Massively parallel sequencing analysis of nondegraded and degraded DNA mixtures using the ForenSeq™ system in combination with EuroForMix software
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Ming-Yih Wu | Hsiang-I Yin | Tsui-Ting Lee | Hsiao-Lin Hwa | T. Ko | H. Hwa | Wan-Chia Chung | Chih-Peng Lin | Hsiang-I Yin | James Chun-I Lee | Tsang-Ming Ko | Ming-Yih Wu | Wan-Chia Chung | Chih-Peng Lin | Tsui-Ting Lee
[1] Bruce Budowle,et al. Flanking region variation of ForenSeq™ DNA Signature Prep Kit STR and SNP loci in Yavapai Native Americans. , 2017, Forensic science international. Genetics.
[2] Michael D. Coble,et al. Evaluation of forensic DNA mixture evidence: protocol for evaluation, interpretation, and statistical calculations using the combined probability of inclusion , 2016, BMC Genetics.
[3] Øyvind Bleka,et al. Open source software EuroForMix can be used to analyse complex SNP mixtures. , 2017, Forensic science international. Genetics.
[4] Titia Sijen,et al. Developmental validation of the HIrisPlex system: DNA-based eye and hair colour prediction for forensic and anthropological usage. , 2014, Forensic science international. Genetics.
[5] Michael D. Coble,et al. Sequence-based analysis of stutter at STR loci: Characterization and utility , 2015 .
[6] James Curran,et al. A discussion of the merits of random man not excluded and likelihood ratios. , 2008, Forensic science international. Genetics.
[7] Jocelyne Bruand,et al. Developmental validation of the MiSeq FGx Forensic Genomics System for Targeted Next Generation Sequencing in Forensic DNA Casework and Database Laboratories. , 2017, Forensic science international. Genetics.
[8] 52 additional reference population samples for the 55 AISNP panel. , 2015, Forensic science international. Genetics.
[9] E. Thompson,et al. Performing the exact test of Hardy-Weinberg proportion for multiple alleles. , 1992, Biometrics.
[10] N. Morling,et al. Characterization of mutations and sequence variants in the D21S11 locus by next generation sequencing. , 2014, Forensic science international. Genetics.
[11] Lilliana I Moreno,et al. Performance and concordance of the ForenSeq™ system for autosomal and Y chromosome short tandem repeat sequencing of reference-type specimens. , 2017, Forensic science international. Genetics.
[12] Walther Parson,et al. Evaluation of the Illumina ForenSeq™ DNA Signature Prep Kit - MPS forensic application for the MiSeq FGx™ benchtop sequencer. , 2017, Forensic science international. Genetics.
[13] Rebecca S Just,et al. Use of the LUS in sequence allele designations to facilitate probabilistic genotyping of NGS-based STR typing results. , 2018, Forensic science international. Genetics.
[14] M. Slatkin. Linkage disequilibrium in growing and stable populations. , 1994, Genetics.
[15] Michael D Coble,et al. Characterization of 26 MiniSTR Loci for Improved Analysis of Degraded DNA Samples , 2007, Journal of forensic sciences.
[16] In Seok Yang,et al. Massively parallel sequencing of 17 commonly used forensic autosomal STRs and amelogenin with small amplicons. , 2016, Forensic science international. Genetics.
[17] Kenneth K. Kidd,et al. SNPs for a universal individual identification panel , 2010, Human Genetics.
[18] Yih-Yuan Chang,et al. Fifteen non-CODIS autosomal short tandem repeat loci multiplex data from nine population groups living in Taiwan , 2012, International Journal of Legal Medicine.
[19] Øyvind Bleka,et al. EuroForMix: An open source software based on a continuous model to evaluate STR DNA profiles from a mixture of contributors with artefacts. , 2016, Forensic science international. Genetics.
[20] H. Hwa,et al. A 1204-single nucleotide polymorphism and insertion-deletion polymorphism panel for massively parallel sequencing analysis of DNA mixtures. , 2018, Forensic science international. Genetics.
[21] Ashley L. Silvia,et al. A preliminary assessment of the ForenSeq™ FGx System: next generation sequencing of an STR and SNP multiplex , 2016, International Journal of Legal Medicine.
[22] Kevin M. Kiesler,et al. Performance of a next generation sequencing SNP assay on degraded DNA. , 2015, Forensic science international. Genetics.
[23] Bruce Budowle,et al. Evaluation of the Illumina(®) Beta Version ForenSeq™ DNA Signature Prep Kit for use in genetic profiling. , 2016, Forensic science international. Genetics.
[24] D. Deforce,et al. Forensic STR analysis using massive parallel sequencing. , 2012, Forensic science international. Genetics.
[25] A. Tillmar,et al. A SNP panel for identity and kinship testing using massive parallel sequencing , 2016, International Journal of Legal Medicine.
[26] David H. Warshauer,et al. Massively parallel sequencing of forensically relevant single nucleotide polymorphisms using TruSeq™ forensic amplicon , 2014, International Journal of Legal Medicine.
[27] Douglas R Storts,et al. Massively parallel sequencing of short tandem repeats-Population data and mixture analysis results for the PowerSeq™ system. , 2016, Forensic science international. Genetics.
[28] Lu Zhang,et al. Massively parallel sequencing of forensic STRs and SNPs using the Illumina® ForenSeq™ DNA Signature Prep Kit on the MiSeq FGx™ Forensic Genomics System. , 2017, Forensic science international. Genetics.
[29] Bruce Budowle,et al. High sensitivity multiplex short tandem repeat loci analyses with massively parallel sequencing. , 2015, Forensic science international. Genetics.
[30] H. Hwa,et al. Genotyping of 75 SNPs using arrays for individual identification in five population groups , 2015, International Journal of Legal Medicine.
[32] Niels Morling,et al. Next generation sequencing and its applications in forensic genetics. , 2015, Forensic science international. Genetics.
[33] David H. Warshauer,et al. Single nucleotide polymorphism typing with massively parallel sequencing for human identification , 2013, International Journal of Legal Medicine.
[34] Paolo Fattorini,et al. Performance of the ForenSeqTM DNA Signature Prep kit on highly degraded samples , 2017, Electrophoresis.
[35] Dieter Deforce,et al. My-Forensic-Loci-queries (MyFLq) framework for analysis of forensic STR data generated by massive parallel sequencing. , 2014, Forensic science international. Genetics.
[36] D. Altman,et al. Multiple significance tests: the Bonferroni method , 1995, BMJ.
[37] P. Gill,et al. Validation of a 21-locus autosomal SNP multiplex for forensic identification purposes. , 2005, Forensic science international.