Literature DB >> 15570103

SNP typing in forensic genetics: a review.

Beatriz Sobrino1, Angel Carracedo.   

Abstract

Single nucleotide polymorphisms (SNPs) are emerging as new markers of interest to the forensic community because of their abundance in the human genome, their low mutation rate, the opportunity they present of analyzing smaller fragments of deoxyribonucleic acid (DNA) than with short tandem repeats--important in degraded DNA samples--and the possibility of automating the analysis with high-throughput technologies. Many new technologies for genotyping SNPs have been developed in the past few years. We describe the principles of the allelic discrimination reactions and the technologies used for each of them. The aim of this chapter is to help in the understanding of the methodologies used in SNP genotyping and in the selection of the most appropriate techniques for forensic purposes.

Entities:  

Mesh:

Year:  2005        PMID: 15570103     DOI: 10.1385/1-59259-867-6:107

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  8 in total

1.  Low-volume amplification on chemically structured chips using the PowerPlex16 DNA amplification kit.

Authors:  Ulrike Schmidt; Sabine Lutz-Bonengel; Hans-Joachim Weisser; Timo Sänger; Stefan Pollak; Ulrike Schön; Thomas Zacher; Wolfgang Mann
Journal:  Int J Legal Med       Date:  2005-10-18       Impact factor: 2.686

2.  Characterization of mtDNA SNP typing and mixture ratio assessment with simultaneous real-time PCR quantification of both allelic states.

Authors:  Harald Niederstätter; Michael D Coble; Petra Grubwieser; Thomas J Parsons; Walther Parson
Journal:  Int J Legal Med       Date:  2005-08-09       Impact factor: 2.686

3.  Low volume amplification and sequencing of mitochondrial DNA on a chemically structured chip.

Authors:  Sabine Lutz-Bonengel; Timo Sänger; Marielle Heinrich; Ulrike Schön; Ulrike Schmidt
Journal:  Int J Legal Med       Date:  2006-11-09       Impact factor: 2.686

4.  Reduced-volume and low-volume typing of Y-chromosomal SNPs to obtain Finnish Y-chromosomal compound haplotypes.

Authors:  Marielle Heinrich; Tina Braun; Timo Sänger; Pekka Saukko; Sabine Lutz-Bonengel; Ulrike Schmidt
Journal:  Int J Legal Med       Date:  2009-08-28       Impact factor: 2.686

5.  Genetic variation and forensic efficiency of 30 indels for three ethnic groups in Guangxi: relationships with other populations.

Authors:  Weian Du; Chunlei Feng; Ting Yao; Cheng Xiao; Hongyan Huang; Weibin Wu; Linnan Zhu; Honghua Qiao; Chao Liu; Ling Chen
Journal:  PeerJ       Date:  2019-05-03       Impact factor: 2.984

6.  Analysis of ancient mtDNA from the medieval archeological site of Amiternum (L'Aquila), central Italy.

Authors:  Anna Poma; Patrizia Cesare; Antonella Bonfigli; Giulia Vecchiotti; Sabrina Colafarina; Francesca Savini; Fabio Redi; Osvaldo Zarivi
Journal:  Heliyon       Date:  2019-10-17

7.  A microarray-based system for the simultaneous analysis of single nucleotide polymorphisms in human genes involved in the metabolism of anti-malarial drugs.

Authors:  Eva Maria Hodel; Serej D Ley; Weihong Qi; Frédéric Ariey; Blaise Genton; Hans-Peter Beck
Journal:  Malar J       Date:  2009-12-09       Impact factor: 2.979

8.  SNP Discovery through Next-Generation Sequencing and Its Applications.

Authors:  Santosh Kumar; Travis W Banks; Sylvie Cloutier
Journal:  Int J Plant Genomics       Date:  2012-11-22
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.