Sentence examples for more genome assemblies from inspiring English sources

As more genome assemblies become available, patterns within many other underrepresented taxonomic groups will be further revealed.

More genome assemblies of bats are needed to determine if this lack of a match is due to sequence divergence of the primer sites or to the lack of filovirus-like NIRVs.

As more genome assemblies become available in underrepresented taxonomic groups, the patterns of compositional biases and restriction site frequencies across the eukaryotic tree of life will become clearer and will improve our understanding of genome evolution.

As more and more draft genome assemblies of species closely related to already sequenced species become available, known gene annotations can be used as starting point for gene predictions.

More complete genome assemblies, or improved and more sensitive algorithms, might detect sequence conservation at these enhancers; while we cannot rule out this possibility, our results were obtained with the best assemblies and computational tools available at the time.

The robustness of our gene-finder was tested across more continuous genome assemblies by using GreenGenie2 to predict a whole-genome gene catalog with the v4 genome assembly.

Our chromosomal coordinates for the human, the mouse, and the rat, obtained from more recent genome assemblies, correct those reported in two earlier studies (Cho et al. 2005; Cho and Zhang 2006).

The authors aligned their scaffolds to the more advanced genome assemblies of chicken and zebra finch (which are a long way away in evolutionary time, circa 90MY, as far as humankind has diverged from a common ancestor with mice).

sinensis beta-keratin genes are shorter due to their more fragmentary genome assemblies, beta-keratin genes with close orthology relationships to Group42 C. picta beta-keratin genes tend to be situated on the same scaffolds, suggesting that they are also located in regions with conserved synteny to microchromosome 25 of chicken (supplementary fig. S3, Supplementary Material online).

These data are an updated version of the data of Patterson et al. (2006), updated and recurated by Burgess and Yang (2008) to incorporate more recent genome assembly sequences and to generate high-quality alignments of genomic regions instead of single variable sites.

Due to the more fragmented genome assembly we expect the true numbers to be closer to the lower bounds.