The goal is to prepare ten-fold redundant Bacterial Artificial Chromosomes (BAC) libraries for species selected by an NIH advisory committee and to disseminate the libraries in accordance with NIH policy. The libraries will be tailored to the scientific community's interest in comparative genomics and be used in support of whole-genome sequencing projects. The project is a continuation of an earlier cooperative agreement between the NIH and the Children's Hospital Oakland Research Institute. The application has four components relevant to preparing (BACs): 1) Library preparation, 2) Clone Arraying & Library Duplication, 3) Characterization, and 4) Research & Development to improve the process efficiency and BAC library quality. During the first year, four BAC libraries will be prepared for genomes having a typical mammalian genome size. This corresponds with an """"""""800,000 BAC clone"""""""" preparation capacity. During years two and three of the program, improvements in BAC construction methods may result in slight increases in throughput. The small size of the continuation program does not offer opportunities for """"""""economy of scale"""""""" improvements. The new libraries will complement the extensive repertoire of BAC clone collections already available for comparative genome analysis. The new clone collections will be analyzed by a standardized set of tests, including screening with a set of genomic markers, limited BAC-end sequencing and insert size determination. Once the libraries pass the quality controls, the new resources will be made available in a format consistent with major applications. To facilitate access to the BAC libraries, a screening service based on cost recovery by user fees has been established. It is expected that the new BAC resources will continue to contribute to better understanding of human gene function and evolution through comparison of human genes with a growing spectrum of animal species. BAC clones will also increasingly be used as tools to create animal models for human diseases. Widespread dissemination of the clones is an essential component of the project. User fees for most libraries cannot cover the costs of maintenance. Hence, minimal funding is requested in support of the maintenance of the new libraries and those generated under the previous program initiative. Information about libraries is available through the website for BACPAC Resources (http://bacpac.chori.org). ? ?
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| (2007) Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature 447:799-816 |
| Carbone, Lucia; Vessere, Gery M; ten Hallers, Boudewijn F H et al. (2006) A high-resolution map of synteny disruptions in gibbon and human genomes. PLoS Genet 2:e223 |
