Sentence examples for many different genomic from inspiring English sources

In addition, researchers search for meaningful events at many different genomic resolution scales, from whole genome to individual base pairs.

Furthermore, NGS has a broad range of possible applications for many different genomic studies, such as species classification and/or gene discovery, de novo assemblies of genomes that have not been sequenced in the past, SNP identification, epigenetic analysis, DNA methylation analysis, and, most notably, transcriptome analyses (RNA-seq) of cells, tissues, and organisms.

The NSCL genetic alterations represented in Table 1 barely scratches the surface in regards to the many different genomic abnormalities that have been identified.

MITEs are widely distributed among eukaryotes [46] and could provide for the emergence of regulatory RNAs, such as miRNAs, siRNAs or other small non-coding RNAs, in many different genomic contexts.

Many different genomic imbalances have been reported in patients with TEF/EA (Felix et al., 2007).

This physical map will greatly facilitate the detailed study of many different genomic regions in channel catfish, and the positional cloning of genes controlling economically important production traits.

Our analysis of the five currently available fish genomes indicates that although the intron content of these genomes is very similar in many respects, different genomic processes appear to be shaping the genomic intron content.

IGV allows researchers to visualize many different types of genomic data together, including NGS data, variant calls, microarray data and genome annotations.

There are many crops with different genomic characteristics that should be considered when identifying the most suited genotyping methodology.

Many loci in different genomic regions also appear to be involved, but nevertheless there appear to be changes across the same set of genomic regions in different, isolated freshwater populations of sticklebacks following invasion (Jones et al. 2012).

Overall, VAS is more efficient and flexible in handling new variant lists since it does not require pre-loading of data, while GEMINI works better in situations where the same list of genetic variants is to be repeatedly analyzed by integrating with many different subsets of genomic data.