Titlebook: Bacterial Artificial Chromosomes; Volume 1: Library Co Shaying Zhao,Marvin Stodolsky Book 2004 Humana Press 2004 BAC.Chromosom.DNA.DNA sequ

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书目名称Bacterial Artificial Chromosomes影响因子(影响力)




书目名称Bacterial Artificial Chromosomes影响因子(影响力)学科排名




书目名称Bacterial Artificial Chromosomes网络公开度




书目名称Bacterial Artificial Chromosomes网络公开度学科排名




书目名称Bacterial Artificial Chromosomes被引频次




书目名称Bacterial Artificial Chromosomes被引频次学科排名




书目名称Bacterial Artificial Chromosomes年度引用




书目名称Bacterial Artificial Chromosomes年度引用学科排名




书目名称Bacterial Artificial Chromosomes读者反馈




书目名称Bacterial Artificial Chromosomes读者反馈学科排名

Rustproof

Cupping

Preparation of BAC Libraries From Bacterial Genomes by In Vitro Packaging,ery low frequency. On the other hand, in vitro packaging limits the size of the DNA based on the phage head stability. However, in vitro package is the most efficient method for introducing large-insert clones.

crescendo

BAC Finishing Strategies,PCI-13 from P. de Jong (.) were fingerprinted, and the resulting maps of these overlapping clones have been integrated with clone maps of individual chromosomes generated by other centers (.). Sets of minimal overlapping clones have been selected for sequencing from the resulting maps.

自制

Projection

George J. Vachtsevanos,Kimon P. Valavanisse it relies on characterization of random clones in libraries comprising YACs or BACs. Even if a YAC or BAC contains an entire gene, the specific recovery of the gene was an arduous process. Often a gene is available as a contiguous set of fragments that must be pieced together.

Ebct207

Sexual Minority Groups and Urban Healthe found that templates produced through RCA yield more consistent and higher-quality sequence than identical templates generated from plasmid-prep methods. The protocol is simple, amenable to high throughput, and currently in use at the DOE Joint Genome Institute (Walnut Creek, CA) for the daily production of 30,000 sequencing templates.

连累

Tree Roots versus Sidewalks and Sewers,e the sequences contained in them. Thus, both physical and functional mapping objectives would be facilitated by an efficient strategy for making nested deletions from one end of the insert DNA in a BAC or PAC clone.

NEX

hidebound

Rolling Circle Amplification for Sequencing Templates,e found that templates produced through RCA yield more consistent and higher-quality sequence than identical templates generated from plasmid-prep methods. The protocol is simple, amenable to high throughput, and currently in use at the DOE Joint Genome Institute (Walnut Creek, CA) for the daily production of 30,000 sequencing templates.