Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christian Hussing"'
Autor:
Christian Hussing, Christina Huber, Rajmonda Bytyci, Helle S. Mogensen, Niels Morling, Claus Børsting
Publikováno v:
Forensic Sciences Research, Vol 3, Iss 2, Pp 111-123 (2018)
The MiSeq FGx™ Forensic Genomics System types 231 genetic markers in one multiplex polymerase chain reaction (PCR) assay. The markers include core forensic short tandem repeats (STRs) as well as identity, ancestry and phenotype informative short nu
Externí odkaz:
https://doaj.org/article/d947b6e816274ee2902b9c67cea75659
Publikováno v:
International Journal of Legal Medicine. 133:325-334
Some STR loci have internal sequence variations, which are not revealed by the standard STR typing methods used in forensic genetics (PCR and fragment length analysis by capillary electrophoresis (CE)). Typing of STRs with next-generation sequencing
Autor:
Rajmonda Bytyci, Claus Børsting, Christina Huber, Niels Morling, Christian Hussing, Helle Smidt Mogensen
Publikováno v:
Forensic Sciences Research, Vol 3, Iss 2, Pp 111-123 (2018)
Forensic sciences research
Forensic sciences research
The MiSeq FGx™ Forensic Genomics System types 231 genetic markers in one multiplex polymerase chain reaction (PCR) assay. The markers include core forensic short tandem repeats (STRs) as well as identity, ancestry and phenotype informative short nu
Autor:
Claus Bøsting, Torben Tvedebrink, Helle Smidt Mogensen, Poul Svante Eriksen, Niels Morling, Søren B. Vilsen, Christian Hussing
Publikováno v:
Vilsen, S B, Tvedebrink, T, Eriksen, P S, Bøsting, C, Hussing, C, Mogensen, H S & Morling, N 2018, ' Stutter analysis of complex STR MPS data ', Forensic Science International: Genetics, vol. 35, pp. 107-112 . https://doi.org/10.1016/j.fsigen.2018.04.003
Stutters are common and well documented artefacts of amplification of short tandem repeat (STR) regions when using polymerase chain reaction (PCR) occurring as strands one or more motifs shorter or longer than the parental allele. Understanding the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f7517ccd994603a41bc162f0fde8a70
https://vbn.aau.dk/da/publications/9c1ab5fb-ab87-4e2e-ab97-70f9391b45f7
https://vbn.aau.dk/da/publications/9c1ab5fb-ab87-4e2e-ab97-70f9391b45f7
Autor:
Helle Smidt Mogensen, Niels Morling, Claus Børsting, Marie-Louise Kampmann, Christian Hussing
Publikováno v:
Forensic Science International: Genetics Supplement Series. 5:e276-e278
To ensure efficient sequencing, the DNA of next-generation sequencing (NGS) libraries must be quantified correctly. Therefore, an accurate, sensitive and stable method for DNA quantification is crucial. In this study, seven different methods for DNA
Autor:
M. de la Puente, Carla Santos, Theresa E. Gross, Christina Strobl, D. Syndercombe Court, J. Uacyisrael, M. V. Lareu, Balázs Egyed, Niels Morling, Walther Parson, Claus Børsting, Christian Hussing, L. Fusco, L. Souto, David Ballard, Christopher Phillips, Angel Carracedo, Peter M. Schneider, Mayra Eduardoff
Publikováno v:
Eduardoff, M, Gross, T E, 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, M V, Schneider, P M, Parson, W & Phillips, C 2016, ' Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™ ', Forensic Science International-Genetics, vol. 23, pp. 178-189 . https://doi.org/10.1016/j.fsigen.2016.04.008
The EUROFORGEN Global ancestry-informative SNP (AIM-SNPs) panel is a forensic multiplex of 128 markers designed to differentiate an individual's ancestry from amongst the five continental population groups of Africa, Europe, East Asia, Native America
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d936fb1b2471eedd80103991e6ed1bd9
https://kclpure.kcl.ac.uk/ws/files/51104537/1_s2.0_S1872497316300643_main.pdf
https://kclpure.kcl.ac.uk/ws/files/51104537/1_s2.0_S1872497316300643_main.pdf
Autor:
Jannik Fonager, Frederik Neess Engsig, Jonas T. Larsson, Christian Hussing, Claus Nielsen, Thea Kølsen Fischer
Publikováno v:
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 73
Background The current widely applied standard method to screen for HIV-1 genotypic resistance is based on Sanger population sequencing (Sseq), which does not allow for the identification of minority variants (MVs) below the limit of detection for th
Publikováno v:
Forensic Science International: Genetics Supplement Series. 5:e449-e450
The Illumina ® ForenSeq™ kit amplifies in one multiplex PCR reaction 59 STRs and 172 SNPs relevant to forensic genetic case work. Typed markers include markers for identification, ancestry identification (AIMs) and pigmentary traits. The products