2011, ISBN: 9781156436837

[ED: Pappeinband], [PU: Bertrams Print On Demand], - Source: Wikipedia. Pages: 37. Chapters: DNA sequencer, Transmission electron microscopy DNA sequencing, Exome sequencing, DNA nanoball… Más…

[ED: Pappeinband], [PU: Bertrams Print On Demand], - Source: Wikipedia. Pages: 37. Chapters: DNA sequencer, Transmission electron microscopy DNA sequencing, Exome sequencing, DNA nanoball sequencing, DNA sequencing theory, 454 Life Sciences, Single molecule fluorescent sequencing, 2 Base Encoding, Ion semiconductor sequencing, Nanopore sequencing, Paired-end Tags, Microfluidic Sanger sequencing, Pyrosequencing, ABI Solid Sequencing, Single molecule real time sequencing, Restriction site associated DNA markers, Sequencing by ligation, Velvet assembler, Sequencing by hybridization, NGSmethDB, BFAST, Peak calling, Restriction fragment mass polymorphism, Standard Flowgram Format, DNA Bank. Excerpt: DNA sequencing includes several methods and technologies that are used for determining the order of the nucleotide bases-adenine, guanine, cytosine, and thymine-in a molecule of DNA. Knowledge of DNA sequences has become indispensable for basic biological research, other research branches utilizing DNA sequencing, and in numerous applied fields such as diagnostic, biotechnology, forensic biology and biological systematics. The advent of DNA sequencing has significantly accelerated biological research and discovery. The rapid speed of sequencing attained with modern DNA sequencing technology has been instrumental in the sequencing of the human genome, in the Human Genome Project. Related projects, often by scientific collaboration across continents, have generated the complete DNA sequences of many animal, plant, and microbial genomes. The first DNA sequences were obtained in the early 1970s by academic researchers using laborious methods based on two-dimensional chromatography. Following the development of dye-based sequencing methods with automated analysis, DNA sequencing has become easier and orders of magnitude faster. RNA sequencing was one of the earliest forms of nucleotide sequencing. The major landmark of RNA sequencing is the sequence of the first complete gene and the complete genome of Bacteriophage MS2, identified and published by Walter Fiers and his coworkers at the University of Ghent (Ghent, Belgium), between 1972 and 1976. Prior to the development of rapid DNA sequencing methods in the early 1970s by Frederick Sanger at the University of Cambridge, in England and Walter Gilbert and Allan Maxam at Harvard, a number of laborious methods were used. For instance, in 1973, Gilbert and Maxam reported the sequence of 24 basepairs using a method known as wandering-spot analysis. The chain-termination method developed by Sanger and coworkers in 1977 soon became the method of choice, owing to its relative ease and reliability. It involves separating DNA base - Besorgungstitel - vorauss. Lieferzeit 3-5 Tage.., [SC: 0.00]<

2011, ISBN: 9781156436837

[ED: Pappeinband], [PU: Bertrams Print On Demand], - Source: Wikipedia. Pages: 37. Chapters: DNA sequencer, Transmission electron microscopy DNA sequencing, Exome sequencing, DNA nanoball… Más…

[ED: Pappeinband], [PU: Bertrams Print On Demand], - Source: Wikipedia. Pages: 37. Chapters: DNA sequencer, Transmission electron microscopy DNA sequencing, Exome sequencing, DNA nanoball sequencing, DNA sequencing theory, 454 Life Sciences, Single molecule fluorescent sequencing, 2 Base Encoding, Ion semiconductor sequencing, Nanopore sequencing, Paired-end Tags, Microfluidic Sanger sequencing, Pyrosequencing, ABI Solid Sequencing, Single molecule real time sequencing, Restriction site associated DNA markers, Sequencing by ligation, Velvet assembler, Sequencing by hybridization, NGSmethDB, BFAST, Peak calling, Restriction fragment mass polymorphism, Standard Flowgram Format, DNA Bank. Excerpt: DNA sequencing includes several methods and technologies that are used for determining the order of the nucleotide bases-adenine, guanine, cytosine, and thymine-in a molecule of DNA. Knowledge of DNA sequences has become indispensable for basic biological research, other research branches utilizing DNA sequencing, and in numerous applied fields such as diagnostic, biotechnology, forensic biology and biological systematics. The advent of DNA sequencing has significantly accelerated biological research and discovery. The rapid speed of sequencing attained with modern DNA sequencing technology has been instrumental in the sequencing of the human genome, in the Human Genome Project. Related projects, often by scientific collaboration across continents, have generated the complete DNA sequences of many animal, plant, and microbial genomes. The first DNA sequences were obtained in the early 1970s by academic researchers using laborious methods based on two-dimensional chromatography. Following the development of dye-based sequencing methods with automated analysis, DNA sequencing has become easier and orders of magnitude faster. RNA sequencing was one of the earliest forms of nucleotide sequencing. The major landmark of RNA sequencing is the sequence of the first complete gene and the complete genome of Bacteriophage MS2, identified and published by Walter Fiers and his coworkers at the University of Ghent (Ghent, Belgium), between 1972 and 1976. Prior to the development of rapid DNA sequencing methods in the early 1970s by Frederick Sanger at the University of Cambridge, in England and Walter Gilbert and Allan Maxam at Harvard, a number of laborious methods were used. For instance, in 1973, Gilbert and Maxam reported the sequence of 24 basepairs using a method known as wandering-spot analysis. The chain-termination method developed by Sanger and coworkers in 1977 soon became the method of choice, owing to its relative ease and reliability. It involves separating DNA base - Besorgungstitel - vorauss. Lieferzeit 3-5 Tage.., [SC: 4.00]<

ISBN: 9781156436837

[ED: Taschenbuch], [PU: Books LLC, Reference Series], Source: Wikipedia. Pages: 37. Chapters: DNA sequencer, Transmission electron microscopy DNA sequencing, Exome sequencing, DNA nanobal… Más…

[ED: Taschenbuch], [PU: Books LLC, Reference Series], Source: Wikipedia. Pages: 37. Chapters: DNA sequencer, Transmission electron microscopy DNA sequencing, Exome sequencing, DNA nanoball sequencing, DNA sequencing theory, 454 Life Sciences, Single molecule fluorescent sequencing, 2 Base Encoding, Ion semiconductor sequencing, Nanopore sequencing, Paired-end Tags, Microfluidic Sanger sequencing, Pyrosequencing, ABI Solid Sequencing, Single molecule real time sequencing, Restriction site associated DNA markers, Sequencing by ligation, Velvet assembler, Sequencing by hybridization, NGSmethDB, BFAST, Peak calling, Restriction fragment mass polymorphism, Standard Flowgram Format, DNA Bank. Excerpt: DNA sequencing includes several methods and technologies that are used for determining the order of the nucleotide bases-adenine, guanine, cytosine, and thymine-in a molecule of DNA. Knowledge of DNA sequences has become indispensable for basic biological research, other research branches utilizing DNA sequencing, and in numerous applied fields such as diagnostic, biotechnology, forensic biology and biological systematics. The advent of DNA sequencing has significantly accelerated biological research and discovery. The rapid speed of sequencing attained with modern DNA sequencing technology has been instrumental in the sequencing of the human genome, in the Human Genome Project. Related projects, often by scientific collaboration across continents, have generated the complete DNA sequences of many animal, plant, and microbial genomes. The first DNA sequences were obtained in the early 1970s by academic researchers using laborious methods based on two-dimensional chromatography. Following the development of dye-based sequencing methods with automated analysis, DNA sequencing has become easier and orders of magnitude faster. RNA sequencing was one of the earliest forms of nucleotide sequencing. The major landmark of RNA sequencing is the sequence of the first complete gene and the complete genome of Bacteriophage MS2, identified and published by Walter Fiers and his coworkers at the University of Ghent (Ghent, Belgium), between 1972 and 1976. Prior to the development of rapid DNA sequencing methods in the early 1970s by Frederick Sanger at the University of Cambridge, in England and Walter Gilbert and Allan Maxam at Harvard, a number of laborious methods were used. For instance, in 1973, Gilbert and Maxam reported the sequence of 24 basepairs using a method known as wandering-spot analysis. The chain-termination method developed by Sanger and coworkers in 1977 soon became the method of choice, owing to its relative ease and reliability. It involves separating DNA baseVersandfertig in 3-5 Tagen, [SC: 0.00]<

2012, ISBN: 1156436834

Kartoniert / Broschiert NATURE / Animals / Insects & Spiders, mit Schutzumschlag neu, [PU:Books LLC, Reference Series]

2012, ISBN: 1156436834

Kartoniert / Broschiert NATURE / Animals / Insects & Spiders, mit Schutzumschlag 11, [PU:Books LLC, Reference Series]