Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 190

1.

Single nucleotide polymorphism typing with massively parallel sequencing for human identification.

Seo SB, King JL, Warshauer DH, Davis CP, Ge J, Budowle B.

Int J Legal Med. 2013 Nov;127(6):1079-86. doi: 10.1007/s00414-013-0879-7. Epub 2013 Jun 5.

PMID:
23736940
2.

Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM™.

Eduardoff M, Santos C, de la Puente M, Gross TE, Fondevila M, Strobl C, Sobrino B, Ballard D, Schneider PM, Carracedo Á, Lareu MV, Parson W, Phillips C.

Forensic Sci Int Genet. 2015 Jul;17:110-21. doi: 10.1016/j.fsigen.2015.04.007. Epub 2015 Apr 15.

PMID:
25955683
3.

Evaluation of the Ion Torrent™ HID SNP 169-plex: A SNP typing assay developed for human identification by second generation sequencing.

Børsting C, Fordyce SL, Olofsson J, Mogensen HS, Morling N.

Forensic Sci Int Genet. 2014 Sep;12:144-54. doi: 10.1016/j.fsigen.2014.06.004. Epub 2014 Jun 14.

PMID:
24997319
4.

Next generation sequencing of SNPs using the HID-Ion AmpliSeq™ Identity Panel on the Ion Torrent PGM™ platform.

Guo F, Zhou Y, Song H, Zhao J, Shen H, Zhao B, Liu F, Jiang X.

Forensic Sci Int Genet. 2016 Nov;25:73-84. doi: 10.1016/j.fsigen.2016.07.021. Epub 2016 Jul 29.

PMID:
27500651
5.

Revealing the challenges of low template DNA analysis with the prototype Ion AmpliSeq™ Identity panel v2.3 on the PGM™ Sequencer.

Elena S, Alessandro A, Ignazio C, Sharon W, Luigi R, Andrea B.

Forensic Sci Int Genet. 2016 May;22:25-36. doi: 10.1016/j.fsigen.2015.07.011. Epub 2015 Jul 19.

PMID:
26828903
6.

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;20:20-9. doi: 10.1016/j.fsigen.2015.09.009. Epub 2015 Sep 21.

PMID:
26433485
7.

Evaluation of the iPLEX® Sample ID Plus Panel designed for the Sequenom MassARRAY® system. A SNP typing assay developed for human identification and sample tracking based on the SNPforID panel.

Johansen P, Andersen JD, Børsting C, Morling N.

Forensic Sci Int Genet. 2013 Sep;7(5):482-7. doi: 10.1016/j.fsigen.2013.04.009. Epub 2013 Jun 28.

PMID:
23948317
8.

Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™.

Eduardoff M, Gross TE, Santos C, de la Puente M, Ballard D, Strobl C, Børsting C, Morling N, Fusco L, Hussing C, Egyed B, Souto L, Uacyisrael J, Syndercombe Court D, Carracedo Á, Lareu MV, Schneider PM, Parson W, Phillips C; EUROFORGEN-NoE Consortium, Parson W, Phillips C.

Forensic Sci Int Genet. 2016 Jul;23:178-89. doi: 10.1016/j.fsigen.2016.04.008. Epub 2016 Apr 21.

PMID:
27208666
9.

Second-generation sequencing of forensic STRs using the Ion Torrent™ HID STR 10-plex and the Ion PGM™.

Fordyce SL, Mogensen HS, Børsting C, Lagacé RE, Chang CW, Rajagopalan N, Morling N.

Forensic Sci Int Genet. 2015 Jan;14:132-40. doi: 10.1016/j.fsigen.2014.09.020. Epub 2014 Oct 5.

PMID:
25450784
10.

Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics.

Tomas C, Stangegaard M, Børsting C, Hansen AJ, Morling N; SNPforID Consortium.

Forensic Sci Int Genet. 2008 Dec;3(1):1-6. doi: 10.1016/j.fsigen.2008.06.007. Epub 2008 Sep 2.

PMID:
19083859
11.

Forensic performance of two insertion-deletion marker assays.

Fondevila M, Phillips C, Santos C, Pereira R, Gusmão L, Carracedo A, Butler JM, Lareu MV, Vallone PM.

Int J Legal Med. 2012 Sep;126(5):725-37. doi: 10.1007/s00414-012-0721-7. Epub 2012 Jun 20.

PMID:
22714117
12.

Whole genome amplification and real-time PCR in forensic casework.

Giardina E, Pietrangeli I, Martone C, Zampatti S, Marsala P, Gabriele L, Ricci O, Solla G, Asili P, Arcudi G, Spinella A, Novelli G.

BMC Genomics. 2009 Apr 14;10:159. doi: 10.1186/1471-2164-10-159.

13.

Developmental validation of a custom panel including 273 SNPs for forensic application using Ion Torrent PGM.

Zhang S, Bian Y, Chen A, Zheng H, Gao Y, Hou Y, Li C.

Forensic Sci Int Genet. 2017 Mar;27:50-57. doi: 10.1016/j.fsigen.2016.12.003. Epub 2016 Dec 7.

PMID:
27951431
14.

Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel.

Phillips C, Fang R, Ballard D, Fondevila M, Harrison C, Hyland F, Musgrave-Brown E, Proff C, Ramos-Luis E, Sobrino B, Carracedo A, Furtado MR, Syndercombe Court D, Schneider PM; SNPforID Consortium.

Forensic Sci Int Genet. 2007 Jun;1(2):180-5. doi: 10.1016/j.fsigen.2007.02.007. Epub 2007 Mar 23.

PMID:
19083752
15.

A SNaPshot of next generation sequencing for forensic SNP analysis.

Daniel R, Santos C, Phillips C, Fondevila M, van Oorschot RA, Carracedo A, Lareu MV, McNevin D.

Forensic Sci Int Genet. 2015 Jan;14:50-60. doi: 10.1016/j.fsigen.2014.08.013. Epub 2014 Aug 30.

PMID:
25282603
16.

Forensic genetic SNP typing of low-template DNA and highly degraded DNA from crime case samples.

Børsting C, Mogensen HS, Morling N.

Forensic Sci Int Genet. 2013 May;7(3):345-52. doi: 10.1016/j.fsigen.2013.02.004. Epub 2013 Mar 19.

PMID:
23523365
17.

Exploring of new Y-chromosome SNP loci using Pyrosequencing and the SNaPshot methods.

Wei W, Luo HB, Yan J, Hou YP.

Int J Legal Med. 2012 Nov;126(6):825-33. doi: 10.1007/s00414-011-0603-4. Epub 2011 Jul 21.

PMID:
21779922
18.

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 SJ, Varlaro J, Stephens KM, Holt CL.

Forensic Sci Int Genet. 2017 May;28:52-70. doi: 10.1016/j.fsigen.2017.01.011. Epub 2017 Jan 27.

19.

SNP detection and prediction of variability between chicken lines using genome resequencing of DNA pools.

Marklund S, Carlborg O.

BMC Genomics. 2010 Nov 25;11:665. doi: 10.1186/1471-2164-11-665.

20.

A low-cost, high-throughput, automated single nucleotide polymorphism assay for forensic human DNA applications.

Pomeroy R, Duncan G, Sunar-Reeder B, Ortenberg E, Ketchum M, Wasiluk H, Reeder D.

Anal Biochem. 2009 Dec 1;395(1):61-7. doi: 10.1016/j.ab.2009.07.041. Epub 2009 Jul 30.

PMID:
19646946

Supplemental Content

Support Center