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Erratum| Volume 33, e17, March 2018

Erratum to “Population and performance analyses of four major populations with Illumina’s FGx Forensic Genomics System” [Forensic Sci. Int.: Genet. 30 (2017) 81–92]

Published:December 19, 2017DOI:https://doi.org/10.1016/j.fsigen.2017.12.007
      The publisher regrets that the supplementary tables for this submission were not included in the original publication. They can now be found by following this link <ADD The publisher would like to apologise for any inconvenience caused.

      Appendix A. Supplementary data

      Linked Article

      • Population and performance analyses of four major populations with Illumina’s FGx Forensic Genomics System
        Forensic Science International: GeneticsVol. 30
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          Numerous studies have illustrated that massively parallel sequencing technologies offer a higher throughput of genetic markers than capillary electrophoresis-based technologies [1–18]. With these data, backward compatibility to current short tandem repeat (STR) marker databases can be maintained while increasing the power of discrimination with additional STRs and identity SNPs, as well as including new types of information with ancestry and phenotype SNPs [4,8,12,13,18,19,20–24]. The smaller amplicons afforded by analyzing SNP markers improve characterization of degraded or challenged samples often encountered in forensic evidence [2,12,19,25,26].
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