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.
137 related articles for article (PubMed ID: 35449468)
21. Inter-laboratory study on standardized MPS libraries: evaluation of performance, concordance, and sensitivity using mixtures and degraded DNA. Müller P; Sell C; Hadrys T; Hedman J; Bredemeyer S; Laurent FX; Roewer L; Achtruth S; Sidstedt M; Sijen T; Trimborn M; Weiler N; Willuweit S; Bastisch I; Parson W; Int J Legal Med; 2020 Jan; 134(1):185-198. PubMed ID: 31745634 [TBL] [Abstract][Full Text] [Related]
22. 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]
23. Impact of DNA degradation on massively parallel sequencing-based autosomal STR, iiSNP, and mitochondrial DNA typing systems. Zavala EI; Rajagopal S; Perry GH; Kruzic I; Bašić Ž; Parsons TJ; Holland MM Int J Legal Med; 2019 Sep; 133(5):1369-1380. PubMed ID: 31267160 [TBL] [Abstract][Full Text] [Related]
24. Validation of the Verogen ForenSeq™ DNA Signature Prep kit/Primer Mix B for phenotypic and biogeographical ancestry predictions using the Micro MiSeq® Flow Cells. Frégeau CJ Forensic Sci Int Genet; 2021 Jul; 53():102533. PubMed ID: 34058534 [TBL] [Abstract][Full Text] [Related]
25. The first GHEP-ISFG collaborative exercise on forensic applications of massively parallel sequencing. Barrio PA; García Ó; Phillips C; Prieto L; Gusmão L; Fernández C; Casals F; Freitas JM; González-Albo MDC; Martín P; Mosquera A; Navarro-Vera I; Paredes M; Pérez JA; Pinzón A; Rasal R; Ruiz-Ramírez J; Trindade BR; Alonso A Forensic Sci Int Genet; 2020 Nov; 49():102391. PubMed ID: 32957016 [TBL] [Abstract][Full Text] [Related]
26. Developmental validation of the ForenSeq® Kintelligence kit, MiSeq FGx® sequencing system and ForenSeq Universal Analysis Software. Antunes J; Walichiewicz P; Forouzmand E; Barta R; Didier M; Han Y; Perez JC; Snedecor J; Zlatkov C; Padmabandu G; Devesse L; Radecke S; Holt CL; Kumar SA; Budowle B; Stephens KM Forensic Sci Int Genet; 2024 Jul; 71():103055. PubMed ID: 38762965 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. 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]
30. 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]
31. Massively parallel sequencing of 165 ancestry-informative SNPs and forensic biogeographical ancestry inference in three southern Chinese Sinitic/Tai-Kadai populations. He G; Liu J; Wang M; Zou X; Ming T; Zhu S; Yeh HY; Wang C; Wang Z; Hou Y Forensic Sci Int Genet; 2021 May; 52():102475. PubMed ID: 33561661 [TBL] [Abstract][Full Text] [Related]
32. Identification of sequence polymorphisms at 58 STRs and 94 iiSNPs in a Tibetan population using massively parallel sequencing. Peng D; Zhang Y; Ren H; Li H; Li R; Shen X; Wang N; Huang E; Wu R; Sun H Sci Rep; 2020 Jul; 10(1):12225. PubMed ID: 32699278 [TBL] [Abstract][Full Text] [Related]
33. Performance and characterization of 94 identity-informative SNPs in Northern Han Chinese using ForenSeq ™ DNA signature prep kit. Guo F; Liu Z; Long G; Zhang B; Liu D; Yu S J Forensic Leg Med; 2024 Apr; 103():102678. PubMed ID: 38522119 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. 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]
36. 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]
37. 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]
38. The forensic landscape and the population genetic analyses of Hainan Li based on massively parallel sequencing DNA profiling. Fan H; Du Z; Wang F; Wang X; Wen SQ; Wang L; Du P; Liu H; Cao S; Luo Z; Han B; Huang P; Zhu B; Qiu P Int J Legal Med; 2021 Jul; 135(4):1295-1317. PubMed ID: 33847803 [TBL] [Abstract][Full Text] [Related]
39. Ancestry Inference Using the ForenSeq Wang NN; Li R; Wu RG; Peng D; Li HX; Shen XF; Sun HY Fa Yi Xue Za Zhi; 2019 Oct; 35(5):560-566. PubMed ID: 31833289 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]