Bulk sequencing settles many cancer questions. However, when researchers need to trace a signal back to the individual cell that generated it—tumor, immune, or stromal—single cell becomes the better choice. Keeping that attribution takes specific choices across sample preparation, sequencing strategy, and bioinformatics. The trade is worth taking, provided the study design is built to capture those populations from the start.
This infographic provides a quick visual framework for scoping a single cell study. Whether researchers are exploring baseline tumor heterogeneity or therapeutic resistance, the resource shows which choices come before preparing the sample.
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- Six molecular readouts available from one cell, from DNA methylation to chromatin accessibility
- Which cancer questions bulk answers well, and which need cell-level data
- The design choices that keep low-abundance cells alive to the sequencer

















