Topics (13) View all

Research experience

  • Nov 2012–
    present
    Research: Conservation genomics
    Australian National University · RSB
    Australia · Canberra
  • Jan 2009–
    Oct 2010
    Research: Guest scientist
    Leibniz Institue for freshwater ecology and inland fisheries
    Germany · Berlin
  • Nov 2002–
    Jun 2012
    Research: Max-Planck-Institut für Entwicklungsbiologie
    Max-Planck-Institut für Entwicklungsbiologie
    Germany · Tübingen
  • May 2001–
    Oct 2002
    Research: Salk Institute
    Salk Institute for Biological Studies
    USA · La Jolla, California

Questions and Answers (3) View all

  • Answer added in Next Generation Sequencing
    11 Does anyone have experience with the Two step PCR amplicon approach?
    By John Leonard · Texas A&M University - Kingsville
    Norman Warthmann · Australian National University
    a) using second generation sequencing for one gene seems a bit overkill to me, unless you do thousands of samples. but if you do thousands of samples,... [more]
  • Answer added in PCR
    28 Any recommendations for a good thermocycler?
    By Elizabeth Traylor · Fred Hutchinson Cancer Research Center
    Norman Warthmann · Australian National University
    we use more than 10 MJ PTC200 (with different block sizes up to 384-well) hooked up to one computer from which you can run your PCR on any machine you... [more]
  • Answer added in Environmental Genomics
    29 What is the best DNA extraction method for Eukaryotes (as universal as possible)?
    By Jennifer Shaw · University of Adelaide
    Norman Warthmann · Australian National University
    Filter your freshwater and then crash the filter wit liquid nitrogen in a bead beater. Then extract your DNA with a soil DNA extraction kit, eg from "... [more]

Publications (32) View all

  • Article: Artificial MicroRNAs for Specific Gene Silencing in Rice.
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    ABSTRACT: Artificial microRNAs (amiRNAs) have been shown to facilitate efficient gene silencing with high specificity to the intended target gene(s). For the plant breeder, gene silencing by artificial miRNAs will certainly accelerate gene discovery, because it allows targeting of all genes in a mapping interval, independent of the genetic background. In addition, beneficial knockout phenotypes can easily be transferred between varieties and across incompatibility barriers. This chapter describes the generation and application of amiRNAs as a gene silencing tool in rice.
    Methods in molecular biology (Clifton, N.J.) 01/2013; 956:131-49.
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    Article: Reference-guided assembly of four diverse Arabidopsis thaliana genomes.
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    ABSTRACT: We present whole-genome assemblies of four divergent Arabidopsis thaliana strains that complement the 125-Mb reference genome sequence released a decade ago. Using a newly developed reference-guided approach, we assembled large contigs from 9 to 42 Gb of Illumina short-read data from the Landsberg erecta (Ler-1), C24, Bur-0, and Kro-0 strains, which have been sequenced as part of the 1,001 Genomes Project for this species. Using alignments against the reference sequence, we first reduced the complexity of the de novo assembly and later integrated reads without similarity to the reference sequence. As an example, half of the noncentromeric C24 genome was covered by scaffolds that are longer than 260 kb, with a maximum of 2.2 Mb. Moreover, over 96% of the reference genome was covered by the reference-guided assembly, compared with only 87% with a complete de novo assembly. Comparisons with 2 Mb of dideoxy sequence reveal that the per-base error rate of the reference-guided assemblies was below 1 in 10,000. Our assemblies provide a detailed, genomewide picture of large-scale differences between A. thaliana individuals, most of which are difficult to access with alignment-consensus methods only. We demonstrate their practical relevance in studying the expression differences of polymorphic genes and show how the analysis of sRNA sequencing data can lead to erroneous conclusions if aligned against the reference genome alone. Genome assemblies, raw reads, and further information are accessible through http://1001genomes.org/projects/assemblies.html.
    Proceedings of the National Academy of Sciences 06/2011; 108(25):10249-54. · 9.68 Impact Factor
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    Article: Major-effect alleles at relatively few loci underlie distinct vernalization and flowering variation in Arabidopsis accessions.
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    ABSTRACT: We have explored the genetic basis of variation in vernalization requirement and response in Arabidopsis accessions, selected on the basis of their phenotypic distinctiveness. Phenotyping of F2 populations in different environments, plus fine mapping, indicated possible causative genes. Our data support the identification of FRI and FLC as candidates for the major-effect QTL underlying variation in vernalization response, and identify a weak FLC allele, caused by a Mutator-like transposon, contributing to flowering time variation in two N. American accessions. They also reveal a number of additional QTL that contribute to flowering time variation after saturating vernalization. One of these was the result of expression variation at the FT locus. Overall, our data suggest that distinct phenotypic variation in the vernalization and flowering response of Arabidopsis accessions is accounted for by variation that has arisen independently at relatively few major-effect loci.
    PLoS ONE 01/2011; 6(5):e19949. · 4.09 Impact Factor
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    Article: Local-scale patterns of genetic variability, outcrossing, and spatial structure in natural stands of Arabidopsis thaliana.
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    ABSTRACT: As Arabidopsis thaliana is increasingly employed in evolutionary and ecological studies, it is essential to understand patterns of natural genetic variation and the forces that shape them. Previous work focusing mostly on global and regional scales has demonstrated the importance of historical events such as long-distance migration and colonization. Far less is known about the role of contemporary factors or environmental heterogeneity in generating diversity patterns at local scales. We sampled 1,005 individuals from 77 closely spaced stands in diverse settings around Tübingen, Germany. A set of 436 SNP markers was used to characterize genome-wide patterns of relatedness and recombination. Neighboring genotypes often shared mosaic blocks of alternating marker identity and divergence. We detected recent outcrossing as well as stretches of residual heterozygosity in largely homozygous recombinants. As has been observed for several other selfing species, there was considerable heterogeneity among sites in diversity and outcrossing, with rural stands exhibiting greater diversity and heterozygosity than urban stands. Fine-scale spatial structure was evident as well. Within stands, spatial structure correlated negatively with observed heterozygosity, suggesting that the high homozygosity of natural A. thaliana may be partially attributable to nearest-neighbor mating of related individuals. The large number of markers and extensive local sampling employed here afforded unusual power to characterize local genetic patterns. Contemporary processes such as ongoing outcrossing play an important role in determining distribution of genetic diversity at this scale. Local "outcrossing hotspots" appear to reshuffle genetic information at surprising rates, while other stands contribute comparatively little. Our findings have important implications for sampling and interpreting diversity among A. thaliana accessions.
    PLoS Genetics 01/2010; 6(3):e1000890. · 8.69 Impact Factor
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    Article: The rate and molecular spectrum of spontaneous mutations in Arabidopsis thaliana.
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    ABSTRACT: To take complete advantage of information on within-species polymorphism and divergence from close relatives, one needs to know the rate and the molecular spectrum of spontaneous mutations. To this end, we have searched for de novo spontaneous mutations in the complete nuclear genomes of five Arabidopsis thaliana mutation accumulation lines that had been maintained by single-seed descent for 30 generations. We identified and validated 99 base substitutions and 17 small and large insertions and deletions. Our results imply a spontaneous mutation rate of 7 x 10(-9) base substitutions per site per generation, the majority of which are G:C-->A:T transitions. We explain this very biased spectrum of base substitution mutations as a result of two main processes: deamination of methylated cytosines and ultraviolet light-induced mutagenesis.
    Science 01/2010; 327(5961):92-4. · 31.20 Impact Factor

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