Base Sequencing of DNA

2018 ◽  
pp. 33-40
Author(s):  
David S. Blackman
Keyword(s):  
Author(s):  
J. P. Langmore ◽  
N. R. Cozzarelli ◽  
A. V. Crewe

A system has been developed to allow highly specific derivatization of the thymine bases of DNA with mercurial compounds wich should be visible in the high resolution scanning electron microscope. Three problems must be completely solved before this staining system will be useful for base sequencing by electron microscopy: 1) the staining must be shown to be highly specific for one base, 2) the stained DNA must remain intact in a high vacuum on a thin support film suitable for microscopy, 3) the arrangement of heavy atoms on the DNA must be determined by the elastic scattering of electrons in the microscope without loss or large movement of heavy atoms.


1986 ◽  
Vol 14 (2) ◽  
pp. 472-472
Author(s):  
J. A. P. EARLE ◽  
R. A. SKUCE ◽  
E. M. HOEY ◽  
S. J. MARTIN

1999 ◽  
Vol 45 (8) ◽  
pp. 686-690 ◽  
Author(s):  
Wouter J Middelhoven ◽  
Gloria Scorzetti ◽  
Jack W Fell

A morphological and physiological description of an anamorphic basidiomycetous yeast species, named Trichosporon guehoae (CBS 8521T), is presented. The ability to assimilate several aliphatic and aromatic compounds as sole source of carbon and energy is reported. The phylogenetic position within the genus, based on nuclear base sequencing of the D1/D2 region of the large subunit of rDNA is discussed.Key words: basidiomycetes, taxonomy, Trichosporon guehoae sp.nov., yeasts.


Author(s):  
Karen P. McCann ◽  
Mohammed T. Akbari ◽  
Adrian C. Williams ◽  
David B. Ramsden

2011 ◽  
Vol 110 (6) ◽  
pp. 1592-1600 ◽  
Author(s):  
K. Haugum ◽  
L.T. Brandal ◽  
I. Løbersli ◽  
G. Kapperud ◽  
B.-A. Lindstedt

2017 ◽  
Author(s):  
Daniel A. Skelly ◽  
John H. McCusker ◽  
Eric A. Stone ◽  
Paul M. Magwene

AbstractInexpensive, high-throughput sequencing has led to the generation of large numbers of sequenced genomes representing diverse lineages in both model and non-model organisms. Such resources are well suited for the creation of new multiparent populations to identify quantitative trait loci that contribute to variation in phenotypes of interest. However, despite significant drops in per-base sequencing costs, the costs of sample handling and library preparation remain high, particularly when many samples are sequenced. We describe a novel method for pooled genotyping of offspring from multiple genetic crosses, such as those that that make up multiparent populations. Our approach, which we call "private haplotype barcoding” (PHB), utilizes private haplotypes to deconvolve patterns of inheritance in individual offspring from mixed pools composed of multiple offspring. We demonstrate the efficacy of this approach by applying the PHB method to whole genome sequencing of 96 segregants from 12 yeast crosses, achieving over a 90% reduction in sample preparation costs relative to non-pooled sequencing. In addition, we implement a hidden Markov model to calculate genotype probabilities for a generic PHB run and a specialized hidden Markov model for the yeast crosses that improves genotyping accuracy by making use of tetrad information. Private haplotype barcoding holds particular promise for facilitating inexpensive genotyping of large pools of offspring in diverse non-model systems.


Genomics ◽  
1995 ◽  
Vol 30 (3) ◽  
pp. 445-449
Author(s):  
Guochun Xie ◽  
Rebecca Lobb ◽  
William J. Bruno ◽  
David C. Torney ◽  
Joe M. Gatewood
Keyword(s):  

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