164 related articles for article (PubMed ID: 38065030)
1. Systematic evaluation of the Precision ID GlobalFiler™ NGS STR panel v2 using single-source samples of various quantity and quality and mixed DNA samples.
Sharma V; Wurmbach E
Forensic Sci Int Genet; 2024 Mar; 69():102995. PubMed ID: 38065030
[TBL] [Abstract][Full Text] [Related]
2. Pilot study for forensic evaluations of the Precision ID GlobalFiler™ NGS STR Panel v2 with the Ion S5™ system.
Tao R; Qi W; Chen C; Zhang J; Yang Z; Song W; Zhang S; Li C
Forensic Sci Int Genet; 2019 Nov; 43():102147. PubMed ID: 31437781
[TBL] [Abstract][Full Text] [Related]
3. Simultaneous sequencing of 102 Y-STRs on Ion Torrent ™ GeneStudio ™ S5 System.
Guo F; Jing G; Lang Y; Liu Z; Yu S
Forensic Sci Int Genet; 2024 Jul; 71():103059. PubMed ID: 38749212
[TBL] [Abstract][Full Text] [Related]
4. Interpreting Mixture Profiles: Comparison between Precision ID GlobalFiler™ NGS STR Panel v2 and Traditional Methods.
Ragazzo M; Carboni S; Caputo V; Buttini C; Manzo L; Errichiello V; Puleri G; Giardina E
Genes (Basel); 2020 May; 11(6):. PubMed ID: 32466613
[TBL] [Abstract][Full Text] [Related]
5. Massively parallel sequencing of 32 forensic markers using the Precision ID GlobalFiler™ NGS STR Panel and the Ion PGM™ System.
Wang Z; Zhou D; Wang H; Jia Z; Liu J; Qian X; Li C; Hou Y
Forensic Sci Int Genet; 2017 Nov; 31():126-134. PubMed ID: 28938153
[TBL] [Abstract][Full Text] [Related]
6. Mixture deconvolution by massively parallel sequencing of microhaplotypes.
Bennett L; Oldoni F; Long K; Cisana S; Madella K; Wootton S; Chang J; Hasegawa R; Lagacé R; Kidd KK; Podini D
Int J Legal Med; 2019 May; 133(3):719-729. PubMed ID: 30758713
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Analyzing degraded DNA and challenging samples using the ForenSeq™ DNA Signature Prep kit.
Sharma V; van der Plaat DA; Liu Y; Wurmbach E
Sci Justice; 2020 May; 60(3):243-252. PubMed ID: 32381241
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Massively parallel sequencing of 17 commonly used forensic autosomal STRs and amelogenin with small amplicons.
Kim EH; Lee HY; Yang IS; Jung SE; Yang WI; Shin KJ
Forensic Sci Int Genet; 2016 May; 22():1-7. PubMed ID: 26799314
[TBL] [Abstract][Full Text] [Related]
11. Evaluation of ArmedXpert software tools, MixtureAce and Mixture Interpretation, to analyze MPS-STR data.
Sharma V; Young B; Armogida L; Khan A; Wurmbach E
Forensic Sci Int Genet; 2022 Jan; 56():102603. PubMed ID: 34673336
[TBL] [Abstract][Full Text] [Related]
12. A novel forensic panel of 186-plex SNPs and 123-plex STR loci based on massively parallel sequencing.
Miao X; Shen Y; Gong X; Yu H; Li B; Chang L; Wang Y; Fan J; Liang Z; Tan B; Li S; Zhang B
Int J Legal Med; 2021 May; 135(3):709-718. PubMed ID: 32851473
[TBL] [Abstract][Full Text] [Related]
13. Development and validation of a novel 133-plex forensic STR panel (52 STRs and 81 Y-STRs) using single-end 400 bp massive parallel sequencing.
Fan H; Wang L; Liu C; Lu X; Xu X; Ru K; Qiu P; Liu C; Wen SQ
Int J Legal Med; 2022 Mar; 136(2):447-464. PubMed ID: 34741666
[TBL] [Abstract][Full Text] [Related]
14. Massively parallel sequence data of 31 autosomal STR loci from 496 Spanish individuals revealed concordance with CE-STR technology and enhanced discrimination power.
Barrio PA; Martín P; Alonso A; Müller P; Bodner M; Berger B; Parson W; Budowle B;
Forensic Sci Int Genet; 2019 Sep; 42():49-55. PubMed ID: 31252251
[TBL] [Abstract][Full Text] [Related]
15. Target capture enrichment of nuclear SNP markers for massively parallel sequencing of degraded and mixed samples.
Bose N; Carlberg K; Sensabaugh G; Erlich H; Calloway C
Forensic Sci Int Genet; 2018 May; 34():186-196. PubMed ID: 29524767
[TBL] [Abstract][Full Text] [Related]
16. Allele frequencies of 31 autosomal short tandem repeat (auSTR) loci obtained using the Precision ID GlobalFiler™ NGS STR Panel v2 in 322 individuals from the Japanese population.
Ohuchi T; Guan X; Hirai E; Hashiyada M; Manabe S; Akane A; Adachi N; Tamaki K; Funayama M
Leg Med (Tokyo); 2022 Nov; 59():102151. PubMed ID: 36191412
[TBL] [Abstract][Full Text] [Related]
17. Application of a probabilistic genotyping software to MPS mixture STR data is supported by similar trends in LRs compared with CE data.
Benschop CCG; van der Gaag KJ; de Vreede J; Backx AJ; de Leeuw RH; Zuñiga S; Hoogenboom J; de Knijff P; Sijen T
Forensic Sci Int Genet; 2021 May; 52():102489. PubMed ID: 33677249
[TBL] [Abstract][Full Text] [Related]
18. A DNA typing panel of 201 genetic markers for degraded samples: development and validation.
Wei H; Qing-Zhen Z; Jing Y; Zhe Z
Yi Chuan; 2024 Apr; 46(4):306-318. PubMed ID: 38632093
[TBL] [Abstract][Full Text] [Related]
19. Assessment of impact of DNA extraction methods on analysis of human remain samples on massively parallel sequencing success.
Zeng X; Elwick K; Mayes C; Takahashi M; King JL; Gangitano D; Budowle B; Hughes-Stamm S
Int J Legal Med; 2019 Jan; 133(1):51-58. PubMed ID: 30341454
[TBL] [Abstract][Full Text] [Related]
20. A sequence-based 74plex microhaplotype assay for analysis of forensic DNA mixtures.
Oldoni F; Bader D; Fantinato C; Wootton SC; Lagacé R; Kidd KK; Podini D
Forensic Sci Int Genet; 2020 Nov; 49():102367. PubMed ID: 32919300
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]