Literature DB >> 17187485

Arrayed identification of DNA signatures.

Max Käller1, Joakim Lundeberg, Afshin Ahmadian.   

Abstract

Over the last few years, several initiatives have described efforts to combine previously invented techniques in molecular biology with parallel detection principles to sequence or genotype DNA signatures. The Infinium system from Illumina and the Affymetrix GeneChips are two systems suitable for whole-genome scoring of variable positions. However, directed candidate-gene approaches are more cost effective and several academic groups and the private sector provide techniques with moderate typing throughput combined with large sample capacity suiting these needs. Recently, whole-genome sequencing platforms based on the sequencing-by-synthesis principle were presented by 454 Life Sciences and Solexa, showing great potential as alternatives to conventional genotyping approaches. In addition to these sequencing initiatives, many efforts are pursuing novel ideas to facilitate fast and cost-effective whole genome sequencing, such as ligation-based sequencing. Reliable methods for routine re-sequencing of human genomes as a tool for personalized medicine, however, remain to be developed.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17187485     DOI: 10.1586/14737159.7.1.65

Source DB:  PubMed          Journal:  Expert Rev Mol Diagn        ISSN: 1473-7159            Impact factor:   5.225


  5 in total

Review 1.  DNA typing in wildlife crime: recent developments in species identification.

Authors:  Shanan S Tobe; Adrian Linacre
Journal:  Forensic Sci Med Pathol       Date:  2010-06-05       Impact factor: 2.007

Review 2.  Keeping up with the next generation: massively parallel sequencing in clinical diagnostics.

Authors:  John R ten Bosch; Wayne W Grody
Journal:  J Mol Diagn       Date:  2008-10-02       Impact factor: 5.568

3.  Sequencing by ligation variation with endonuclease V digestion and deoxyinosine-containing query oligonucleotides.

Authors:  Antoine Ho; Maurice Murphy; Susan Wilson; Susan R Atlas; Jeremy S Edwards
Journal:  BMC Genomics       Date:  2011-12-12       Impact factor: 3.969

4.  GeneWiz browser: An Interactive Tool for Visualizing Sequenced Chromosomes.

Authors:  Peter F Hallin; Hans-Henrik Stærfeldt; Eva Rotenberg; Tim T Binnewies; Craig J Benham; David W Ussery
Journal:  Stand Genomic Sci       Date:  2009-09-25

5.  Association study between BDNF gene polymorphisms and autism by three-dimensional gel-based microarray.

Authors:  Lu Cheng; Qinyu Ge; Pengfeng Xiao; Beili Sun; Xiaoyan Ke; Yunfei Bai; Zuhong Lu
Journal:  Int J Mol Sci       Date:  2009-06-02       Impact factor: 6.208

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.