Publikationen von A. Dahl

Colonna, V.; Ayub, Q.; Chen, Y.; Pagani, L.; Luisi, P.; Pybus, M.; Garrison, E.; Xue, Y.; Tyler-Smith, C.; 1000 Genomes Project, C. et al.; Sudbrak, R.; Albrecht, M.; Amstislavskiy, V.; Borodina, T. A.; Dahl, A.; Davydov, A.; Herwig, R.; Marquardt, P.; Mertes, F.; Nietfeld, W.; Parkhomchuk, D.; Soldatov, A. V.; Timmermann, B.; Tolzmann, M.; Lehrach, H.; Yaspo, M. L.: Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences. Genome Biology: Biology for the Post-Genomic Era 15 (6), R88 (2014)

The 1000 Genomes Project Consortium; Sudbrak, R.; Albrecht, M.; Amstislavskiy, V.; Borodina, T. A.; Dahl, A.; Davydov, A.; Herwig, R.; Marquardt, P.; Mertes, F. et al.; Nietfeld, W.; Parkhomchuk, D.; Soldatov, A.; Timmermann, B.; Tolzmann, M.; Lehrach, H.: The 1000 Genomes Project: data management and community access. Nature methods 9 (5), S. 459 - 462 (2012)

MacArthur, D. G.; Balasubramanian, S.; Frankish, A.; 1000 Genomes Project, C.; Sudbrak, R.; Albrecht , M. W.; Amstislavskiy, V.; Borodina, T. A.; Dahl, A.; Davydov, A. et al.; Herwig, R.; Marquardt, P.; Mertes, F.; Nietfeld, W.; Parkhomchuk, D.; Soldatov, A.; Timmermann, B.; Tolzmann, M.; Lehrach, H.: A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science 335 (6070), S. 823 - 828 (2012)

Bormann, F.; Sers, C.; Seliger, B.; Handke, D.; Bergmann, T.; Seibt, S.; Lehrach, H.; Dahl, A.: Methylation-specific ligation detection reaction (msLDR): a new approach for multiplex evaluation of methylation patterns. Molecular Genetics and Genomics: MGG 286 (3-4), S. 279 - 91 (2011)

von Keyserling, H.; Bergmann, T.; Schuetz, M.; Schiller, U.; Stanke, J.; Hoffmann, C.; Schneider, A.; Lehrach, H.; Dahl, A.; Kaufmann, A. M.: Analysis of 4 single-nucleotide polymorphisms in relation to cervical dysplasia and cancer development using a high-throughput ligation-detection reaction procedure. International Journal of Gynecological Cancer: Official Journal of the International Gynecological Cancer Society 21 (9), S. 1664 - 71 (2011)

Mertes, F.; Biens, K.; Lehrach, H.; Wagner, M.; Dahl, A.: High-throughput Universal Probe Salmonella Serotyping (UPSS) by nanoPCR. J Microbiol Methods 83 (2), S. 217 - 223 (2010)

Krawitz, P. M.; Schweiger, M. R.; Rödelsperger, C.; Marcelis, C.; Kölsch, U.; Meisel, C.; Stephani, F.; Kinoshita, T.; Murakami, Y.; Bauer, S. et al.; Isau, M.; Fischer, A.; Dahl, A.; Kerick, M.; Hecht, J.; Köhler, S.; Jager, M.; Grünhagen, J.; de Condor, B. J.; Doelken, S.; Brunner, H. G.; Meinecke, P.; Passarge, E.; Thompson, M. D.; Cole, D. E.; Horn, D.; Roscioli, T.; Mundlos, S.; Robinson, P. N.: Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 42 (10), S. 827 - 829 (2010)

Krawitz, P. M.; Schweiger, M. R.; Rödelsperger, C.; Marcelis, C.; Kölsch, U.; Meisel, C.; Stephani, F.; Kinoshita, T.; Murakami, Y.; Bauer, S. et al.; Isau, M.; Fischer, A.; Dahl, A.; Kerick, M.; Hecht, J.; Köhler, S.; Jager, M.; Grünhagen, J.; de Condor, B. J.; Doelken, S.; Brunner, H. G.; Meinecke, P.; Passarge, E.; Thompson, M. D.; Cole, D. E.; Horn, D.; Roscioli, T.; Mundlos, S.; Robinson, P. N.: Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 42 (10), S. 827 - 829 (2010)

Krawitz, P. M.; Schweiger, M. R.; Rödelsperger, C.; Marcelis, C.; Kölsch, U.; Meisel, C.; Stephani, F.; Kinoshita, T.; Murakami, Y.; Bauer, S. et al.; Isau, M.; Fischer, A.; Dahl, A.; Kerick, M.; Hecht, J.; Köhler, S.; Jager, M.; Grünhagen, J.; de Condor, B. J.; Doelken, S.; Brunner, H. G.; Meinecke, P.; Passarge, E.; Thompson, M. D.; Cole, D. E.; Horn, D.; Roscioli, T.; Mundlos, S.; Robinson, P. N.: Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 42 (10), S. 827 - 829 (2010)

Dahl, A.; Mertes, F.; Timmermann, B.; Lehrach, H.: The application of massively parallel sequencing technologies in diagnostics. F1000 Biology Reports 2, S. 2:59 - 2:59 (2010)

Scholz, A.-K.; Klebl, B. M.; Morkel, M.; Lehrach, H.; Dahl, A.; Lange, B. M.H.: A Flexible Multiwell Format for Immunofluorescence Screening Microscopy of Small-Molecule Inhibitors. Assay and Drug Development Technologies. 8 (5), S. 571 - 580 (2010)

McMeekin, T. A.; Hill, C.; Wagner, M.; Dahl, A.; Ross, T.: Ecophysiology of food-borne pathogens: Essential knowledge to improve food safety. International Journal of Food Microbiology 139 (Suppl 1), S. S64 - 78 (2010)

Dahl, A.; Mertes, F.; Marchfelder, U.; Boerno, S.; Fischer, A.; Schweiger, M.; Lehrach, H.: Bewertung der SOLiD-Sequenzierungsplattform aus Nutzerperspektive. Laborwelt 11 (1), S. 8 - 10 (2010)

Kepper, P.; Reinhardt, R.; Dahl, A.; Lehrach, H.; Sauer, S.: Matrix-Assisted Laser Desorption/Ionization Mass Spectrometric Analysis of DNA on Microarrays. Clinical Chemistry: International Journal of Molecular Diagnostics and Laboratory Medicine 52 (7), S. 1303 - 1310 (2007)

Dahl, A.; Sultan, M.; Jung, A.; Schwartz, R.; Lange, M.; Steinwand, M.; Livak, K. J.; Lehrach, H.; Nyarsik, L.: Quantitative PCR based expression analysis on a nanoliter scale using polymer nano-well chips. Biomedical Microdevices 9 (3), S. 307 - 314 (2007)

Sauer, S.; Kepper, P.; Smyra, A.; Dahl, A.; Ferse, F.-T.; Lehrach, H.; Reinhardt, R.: Automated solid-phase extraction for purification of single nucleotide polymorphism genotyping products prior to matrix-assisted laser desorption/ionisation time-of-flight mass spectrometric analysis. Journal of Chromatography A 1049 (1-2), S. 9 - 16 (2004)

Timmermann, B.; Sauer, S.; Dahl, A.; Reinhardt, R.: Genetische Variabilität des Menschen: Hochdurchsatz- Technologien und Datenanalyse. Laborwelt 5 (5), S. 31 - 32 (2004)

Dahl, A.: Development of a miniaturised platform for PCR based assays with application in gene expression analysis and SNP genotyping. Dissertation, Freie Universität, Berlin (2007)