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Transcriptomic and epigenomic data integration software tools | RNA sequencing analysis

Transcriptomic and epigenomic data integration software tools | RNA sequencing analysis A variety of NGS-based techniques have been developed. For example, chromatin immunoprecipitation coupled with parallel sequencing (ChIP-seq) is widely used to assess the binding of proteins to the genome. RNA sequencing (RNA-seq) can estimate the abundance of whole transcripts and their isoforms. Genome-wide nucleosome positioning and open chromatin can be captured by MNase-seq and DNase-seq, respectively. As the demand for NGS has increased, several thousand NGS-based data sets have been deposited in public data repositories such as gene expression omnibus (GEO). Notably, novel findings frequently emerge from reanalyzing available NGS-based data sets. However, there is no easy way to access, download, and process a large set of original (raw) NGS-based data for comparative and integrative analysis, although some web-based applications have been developed to resolve the issue.
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