These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
202 related articles for article (PubMed ID: 30483659)
1. Sequencing of 231 forensic genetic markers using the MiSeq FGx™ forensic genomics system - an evaluation of the assay and software. Hussing C; Huber C; Bytyci R; Mogensen HS; Morling N; Børsting C Forensic Sci Res; 2018; 3(2):111-123. PubMed ID: 30483659 [TBL] [Abstract][Full Text] [Related]
2. Developmental validation of the MiSeq FGx Forensic Genomics System for Targeted Next Generation Sequencing in Forensic DNA Casework and Database Laboratories. Jäger AC; Alvarez ML; Davis CP; Guzmán E; Han Y; Way L; Walichiewicz P; Silva D; Pham N; Caves G; Bruand J; Schlesinger F; Pond SJK; Varlaro J; Stephens KM; Holt CL Forensic Sci Int Genet; 2017 May; 28():52-70. PubMed ID: 28171784 [TBL] [Abstract][Full Text] [Related]
3. Massively parallel sequencing of forensic STRs and SNPs using the Illumina Guo F; Yu J; Zhang L; Li J Forensic Sci Int Genet; 2017 Nov; 31():135-148. PubMed ID: 28938154 [TBL] [Abstract][Full Text] [Related]
4. A preliminary assessment of the ForenSeq™ FGx System: next generation sequencing of an STR and SNP multiplex. Silvia AL; Shugarts N; Smith J Int J Legal Med; 2017 Jan; 131(1):73-86. PubMed ID: 27785563 [TBL] [Abstract][Full Text] [Related]
5. Genetic analysis of the Yavapai Native Americans from West-Central Arizona using the Illumina MiSeq FGx™ forensic genomics system. Wendt FR; Churchill JD; Novroski NMM; King JL; Ng J; Oldt RF; McCulloh KL; Weise JA; Smith DG; Kanthaswamy S; Budowle B Forensic Sci Int Genet; 2016 Sep; 24():18-23. PubMed ID: 27243782 [TBL] [Abstract][Full Text] [Related]
6. Evaluation of the Illumina ForenSeq™ DNA Signature Prep Kit - MPS forensic application for the MiSeq FGx™ benchtop sequencer. Xavier C; Parson W Forensic Sci Int Genet; 2017 May; 28():188-194. PubMed ID: 28279935 [TBL] [Abstract][Full Text] [Related]
7. Sequencing of human identification markers in an Uyghur population using the MiSeq FGx Simayijiang H; Morling N; Børsting C Forensic Sci Res; 2022; 7(2):154-162. PubMed ID: 35784409 [TBL] [Abstract][Full Text] [Related]
8. Parallel sequencing of 87 STR and 294 SNP markers using the prototype of the SifaMPS panel on the MiSeq FGx™ system. Tao R; Wang S; Chen A; Xia R; Zhang X; Yang Q; Qu Y; Zhang S; Li C Forensic Sci Int Genet; 2021 May; 52():102490. PubMed ID: 33689955 [TBL] [Abstract][Full Text] [Related]
9. Global patterns of STR sequence variation: Sequencing the CEPH human genome diversity panel for 58 forensic STRs using the Illumina ForenSeq DNA Signature Prep Kit. Phillips C; Devesse L; Ballard D; van Weert L; de la Puente M; Melis S; Álvarez Iglesias V; Freire-Aradas A; Oldroyd N; Holt C; Syndercombe Court D; Carracedo Á; Lareu MV Electrophoresis; 2018 Nov; 39(21):2708-2724. PubMed ID: 30101987 [TBL] [Abstract][Full Text] [Related]
10. The Danish STR sequence database: duplicate typing of 363 Danes with the ForenSeq™ DNA Signature Prep Kit. Hussing C; Bytyci R; Huber C; Morling N; Børsting C Int J Legal Med; 2019 Mar; 133(2):325-334. PubMed ID: 29797283 [TBL] [Abstract][Full Text] [Related]
11. Evaluation of the Illumina(®) Beta Version ForenSeq™ DNA Signature Prep Kit for use in genetic profiling. Churchill JD; Schmedes SE; King JL; Budowle B Forensic Sci Int Genet; 2016 Jan; 20():20-29. PubMed ID: 26433485 [TBL] [Abstract][Full Text] [Related]
12. Qualitative and quantitative assessment of Illumina's forensic STR and SNP kits on MiSeq FGx™. Sharma V; Chow HY; Siegel D; Wurmbach E PLoS One; 2017; 12(11):e0187932. PubMed ID: 29121662 [TBL] [Abstract][Full Text] [Related]
13. Evaluation of a custom GeneRead™ massively parallel sequencing assay with 210 ancestry informative SNPs using the Ion S5™ and MiSeq platforms. Truelsen D; Pereira V; Phillips C; Morling N; Børsting C Forensic Sci Int Genet; 2021 Jan; 50():102411. PubMed ID: 33176271 [TBL] [Abstract][Full Text] [Related]
14. Systematic assessment of the performance of illumina's MiSeq FGx™ forensic genomics system. Almalki N; Chow HY; Sharma V; Hart K; Siegel D; Wurmbach E Electrophoresis; 2017 Mar; 38(6):846-854. PubMed ID: 27943350 [TBL] [Abstract][Full Text] [Related]
15. High-resolution genotyping of 58 STRs in 635 Northern Han Chinese with MiSeq FGx ® Forensic Genomics System. Guo F; Liu Z; Long G; Zhang B; Dong X; Liu D; Yu S Forensic Sci Int Genet; 2023 Jul; 65():102879. PubMed ID: 37150076 [TBL] [Abstract][Full Text] [Related]
16. STRinNGS v2.0: Improved tool for analysis and reporting of STR sequencing data. Jønck CG; Qian X; Simayijiang H; Børsting C Forensic Sci Int Genet; 2020 Sep; 48():102331. PubMed ID: 32623352 [TBL] [Abstract][Full Text] [Related]
17. Utility of ForenSeq™ DNA Signature Prep Kit in the research of pairwise 2nd-degree kinship identification. Xu M; Du Q; Ma G; Chen Z; Liu Q; Fu L; Cong B; Li S Int J Legal Med; 2019 Nov; 133(6):1641-1650. PubMed ID: 30687898 [TBL] [Abstract][Full Text] [Related]
18. Concordance study on Y-STRs typing between SeqStudio™ genetic analyzer for HID and MiSeq™ FGx forensic genomics system. Soldati G; Turrina S; Treccani M; Saccardo C; Ausania F; De Leo D Mol Biol Rep; 2023 Dec; 50(12):9779-9789. PubMed ID: 37812349 [TBL] [Abstract][Full Text] [Related]
19. Performance and concordance of the ForenSeq™ system for autosomal and Y chromosome short tandem repeat sequencing of reference-type specimens. Just RS; Moreno LI; Smerick JB; Irwin JA Forensic Sci Int Genet; 2017 May; 28():1-9. PubMed ID: 28126691 [TBL] [Abstract][Full Text] [Related]
20. Inter-laboratory validation study of the ForenSeq™ DNA Signature Prep Kit. Köcher S; Müller P; Berger B; Bodner M; Parson W; Roewer L; Willuweit S; Forensic Sci Int Genet; 2018 Sep; 36():77-85. PubMed ID: 29945120 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]