EPIANNO: ePIgenomics ANNOtation tool.
Ontology highlight
ABSTRACT: Recently, with the development of next generation sequencing (NGS), the combination of chromatin immunoprecipitation (ChIP) and NGS, namely ChIP-seq, has become a powerful technique to capture potential genomic binding sites of regulatory factors, histone modifications and chromatin accessible regions. For most researchers, additional information including genomic variations on the TF binding site, allele frequency of variation between different populations, variation associated disease, and other neighbour TF binding sites are essential to generate a proper hypothesis or a meaningful conclusion. Many ChIP-seq datasets had been deposited on the public domain to help researchers make new discoveries. However, researches are often intimidated by the complexity of data structure and largeness
SUBMITTER: Liu CH
PROVIDER: S-EPMC4747527 | biostudies-literature | 2016
REPOSITORIES: biostudies-literature
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