Sentence examples for genomic evolution have from inspiring English sources

Recently, as increasing numbers of plasmid genomic sequences have become available, systematic analyses of the dynamics and relationships among plasmids and their contributions to bacterial genomic evolution have become feasible.

Further sequencing and physiological experiments will be necessary to identify particular genomic differences associated with living in different environments, but the data presented here indicate that substantial genomic evolution has occurred since the divergence of these two lineages.

Certainly, the prevalence and importance of duplication in genomic evolution has only recently become clear [ 11] and is among the major insights delivered by whole genome sequencing.

Taken together, these results indicate that much genomic evolution has occurred in the seed plant lineage before the split between gymnosperms and angiosperms, and that the pace of evolution of the genome macro-structure has been much slower in the gymnosperm lineage leading to extent conifers than that seen for the same period of time in flowering plants.

These tremendous amounts of data have not only enabled advances in fundamental biology, helping to understand the pathogenesis of microorganisms and their genomic evolution, but have also had implications for clinical microbiology.

The conservation of these sequences in significant number of bacterial genomes despite limitation on their genomic size during evolution have therefore suggested their functions are essential in regulation of cellular activities in prokaryotes, as in their eukaryotic counterparts.

However, the study of genomic island evolution has been mostly performed at the sequence level using computer software or hybridization analysis to compare different bacterial genomic sequences.

This pattern of genomic drift evolution has two important implications for the FBX gene superfamily.

These results support that CNA patterns in myeloma, such as the eight characteristic trisomy chromosomes in about half of all myeloma patients, are not a by-product of myeloma genomic evolution but have functional and consequential effects that contribute to the pathogenesis of myeloma.

The dynamics of both phenotypic [ 13- 19] and genomic [ 20- 26] evolution have been characterized in a variety of ways.

Debates about organellar evolution have been revitalized and streamlined during the post-genomic revolution.