Publikationen von Peter F. Arndt

Busse, C. E.; Czogiel, I.; Braun, P.; Arndt, P. F.; Wardemann, H.: Single-cell based high-throughput sequencing of full-length immunoglobulin heavy and light chain genes. European Journal of Immunology 44 (2), S. 597 - 603 (2014)

Ebert, G.; Steininger, A.; Weissmann, R.; Boldt, V.; Lind-Thomsen, A.; Grune, J.; Badelt, S.; Hessler, M.; Peiser, M.; Hitzler, M. et al.; Jensen, L. R.; Müller, I.; Hu, H.; Arndt, P. F.; Kuss, A. W.; Tebel, K.; Ullmann, R.: Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7. BMC Genomics 15, S. 15:537 - 15:537 (2014)

Mugal, C. F.; Arndt, P. F.; Ellegren, H.: Twisted signatures of GC-biased gene conversion embedded in an evolutionary stable karyotype. Molecular Biology and Evolution 30 (7), S. 1700 - 1712 (2013)

Massip, F.; Arndt, P. F.: Neutral Evolution of Duplicated DNA: An Evolutionary Stick-Breaking Process Causes Scale-Invariant Behavior. Physical Review Letters 110 (14), S. 148101 - 148101 (2013)

Schütze, T.; Wilhelm, B.; Greiner, N.; Braun, H.; Peter, F.; Mörl, M.; Erdmann, V. A.; Lehrach, H.; Konthur, Z.; Menger, M. et al.; Arndt, P. F.; Glökler, J.: Probing the SELEX Process with Next-Generation Sequencing. PLoS ONE 6 (12), e29604 (2011)

Clement, Y.; Arndt, P. F.: Substitution patterns are under different influences in primates and rodents. Genome Biol Evol 3, S. 236 - 45 (2011)

Cusack, B. P.; Arndt, P. F.; Duret, L.; Roest Crollius, H.: Preventing dangerous nonsense: selection for robustness to transcriptional error in human genes. PLoS Genet 7 (10), S. e1002276 (2011)

Schutze, T.; Wilhelm, B.; Greiner, N.; Braun, H.; Peter, F.; Morl, M.; Erdmann, V. A.; Lehrach, H.; Konthur, Z.; Menger, M. et al.; Arndt, P. F.; Glokler, J.: Probing the SELEX Process with Next-Generation Sequencing. PLoS ONE 6 (12), S. e29604 - e29604 (2011)

Zemojtel, T.; Kielbasa, S. M.; Arndt, P. F.; Behrens, S.; Bourque, G.; Vingron, M.: CpG deamination creates transcription factor-binding sites with high efficiency. Genome Biol Evol 3, S. 1304 - 11 (2011)

Schütze, T.; Arndt, P. F.; Menger, M.; Wochner, A.; Vingron, M.; Erdmann, V. A.; Lehrach, H.; Kaps, C.; Glökler, J.: A calibrated diversity assay for nucleic acid libraries using DiStRO-a Diversity Standard of Random Oligonucleotides. Nucleic Acids Research 38 (4), S. e23 - e23 (2010)

Polak, P.; Querfurth, R.; Arndt, P. F.: The evolution of transcription-associated biases of mutations across vertebrates. BMC Evolutionary Biology 10, S. 10:187 - 10:187 (2010)

Zemojtel, T.; Kielbasa, S. M.; Arndt, P. F.; Chung, H.-R.; Vingron, M.: Methylation and deamination of CpGs generate p53-binding sites on a genomic scale. Trends in Genetics 25 (2), S. 63 - 66 (2009)

Squartini, F.; Arndt, P. F.: Quantifying the stationarity and time reversibility of the nucleotide substitution process. Molecular Biology and Evolution 25 (12), S. 2525 - 2535 (2008)

Duret, L.; Arndt, P. F.: The Impact of Recombination on Nucleotide Substitutions in the Human Genome e1000071 (2008). PLoS Genetics 4 (5), S. e1000071 - e1000071 (2008)

Polak, P.; Arndt, P. F.: Transcription induces strand-specific mutations at the 5? end of human genes. Genome Research 18 (8), S. 1216 - 1223 (2008)

Arndt, P. F.; Vingron, M.: The Otto Warburg International Summer School and Workshop on Networks and Regulation. BMC Bioinformatics 8 (Suppl) (6), S. S1 - S1 (2007)

de la Chaux, N.; Messer, P. W.; Arndt, P.: DNA indels in coding regions reveal selective constraints on protein evolution in the human lineage. BMC Evolutionary Biology 7, S. 191 - 102 (2007)

Messer, P. W.; Bundschuh, R.; Vingron, M.; Arndt, P. F.: Effects of Long-Range Correlations in DNA on Sequence Alignment Score Statistics. Journal of Computational Biology: A Journal of Computational Molecular Cell Biology 14 (5), S. 655 - 668 (2007)

Messer, P. W.; Arndt, P. F.: The Majority of Recent Short DNA Insertions in the Human Genome Are Tandem Duplications. Molecular Biology and Evolution: MBE 24 (5), S. 1190 - 1197 (2007)

Messer, P. W.; Arndt, P. F.: CorGen-measuring and generating long-range correlations for DNA sequence analysis. Nucleic Acids Research 34, S. W692 - W695 (2006)