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Heinz Himmelbauer

Researcher at University of Natural Resources and Life Sciences, Vienna

Publications -  146
Citations -  15900

Heinz Himmelbauer is an academic researcher from University of Natural Resources and Life Sciences, Vienna. The author has contributed to research in topics: Genome & Gene. The author has an hindex of 40, co-authored 140 publications receiving 14761 citations. Previous affiliations of Heinz Himmelbauer include Lincoln's Inn & Max Planck Society.

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Genome sequence of the Brown Norway rat yields insights into mammalian evolution

Richard A. Gibbs, +242 more
- 01 Apr 2004 - 
TL;DR: This first comprehensive analysis of the genome sequence of the Brown Norway (BN) rat strain is reported, which is the third complete mammalian genome to be deciphered, and three-way comparisons with the human and mouse genomes resolve details of mammalian evolution.

Genome sequence of the Brown Norway rat yields insights into mammalian evolutionRat Genome Sequencing Project ConsortiumNature200442849352115057822

Richard A. Gibbs, +226 more
Abstract: The laboratory rat (Rattus norvegicus) is an indispensable tool in experimental medicine and drug development, having made inestimable contributions to human health. We report here the genome sequence of the Brown Norway (BN) rat strain. The sequence represents a high-quality ‘draft’ covering over 90% of the genome. The BN rat sequence is the third complete mammalian genome to be deciphered, and three-way comparisons with the human and mouse genomes resolve details of mammalian evolution. This first comprehensive analysis includes genes and proteins and their relation to human disease, repeated sequences, comparative genome-wide studies of mammalian orthologous chromosomal regions and rearrangement breakpoints, reconstruction of ancestral karyotypes and the events leading to existing species, rates of variation, and lineage-specific and lineage-independent evolutionary events such as expansion of gene families, orthology relations and protein evolution.
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Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

TL;DR: The patterns of somatic mutation, supported by functional and clinical analyses, strongly indicate that the recurrent NOTCH1, MYD88 and XPO1 mutations are oncogenic changes that contribute to the clinical evolution of the disease.
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Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

TL;DR: The results show different types of biases and ways to detect, which have implications on the use and interpretation of Solexa data, for de novo sequencing, re-sequencing, the identification of single nucleotide polymorphisms and DNA methylation sites, as well as for transcriptome analysis.
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The Collaborative Cross, a community resource for the genetic analysis of complex traits

Gary A. Churchill, +113 more
- 01 Nov 2004 - 
TL;DR: The Collaborative Cross will provide a common reference panel specifically designed for the integrative analysis of complex systems and will change the way the authors approach human health and disease.