about
More comprehensive forensic genetic marker analyses for accurate human remains identification using massively parallel DNA sequencing.Novel Y-chromosome Short Tandem Repeat Variants Detected Through the Use of Massively Parallel Sequencing.Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosaExome-based mapping and variant prioritization for inherited Mendelian disorders.Characterization of genetic sequence variation of 58 STR loci in four major population groups.Genetic analysis of the Yavapai Native Americans from West-Central Arizona using the Illumina MiSeq FGx™ forensic genomics system.Erratum to: More Comprehensive Forensic Genetic Marker Analyses for Accurate Human Remains Identification Using Massively Parallel DNA Sequencing.Massively parallel sequencing-enabled mixture analysis of mitochondrial DNA samples.Increasing the discrimination power of ancestry- and identity-informative SNP loci within the ForenSeq™ DNA Signature Prep KitParsing apart the contributors of mitochondrial DNA mixtures with massively parallel sequencing dataWorking towards implementation of whole genome mitochondrial DNA sequencing into routine caseworkMassively parallel sequencing of 68 insertion/deletion markers identifies novel microhaplotypes for utility in human identity testing
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description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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prefLabel
Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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Jennifer D. Churchill
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jennifer-churchill
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0000-0001-9796-193X