Mar 10, 2007

Consistent treatment of length variants in the human mtDNA control region: a reappraisal

International Journal of Legal Medicine
H J Bandelt, Walther Parson

Abstract

In forensic science, as well as in molecular anthropology and medical genetics, human mitochondrial DNA (mtDNA) variation is being recorded by aligning mtDNA sequences to the revised Cambridge reference sequence (rCRS). This task is straightforward for the vast majority of nucleotide positions but appears to be difficult for some short sequence stretches, namely, in regions displaying length variation. Earlier guidelines for imposing a unique alignment relied on binary alignment to a standard sequence (the rCRS) and used additional priority rules for resolving ambiguities. It turns out, however, that these rules have not been applied rigorously and led to inconsistent nomenclature. There is no way to adapt the priority rules in a reasonable way because binary alignment to a standard sequence is bound to produce artificial alignments that may place sequences separated by a single mutation at mismatch distance larger than 1. To remedy the situation, we propose a phylogenetic approach for multiple alignment and resulting notation.

Mentioned in this Paper

DNA, Mitochondrial
Medical Genetics Specialty
Spastic Syndrome
Phylogeny
Nucleotides
Forensic Genetics
Nomenclature
Genetic Fingerprinting
Mitochondrial DNA Location
Mutation Abnormality

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