4.8 Article

seqMINER: an integrated ChIP-seq data interpretation platform

Journal

NUCLEIC ACIDS RESEARCH
Volume 39, Issue 6, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkq1287

Keywords

-

Funding

  1. INSERM-Region Alsace
  2. Association pour la Recherche sur le Cancer (ARC)
  3. French Ministry of Education, Research and Technology (MNERT)
  4. ANR (GenomATAC) [ANR-09-BLAN-0266]
  5. EU [LSHG-CT-2007-037445]
  6. Ligue National contre le cancer
  7. Institut National du Cancer
  8. Ligue National contre le cancer, equipe labelisee
  9. Agence Nationale de la Recherche (ANR) [ANR-09-BLAN-0266] Funding Source: Agence Nationale de la Recherche (ANR)

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available