Sentence examples for multiple genomic and from inspiring English sources

PDMeth provides integrated gene methylation data based on cross dataset analysis for disease and normal samples and includes a user friendly and configurable genome browser in which multiple genomic and epigenomic resources can be visualized simultaneously.

Cancer cells harbor multiple genomic and epigenetic abnormalities.

Our work integrated multiple genomic and genetic data types within the Luminal A breast cancer subtype and spanned multiple data sets.

Several evidences depict that the expressions of miRNAs are remarkably modulated in malignant tissues due to multiple genomic and epigenetic alterations.

As described, ERα can mediate estrogenic response through multiple genomic and non-genomic mechanisms, many of which affect proteins and pathways not necessarily directly or exclusively associated with ERα.

Due to the low incidence and limited amounts of biopsy materials, clinical OS samples available for research are particularly scarce, making it extremely difficult to analyze the tumor samples using multiple genomic and proteomic platforms [ 9].

The uptake of multiple genomic islands and modules and resistance determinants is in agreement with the hypothesis of genetic capitalism, which states that successful integration and selection of a foreign genetic element increases the number of possible genetic transfer events in the future [17].

Of the clean reads, more than 62% matched either to a unique or multiple genomic positions, and 4,106,692 and 3,922,411 uniquely matched reads were used for gene expression analysis of each library.

This work demonstrates a systematic approach to integrate multiple genomic datasets and to infer TF and miRNA regulatory networks, which may be used to better understand coordinated gene regulation by TFs and miRNAs in complex biological systems.

Systems biology approaches can help genomics studies through systematic and integrative approaches to incorporate multiple genomic data and assemble the information toward cellular or physiological behaviours related to a particular biological phenotype such as disease.

Two SNPs (BIEC2_403636 and BIEC2_424368) were excluded because they showed evidence of probe hybridization to multiple genomic locations, and two other SNPs (BIEC2_346860 and BIEC2_840760) were excluded due to low duplicate concordance rates.