Research experience
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Nov 2012–
presentResearch: Conservation genomics
Australian National University · RSBAustralia · Canberra -
Jan 2009–
Oct 2010Research: Guest scientist
Leibniz Institue for freshwater ecology and inland fisheriesGermany · Berlin -
Nov 2002–
Jun 2012Research: Max-Planck-Institut für Entwicklungsbiologie
Max-Planck-Institut für EntwicklungsbiologieGermany · Tübingen -
May 2001–
Oct 2002Research: Salk Institute
Salk Institute for Biological StudiesUSA · La Jolla, California
Questions and Answers (3) View all
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Answer added in Next Generation Sequencing11 Does anyone have experience with the Two step PCR amplicon approach?By John Leonard · Texas A&M University - KingsvilleNorman Warthmann · Australian National Universitya) 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]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, then you are probably interested in the allele frequencies across populations. In this case you may want to be careful about the biases you are introducing by doing 2 subsequent PCR reactions. On the other hand: if you are not doing only one gene, but several to hundreds, then adding a common sequence to the PCR primers is not your most cost-effective option. Then you are better off performing PCR reactions with standard primers, pool the PCR products per individual and then go through standard library preps. b) an important point was raised by Colin: make sure your sequences do not start with identical sequence. However, since you are probably only after a few million reads, then, instead of wasting 50 % or more of your lane with PhiX, you may want to just spike little amounts of your sample into a sequencing lane with an unrelated (unbiased) sample.Following
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Answer added in PCR28 Any recommendations for a good thermocycler?By Elizabeth Traylor · Fred Hutchinson Cancer Research CenterNorman Warthmann · Australian National Universitywe 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]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 want. This is efficient. No idea why most PCR machine manufacturers make integrated systems with fancy touch screens. Seems they really want you to punch your programs directly into the machine. My advise: not an integrated system, but high max and adjustable ramping speed. If it is really true that they don't make those PTC200 anymore that would be a pity, they gotten high milage in our lab and still work great.Following
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Answer added in Environmental Genomics29 What is the best DNA extraction method for Eukaryotes (as universal as possible)?By Jennifer Shaw · University of AdelaideNorman Warthmann · Australian National UniversityFilter 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]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 "mo bio" or "epicentre"Following
Publications (32) View all
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Article: Artificial MicroRNAs for Specific Gene Silencing in Rice.
[show abstract] [hide abstract]
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. -
SourceAvailable from: Detlef Weigel
Article: Reference-guided assembly of four diverse Arabidopsis thaliana genomes.
Korbinian Schneeberger, Stephan Ossowski, Felix Ott, Juliane D Klein, Xi Wang, Christa Lanz, Lisa M Smith, Jun Cao, Joffrey Fitz, Norman Warthmann, Stefan R Henz, Daniel H Huson, Detlef Weigel[show abstract] [hide abstract]
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 -
SourceAvailable from: Magnus Nordborg
Article: Major-effect alleles at relatively few loci underlie distinct vernalization and flowering variation in Arabidopsis accessions.
Amy Strange, Peijin Li, Clare Lister, Jillian Anderson, Norman Warthmann, Chikako Shindo, Judith Irwin, Magnus Nordborg, Caroline Dean[show abstract] [hide abstract]
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 -
SourceAvailable from: Sang-Tae Kim
Article: Local-scale patterns of genetic variability, outcrossing, and spatial structure in natural stands of Arabidopsis thaliana.
Kirsten Bomblies, Levi Yant, Roosa A Laitinen, Sang-Tae Kim, Jesse D Hollister, Norman Warthmann, Joffrey Fitz, Detlef Weigel[show abstract] [hide abstract]
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 -
SourceAvailable from: Detlef Weigel
Article: The rate and molecular spectrum of spontaneous mutations in Arabidopsis thaliana.
Stephan Ossowski, Korbinian Schneeberger, José Ignacio Lucas-Lledó, Norman Warthmann, Richard M Clark, Ruth G Shaw, Detlef Weigel, Michael Lynch[show abstract] [hide abstract]
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