Literature DB >> 14500830

Advanced computational techniques for re-sequencing DNA with polymerase signaling assay arrays.

Itsik Pe'er1, Naama Arbili, Yi Liu, Colby Enck, Craig A Gelfand, Ron Shamir.   

Abstract

Re-sequencing, the identification of the specific variants in a sequence of interest compared with a known genomic sequence, is a ubiquitous task in today's biology. Universal arrays, which interrogate all possible oligonucleotides of a certain length in a target sequence, have been suggested for computationally determining a polynucleotide sequence from its oligonucleotide content. We present here new methods that use such arrays for re-sequencing. Our methods are applied to data obtained by the polymerase signaling assay, which arrays single-based primer extension reactions for either universal or partial arrays of pentanucleotides. The computational analysis uses the spectrum alignment algorithm, which is refined and enhanced here in order to overcome noise incurred by the use of such short primers. We present accurate re-sequencing results for both synthetic and amplified DNA molecules.

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Year:  2003        PMID: 14500830      PMCID: PMC206457          DOI: 10.1093/nar/gkg757

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  21 in total

1.  Optimal reconstruction of a sequence from its probes.

Authors:  A M Frieze; F P Preparata; E Upfal
Journal:  J Comput Biol       Date:  1999 Fall-Winter       Impact factor: 1.479

2.  Sequencing-by-hybridization at the information-theory bound: an optimal algorithm.

Authors:  F P Preparata; E Upfal
Journal:  J Comput Biol       Date:  2000       Impact factor: 1.479

3.  DNA sequencing by hybridization with arrays of samples or probes.

Authors:  R Drmanac; S Drmanac; J Baier; G Chui; D Coleman; R Diaz; D Gietzen; A Hou; H Jin; T Ukrainczyk; C Xu
Journal:  Methods Mol Biol       Date:  2001

Review 4.  Sequencing by hybridization arrays.

Authors:  R Drmanac; S Drmanac
Journal:  Methods Mol Biol       Date:  2001

Review 5.  Advances in the analysis of DNA sequence variations using oligonucleotide microchip technology.

Authors:  S V Tillib; A D Mirzabekov
Journal:  Curr Opin Biotechnol       Date:  2001-02       Impact factor: 9.740

6.  Spectrum alignment: efficient resequencing by hybridization.

Authors:  I Pe'er; R Shamir
Journal:  Proc Int Conf Intell Syst Mol Biol       Date:  2000

Review 7.  Tech.sight. Genetic testing--present and future.

Authors:  H Yan; K W Kinzler; B Vogelstein
Journal:  Science       Date:  2000-09-15       Impact factor: 47.728

8.  Mutation detection by ligation to complete n-mer DNA arrays.

Authors:  K L Gunderson; X C Huang; M S Morris; R J Lipshutz; D J Lockhart; M S Chee
Journal:  Genome Res       Date:  1998-11       Impact factor: 9.043

9.  Accurate sequencing by hybridization for DNA diagnostics and individual genomics.

Authors:  S Drmanac; D Kita; I Labat; B Hauser; C Schmidt; J D Burczak; R Drmanac
Journal:  Nat Biotechnol       Date:  1998-01       Impact factor: 54.908

10.  A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.

Authors:  R Sachidanandam; D Weissman; S C Schmidt; J M Kakol; L D Stein; G Marth; S Sherry; J C Mullikin; B J Mortimore; D L Willey; S E Hunt; C G Cole; P C Coggill; C M Rice; Z Ning; J Rogers; D R Bentley; P Y Kwok; E R Mardis; R T Yeh; B Schultz; L Cook; R Davenport; M Dante; L Fulton; L Hillier; R H Waterston; J D McPherson; B Gilman; S Schaffner; W J Van Etten; D Reich; J Higgins; M J Daly; B Blumenstiel; J Baldwin; N Stange-Thomann; M C Zody; L Linton; E S Lander; D Altshuler
Journal:  Nature       Date:  2001-02-15       Impact factor: 49.962

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