Titlebook: Bacterial Artificial Chromosomes; Volume 2: Functional Shaying Zhao,Marvin Stodolsky Book 2004 Humana Press 2004

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書目名稱Bacterial Artificial Chromosomes影響因子(影響力)




書目名稱Bacterial Artificial Chromosomes影響因子(影響力)學(xué)科排名




書目名稱Bacterial Artificial Chromosomes網(wǎng)絡(luò)公開度




書目名稱Bacterial Artificial Chromosomes網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Bacterial Artificial Chromosomes被引頻次




書目名稱Bacterial Artificial Chromosomes被引頻次學(xué)科排名




書目名稱Bacterial Artificial Chromosomes年度引用




書目名稱Bacterial Artificial Chromosomes年度引用學(xué)科排名




書目名稱Bacterial Artificial Chromosomes讀者反饋




書目名稱Bacterial Artificial Chromosomes讀者反饋學(xué)科排名

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Exon Trapping for Positional Cloning and Fingerprinting,ies, or phenotypes, to a quantitative trait locus (QTL), a genomic region no smaller than 1 centiMorgan (cM) or megabase (Mb) in length. Physical mapping can then provide a map of higher resolution. Physical maps are constructed from clones identified by screening genomic libraries. Genomic clones c

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Isolation of CpG Islands From BAC Clones Using a Methyl-CpG Binding Column,ize, which are free of methylation and these are known as CpG islands (. . . and . for reviews). In addition to distinctive DNA characteristics, CpG islands have an open chromatin structure in that they are hyperacetylated, lack histone H1, and have a nucleosome-free region (.). The major reason for

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BAC Microarray-Based Comparative Genomic Hybridization,ridization (array CGH) provides a high throughput means to measure and map copy number aberrations on a genome-wide scale and to link them directly to genome sequence. For applications involving the analysis of tumors, the technology must provide reliable detection of single copy gains and losses in

conformity

Large DNA Transformation in Plants,). Both methods used modified bacterial artificial chromosomes (BACs) such as BIBAC or pBACwich. BIBAC vector (used in tomato) is capable of transferring large DNA fragments from . into plants. pBACwich (used in tobacco) utilizes a Cre/. site-specific recombination system to integrate large DNA frag

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BAC Modification Using a RecA Expressing Shuttle Vector System,BACs have the capacity for maintaining large, often more than 300 kb fragments of mammalian DNA as stable inserts and avoid much of the insert chimerism which characterizes yeast artificial chromosomes (YACs). Isolation of BAC DNA is easy because they exist as supercoiled circular plasmids that are

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館長

BAC Engineering for the Generation of ES Cell-Targeting Constructs and Mouse Transgenes,b), which can accommodate most eukaryotic genes along with their full set of regulatory elements, and to their greater convenience in handling over other large cloning vectors like P1-based artificial chromosomes (PACs) and yeast artificial chromosomes (YACs). Two key advances for harnessing the ful