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      Partial correlation analysis indicates causal relationships between GC-content, exon density and recombination rate in the human genome

      research-article
      1 , 2 , 3 , 1 ,
      BMC Bioinformatics
      BioMed Central
      The Seventh Asia Pacific Bioinformatics Conference (APBC 2009)
      13–16 January 2009

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          Abstract

          Background

          Several features are known to correlate with the GC-content in the human genome, including recombination rate, gene density and distance to telomere. However, by testing for pairwise correlation only, it is impossible to distinguish direct associations from indirect ones and to distinguish between causes and effects.

          Results

          We use partial correlations to construct partially directed graphs for the following four variables: GC-content, recombination rate, exon density and distance-to-telomere. Recombination rate and exon density are unconditionally uncorrelated, but become inversely correlated by conditioning on GC-content. This pattern indicates a model where recombination rate and exon density are two independent causes of GC-content variation.

          Conclusion

          Causal inference and graphical models are useful methods to understand genome evolution and the mechanisms of isochore evolution in the human genome.

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          Most cited references36

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          A high-resolution recombination map of the human genome.

          Determination of recombination rates across the human genome has been constrained by the limited resolution and accuracy of existing genetic maps and the draft genome sequence. We have genotyped 5,136 microsatellite markers for 146 families, with a total of 1,257 meiotic events, to build a high-resolution genetic map meant to: (i) improve the genetic order of polymorphic markers; (ii) improve the precision of estimates of genetic distances; (iii) correct portions of the sequence assembly and SNP map of the human genome; and (iv) build a map of recombination rates. Recombination rates are significantly correlated with both cytogenetic structures (staining intensity of G bands) and sequence (GC content, CpG motifs and poly(A)/poly(T) stretches). Maternal and paternal chromosomes show many differences in locations of recombination maxima. We detected systematic differences in recombination rates between mothers and between gametes from the same mother, suggesting that there is some underlying component determined by both genetic and environmental factors that affects maternal recombination rates.
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            The fine-scale structure of recombination rate variation in the human genome.

            The nature and scale of recombination rate variation are largely unknown for most species. In humans, pedigree analysis has documented variation at the chromosomal level, and sperm studies have identified specific hotspots in which crossing-over events cluster. To address whether this picture is representative of the genome as a whole, we have developed and validated a method for estimating recombination rates from patterns of genetic variation. From extensive single-nucleotide polymorphism surveys in European and African populations, we find evidence for extreme local rate variation spanning four orders in magnitude, in which 50% of all recombination events take place in less than 10% of the sequence. We demonstrate that recombination hotspots are a ubiquitous feature of the human genome, occurring on average every 200 kilobases or less, but recombination occurs preferentially outside genes.
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              • Book: not found

              Cause and Correlation in Biology

                Author and article information

                Conference
                BMC Bioinformatics
                BMC Bioinformatics
                BioMed Central
                1471-2105
                2009
                30 January 2009
                : 10
                : Suppl 1
                : S66
                Affiliations
                [1 ]The Robert S Boas Center for Genomics and Human GeneticsFeinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA
                [2 ]Plant Biology Division, The Samuel Roberts Noble Foundation, Ardmore, OK 73401, USA
                [3 ]Department of Statistics and Finance, University of Science and Technology of China, Anhui 230026, Hefei, PR China
                Article
                1471-2105-10-S1-S66
                10.1186/1471-2105-10-S1-S66
                2648766
                19208170
                f23b0553-c191-40da-98fb-e260b1bfa2e5
                Copyright © 2009 Freudenberg et al; licensee BioMed Central Ltd.

                This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                The Seventh Asia Pacific Bioinformatics Conference (APBC 2009)
                Beijing, China
                13–16 January 2009
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                Research

                Bioinformatics & Computational biology
                Bioinformatics & Computational biology

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