9 results match your criteria: "Stanford DNA Sequencing and Technology Center[Affiliation]"
Proc Natl Acad Sci U S A
December 2000
Department of Genetics, University of Dublin, Trinity College, Dublin 2, Ireland; Stanford DNA Sequencing and Technology Center, 855 California Avenue, Palo Alto, CA 94304, USA.
Gene order evolution in two eukaryotes was studied by comparing the Saccharomyces cerevisiae genome sequence to extensive new data from whole-genome shotgun and cosmid sequencing of Candida albicans. Gene order is substantially different between these two yeasts, with only 9% of gene pairs that are adjacent in one species being conserved as adjacent in the other. Inversion of small segments of DNA, less than 10 genes long, has been a major cause of rearrangement, which means that even where a pair of genes has been conserved as adjacent, the transcriptional orientations of the two genes relative to one another are often different.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
June 2000
Stanford DNA Sequencing and Technology Center, 855 California Avenue, Palo Alto, CA 94304, USA.
Some insight into human evolution has been gained from the sequencing of four Y chromosome genes. Primary genomic sequencing determined gene SMCY to be composed of 27 exons that comprise 4,620 bp of coding sequence. The unfinished sequencing of the 5' portion of gene UTY1 was completed by primer walking, and a total of 20 exons were found.
View Article and Find Full Text PDFNucleic Acids Res
January 2000
Stanford DNA Sequencing and Technology Center, 855 California Avenue, Palo Alto, CA 94304, USA.
The Database of Arabidopsis thaliana Annotation (D At A) was created to enable easy access to and analysis of all the Arabidopsis genome project annotation. The database was constructed using the completed A.thaliana genomic sequence data currently in GenBank.
View Article and Find Full Text PDFGenome Res
May 1999
Stanford DNA Sequencing and Technology Center, Palo Alto, California 94304, USA.
Recent advances in DNA sequencing technologies, both in the form of high lane-density gels and automated capillary systems, will lead to an increased requirement for sample preparation systems that operate at low cost and high throughput. As part of the development of a fully automated sequencing system, we have developed an automated subsystem capable of producing 10,000 sequence-ready ssDNA templates per day from libraries of M13 plaques at a cost of $0.29 per sample.
View Article and Find Full Text PDFNat Genet
April 1999
Stanford DNA Sequencing and Technology Center, Stanford University, California 94305, USA.
Chlamydia are obligate intracellular eubacteria that are phylogenetically separated from other bacterial divisions. C. trachomatis and C.
View Article and Find Full Text PDFGenet Anal
February 1999
Stanford DNA Sequencing and Technology Center, Stanford University, CA 94305, USA.
A highly reliable and efficient technology has been developed for high-throughput DNA polymorphism screening and large-scale genotyping. Photolithographic synthesis has been used to generate miniaturized, high-density oligonucleotide arrays. Dedicated instrumentation and software have been developed for array hybridization, fluorescent detection, and data acquisition and analysis.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
January 1999
Stanford DNA Sequencing and Technology Center, 855 California Avenue, Palo Alto, CA 94304, USA.
A compact, flow-through centrifugation system has been developed specifically for high-throughput centrifugation of large numbers of samples. The instrument is based on multiple high-speed rotors that also serve as sample holders. The small size of the rotors allows them to be arrayed in a standard 96-well microtiter plate spacing, making this device ideal for highly parallel automated instrumentation.
View Article and Find Full Text PDFGenome Res
August 1998
Stanford DNA Sequencing and Technology Center, Palo Alto, California 94304, USA.
An automated, inexpensive, easy-to-use, and reproducible technique for controlled, random DNA fragmentation has been developed. The technique is based on point-sink hydrodynamics that result when a DNA sample is forced through a small hole by a syringe pump. Commercially available components are used to reduce the cost and complexity of the instrument.
View Article and Find Full Text PDFNature
May 1997
Stanford DNA Sequencing and Technology Center, Palo Alto, California 94304, USA.
Here we report the sequence of 569,202 base pairs of Saccharomyces cerevisiae chromosome V. Analysis of the sequence revealed a centromere, two telomeres and 271 open reading frames (ORFs) plus 13 tRNAs and four small nuclear RNAs. There are two Tyl transposable elements, each of which contains an ORF (included in the count of 271).
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