Spark: A navigational paradigm for genomic data exploration

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Figure 2.
Figure 2.

Clustering analysis at annotated TSSs. (A) Histogram indicates the number of regions in each cluster, and the overlaid dendrogram traces the interactive cluster splitting events (initial clustering with k = 2, followed by one manual split of cluster c1 into c1-1 and c1-2). Chromatin modification (blue), DNA methylation (green; MeDIP and MRE indicate methylated and unmethylated CpGs, respectively), and RNA-seq (orange) data from H1 hESCs together with genomic CpG density values (gray) were clustered using a bin size of 300 bp across 6-kb windows centered on RefSeq transcriptional start sites (TSSs). (B) Further exploration and interactive refinement of the clusters from A.

This Article

  1. Genome Res. 22: 2262-2269

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