Recent publications published by researchers at the MRC WIMM.
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases.
Journal article
Pagnamenta AT. et al, (2023), Genome Med, 15
MAGNETO: Cell type marker panel generator from single-cell transcriptomic data.
Journal article
Tangherloni A. et al, (2023), J Biomed Inform, 147
CATCH-UP: A High-Throughput Upstream-Pipeline for Bulk ATAC-Seq and ChIP-Seq Data.
Journal article
Riva SG. et al, (2023), J Vis Exp
MLL-AF4 cooperates with PAF1 and FACT to drive high-density enhancer interactions in leukemia.
Journal article
Crump NT. et al, (2023), Nat Commun, 14
GTAC enables parallel genotyping of multiple genomic loci with chromatin accessibility profiling in single cells.
Journal article
Turkalj S. et al, (2023), Cell Stem Cell, 30, 722 - 740.e11
Active regulatory elements recruit cohesin to establish cell-specific chromatin domains
Preprint
Georgiades E. et al, (2023)
Consensus Clustering Strategy for Cell Type Assignments of scRNA-seq Data
Conference paper
Riva SG. et al, (2023), CIBCB 2023 - 20th IEEE Conference on Computational Intelligence in Bioinformatics and Computational Biology
COVID-19 BEDS OCCUPANCY AND HOSPITAL COMPLAINTS: A PREDICTIVE MODEL
Conference paper
Foglia E. et al, (2022), VALUE IN HEALTH, 25, S356 - S356
IRX3 Oncogene Activation in T-ALL through Enhancer Hijacking Caused By fto Intron 8 Deletions
Conference paper
Rahman S. et al, (2022), BLOOD, 140, 1009 - 1010