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Sampling sequence

Program the pump to purge out the column and shut down the pump automatically after the sample sequence. [Pg.259]

In order to show that the selectivity of the separation remained constant throughout the entire sample sequence, the selectivity solution is re-injected after each 10 sample injections and at the end of the sequence. [Pg.66]

Figure 3.30 (A) Current-time curves illustrating the sampling sequence for current-sampled polarography if, diffusion-controlled faradaic current id), double-layer charging current it = if + idl. (B) Current-sampled polarogram. Figure 3.30 (A) Current-time curves illustrating the sampling sequence for current-sampled polarography if, diffusion-controlled faradaic current id), double-layer charging current it = if + idl. (B) Current-sampled polarogram.
The Crochiere and Rabiner equation for interpolation/decimation by a fixed factor of L IM is summarized here. The output sample sequence y m is formed by the convolution ... [Pg.180]

The filters hk(n) can be desingned to satisfy a perfect reconstruction constraint f k (n) — (n) where 8( ) is the unit sample sequence. One sufficient condition for perfect reconstruction is that the length of h ri) be less than the frequency sampling factor, i.e., S[Pg.507]

After a sample sequence has been analyzed, the analyst evaluates a computer printout with the raw analytical data and the computer-calculated analytical results. The analyst verifies that the QC acceptance criteria for daily calibration verifications, the surrogate and internal standards, and laboratory QC samples have been met. This review enables the analyst to determine whether reanalysis of samples will be required. Sample dilutions may be also needed if analyte concentrations in samples exceed the instrument calibration range. [Pg.196]

To discover new fitness peaks, the neutral network must be sufficiently extended, allowing neutral drift to effectively sample sequence space. A neutral network can be characterized by a mean fraction of neutral neighbors A (Reidys et al., 1997). If A exceeds a threshold A,., then the network is connected and dense, making it more likely the network percolates through sequence space. If A < Ac, the networks are partitioned into components. Using random graph theory, the threshold is derived analytically as... [Pg.144]

As already noted, the properties of convolution and correlation are the same, whether or not a continuous or discrete transformation is used, but because of the cyclic nature of sampled sequences discussed previously, the mechanics of calculating correlation and convolution of functions are somewhat different. The discrete convolution property is applied to a periodic signal 5 and a finite, but periodic, sequence r. The period of 5 is N, so that 5 is completely determined by the N samples s0, Sj,. .., %. The duration of the finite sequence r is assumed to be the same as the period of the data N samples. Then, the convolution of 5 and r is... [Pg.392]

HPLC itself is now considered to be a fuUy automated system. Once the solutions are placed in vials and sample sequence is programmed into the software, the auto-injector injects as stated in the sample sequence and it runs as specified in the instrument method. Many types of software, once programmed, also allow integration, processing, and reporting of an entire HPLC run to be performed automatically once the run is completed. [Pg.719]

It is also possible to use antibody based approaches to assay the accumulation of enzymes involved in denitrification pathways in environmental samples. Ward and Cockroft (1993) developed antisera to nitrite reductase from a marine Pseudomonas stutzeri isolate, and assayed sediment, water column and microbial mat samples. The antibody identified nitrite reductase in mat samples and was more specific than a DNA probe designed against the same species (Ward and Cockroft, 1993). JVIore recently, other strains of denitrifiers have been isolated from both sediment and water column samples. Sequence information regarding the denitrifying genes should prove invaluable for future refinement of both sequence based approaches and the development of additional antibodies to denitrifiers important in the marine environment. [Pg.1326]

Sample Sequence Expected monoisotopic mass Observed mass (amu)... [Pg.407]

From these arrangement results two groups of test samples each with three TRIOs randomly distributed. One group starts on the left with the A sample, sequence is AAB, ABA, ABB, and the other on the left with the B sample, i.e. BAA, BAB, BBA. [Pg.581]

Limits of Quantitation. The system s ability to detect the LOQ should be evaluated with each sample sequence. An injection of the LOQ concentration during SS evaluation may also be used as a rough check of the linearity of the system over the range from LOQ to 100% of the target active concentration. [Pg.426]

If there is no company policy, a suggested sample sequence scheme, including order and number of injections of standards, blanks, system suitability, controls, and samples... [Pg.427]

Fig. 5.64. Interactive exploring (sample sequence trace) and aggregation of subsequences (phase 2)... Fig. 5.64. Interactive exploring (sample sequence trace) and aggregation of subsequences (phase 2)...
Fig. 2. Probe overlaps and assembly branches. A A sample sequence containing known primer sequences PPPPPPP at each end and two 7-mer repeat sequences is shown. B Assembly using overlapped probes is initiated at the 5 end by first selecting a positive probe that corresponds to the primer sequence. Sequence extension continues in the 3 direction until the first branching point, where two possible options for further extension occur (GGTCCCTc and GGTCCCTa). The branching process (C) leads to many alternative sequences. Requiring that the sequence must end with the 3 primer and that sequence sub-fragments between branching points occur only once results in assembly of two possible sequences (D), which differ in placement of CAA and AAT sub-sequences... Fig. 2. Probe overlaps and assembly branches. A A sample sequence containing known primer sequences PPPPPPP at each end and two 7-mer repeat sequences is shown. B Assembly using overlapped probes is initiated at the 5 end by first selecting a positive probe that corresponds to the primer sequence. Sequence extension continues in the 3 direction until the first branching point, where two possible options for further extension occur (GGTCCCTc and GGTCCCTa). The branching process (C) leads to many alternative sequences. Requiring that the sequence must end with the 3 primer and that sequence sub-fragments between branching points occur only once results in assembly of two possible sequences (D), which differ in placement of CAA and AAT sub-sequences...
The second test, which required N 3 20, is a graphical method for detecting trends in sample compositions when the latter are plotted versus sample sequence. Seven successive results on one side of the mean m, indicate that there is a trend in the sample compositions rather than a purely random arrangement. The authors advise a repetition of this test to confirm whether this trend exists. If the trend is still indicated the batch is not well blended. [Pg.269]

Use vials with thin septa to prevent sample evaporation particularly if the sample solvent is volatile. Avoid sampling the same standard vial excessively. Use multiple standard vials for long sample sequences. [Pg.123]

When a new sample is inserted into the sample table, only the sample. cid need be specified. The default value for id will cause a new sample.id to be taken from the uniq samples sequence. The default value for sample.prepared will cause the current time to be inserted into that column. If a further specification of the same sample needs to be made, the following SQL will suffice to add compound id 55. [Pg.164]


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See also in sourсe #XX -- [ Pg.157 ]




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Protein sequence-structure sample structures

Sequencing with large samples

Sequencing with small samples

Sequencing, proteins sample preparation

Transition path sampling sequences

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