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.
428 related articles for article (PubMed ID: 29679929)
1. A phylogenetic framework facilitates Y-STR variant discovery and classification via massively parallel sequencing. Huszar TI; Jobling MA; Wetton JH Forensic Sci Int Genet; 2018 Jul; 35():97-106. PubMed ID: 29679929 [TBL] [Abstract][Full Text] [Related]
2. Investigation into the sequence structure of 23 Y chromosomal STR loci using massively parallel sequencing. Kwon SY; Lee HY; Kim EH; Lee EY; Shin KJ Forensic Sci Int Genet; 2016 Nov; 25():132-141. PubMed ID: 27591816 [TBL] [Abstract][Full Text] [Related]
3. Sequencing of autosomal, mitochondrial and Y-chromosomal forensic markers in the People of the British Isles cohort detects population structure dominated by patrilineages. Huszar TI; Bodmer WF; Hutnik K; Wetton JH; Jobling MA Forensic Sci Int Genet; 2022 Jul; 59():102725. PubMed ID: 35640311 [TBL] [Abstract][Full Text] [Related]
4. Genetic analysis of Southern Brazil subjects using the PowerSeq™ AUTO/Y system for short tandem repeat sequencing. Silva DSBS; Sawitzki FR; Scheible MKR; Bailey SF; Alho CS; Faith SA Forensic Sci Int Genet; 2018 Mar; 33():129-135. PubMed ID: 29275088 [TBL] [Abstract][Full Text] [Related]
5. Evaluation of Promega PowerSeq™ Auto/Y systems prototype on an admixed sample of Rio de Janeiro, Brazil: Population data, sensitivity, stutter and mixture studies. Moura-Neto R; King JL; Mello I; Dias V; Crysup B; Woerner AE; Budowle B; Silva R Forensic Sci Int Genet; 2021 Jul; 53():102516. PubMed ID: 33878618 [TBL] [Abstract][Full Text] [Related]
6. Characterization of genetic sequence variation of 58 STR loci in four major population groups. Novroski NMM; King JL; Churchill JD; Seah LH; Budowle B Forensic Sci Int Genet; 2016 Nov; 25():214-226. PubMed ID: 27697609 [TBL] [Abstract][Full Text] [Related]
7. Massively parallel sequencing of sex-chromosomal STRs in Saudi Arabia reveals patrilineage-associated sequence variants. Khubrani YM; Jobling MA; Wetton JH Forensic Sci Int Genet; 2020 Nov; 49():102402. PubMed ID: 33035796 [TBL] [Abstract][Full Text] [Related]
8. Characterization of sequence variations in the extended flanking regions using massively parallel sequencing in 21 A-STRs and 21 Y-STRs. Li H; Li B; Liu Y; Yang F; Cao Y; Xie J; Liu X; Zhao Z; Li C BMC Genomics; 2024 Sep; 25(1):841. PubMed ID: 39244600 [TBL] [Abstract][Full Text] [Related]
9. Flanking region variation of ForenSeq™ DNA Signature Prep Kit STR and SNP loci in Yavapai Native Americans. Wendt FR; King JL; Novroski NMM; Churchill JD; Ng J; Oldt RF; McCulloh KL; Weise JA; Smith DG; Kanthaswamy S; Budowle B Forensic Sci Int Genet; 2017 May; 28():146-154. PubMed ID: 28273507 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Sequence Variations of 31 Υ-Chromosomal Short Tandem Repeats Analyzed by Massively Parallel Sequencing in Three U.S. Population Groups and Korean Population. Moon MH; Hong SR; Shin KJ J Korean Med Sci; 2022 Feb; 37(6):e40. PubMed ID: 35166077 [TBL] [Abstract][Full Text] [Related]
12. Filipino DNA variation at 12 X-chromosome short tandem repeat markers. Salvador JM; Apaga DLT; Delfin FC; Calacal GC; Dennis SE; De Ungria MCA Forensic Sci Int Genet; 2018 Sep; 36():e8-e12. PubMed ID: 29909139 [TBL] [Abstract][Full Text] [Related]
13. Massively parallel sequencing of forensic STRs: Considerations of the DNA commission of the International Society for Forensic Genetics (ISFG) on minimal nomenclature requirements. Parson W; Ballard D; Budowle B; Butler JM; Gettings KB; Gill P; Gusmão L; Hares DR; Irwin JA; King JL; Knijff P; Morling N; Prinz M; Schneider PM; Neste CV; Willuweit S; Phillips C Forensic Sci Int Genet; 2016 May; 22():54-63. PubMed ID: 26844919 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Massively parallel sequencing of autosomal STRs and identity-informative SNPs highlights consanguinity in Saudi Arabia. Khubrani YM; Hallast P; Jobling MA; Wetton JH Forensic Sci Int Genet; 2019 Nov; 43():102164. PubMed ID: 31585345 [TBL] [Abstract][Full Text] [Related]
17. An evaluation of the PowerSeq™ Auto System: A multiplex short tandem repeat marker kit compatible with massively parallel sequencing. Zeng X; King J; Hermanson S; Patel J; Storts DR; Budowle B Forensic Sci Int Genet; 2015 Nov; 19():172-179. PubMed ID: 26240968 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Concordance and characterization of massively parallel sequencing at 58 STRs in a Tibetan population. Li H; Zhang C; Song G; Ma K; Cao Y; Zhao X; Yang Q; Xie J Mol Genet Genomic Med; 2021 Apr; 9(4):e1626. PubMed ID: 33630413 [TBL] [Abstract][Full Text] [Related]
20. Novel Y-chromosome short tandem repeat sequence variation for loci DYS710, DYS518, DYS385, DYS644, DYS612, DYS626, DYS504, DYS481, DYS447 and DYS449. Kasu M; Fredericks J; Fraser M; Labuschagne C; Lesaoana M; D'Amato ME Int J Legal Med; 2019 Nov; 133(6):1681-1689. PubMed ID: 30982129 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]