Forensic performance of insertion-deletion marker systems

Forensic Science International: Genetics Supplement Series

Volumn 3, Issue 1, 2011, Pages

  Fondevila, Manuel ^a,c   Pereira, Rui ^a,b   Gusmão, Leonor ^b   Phillips, Christopher ^a   Lareu, Maria Victoria ^a   Carracedo, Angel ^a   Butler, John M ^c   Vallone, Peter M ^c  

^a UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

^b UNIVERSITY OF PORTO   (Portugal)

^c NATIONAL INSTITUTE OF STANDARDS AND TECHNOLOGY   (United States)

Author keywords

InDel; Multiplex; Short amplicon; Uncharted variation

Indexed keywords

DNA;

ALLELE; AMPLICON; AMPLIFIED FRAGMENT LENGTH POLYMORPHISM; ARTICLE; DNA DEGRADATION; FORENSIC GENETICS; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; GENOTYPE; HUMAN; INDEL MUTATION; MUTATION RATE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 82455164190     PISSN: 18751768     EISSN: 1875175X     Source Type: Journal    
DOI: 10.1016/j.fsigss.2011.09.083     Document Type: Article

References (5)

1. Weber J.L., David D., Heil J., et al. Human diallelic insertion/deletion polymorphisms. Am. J. Hum. Genet. 2002, 71:854-862.
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3. Syvänen A.C. Accessing genetic variation: genotyping single nucleotide polymorphisms. Nat. Rev. Genet. 2001, 12:930-942.
4. http://www.qiagen.com/products/investigatordipplexkit.aspx.
5. Kline M.C., Hill C.R., Decker A.E., et al. STR sequence analysis for characterizing normal, variant, and null alleles. FSI: Genet. 2011, 5(4):329-332.