936 resultados para Direct-sequence code division multiple access
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Mode of access: Internet.
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"September 1977."
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Mode of access: Internet.
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Vols. for 1970-1972 published by the Public Health Service; 1976- by the Public Health Service, Food and Drug Administration; 1980- by the U.S. Dept. of Health and Human Services, Public Health Service, Food and Drug Administration.
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Mode of access: Internet.
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The ed. issued by the Board of Fish and Game Commissioners (the under its earlier name: State Board of Fish Commissioners); -28th, 35th- by the Division of Fish and Game of the Dept. of Natural Resources (on cover of 27th ed.: Pub. by the Fish and Game Commission); 29th-34th comp. by the Bureau of Game Conservation of the Division of Fish and Game
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Supplements accompany some vols.
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Has supplements.
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Title varies slightly.
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Later editions issued in three parts: State government, Government of counties, Government of cities and local agencies. In this library, the latter two are cataloged separately: Government of counties: KFC758.A29C3; Government of cities and local agencies: KFC752.A29A3.
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Background: This paper describes SeqDoC, a simple, web-based tool to carry out direct comparison of ABI sequence chromatograms. This allows the rapid identification of single nucleotide polymorphisms (SNPs) and point mutations without the need to install or learn more complicated analysis software. Results: SeqDoC produces a subtracted trace showing differences between a reference and test chromatogram, and is optimised to emphasise those characteristic of single base changes. It automatically aligns sequences, and produces straightforward graphical output. The use of direct comparison of the sequence chromatograms means that artefacts introduced by automatic base-calling software are avoided. Homozygous and heterozygous substitutions and insertion/deletion events are all readily identified. SeqDoC successfully highlights nucleotide changes missed by the Staden package 'tracediff' program. Conclusion: SeqDoC is ideal for small-scale SNP identification, for identification of changes in random mutagenesis screens, and for verification of PCR amplification fidelity. Differences are highlighted, not interpreted, allowing the investigator to make the ultimate decision on the nature of the change.
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A series of highly functionalized cyclic enones were obtained from Mannich, Morita-Baylis-Hiliman and elimination reaction with cyclic enones.