Is mammalian chromosomal evolution driven by regions of genome fragility?
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* Corresponding author: Terence J Robinson tjr@sun.ac.za
1 Evolutionary Genomics Group, Department of Botany & Zoology, University of Stellenbosch, Private Bag X1, Matieland 7602, South Africa
2 Institut de Biologia Molecular de Barcelona, CSIC, Department of Physiology and Molecular Biodiversity, Jordi Girona 18, 08034 Barcelona, Spain
Genome Biology 2006, 7:R115 doi:10.1186/gb-2006-7-12-r115
Published: 8 December 2006Additional files
Additional data file 1:
Multispecies alignments to all human chromosomes.
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Additional data file 2:
Distribution of base pair tandem repeats along all human chromosomes represented as windows of 250,000 bp each.
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Additional data file 3:
Base pairs implicated in tandem repeats per chromosome.
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Additional data file 4:
List of all of the homologous syntenic blocks (HSB) detected.
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Additional data file 5:
List of evolutionary breakpoint regions (EBR) less than 4 Mb and their chromosomal positions in the human genome.
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Additional data file 6:
List of evolutionary chromosomal bands detected.
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Additional data file 7:
List of all human fragile sites described in the literature.
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Additional data file 8:
List of common human fragile sites that have been cloned and analyzed at the molecular level.
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Additional data file 9:
Human genome divided into windows of 0.250 Mb.
Format: PDF Size: 387KB Download file
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