Publication | Closed Access
Characterization of New MiniSTR Loci to Aid Analysis of Degraded DNA
317
Citations
32
References
2004
Year
Genetic TestingDnaDegraded DnaGeneticsGenetic EpidemiologyDna AnalysisMolecular BiologyPathologyNucleic Acid Amplification TestMolecular GeneticsAid AnalysisGenomicsReal-time Polymerase Chain ReactionPolymerase Chain ReactionMolecular EcologyBiostatisticsNew Pcr PrimersDegraded Dna SpecimensPublic HealthCodis MarkersDna SequencingDna ReplicationStatistical GeneticsNew Ministr LociForensic IdentificationNucleic Acid AmplificationMedicineGenome Editing
A number of studies have demonstrated that successful analysis of degraded DNA specimens from mass disasters or forensic evidence improves with smaller sized polymerase chain reaction (PCR) products. We have scanned the literature for new STR loci, unlinked from the CODIS markers, which can generate amplicons less than 125 bp in size and would therefore be helpful in testing degraded DNA samples. New PCR primers were designed and tested for the STR loci D1S1677, D2S441, D4S2364, D10S1248, D14S1434, and D22S1045, arranged into two miniSTR triplexes. All loci show a moderate degree of polymorphism among 474 U.S. population samples tested and were reliable and sensitive to at least 100 pg of DNA template under controlled laboratory conditions and pristine DNA samples. The utility of these new loci were confirmed in comparing the success of the miniSTR assays for typing degraded bone samples while partial profiles were observed with the majority of the samples using a commercial STR kit.
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