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Robert W Allen

Publications and source records attributed to Robert W Allen.

4 recordsLinked to original sources

Characteristics of mutations at the D5S818 locus studied with a tightly linked marker.

BACKGROUND: Mutations to STR alleles are not well understood in terms of the mechanism(s) underlying such mutations or their relative frequency among different alleles at the locus. STUDY DESIGN AND METHODS: A cytosine/thymosine (C/T) polymorphism was discovered 13 nucleotides upstream from the 5'-end of the tandem array of the D5S818 locus (-13SNP). The -13SNP coincidentally creates a restriction site polymorphism for the restriction endonuclease SnaBI that is tightly linked to the tandem array of D5S818. Forty D5S818 addition/deletion mutations in the tandem array were characterized with RFLP analysis with SnaBI. RESULTS: Among 40 mutations studied, 34 (approximately 85%) were of paternal origin, 1 ( approximately 3%) was of maternal origin, and 5 (approximately 13%) had an unclear lineage of origin. In 26 cases where the magnitude of the repeat change could be determined, 23 (88%) involved changes of a single repeat unit, whereas 3 (12%) involved changes of 2 or more repeats. The number of additions to the tandem array was roughly equal to the number of deletions from the tandem array. In 19 instances it was possible to identify the parental allele that underwent the mutation. Alleles 13 and 14 were prone to mutation, whereas Allele 11 was resistant. Thus, there is an unequal sensitivity to mutation among D5S818 alleles. CONCLUSIONS: The use of the linked -13SNP marker has revealed several features of mutations at the D5S818 locus: 1) Single repeat changes are the most commonly observed. 2) Mutations are more likely in the paternal lineage. 3) Not all alleles undergo mutation with equal frequency.

Adult↗

Resolution of a serum sample mix-up through the use of short tandem repeat DNA typing.

BACKGROUND: A sample mix-up occurred in a tissue procurement laboratory in which aliquots of serum from two tissue donors were accidentally mislabeled. The clues to the apparent mixup involved discrepant Hepatitis C test results. In an attempt to resolve the apparent mix up, DNA typing was performed using serum samples as a possible source of genomic DNA. STUDY DESIGN AND METHODS: Two hundred microliter aliquots of two reference sera and aliquots prepared from them were subjected to DNA extraction. PCR amplification of 9 STR loci was performed on the extracts and amplicons were analyzed by capillary electrophoresis. RESULTS: About 1 microg/ml of DNA was recovered from all serum samples and was of sufficient quality to direct the amplification of most, if not all STR loci allowing the mislabeled specimens to be traced to the proper tissue donor. CONCLUSIONS: Serum is a useful source of genomic DNA for STR analysis in situations in which such samples are the only source of DNA for testing. Interestingly, one of the tissue donors on life support and repeatedly receiving blood products, exhibited a mixed DNA profile indicative of the presence of DNA from multiple individuals in the bloodstream.

DNA↗

Paternity Testing Commission of the International Society of Forensic Genetics: recommendations on genetic investigations in paternity cases.

The International Society for Forensic Genetics (ISFG) has established a Paternity Testing Commission (PTC) with the purpose of formulating international recommendations concerning genetic investigations in paternity testing. The PTC recommends that paternity testing be performed in accordance with the ISO 17025 standards. The ISO 17025 standards are general standards for testing laboratories and the PTC offers explanations and recommendations concerning selected areas of special importance to paternity testing.

Equipment and Supplies↗