Kasper Nielsen
Technical University of Denmark
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Publication
Featured researches published by Kasper Nielsen.
Nature | 2010
Morten Rasmussen; Yingrui Li; Stinus Lindgreen; Jakob Skou Pedersen; Anders Albrechtsen; Ida Moltke; Mait Metspalu; Ene Metspalu; Toomas Kivisild; Ramneek Gupta; Marcelo Bertalan; Kasper Nielsen; M. Thomas P. Gilbert; Yong Wang; Maanasa Raghavan; Paula F. Campos; Hanne Munkholm Kamp; Andrew S. Wilson; Andrew Gledhill; Silvana R. Tridico; Michael Bunce; Eline D. Lorenzen; Jonas Binladen; Xiaosen Guo; Jing Zhao; Xiuqing Zhang; Hao Zhang; Zhuo Li; Minfeng Chen; Ludovic Orlando
We report here the genome sequence of an ancient human. Obtained from ∼4,000-year-old permafrost-preserved hair, the genome represents a male individual from the first known culture to settle in Greenland. Sequenced to an average depth of 20×, we recover 79% of the diploid genome, an amount close to the practical limit of current sequencing technologies. We identify 353,151 high-confidence single-nucleotide polymorphisms (SNPs), of which 6.8% have not been reported previously. We estimate raw read contamination to be no higher than 0.8%. We use functional SNP assessment to assign possible phenotypic characteristics of the individual that belonged to a culture whose location has yielded only trace human remains. We compare the high-confidence SNPs to those of contemporary populations to find the populations most closely related to the individual. This provides evidence for a migration from Siberia into the New World some 5,500 years ago, independent of that giving rise to the modern Native Americans and Inuit.
Science | 2011
Morten Rasmussen; Xiaosen Guo; Yong Wang; Kirk E. Lohmueller; Simon Rasmussen; Anders Albrechtsen; Line Skotte; Stinus Lindgreen; Mait Metspalu; Thibaut Jombart; Toomas Kivisild; Weiwei Zhai; Anders Eriksson; Andrea Manica; Ludovic Orlando; Francisco M. De La Vega; Silvana R. Tridico; Ene Metspalu; Kasper Nielsen; María C. Ávila-Arcos; J. Víctor Moreno-Mayar; Craig Muller; Joe Dortch; M. Thomas P. Gilbert; Ole Lund; Agata Wesolowska; Monika Karmin; Lucy A. Weinert; Bo Wang; Jun Li
Whole-genome data indicate that early modern humans expanded into Australia 62,000 to 75,000 years ago. We present an Aboriginal Australian genomic sequence obtained from a 100-year-old lock of hair donated by an Aboriginal man from southern Western Australia in the early 20th century. We detect no evidence of European admixture and estimate contamination levels to be below 0.5%. We show that Aboriginal Australians are descendants of an early human dispersal into eastern Asia, possibly 62,000 to 75,000 years ago. This dispersal is separate from the one that gave rise to modern Asians 25,000 to 38,000 years ago. We also find evidence of gene flow between populations of the two dispersal waves prior to the divergence of Native Americans from modern Asian ancestors. Our findings support the hypothesis that present-day Aboriginal Australians descend from the earliest humans to occupy Australia, likely representing one of the oldest continuous populations outside Africa.
Nature Genetics | 2014
Klaus Bønnelykke; Patrick Sleiman; Kasper Nielsen; Eskil Kreiner-Møller; Josep M. Mercader; Danielle Belgrave; Herman T. den Dekker; Anders Husby; Astrid Sevelsted; Grissel Faura-Tellez; Li Mortensen; Lavinia Paternoster; Richard Flaaten; Anne Mølgaard; David E. Smart; Philip Francis Thomsen; Morten Rasmussen; Sílvia Bonàs-Guarch; Claus Holst; Ellen Aagaard Nohr; Rachita Yadav; Michael March; Thomas Blicher; Peter M. Lackie; Vincent W. V. Jaddoe; Angela Simpson; John W. Holloway; Liesbeth Duijts; Adnan Custovic; Donna E. Davies
Asthma exacerbations are among the most frequent causes of hospitalization during childhood, but the underlying mechanisms are poorly understood. We performed a genome-wide association study of a specific asthma phenotype characterized by recurrent, severe exacerbations occurring between 2 and 6 years of age in a total of 1,173 cases and 2,522 controls. Cases were identified from national health registries of hospitalization, and DNA was obtained from the Danish Neonatal Screening Biobank. We identified five loci with genome-wide significant association. Four of these, GSDMB, IL33, RAD50 and IL1RL1, were previously reported as asthma susceptibility loci, but the effect sizes for these loci in our cohort were considerably larger than in the previous genome-wide association studies of asthma. We also obtained strong evidence for a new susceptibility gene, CDHR3 (encoding cadherin-related family member 3), which is highly expressed in airway epithelium. These results demonstrate the strength of applying specific phenotyping in the search for asthma susceptibility genes.
Cell | 2015
Simon Rasmussen; Morten E. Allentoft; Kasper Nielsen; Ludovic Orlando; Martin Sikora; Karl-Göran Sjögren; Anders Gorm Pedersen; Mikkel Schubert; Alex Van Dam; Christian Moliin Outzen Kapel; Henrik Bjørn Nielsen; Søren Brunak; Pavel Avetisyan; Andrey Epimakhov; Mikhail Viktorovich Khalyapin; Artak Gnuni; Aivar Kriiska; Irena Lasak; Mait Metspalu; Vyacheslav Moiseyev; Andrei Gromov; Dalia Pokutta; Lehti Saag; Liivi Varul; Levon Yepiskoposyan; Thomas Sicheritz-Pontén; Robert Foley; Marta Mirazón Lahr; Rasmus Nielsen; Kristian Kristiansen
Summary The bacteria Yersinia pestis is the etiological agent of plague and has caused human pandemics with millions of deaths in historic times. How and when it originated remains contentious. Here, we report the oldest direct evidence of Yersinia pestis identified by ancient DNA in human teeth from Asia and Europe dating from 2,800 to 5,000 years ago. By sequencing the genomes, we find that these ancient plague strains are basal to all known Yersinia pestis. We find the origins of the Yersinia pestis lineage to be at least two times older than previous estimates. We also identify a temporal sequence of genetic changes that lead to increased virulence and the emergence of the bubonic plague. Our results show that plague infection was endemic in the human populations of Eurasia at least 3,000 years before any historical recordings of pandemics.
Plant Physiology | 2009
Svend Secher Dam; Brian S. Laursen; Jane H. Ørnfelt; Bjarne Jochimsen; Hans Henrik Stærfeldt; Carsten Friis; Kasper Nielsen; Nicolas Goffard; Søren Besenbacher; Lene Krusell; Shusei Sato; Satoshi Tabata; Ida B. Thøgersen; Jan J. Enghild; Jens Stougaard
We have characterized the development of seeds in the model legume Lotus japonicus. Like soybean (Glycine max) and pea (Pisum sativum), Lotus develops straight seed pods and each pod contains approximately 20 seeds that reach maturity within 40 days. Histological sections show the characteristic three developmental phases of legume seeds and the presence of embryo, endosperm, and seed coat in desiccated seeds. Furthermore, protein, oil, starch, phytic acid, and ash contents were determined, and this indicates that the composition of mature Lotus seed is more similar to soybean than to pea. In a first attempt to determine the seed proteome, both a two-dimensional polyacrylamide gel electrophoresis approach and a gel-based liquid chromatography-mass spectrometry approach were used. Globulins were analyzed by two-dimensional polyacrylamide gel electrophoresis, and five legumins, LLP1 to LLP5, and two convicilins, LCP1 and LCP2, were identified by matrix-assisted laser desorption ionization quadrupole/time-of-flight mass spectrometry. For two distinct developmental phases, seed filling and desiccation, a gel-based liquid chromatography-mass spectrometry approach was used, and 665 and 181 unique proteins corresponding to gene accession numbers were identified for the two phases, respectively. All of the proteome data, including the experimental data and mass spectrometry spectra peaks, were collected in a database that is available to the scientific community via a Web interface (http://www.cbs.dtu.dk/cgi-bin/lotus/db.cgi). This database establishes the basis for relating physiology, biochemistry, and regulation of seed development in Lotus. Together with a new Web interface (http://bioinfoserver.rsbs.anu.edu.au/utils/PathExpress4legumes/) collecting all protein identifications for Lotus, Medicago, and soybean seed proteomes, this database is a valuable resource for comparative seed proteomics and pathway analysis within and beyond the legume family.
Journal of Proteome Research | 2010
Gitte Nautrup-Pedersen; Svend Secher Dam; Brian S. Laursen; Astrid L. Siegumfeldt; Kasper Nielsen; Nicolas Goffard; Hans Henrik Stærfeldt; Carsten Friis; Shusei Sato; Satoshi Tabata; Andrea Lorentzen; Peter Roepstorff; Jens Stougaard
Legume pods serve important functions during seed development and are themselves sources of food and feed. Compared to seeds, the metabolism and development of pods are not well-defined. The present characterization of pods from the model legume Lotus japonicus, together with the detailed analyses of the pod and seed proteomes in five developmental stages, paves the way for comparative pathway analysis and provides new metabolic information. Proteins were analyzed by two-dimensional gel electrophoresis and tandem-mass spectrometry. These analyses lead to the identification of 604 pod proteins and 965 seed proteins, including 263 proteins distinguishing the pod. The complete data set is publicly available at http://www.cbs.dtu.dk/cgi-bin/lotus/db.cgi , where spots in a reference map are linked to experimental data, such as matched peptides, quantification values, and gene accessions. Identified pod proteins represented enzymes from 85 different metabolic pathways, including storage globulins and a late embryogenesis abundant protein. In contrast to seed maturation, pod maturation was associated with decreasing total protein content, especially proteins involved in protein biosynthesis and photosynthesis. Proteins detected only in pods included three enzymes participating in the urea cycle and four in nitrogen and amino group metabolism, highlighting the importance of nitrogen metabolism during pod development. Additionally, five legume seed proteins previously unassigned in the glutamate metabolism pathway were identified.
Nature Genetics | 2017
Zhaoming Wang; Katherine A. McGlynn; Ewa Rajpert-De Meyts; D. Timothy Bishop; Charles C. Chung; Marlene Danner Dalgaard; Mark H. Greene; Ramneek Gupta; Tom Grotmol; Trine B. Haugen; Robert Karlsson; Kevin Litchfield; Nandita Mitra; Kasper Nielsen; Louise C. Pyle; Stephen M. Schwartz; Vesteinn Thorsson; Saran Vardhanabhuti; Fredrik Wiklund; Clare Turnbull; Stephen J. Chanock; Peter A. Kanetsky; Katherine L. Nathanson
The international Testicular Cancer Consortium (TECAC) combined five published genome-wide association studies of testicular germ cell tumor (TGCT; 3,558 cases and 13,970 controls) to identify new susceptibility loci. We conducted a fixed-effects meta-analysis, including, to our knowledge, the first analysis of the X chromosome. Eight new loci mapping to 2q14.2, 3q26.2, 4q35.2, 7q36.3, 10q26.13, 15q21.3, 15q22.31, and Xq28 achieved genome-wide significance (P < 5 × 10−8). Most loci harbor biologically plausible candidate genes. We refined previously reported associations at 9p24.3 and 19p12 by identifying one and three additional independent SNPs, respectively. In aggregate, the 39 independent markers identified to date explain 37% of father-to-son familial risk, 8% of which can be attributed to the 12 new signals reported here. Our findings substantially increase the number of known TGCT susceptibility alleles, move the field closer to a comprehensive understanding of the underlying genetic architecture of TGCT, and provide further clues to the etiology of TGCT.
Journal of Graphics Tools | 2002
Kasper Nielsen; Niels Jørgen Christensen
Abstract This paper describes a method that speeds up hemicube rendering by using texture maps to discretize a scene instead of geometric meshing. The method avoids subdivision of input surfaces and takes advantage of hardware texture mapping in order to accelerate form factor calculations. By using the method, we are able to compute finite-element progressive radiosity significantly faster than when using traditional meshing.
Proteomics | 2014
Svend Secher Dam; Thomas F. Dyrlund; Anna Ussatjuk; Bjarne Jochimsen; Kasper Nielsen; Nicolas Goffard; Miguel Ventosa; Andrea Lorentzen; Vikas Gupta; Stig U. Andersen; Jan J. Enghild; Clive W. Ronson; Peter Roepstorff; Jens Stougaard
Legume symbiosis with rhizobia results in the formation of a specialized organ, the root nodule, where atmospheric dinitrogen is reduced to ammonia. In Lotus japonicus (Lotus), several genes involved in nodule development or nodule function have been defined using biochemistry, genetic approaches, and high‐throughput transcriptomics. We have employed proteomics to further understand nodule development. Two developmental stages representing nodules prior to nitrogen fixation (white) and mature nitrogen fixing nodules (red) were compared with roots. In addition, the proteome of a spontaneous nodule formation mutant (snf1) was determined. From nodules and roots, 780 and 790 protein spots from 2D gels were identified and approximately 45% of the corresponding unique gene accessions were common. Including a previous proteomics set from Lotus pod and seed, the common gene accessions were decreased to 7%. Interestingly, an indication of more pronounced PTMs in nodules than in roots was determined. Between the two nodule developmental stages, higher levels of pathogen‐related 10 proteins, HSPs, and proteins involved in redox processes were found in white nodules, suggesting a higher stress level at this developmental stage. In contrast, protein spots corresponding to nodulins such as leghemoglobin, asparagine synthetase, sucrose synthase, and glutamine synthetase were prevalent in red nodules. The distinct biochemical state of nodules was further highlighted by the conspicuous presence of several nitrilases, ascorbate metabolic enzymes, and putative rhizobial effectors.
Journal of Proteomics | 2014
Svend Secher Dam; Thomas F. Dyrlund; Anna Ussatjuk; Bjarne Jochimsen; Kasper Nielsen; Nicolas Goffard; Miguel Ventosa; Andrea Lorentzen; Vikas Gupta; Stig U. Andersen; Jan J. Enghild; Clive W. Ronson; Peter Roepstorff; Jens Stougaard
Legume symbiosis with rhizobia results in the formation of a specialized organ, the root nodule, where atmospheric dinitrogen is reduced to ammonia. In Lotus japonicus (Lotus), several genes involved in nodule development or nodule function have been defined using biochemistry, genetic approaches, and high‐throughput transcriptomics. We have employed proteomics to further understand nodule development. Two developmental stages representing nodules prior to nitrogen fixation (white) and mature nitrogen fixing nodules (red) were compared with roots. In addition, the proteome of a spontaneous nodule formation mutant (snf1) was determined. From nodules and roots, 780 and 790 protein spots from 2D gels were identified and approximately 45% of the corresponding unique gene accessions were common. Including a previous proteomics set from Lotus pod and seed, the common gene accessions were decreased to 7%. Interestingly, an indication of more pronounced PTMs in nodules than in roots was determined. Between the two nodule developmental stages, higher levels of pathogen‐related 10 proteins, HSPs, and proteins involved in redox processes were found in white nodules, suggesting a higher stress level at this developmental stage. In contrast, protein spots corresponding to nodulins such as leghemoglobin, asparagine synthetase, sucrose synthase, and glutamine synthetase were prevalent in red nodules. The distinct biochemical state of nodules was further highlighted by the conspicuous presence of several nitrilases, ascorbate metabolic enzymes, and putative rhizobial effectors.