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Stutter analysis of complex STR MPS data.
Forensic Sci Int Genet. 2018 Jul;35:107-112. doi: 10.1016/j.fsigen.2018.04.003. Epub 2018 Apr 20.
Forensic Sci Int Genet. 2018.
PMID: 29702330
Modelling allelic drop-outs in STR sequencing data generated by MPS.
Vilsen SB, Tvedebrink T, Eriksen PS, Hussing C, Børsting C, Morling N.
Vilsen SB, et al. Among authors: hussing c.
Forensic Sci Int Genet. 2018 Nov;37:6-12. doi: 10.1016/j.fsigen.2018.07.017. Epub 2018 Jul 25.
Forensic Sci Int Genet. 2018.
PMID: 30071494
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Quantification of massively parallel sequencing libraries - a comparative study of eight methods.
Hussing C, Kampmann ML, Mogensen HS, Børsting C, Morling N.
Hussing C, et al.
Sci Rep. 2018 Jan 18;8(1):1110. doi: 10.1038/s41598-018-19574-w.
Sci Rep. 2018.
PMID: 29348673
Free PMC article.
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Sequencing of 231 forensic genetic markers using the MiSeq FGx™ forensic genomics system - an evaluation of the assay and software.
Hussing C, Huber C, Bytyci R, Mogensen HS, Morling N, Børsting C.
Hussing C, et al.
Forensic Sci Res. 2018 Apr 9;3(2):111-123. doi: 10.1080/20961790.2018.1446672. eCollection 2018.
Forensic Sci Res. 2018.
PMID: 30483659
Free PMC article.
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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.
Eduardoff M, et al. Among authors: hussing c.
Forensic Sci Int Genet. 2016 Jul;23:178-189. doi: 10.1016/j.fsigen.2016.04.008. Epub 2016 Apr 21.
Forensic Sci Int Genet. 2016.
PMID: 27208666
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The Danish STR sequence database: duplicate typing of 363 Danes with the ForenSeq™ DNA Signature Prep Kit.
Hussing C, Bytyci R, Huber C, Morling N, Børsting C.
Hussing C, et al.
Int J Legal Med. 2019 Mar;133(2):325-334. doi: 10.1007/s00414-018-1854-0. Epub 2018 May 24.
Int J Legal Med. 2019.
PMID: 29797283
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Identification of minority resistance mutations in the HIV-1 integrase coding region using next generation sequencing.
Fonager J, Larsson JT, Hussing C, Neess Engsig F, Nielsen C, Fischer TK.
Fonager J, et al. Among authors: hussing c.
J Clin Virol. 2015 Dec;73:95-100. doi: 10.1016/j.jcv.2015.11.009. Epub 2015 Nov 10.
J Clin Virol. 2015.
PMID: 26587787
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