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D. Syndercombe Court

Researcher at King's College London

Publications -  42
Citations -  1075

D. Syndercombe Court is an academic researcher from King's College London. The author has contributed to research in topics: Population & SNP genotyping. The author has an hindex of 17, co-authored 39 publications receiving 967 citations. Previous affiliations of D. Syndercombe Court include Queen Mary University of London.

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Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel

TL;DR: A novel 49plex assay has been developed based on the Genplex typing system, a modification of SNPlex chemistry using oligo-ligation of pre-amplified DNA and dye-labeled, mobility modified detection probes to allow detection with standard capillary electrophoresis analyzers.
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RNA/DNA co-analysis from human saliva and semen stains--results of a third collaborative EDNAP exercise

TL;DR: The results of this collaborative exercise involving an RNA/DNA co-extraction strategy support the potential use of an mRNA based system for the identification of saliva and semen in forensic casework that is compatible with current DNA analysis methodologies.
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RNA/DNA co-analysis from human menstrual blood and vaginal secretion stains: Results of a fourth and fifth collaborative EDNAP exercise

TL;DR: Results of this and the previous collaborative RNA exercises support RNA profiling as a reliable body fluid identification method that can easily be combined with current STR typing technology.
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Investigation of the STR locus HUMTH01 using PCR and two electrophoresis formats: UK and Galician Caucasian population surveys and usefulness in paternity investigations

TL;DR: The use of PCR followed by electrophoresis in either gel format appears to provide a quick and straightforward method for investigating the HUMTH01 locus.
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The recombination landscape around forensic STRs: Accurate measurement of genetic distances between syntenic STR pairs using HapMap high density SNP data

TL;DR: The detailed analysis of recombination rates made for autosomal forensic STRs was extended to the more than 50 X chromosome STRs established or in development for complex kinship analyses, allowing all current STR sets or their combinations to be used in supplemented paternity analyses without the need for further adjustment for physical linkage.