Sentence examples for genomic evolution has from inspiring English sources

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.

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.

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 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 genomic approach to understanding how evolution has generated the extraordinary diversity of flowers is to assemble a floral EST database for several missing-link taxa and then use gene phylogenies and expression data to identify genes that are important in flower evolution.

However, our genomic studies have shown that rapid evolution has produced a distinct repertoire of PLUNC genes in mammals characterised by low sequence similarity, an observation that is often found in host defence protein families (Bingle et al. 2004; Wheeler et al. 2007).

An important role for genomic copy-number variation in human evolution has also been postulated (Dumas et al. 2007), given that about one-third of over 24 000 genes analyzed have been found to exhibit copy-number variation among species of humans and other primates (Dumas et al. 2007), with humans and chimpanzees in particular differing by over 6% in their complements of genes (Demuth et al. 2006).

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.