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.
Pagnamenta AT. et al, (2023), Genome Med, 15
MAGNETO: Cell type marker panel generator from single-cell transcriptomic data.
Tangherloni A. et al, (2023), J Biomed Inform, 147
CATCH-UP: A High-Throughput Upstream-Pipeline for Bulk ATAC-Seq and ChIP-Seq Data.
Riva SG. et al, (2023), J Vis Exp
MLL-AF4 cooperates with PAF1 and FACT to drive high-density enhancer interactions in leukemia.
Crump NT. et al, (2023), Nat Commun, 14
GTAC enables parallel genotyping of multiple genomic loci with chromatin accessibility profiling in single cells.
Turkalj S. et al, (2023), Cell Stem Cell, 30, 722 - 740.e11
Active regulatory elements recruit cohesin to establish cell-specific chromatin domains
Georgiades E. et al, (2023)
Consensus Clustering Strategy for Cell Type Assignments of scRNA-seq Data
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
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
Rahman S. et al, (2022), BLOOD, 140, 1009 - 1010