Literature DB >> 15177688

Representing GC variation along eukaryotic chromosomes.

Jan Paces1, Radek Zíka, Václav Paces, Adam Pavlícek, Oliver Clay, Giorgio Bernardi.   

Abstract

Genome sequencing now permits direct visual representation, at any scale, of GC heterogeneity along the chromosomes of several higher eukaryotes. Plots can be easily obtained from the chromosomal sequences, yet sequence releases of mammalian or plant chromosomes still tend to use small scales or window sizes that obscure important large-scale compositional features. To faithfully reveal, at one glance, the compositional variation at a given scale, we have devised a simple scheme that combines line plots with color-coded shading of the regions underneath the plots. The scheme can be applied to different eukaryotic genomes to facilitate their comparison, as illustrated here for a sample of chromosomes chosen from seven selected species. As a complement to a previously published compact view of isochores in the human genome sequence, we include here an analogous map for the recently sequenced mouse genome, and discuss the contribution of repetitive DNA to the GC variation along the plots. Supplementary information, including a database of color-coded GC profiles for all recently sequenced eukaryotes and the program draw_chromosomes_gc.pl used to obtain them, are available at.

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Year:  2004        PMID: 15177688     DOI: 10.1016/j.gene.2004.02.041

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  18 in total

1.  Unraveling cell type-specific and reprogrammable human replication origin signatures associated with G-quadruplex consensus motifs.

Authors:  Emilie Besnard; Amélie Babled; Laure Lapasset; Ollivier Milhavet; Hugues Parrinello; Christelle Dantec; Jean-Michel Marin; Jean-Marc Lemaitre
Journal:  Nat Struct Mol Biol       Date:  2012-07-01       Impact factor: 15.369

2.  Amplification of whole tumor genomes and gene-by-gene mapping of genomic aberrations from limited sources of fresh-frozen and paraffin-embedded DNA.

Authors:  Markus Bredel; Claudia Bredel; Dejan Juric; Young Kim; Hannes Vogel; Griffith R Harsh; Lawrence D Recht; Jonathan R Pollack; Branimir I Sikic
Journal:  J Mol Diagn       Date:  2005-05       Impact factor: 5.568

3.  The biased distribution of Alus in human isochores might be driven by recombination.

Authors:  Michael Hackenberg; Pedro Bernaola-Galván; Pedro Carpena; José L Oliver
Journal:  J Mol Evol       Date:  2005-03       Impact factor: 2.395

4.  Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations.

Authors:  Marzena Gajecka; Adam Pavlicek; Caron D Glotzbach; Blake C Ballif; Malgorzata Jarmuz; Jerzy Jurka; Lisa G Shaffer
Journal:  Hum Genet       Date:  2006-07-18       Impact factor: 4.132

5.  An isochore map of human chromosomes.

Authors:  Maria Costantini; Oliver Clay; Fabio Auletta; Giorgio Bernardi
Journal:  Genome Res       Date:  2006-04       Impact factor: 9.043

6.  A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting RAB11FIP5 identifies a potential candidate gene for autism spectrum disorder.

Authors:  Jasmin Roohi; David H Tegay; John C Pomeroy; Sandra Burkett; Gary Stone; Roscoe Stanyon; Eli Hatchwell
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2008-06-05       Impact factor: 3.568

7.  Classifying coding DNA with nucleotide statistics.

Authors:  Nicolas Carels; Diego Frías
Journal:  Bioinform Biol Insights       Date:  2009-10-28

8.  The isochore patterns of invertebrate genomes.

Authors:  Rosalia Cammarano; Maria Costantini; Giorgio Bernardi
Journal:  BMC Genomics       Date:  2009-11-18       Impact factor: 3.969

9.  Two common profiles exist for genomic oligonucleotide frequencies.

Authors:  Shang-Hong Zhang; Lei Wang
Journal:  BMC Res Notes       Date:  2012-11-17

10.  The evolution of isochore patterns in vertebrate genomes.

Authors:  Maria Costantini; Rosalia Cammarano; Giorgio Bernardi
Journal:  BMC Genomics       Date:  2009-04-03       Impact factor: 3.969

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