Massively parallel sequencing of short tandem repeats—Population data and mixture analysis results for the PowerSeq™ system
Tài liệu tham khảo
Altshuler, 2010, Integrating common and rare genetic variation in diverse human populations, Nature, 467, 52, 10.1038/nature09298
Anvar, 2014, TSSV: a tool for characterization of complex allelic variants in pure and mixed genomes, Bioinformatics, 30, 1651, 10.1093/bioinformatics/btu068
Brookes, 2012, Characterising stutter in forensic STR multiplexes, Forensic Sci. Int. Genet., 6, 58, 10.1016/j.fsigen.2011.02.001
Budowle, 2009, Mixture interpretation: defining the relevant features for guidelines for the assessment of mixed DNA profiles in forensic casework, J. Forensic Sci., 54, 810, 10.1111/j.1556-4029.2009.01046.x
Cann, 2002, A human genome diversity cell line panel, Science, 296, 261, 10.1126/science.296.5566.261b
Gelardi, 2014, Second generation sequencing of three STRs D3S1358, D12S391 and D21S11 in Danes and a new nomenclature for sequenced STR alleles, Forensic Sci. Int. Genet., 12, 38, 10.1016/j.fsigen.2014.04.016
Gettings, 2015, STR allele sequence variation: current knowledge and future issues, Forensic Sci. Int. Genet., 18, 118, 10.1016/j.fsigen.2015.06.005
Kline, 2011, STR sequence analysis for characterizing normal, variant, and null alleles, Forensic Sci. Int. Genet., 5, 329, 10.1016/j.fsigen.2010.09.005
P. de Knijff, J. Pijpe, Population genetics of an African Pygmy population, 2015, Ref. Type: Unpublished work.
Kraaijenbrink, 2014, A linguistically informed autosomal STR survey of human populations residing in the greater Himalayan region, PLoS One, 9, e91534, 10.1371/journal.pone.0091534
Magoc, 2011, FLASH: fast length adjustment of short reads to improve genome assemblies, Bioinformatics, 27, 2957, 10.1093/bioinformatics/btr507
Oostdik, 2014, Developmental validation of the PowerPlex((R)) Fusion System for analysis of casework and reference samples: a 24-locus multiplex for new database standards, Forensic Sci. Int. Genet., 12, 69, 10.1016/j.fsigen.2014.04.013
Promega Corporation. Powerstats v12, 2015, Ref. Type: Unpublished work.
Promega Corporation Technical Manual, PowerPlex® Fusion System, 2015, Ref. Type: Unpublished work.
Scheible, 2014, Short tandem repeat typing on the 454 platform: strategies and considerations for targeted sequencing of common forensic markers, Forensic Sci. Int. Genet., 12, 107, 10.1016/j.fsigen.2014.04.010
Schirmer, 2015, Insight into biases and sequencing errors for amplicon sequencing with the Illumina MiSeq platform, Nucleic Acids Res., 43, e37, 10.1093/nar/gku1341
van der Gaag, 2015, Forensic nomenclature for short tandem repeats updated for sequencing, Forensic Sci. Int. Genet. Suppl. Ser., 4
Warshauer, 2015, STRait Razor v2.0: the improved STR Allele identification Tool–Razor, Forensic Sci. Int. Genet., 14, 182, 10.1016/j.fsigen.2014.10.011
Westen, 2012, Assessment of the stochastic threshold, back- and forward stutter filters and low template techniques for NGM, Forensic Sci. Int. Genet., 6, 708, 10.1016/j.fsigen.2012.05.001
Westen, 2014, Comparing six commercial autosomal STR kits in a large Dutch population sample, Forensic Sci. Int. Genet., 10, 55, 10.1016/j.fsigen.2014.01.008
Zeng, 2015, High sensitivity multiplex short tandem repeat loci analyses with massively parallel sequencing, Forensic Sci. Int. Genet., 16, 38, 10.1016/j.fsigen.2014.11.022