Consequences and opportunities arising due to sparser single-cell RNA-seq datasets

Identifying Aging and Alzheimer Disease–Associated Somatic Variations in Excitatory Neurons From the Human Frontal Cortex

Cell type deconvolution of methylated cell-free DNA at the resolution of individual reads

Cell type matching across species using protein embeddings and transfer learning

scMoC: single-cell multi-omics clustering

CHOP: Haplotype-aware path indexing in population graphs

PCADD: SNV prioritisation in Sus scrofa

Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease

SpaGE: Spatial Gene Enhancement using scRNA-seq

Predicting variant deleteriousness in non-human species: Applying the CADD approach in mouse

Co-expression Patterns between ATN1 and ATXN2 Coincide with Brain Regions Affected in Huntington’s Disease

Pan-cancer subtyping in a 2D-map shows substructures that are driven by specific combinations of molecular characteristics

2D Representation of Transcriptomes by t-SNE Exposes Relatedness between Human Tissues

Comparison of the indoor performance of 12 commercial PV products by a simple model

Proteny: Discovering and visualizing statistically significant syntenic clusters at the proteome level

Unbiased Quantitative Models of Protein Translation Derived from Ribosome Profiling Data

Hi-C Chromatin Interaction Networks Predict Co-expression in the Mouse Cortex

Insight into neutral and disease-associated human genetic variants through interpretable predictors

Integration of gene expression and DNA-methylation profiles improves molecular subtype classification in acute myeloid leukemia

An integrated approach of gene expression and DNA-methylation profiles of WNT signaling genes uncovers novel prognostic markers in Acute Myeloid Leukemia