seqMINER: an integrated ChIP-seq data interpretation platform
By T. Ye, A. Krebs, M. Choukrallah, C. Keime, F. Plewniak, I. Davidson, L. Tora. Nucleic Acids Research, 2010
430 citations recorded by the source corpus.
In a single experiment, chromatin immunoprecipitation combined with high throughput sequencing (ChIP-seq) provides genome-wide information about a given covalent histone modification or transcription factor occupancy. However, time efficient bioinformatics resources for extracting biological meaning out of these gigabyte-scale datasets are often a limiting factor for data interpretation by biologists. We created an integrated portable ChIP-seq data interpretation platform called seqMINER, with optimized performances for efficient handling of multiple genome-wide datasets. seqMINER allows comparison and integration of multiple ChIP-seq datasets and extraction of qualitative as well as quantitative information. seqMINER can handle the biological complexity of most experimental situations and proposes methods to the user for data classification according to the analysed features. In addition, through multiple graphical representations, seqMINER allows visualization and modelling of general as well as specific patterns in a given dataset. To demonstrate the efficiency of seqMINER, we have carried out a comprehensive analysis of genome-wide chromatin modification data in mouse embryonic stem cells to understand the global epigenetic landscape and its change through cellular differentiation.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/75872cef4875796a9f87791b838df9b1d5c335a2
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
Citations in the corpus
- Cistrome: an integrative platform for transcriptional regulation studies (2011, background): “recently published seqMINER platform [4].”
- ngs.plot: Quick mining and visualization of next-generation sequencing data by integrating genomic databases (2014, methodology): “Several programs [18-20] with graphical interfaces have been developed, featuring a point-and-click workflow to perform these tasks.”