Similar articles for PMID: 28666376

Year	Number of Results
2001	1
2003	1
2005	1
2009	1
2010	2
2011	2
2012	5
2013	13
2014	13
2015	17
2016	23
2017	28
2018	27
2019	21
2020	12
2021	9
2022	11
2023	1
2024	0

1

A massively parallel strategy for STR marker development, capture, and genotyping.

Kistler L, Johnson SM, Irwin MT, Louis EE, Ratan A, Perry GH. Kistler L, et al. Nucleic Acids Res. 2017 Sep 6;45(15):e142. doi: 10.1093/nar/gkx574. Nucleic Acids Res. 2017. PMID: 28666376 Free PMC article.

2

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. Phillips C, et al. Electrophoresis. 2018 Nov;39(21):2708-2724. doi: 10.1002/elps.201800117. Epub 2018 Sep 3. Electrophoresis. 2018. PMID: 30101987

3

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. Peng D, et al. Sci Rep. 2020 Jul 22;10(1):12225. doi: 10.1038/s41598-020-69137-1. Sci Rep. 2020. PMID: 32699278 Free PMC article.

4

Introduction of the Python script STRinNGS for analysis of STR regions in FASTQ or BAM files and expansion of the Danish STR sequence database to 11 STRs.

Friis SL, Buchard A, Rockenbauer E, Børsting C, Morling N. Friis SL, et al. Forensic Sci Int Genet. 2016 Mar;21:68-75. doi: 10.1016/j.fsigen.2015.12.006. Epub 2015 Dec 12. Forensic Sci Int Genet. 2016. PMID: 26722765

5

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. Parson W, et al. Forensic Sci Int Genet. 2016 May;22:54-63. doi: 10.1016/j.fsigen.2016.01.009. Epub 2016 Jan 21. Forensic Sci Int Genet. 2016. PMID: 26844919

6

Accurate typing of short tandem repeats from genome-wide sequencing data and its applications.

Fungtammasan A, Ananda G, Hile SE, Su MS, Sun C, Harris R, Medvedev P, Eckert K, Makova KD. Fungtammasan A, et al. Genome Res. 2015 May;25(5):736-49. doi: 10.1101/gr.185892.114. Epub 2015 Mar 30. Genome Res. 2015. PMID: 25823460 Free PMC article.

7

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. Wendt FR, et al. Forensic Sci Int Genet. 2017 May;28:146-154. doi: 10.1016/j.fsigen.2017.02.014. Epub 2017 Feb 27. Forensic Sci Int Genet. 2017. PMID: 28273507

8

CRISPR-Cas9-targeted fragmentation and selective sequencing enable massively parallel microsatellite analysis.

Shin G, Grimes SM, Lee H, Lau BT, Xia LC, Ji HP. Shin G, et al. Nat Commun. 2017 Feb 7;8:14291. doi: 10.1038/ncomms14291. Nat Commun. 2017. PMID: 28169275 Free PMC article.

9

Massively parallel sequencing of 25 short tandem repeat loci including the SE33 marker in Koreans.

Lee JH, Kim J, Kim H, Kim HS, Kim E. Lee JH, et al. Genes Genomics. 2021 Feb;43(2):133-140. doi: 10.1007/s13258-020-01033-4. Epub 2021 Jan 22. Genes Genomics. 2021. PMID: 33481226

10

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. Silva DSBS, et al. Forensic Sci Int Genet. 2018 Mar;33:129-135. doi: 10.1016/j.fsigen.2017.12.008. Epub 2017 Dec 16. Forensic Sci Int Genet. 2018. PMID: 29275088

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