Big data in forensic genetics.
暂无分享,去创建一个
[1] W Parson,et al. Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM™. , 2015, Forensic science international. Genetics.
[2] Yaran Yang,et al. Application of Next-generation Sequencing Technology in Forensic Science , 2014, Genom. Proteom. Bioinform..
[4] T Egeland,et al. Beyond traditional paternity and identification cases. Selecting the most probable pedigree. , 2000, Forensic science international.
[5] Xavier Estivill,et al. Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies , 2022 .
[6] J. V. van Meurs,et al. A SNP panel for identification of DNA and RNA specimens , 2018, BMC Genomics.
[7] B. Weir,et al. A genome-wide study of Hardy–Weinberg equilibrium with next generation sequence data , 2017, Human Genetics.
[8] A. Scally. Global clues to the nature of genomic mutations in humans , 2017, eLife.
[9] A. Dawid,et al. Non-fatherhood or mutation? A probabilistic approach to parental exclusion in paternity testing. , 2001, Forensic science international.
[10] Pedro V. Silva,et al. General Derivation of the Sets of Pedigrees with the Same Kinship Coefficients , 2010, Human Heredity.
[11] Lorena Pantano,et al. InvFEST, a database integrating information of polymorphic inversions in the human genome , 2013, Nucleic Acids Res..
[12] Jeffrey D. Wall,et al. Detecting Recombination Hotspots from Patterns of Linkage Disequilibrium , 2016, G3: Genes, Genomes, Genetics.
[13] Svante Pääbo,et al. The mosaic that is our genome , 2003, Nature.
[14] Robert C. Elston,et al. Will Formal Genetics Become Dispensable? , 2013, Human Heredity.
[15] S. Cebrat,et al. Distribution of Recombination Hotspots in the Human Genome – A Comparison of Computer Simulations with Real Data , 2013, PloS one.
[16] P. Donnelly,et al. The Fine-Scale Structure of Recombination Rate Variation in the Human Genome , 2004, Science.
[17] R. Redfield. “Why Do We Have to Learn This Stuff?”—A New Genetics for 21st Century Students , 2012, PLoS biology.
[18] Niels Morling,et al. ISFG: Recommendations on biostatistics in paternity testing. , 2007, Forensic science international. Genetics.
[19] J. Koehler,et al. The Coming Paradigm Shift in Forensic Identification Science , 2005, Science.
[20] T. Egeland,et al. DNA Commission of the International Society for Forensic Genetics (ISFG): Guidelines on the use of X-STRs in kinship analysis. , 2017, Forensic science international. Genetics.
[21] Gabor T. Marth,et al. A global reference for human genetic variation , 2015, Nature.
[22] Toshihiro Tanaka. The International HapMap Project , 2003, Nature.
[23] A. Dawid,et al. Response to: DNA identification by pedigree likelihood ratio accommodating population substructure and mutations , 2011, Investigative Genetics.
[24] N. Pinto,et al. Mutation and mutation rates at Y chromosome specific Short Tandem Repeat Polymorphisms (STRs): a reappraisal. , 2014, Forensic science international. Genetics.
[25] Kelly A Meiklejohn,et al. An automated independent workflow for the analysis of massively parallel sequence data from forensic SNP assays , 2018, Electrophoresis.
[26] Amanda B. Hepler,et al. Genetic relatedness analysis: modern data and new challenges , 2006, Nature Reviews Genetics.
[27] M. Cáceres,et al. Human inversions and their functional consequences , 2015, Briefings in functional genomics.
[28] Heterozygosity increases microsatellite mutation rate , 2016, Biology Letters.
[29] María del Mar González,et al. Frequency and Pattern of Heteroplasmy in the Complete Human Mitochondrial Genome , 2013, PloS one.
[30] Martin Krzywinski,et al. The curse(s) of dimensionality , 2018, Nature Methods.
[31] Yuan-ming Wu,et al. Tri-allelic pattern of short tandem repeats identifies the murderer among identical twins and suggests an embryonic mutational origin. , 2015, Forensic science international. Genetics.
[32] Wentian Li,et al. Mappability and read length , 2014, Front. Genet..
[33] Michael J. Dougherty,et al. Assessing the Genetics Content in the Next Generation Science Standards , 2015, PloS one.
[34] A. Amorim,et al. Tri-allelic pattern at the TPOX locus: a familial study. , 2014, Gene.
[35] Hoi Yan Chow,et al. Qualitative and quantitative assessment of Illumina’s forensic STR and SNP kits on MiSeq FGx™ , 2017, PloS one.
[36] B. Payseur,et al. Effects of Demographic History on the Detection of Recombination Hotspots from Linkage Disequilibrium , 2017, Molecular biology and evolution.
[37] Bruce Budowle,et al. Increasing the reach of forensic genetics with massively parallel sequencing , 2017, Forensic Science, Medicine and Pathology.
[38] Roded Sharan,et al. To Embed or Not: Network Embedding as a Paradigm in Computational Biology , 2019, Front. Genet..
[39] L. Chikhi,et al. Send Orders of Reprints at Reprints@benthamscience.org on the Structural Plasticity of the Human Genome: Chromosomal Inver- Sions Revisited , 2022 .
[40] W. Rojas,et al. Evaluating the X Chromosome-Specific Diversity of Colombian Populations Using Insertion/Deletion Polymorphisms , 2014, PloS one.
[41] Arthur Wuster,et al. Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes , 2017, Nature Communications.
[42] Jacqueline Weber-Lehmann,et al. Finding the needle in the haystack: differentiating "identical" twins in paternity testing and forensics by ultra-deep next generation sequencing. , 2014, Forensic science international. Genetics.