Our major goals are simple: we intend to determine a major fraction (see below) of the sequence of the genome of budding yeast (Saccharomyces cerevisiae). As an integral part of this effort, we intend to improve the speed and reduce the cost of production sequencing, largely through automation. We want to integrate development of new methods and their implementation in production so that new processes are continually tested and applied in such a way as to minimize the """"""""down-time"""""""". Limited sequencing of human DNA will be done as well, in order to assess the generality of our evolving methods. We plan to apply novel methods of testing the accuracy of sequences obtained in production. We propose to explore new ways in which knowledge of sequence can be used, on a genome- wide basis, to get some idea of the biological functions of yeast genes. As we approach the end of the yeast genome, we propose to phase into production sequencing of carefully chosen megabase-scale segments from chromosome 4 of the human.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Program Projects (P01)
Project #
5P01HG000205-05
Application #
2208629
Study Section
Special Emphasis Panel (SRC (02))
Project Start
1990-09-28
Project End
1998-07-31
Budget Start
1994-08-01
Budget End
1995-07-31
Support Year
5
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Stanford University
Department
Genetics
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Tóth, Eszter N; Lohith, Akshar; Mondal, Manas et al. (2018) Single-cell nanobiopsy reveals compartmentalization of mRNAs within neuronal cells. J Biol Chem 293:4940-4951
Jalili, Roxana; Horecka, Joe; Swartz, James R et al. (2018) Streamlined circular proximity ligation assay provides high stringency and compatibility with low-affinity antibodies. Proc Natl Acad Sci U S A 115:E925-E933
Roy, Kevin R; Smith, Justin D; Vonesch, Sibylle C et al. (2018) Multiplexed precision genome editing with trackable genomic barcodes in yeast. Nat Biotechnol 36:512-520
Emaminejad, Sam; Gao, Wei; Wu, Eric et al. (2017) Autonomous sweat extraction and analysis applied to cystic fibrosis and glucose monitoring using a fully integrated wearable platform. Proc Natl Acad Sci U S A 114:4625-4630
Smith, Justin D; Schlecht, Ulrich; Xu, Weihong et al. (2017) A method for high-throughput production of sequence-verified DNA libraries and strain collections. Mol Syst Biol 13:913
Jensen, Michael; Davis, Ronald (2017) RecJ 5' Exonuclease Digestion of Oligonucleotide Failure Strands: A ""Green"" Method of Trityl-On Purification. Biochemistry 56:2417-2424
Lau, Billy T; Ji, Hanlee P (2017) Single molecule counting and assessment of random molecular tagging errors with transposable giga-scale error-correcting barcodes. BMC Genomics 18:745
Shin, GiWon; Grimes, Susan M; Lee, HoJoon et al. (2017) CRISPR-Cas9-targeted fragmentation and selective sequencing enable massively parallel microsatellite analysis. Nat Commun 8:14291
Celaj, Albi; Schlecht, Ulrich; Smith, Justin D et al. (2017) Quantitative analysis of protein interaction network dynamics in yeast. Mol Syst Biol 13:934
Esfandyarpour, Rahim; DiDonato, Matthew J; Yang, Yuxin et al. (2017) Multifunctional, inexpensive, and reusable nanoparticle-printed biochip for cell manipulation and diagnosis. Proc Natl Acad Sci U S A 114:E1306-E1315

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