Searching journal content for articles similar to Vandepoele et al. 12 (11): 1792.

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  1. ...larger in maize than in rice. Since the BESs and markers in the FPC map do not cover the , there will be many possible anchors that cannot be detected. Therefore, there will be many genes in rice that do not appear to have a homologous sequence in maize. Moreover, the hybridized markers in FPC...
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  2. ...of intragenomic and intergenomic homologous genes were determined using the method of Rost ( 1999 ). Consequently, i-ADHoRe was run on the Arabidopsis and rice data sets separately and on a combined Arabidopsisrice data set. We used a gap size of 30, a quality factor of 0.9, and a probability cutoff of 0...
  3. ...functionalities. Results Identifying sister chromosome regions based on conserved gene order Paralogs derived from WGD are expected to be located in chromosome regions of shared ancestry. To help identify such regions, we first determined fish–human gene homology relationships by exhaustive, ‘‘all...
  4. ...on information from only one species. New angiosperm sequences ( Table 1 ) promise to qualitatively improve our deductions about the evolution of angiosperm gene repertoire and arrangement. Arabidopsis ( Arabidopsis Genome Initiative 2000 ), rice ( Oryza sativa ) ( International Rice Genome Sequencing Project...
  5. ...the average Arabidopsis gene density of 1 gene per 4.5 kb of sequence ( The Arabidopsis Genome Initiative 2000 ) and similar to the average gene density in rice ( Rice Chromosome 10 Sequencing Consortium 2003 ). The CesA1 region appears to be part of a gene island, as the gene density is fairly high...
  6. ...( Vandepoele et al. 2002 ) to study a higher-confidence subset of 1459 orthologous pairs to identify regions in the two large halophilic archaeal chromosomes with conserved gene order and orientation (for a description of the ADHoRe software, see Supplemental material). The regions of micro-colinearity...
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