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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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31#
發(fā)表于 2025-3-26 21:32:53 | 只看該作者
Bacterial Artificial Chromosomes978-1-59259-752-9Series ISSN 1064-3745 Series E-ISSN 1940-6029
32#
發(fā)表于 2025-3-27 04:39:06 | 只看該作者
https://doi.org/10.1385/1592597521BAC; Chromosom; DNA; DNA sequencing; PAC; hybridization; reproducible techniques
33#
發(fā)表于 2025-3-27 06:35:19 | 只看該作者
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發(fā)表于 2025-3-27 12:54:06 | 只看該作者
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發(fā)表于 2025-3-28 01:55:40 | 只看該作者
Caitlin Powers,Daniel Mellinger,Vijay Kumar DNA from different species. These BAC libraries are constructed by insertion of DNA fragments from different species into a vector, which can be replicated in a bacterial host. Choosing . as the model host has many advantages: rapid growth of the host, high stability of the DNA fragment when inside
38#
發(fā)表于 2025-3-28 03:21:29 | 只看該作者
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發(fā)表于 2025-3-28 09:07:40 | 只看該作者
A Systematic Examination of the Handonventional methods to screen large-insert clone libraries for specific clones within a defined chromosomal interval are polymerase chain reaction (PCR) based using microsatellite markers. This strategy is labor- and cost-intensive and requires the PCR amplification of several thousands of DNA sampl
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發(fā)表于 2025-3-28 13:21:26 | 只看該作者
A Systematic Examination of the Handrstanding disease, development and evolution. To accomplish this goal and a broad spectrum of applications requires integration of genome sequence information to genetic markers (expressed sequence tag/cDNA/gene transcripts content) and to reagents that can be seen through a microscope and linked to
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