Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants

Enhanced detection of RNA modifications with high-accuracy nanopore RNA basecalling models

Transcriptome wide identification of Dicer binding in human and C. elegans reveals a variety of substrates

Interferon inducible pseudouridine modification in human mRNA by quantitative nanopore profiling (Illumina)

Interferon inducible pseudouridine modification in human mRNA by quantitative nanopore profiling

Maximal interferon induction in the absence of influenza NS1 is infrequent owing to requirements for replication and export

High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency

Variant specific global loss of cellular m6A RNA methylation during SARS-CoV-2 infection

Position-dependent function of human sequence-specific transcription factors

Repriming limits R-loop formation at DNA secondary structures during S phase

CDK12 and CDK13

Quantifying Biopolymer Sequence Recognition using Biophysically Informed Machine Learning

Assessment of Variant Abundance by Massively Parallel Sequencing for PTEN and TPMT

Assaying RNA Structure with LASER-seq

Identification of functional regulatory variants implicates distinct transcriptional networks in dementia

Massively parallel characterization of CYP2C9 variant enzyme activity and abundance

A single-cell massively parallel reporter assay detects cell type specific cis-regulatory activity

Analysis of queuosine and 2-thio tRNA modifications by high throughput sequencing

Joint epigenome profiling reveals cell-type-specific gene regulatory programs in human cortical organoids

A Transcription Factor Atlas of Directed Differentiation