Claus Børsting
Senior Researcher
Section of Forensic Genetics
Frederik V's Vej 11
2100 København Ø
- 2017
- Published
Reproducibility of methylated CpG typing with the Illumina MiSeq
Kampmann, Marie-Louise, Meyer, Olivia Luxford, Schmidt, Suzanne, Børsting, Claus & Morling, Niels, 2017, In: Forensic Science International: Genetics. Supplement Series. 6, p. e430-e432 2 p.Research output: Contribution to journal › Conference article › Research › peer-review
- Published
Typing of two Middle Eastern populations with the Precision ID Ancestry Panel.
Hegner, Ditte Truelsen, Farzad, M. S., Mogensen, Helle Smidt, Pereira, Vania, Børsting, Claus & Morling, Niels, 2017, In: Forensic Science International: Genetics. Supplement Series. 6, p. e302-e303Research output: Contribution to journal › Conference article › Research › peer-review
- 2016
- Published
A study of the peopling of Greenland using next generation sequencing of complete mitochondrial genomes
Lopopolo, M., Børsting, Claus, Pereira, Vania & Morling, Niels, Dec 2016, In: American Journal of Physical Anthropology. 161, 4, p. 698-704Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Evaluation of the iPLEX® ADME PGx Pro Panel and allele frequencies of pharmacogenetic markers in Danes
Jensen, L., Børsting, Claus, Dalhoff, Kim & Morling, Niels, Nov 2016, In: Clinical Biochemistry. 49, 16-17, p. 1299–1301 3 p.Research output: Contribution to journal › Letter › Research › peer-review
- Published
ISO 17025 validation of a next-generation sequencing assay for relationship testing
Buchard, Anders, Kampmann, Marie-Louise, Poulsen, L., Børsting, Claus & Morling, Niels, Nov 2016, In: Electrophoresis. 37, 21, p. 2822-2831 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Thirty autosomal insertion-deletion polymorphisms analyzed using the Investigator(®) DIPplex Kit in populations from Iraq, Lithuania, Slovenia, and Turkey
Tomas Mas, Carmen, Poulsen, L., Drobnič, K., Ivanova, V., Jankauskiene, J., Bunokiene, D., Børsting, Claus & Morling, Niels, Nov 2016, In: Forensic science international. Genetics. 25, p. 142-144 3 p.Research output: Contribution to journal › Letter › Research › peer-review
- Published
High-throughput sequencing of forensic genetic samples using punches of FTA cards with buccal swabs
Kampmann, Marie-Louise, Buchard, Anders, Børsting, Claus & Morling, Niels, Sep 2016, In: BioTechniques. 61, 3, p. 149-151 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genomic applications in forensic medicine
Børsting, Claus & Morling, Niels, 1 Jul 2016, Medical and Health Genomics. Kumar, D. & Antonarakis, S. (eds.). Academic Press, p. 295-309 15 p.Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review
- Published
Importance of non-synonymous OCA2 variants in human eye colour prediction
Andersen, Jeppe Dyrberg, Pietroni, Carlotta, Johansen, P., Andersen, M. M., Pereira, Vania, Børsting, Claus & Morling, Niels, Jul 2016, In: Molecular Genetics & Genomic Medicine. 4, 4, p. 420-430 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™
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., EUROFORGEN-NoE Consortium & 2 others, , Jul 2016, In: Forensic Science International: Genetics. 23, p. 178-189 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 542383
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Biomek®-3000 and GenPlex in Forensic Genetics
Research output: Contribution to conference › Poster › Research
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4146
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Evaluation of the Ion Torrent™ HID SNP 169-plex: A SNP typing assay developed for human identification by second generation sequencing
Research output: Contribution to journal › Journal article › Research › peer-review
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2935
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Characterization of mutations and sequence variants in the D21S11 locus by next generation sequencing
Research output: Contribution to journal › Journal article › Research › peer-review
Published