Ronald W. Davis
教授
Department of Biochemistry
Stanford University;Department of Genetics, Stanford University;School of Medicine, Stanford University;Genome Technology Center, Stanford University;Maternal and Child Health Research Institute, Stanford University;Cancer Institute, Stanford University
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We are using Saccharomyces cerevisiae and Human to conduct whole genome analysis projects. The yeast genome sequence has approximately 6,000 genes. We have made a set of haploid and diploid strains (21,000) containing a complete deletion of each gene. In order to facilitate whole genome analysis each deletion is molecularly tagged with a unique 20-mer DNA sequence. This sequence acts as a molecular bar code and makes it easy to identify the presence of each deletion. The mixture of all such tag strains then allows for the analysis of the entire genome with the manipulation of a single culture. During growth under a variety of conditions the loss of a tag indicates the loss of a deletion from the population. The concentration of each tag is determined by PCR amplification of the tags and hybridization to an Affymetrix DNA chip that contains the complement to all of the DNA sequence tags. This approach is being applied to other microorganisms.
We have identified a number of wild isolates of yeast that grow at much higher temperatures than is typical for Saccharomyces cerevisiae and are pathogenic and can kill a mouse. Microarrays have been used to map complex genetic traits such as virulence traits in pathogenic Saccharomyces cerevisiae using hybridization to detect single nucleotide polymorphisms. We have developed a new technology termed Reciprocal Hemizygosity Scanning that allows the determination of the contribution to the phenotype of all pair wise alleles for the whole genome from 2 independent strains. Using this technology we can map and quantitate all of the alleles in the genome for any complex quantitative trait in a single tube assay. These technologies will allow us to explore allelic contributions in complex mixed culture real environments and to investigate ecology at the genome level.
We have identified a number of wild isolates of yeast that grow at much higher temperatures than is typical for Saccharomyces cerevisiae and are pathogenic and can kill a mouse. Microarrays have been used to map complex genetic traits such as virulence traits in pathogenic Saccharomyces cerevisiae using hybridization to detect single nucleotide polymorphisms. We have developed a new technology termed Reciprocal Hemizygosity Scanning that allows the determination of the contribution to the phenotype of all pair wise alleles for the whole genome from 2 independent strains. Using this technology we can map and quantitate all of the alleles in the genome for any complex quantitative trait in a single tube assay. These technologies will allow us to explore allelic contributions in complex mixed culture real environments and to investigate ecology at the genome level.
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Vishnu Shankar,Julie Wilhelmy,Basil Michael, Layla Cervantes,Vamsee Mallajosyula,Ronald Davis,Michael Snyder,Shady Younis, William H Robinson,Sadasivan Shankar,Paul Mischel, Hector Bonilla,
crossref(2024)
Fereshteh Jahanbani,Justin Cyril Sing, Rajan Douglas Maynard,Shaghayegh Jahanbani, Janet Dafoe,Whitney Dafoe, Nathan Jones, Kelvin J. Wallace, Azuravesta Rastan,Holden T. Maecker,Hannes L. Röst,Michael P. Snyder,
Frontiers in Immunology (2024)
Fereshteh Jahanbani,Justin Cyril Sing, Rajan Douglas Maynard,Shaghayegh Jahanbani, Janet Dafoe,Whitney Dafoe, Nathan Jones, Kelvin J. Wallace, Azuravesta Rastan,Holden T. Maecker,Hannes L. Röst,Michael P. Snyder,
Frontiers in Immunology (2024)
Fereshteh Jahanbani,Justin Cyril Sing, Rajan Douglas Maynard,Shaghayegh Jahanbani, Janet Dafoe,Whitney Dafoe, Nathan Jones, Kelvin J Wallace, Azuravesta Rastan,Holden T Maecker,Hannes L Röst,Michael P Snyder,
Fereshteh Jahanbani,Justin Cyril Sing, Rajan Douglas Maynard,Shaghayegh Jahanbani, Janet Dafoe,Whitney Dafoe, Nathan Jones, Kelvin J. Wallace, Azuravesta Rastan,Holden T. Maecker,Hannes L. Rost,Michael P. Snyder,
FRONTIERS IN IMMUNOLOGY (2024)
Z.S. Mayo,C.A. Reddy, C. Billena, E.M. Davies, A. Bommireddy,R.W. Davis,E.S. Murphy,J.H. Suh,E.H. Balagamwala,T.A. Chan, J.S. Yu,G.H. Barnett,
International journal of radiation oncology, biology, physicsno. 2 (2023): e137-E137
Journal of applied physicsno. 11 (2023): 113104-113104
A. Bommireddy, C. Billena,Z. S. Mayo, S. Koro,R. W. Davis,S. T. Chao,E. S. Murphy,J. H. Suh,T. A. Chan,J. S. Yu,G. H. Barnett,A. M. Mohammadi,
International journal of radiation oncology, biology, physicsno. 2 (2023): E90-E90
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