scTEM-seq: Single-cell analysis of transposable element methylation to link global epigenetic heterogeneity with transcriptional programs

- Hunt, Kooper V., Burnard, Sean M., Roper, Ellise A., Bond, Danielle R., Dun, Matthew D., Verrills, Nicole M., Enjeti, Anoop K., Lee, Heather J.

Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes

- Xavier, Alexandre, Scott, Rodney J., Talseth-Palmer, Bente

Identification of new causative genes in inherited colorectal cancer

- Xavier, Alexandre

Single-cell epigenomics in cancer: Charting a course to clinical impact

- Bond, Danielle R., Uddipto, Kumar, Enjeti, Anoop K., Lee, Heather J.

Characterising transcriptional perturbations arising from altered expression of schizophrenia-associated microRNA

- Geaghan, Michael

ScNMT-seq enables joint profiling of chromatin accessibility DNA methylation and transcription in single cells

- Clark, Stephen J., Argelaguet, Ricard, Stegle, Oliver, Reik, Wolf, Kapourani, Chantriolnt-Andreas, Stubbs, Thomas M., Lee, Heather J., Alda-Catalinas, Celia, Krueger, Felix, Sanguinetti, Guido, Kelsey, Gavin, Marioni, John C.

Hypermutation in pancreatic cancer

- Humphris, Jeremy L., Patch, Ann-Marie, Quinn, Michael C. J., Bruxner, Timothy J. C., Christ, Angelika N., Harliwong, Ivon, Idrisoglu, Senel, Manning, Suzanne, Nourse, Craig, Nourbakhsh, Ehsan, Stone, Andrew, Wilson, Peter J., Nones, Katia, Scarlett, Christopher J., Bailey, Peter J., Johns, Amber L., McKay, Skye, Chang, David K., Miller, David K., Pajic, Marina, Kassahn, Karin S.

Mixed integer linear programming models for machine scheduling

- Clement, Riley

Neoadjuvant chemotherapy: what does it take to tAnGo?

- Zdenkowski, Nicholas, McCarthy, Nicole