177 related articles for article (PubMed ID: 37336821)
1. Comparison of three massively parallel sequencing platforms for single nucleotide polymorphism (SNP) genotyping in forensic genetics.
Li R; Wang Q; Yang J; Zhu J; Liu J; Wu R; Sun H
Int J Legal Med; 2023 Sep; 137(5):1361-1372. PubMed ID: 37336821
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Next-Generation Sequencing: ForenSeq™ DNA Signature Prep Kit with the Illumina MiSeq FGx.
Foley MM
Methods Mol Biol; 2023; 2685():397-427. PubMed ID: 37439995
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Developmental validation of the MGIEasy Signature Identification Library Prep Kit, an all-in-one multiplex system for forensic applications.
Li R; Shen X; Chen H; Peng D; Wu R; Sun H
Int J Legal Med; 2021 May; 135(3):739-753. PubMed ID: 33523251
[TBL] [Abstract][Full Text] [Related]
10. Comparison of Two Massively Parallel Sequencing Platforms using 83 Single Nucleotide Polymorphisms for Human Identification.
Apaga DL; Dennis SE; Salvador JM; Calacal GC; De Ungria MC
Sci Rep; 2017 Mar; 7(1):398. PubMed ID: 28341840
[TBL] [Abstract][Full Text] [Related]
11. Validation and beyond: Next generation sequencing of forensic casework samples including challenging tissue samples from altered human corpses using the MiSeq FGx system.
Senst A; Caliebe A; Scheurer E; Schulz I
J Forensic Sci; 2022 Jul; 67(4):1382-1398. PubMed ID: 35318655
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. Evaluation of the VISAGE Basic Tool for Appearance and Ancestry Prediction Using PowerSeq Chemistry on the MiSeq FGx System.
Palencia-Madrid L; Xavier C; de la Puente M; Hohoff C; Phillips C; Kayser M; Parson W
Genes (Basel); 2020 Jun; 11(6):. PubMed ID: 32604780
[TBL] [Abstract][Full Text] [Related]
17. Increasing the discrimination power of ancestry- and identity-informative SNP loci within the ForenSeq™ DNA Signature Prep Kit.
King JL; Churchill JD; Novroski NMM; Zeng X; Warshauer DH; Seah LH; Budowle B
Forensic Sci Int Genet; 2018 Sep; 36():60-76. PubMed ID: 29935396
[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. Optimizing DNA recovery and forensic typing of degraded blood and dental remains using a specialized extraction method, comprehensive qPCR sample characterization, and massively parallel sequencing.
Carrasco P; Inostroza C; Didier M; Godoy M; Holt CL; Tabak J; Loftus A
Int J Legal Med; 2020 Jan; 134(1):79-91. PubMed ID: 31414202
[TBL] [Abstract][Full Text] [Related]
20. Operationalisation of the ForenSeq® Kintelligence Kit for Australian unidentified and missing persons casework.
Watson J; McNevin D; Grisedale K; Spiden M; Seddon S; Ward J
Forensic Sci Int Genet; 2024 Jan; 68():102972. PubMed ID: 37918284
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
