Though scientists underscore the importance of their accomplishment by calling the genome a "portrait of who we are," they quickly append that: people are not, and never will be, mere products of their genes.
Overall, our results provide a genome-wide portrait of divergence and introgression associated with adaptation and speciation in an iconic butterfly radiation.
The results presented here provide a comprehensive, genome-wide portrait of transcripts encompassing the BvgAS regulon, while also providing data validating the usefulness of utilizing the long-oligonucleotide microarray described here for studying gene expression in B. bronchiseptica.
The results presented here provide a comprehensive, genome-wide portrait of transcripts encompassing the BvgAS regulon, and provide data validating the use of the long-oligonucleotide microarray described here for studying gene expression in Bordetella bronchiseptica.
The results presented here provide a comprehensive, genome-wide portrait of transcripts encompassing the BvgAS regulon, while also providing data validating the long-oligonucleotide microarray described here for studying gene expression in Bordetella bronchiseptica.
A genome-wide quantitative portrait of each individual NFR, with their starting and ending positions, lengths, and degrees of nucleosome depletion is critical for revealing the heterogeneity of gene regulation and chromatin organization.
The genome-wide expression portrait of MSCs that we presented in this work comprises the largest non-relative profile released for this human primary cell type.
In this way, the RNA deep sequencing assays here presented were performed on well-controlled human cell populations, and allowed quantitative determination of a human MSCs genome-wide expression portrait that includes a compendium of 5,271 protein-coding genes.
Therein, integrated analysis of genome and transcriptome portraits resulted in the robust identification of 10 subgroups, each being reproducible in the validation cohort and thus representing trustable tumor subtypes.
DFR analysis turns to be an efficient and inexpensive method to portrait the genome plasticity of Y. pestis based on horizontal gene transfer (HGT).
