J
Jonathan L. King
Researcher at University of North Texas Health Science Center
Publications - 103
Citations - 3135
Jonathan L. King is an academic researcher from University of North Texas Health Science Center. The author has contributed to research in topics: Population & Massive parallel sequencing. The author has an hindex of 28, co-authored 98 publications receiving 2551 citations. Previous affiliations of Jonathan L. King include University of North Texas.
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Journal ArticleDOI
Evaluation of the Illumina® Beta Version ForenSeq™ DNA Signature Prep Kit for use in genetic profiling
TL;DR: This set of experiments indicates the beta version of the ForenSeq DNA Signature Prep Kit is a valid tool for forensic DNA typing and warrants full validation studies of this MPS technology.
Journal ArticleDOI
Massively parallel sequencing of forensic STRs: Considerations of the DNA commission of the International Society for Forensic Genetics (ISFG) on minimal nomenclature requirements
Walther Parson,Walther Parson,David Ballard,Bruce Budowle,John M. Butler,Katherine Butler Gettings,Peter Gill,Leonor Gusmão,Douglas R. Hares,Jodi A. Irwin,Jonathan L. King,Peter de Knijff,Niels Morling,Mechthild Prinz,Peter M. Schneider,Christophe Van Neste,Sascha Willuweit,Christopher Phillips +17 more
TL;DR: A sequence (text) string format is proposed the minimal requirement of data storage that laboratories should follow when adopting MPS of STRs and the variant annotation and sequence comparison framework necessary to maintain compatibility among established and future data is discussed.
Journal ArticleDOI
High-quality and high-throughput massively parallel sequencing of the human mitochondrial genome using the Illumina MiSeq.
Jonathan L. King,Bobby LaRue,Nicole M.M. Novroski,Monika Stoljarova,Seung Bum Seo,Xiangpei Zeng,David H. Warshauer,Carey Davis,Walther Parson,Antti Sajantila,Bruce Budowle +10 more
TL;DR: An overall increase in haplotype or genetic diversity and random match probability, as well as better haplogroup assignment demonstrates that MPS of the mtGenome using the Illumina MiSeq system is a viable and reliable methodology.
Journal ArticleDOI
Characterization of genetic sequence variation of 58 STR loci in four major population groups.
Nicole M.M. Novroski,Jonathan L. King,Jennifer D. Churchill,Lay Hong Seah,Bruce Budowle,Bruce Budowle +5 more
TL;DR: These population data illustrate the genetic variation that exists in the commonly used STR markers in the selected population samples and provide allele frequencies for statistical calculations related to STR profiling with MPS data.
Journal ArticleDOI
Single nucleotide polymorphism typing with massively parallel sequencing for human identification
Seung Bum Seo,Jonathan L. King,David H. Warshauer,Carey Davis,Jianye Ge,Bruce Budowle,Bruce Budowle +6 more
TL;DR: Overall, the data support that genotyping a large battery of SNPs is feasible with massively parallel sequencing and more comprehensive rapid genotypes and more cost-effective results may be obtained from multiple samples in one analysis than are possible with current typing and capillary electrophoresis systems.