove to be more susceptible to skin cancer, infection, or even premature wrinkling after 20 or 30 years.

drexp(ikd' r)

Draw graphics anywhere on your forms where you want to add some visual effects or draw the user s attention

(7.3.43)

2 f! (k s, ki ) 1 )

(raj - ral)))

(7.3.44a)

Tools provided with Visual Studio and third-party products can help you build and print reports But what if the users just want to print the contents of their forms A new method in the NET Framework makes printing forms relatively easy

:! 1

lij drajl dr allfl exp(ikd (raj - r al))9s(raj, ral.) (7.3.44b)

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Computing is an enabling technology at the core of the biotech revolution Virtually all of the advances in molecular biology over the last two decades have been due in part to the introduction and rapid evolution of the per sonal computer, high-speed international and local networks, and innova tive software The acceleration in the quantity of holdings in the online biological databases re ects the rapid growth of the Internet, constantly in creasing processor power, and a drop in the cost of computing power Whether the task is diagnose and treat genetic diseases or to develop new pharmaceuticals, there is simply too much biological data to search through, manage and manipulate manually What s more, not only is there more data than can reasonably be analyzed without computer-based tools, but also in some areas the data are still multiplying exponentially.

where the joint probability density function of secondary scatterers is, analogous to (7.3.8c),

(7.3.45)

with 9s being the pair distribution function of secondary scatterers. To illustrate, we consider a special case with 9p = 1,9s = 1, and let v p be a cubic volume of l~. Then the integrals in (7.3.43) and (7.3.44) can be carried out readily. Putting the results into (7.3.42) gives

4

p(ks , ki ) =

(7.3.46)

(7.3.22), where the particles are not in clusters. In some cases, the result of (7.3.46) can be much larger than that of (7.3.22). This shows that when small point scatterers cluster to form "larger" particles, the scattering can be much larger even when the total number of small point scatteren, remain the same.

In this section we illustrate Monte Carlo simulations of scattering by point scatterers. We calculate the extinction coefficients and phase functions for the cases of uniformly random distribution and the case of clustered random distributions. Consider an incident wave impinging upon N scatterers (7.4.1)

If you implemented your MDI parent form using the MDI Parent Form template, you already have Print, Print Preview, and Print Setup options on the File menu and Print and Print Preview icons on the toolbar You can either remove the options and icons or write code to support them This section provides the code you need to implement them

(7.4.2)

Consider the growth of the freely accessible online gene database, GenBank, maintained by the federally funded US National Center for Biotechnology Information (NCBI), as illustrated in Figure 16 GenBank was started in 1982 with a holding of only about 600 DNA sequences, all sequenced through manual methods Thanks to automated gene-sequencing machines and highly publicized race between Celera Genomics and the government-funded Human Genome Project to map the human genome, GenBank has grown exponentially since about 1998, when it contained data on about three million entries Similarly, Swiss-Prot, a protein data base that is funded and maintained by the Swiss Institute of Bioinformatics (SIB) and the European Bioinformatics Institute (EBI), has roughly doubled in size every ve years since 1986, when there were only a few hundred en tries in the database.

We start by putting N particles in a cubic box of size V = L3. The coordinates rj = (Xj,Yj,Zj),j = 1,2, ... ,N, are determined by choosing three random numbers between 0 and 1 and then multiplying them by L. Once the positions of the N particles are given, we can solve the Foldy-Lax multiple scattering equations

= E-

(-.)

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