Principle
Integrate RNA-Seq, ATAC-Seq, ChIP-Seq, CUT&Tag, DNA methylation or Hi-C around one research question. Sample correspondence, experimental conditions and data quality guide comparisons and candidate regulatory hypotheses. This service covers sequencing-based integration; proteomics and metabolomics are described separately.
Applications
- Relate expression to accessibility, histone modifications or methylation
- Integrate chromatin interactions with candidate regulatory elements
- Develop cross-omics hypotheses from matched samples and comparable conditions
Method features
- Select combinations around the research question and sample matching
- Covers transcriptomic, epigenetic and three-dimensional genome sequencing
- Evaluate candidate associations using independent data or follow-up experiments
Workflow
- 01
Define the question, assay combination and sample correspondence
- 02
Assess and process each sequencing dataset
- 03
Integrate signals, prioritize candidate mechanisms and visualize results
- 04
Discuss interpretation, scope and follow-up validation
This is a workflow overview. Experimental and analytical details depend on sample conditions and research objectives.