Inherited functional regulatory risk variants for common human cancers [MPRA]

Set2: ERCC bulk short-read RNA-seq by Illumina NextSeq platform

Utility analyses of AVITI sequencing platforms

Set7: ERCC bulk short-read RNA-seq by Illumina NextSeq platform, additional samples

Systematic characterization of indel variants using a yeast-based protein folding sensor

Iterative deep learning-design of human enhancers exploits condensed sequence grammar to achieve cell type-specificity [RNA-Seq]

Genomic context sensitizes regulatory elements to genetic disruption [DNA]

Genomic context sensitizes regulatory elements to genetic disruption

Characterizing glucokinase variant mechanisms using a multiplexed abundance assay

Spatial Transcriptomics of Liver tissue with Bcatenin exon3 genetic mutations.

Optimized CRISPR guide RNA library cloning reduces skew and enables more compact genetic screens

Differential Whole Genome CRISPR Screening Strategy for SARS-CoV-2 Spike and VSV-G Mediated Pseudoviral Entry

Multiplexed assessment of human glucokinase variant activity

Transcription factor paralogs orchestrate alternative gene regulatory networks by context-dependent cooperation with multiple cofactors

DeepSTARR predicts enhancer activity from DNA sequence and enables the de novo design of synthetic enhancers [Drosophila genome-wide UMI-STARR-seq]

DeepSTARR predicts enhancer activity from DNA sequence and enables the de novo design of synthetic enhancers [Human oligo UMI-STARR-seq]

DeepSTARR predicts enhancer activity from DNA sequence and enables the de novo design of synthetic enhancers

Whole genome functional characterization of RE1 silencers using a modified massively parallel reporter assay

Sequencing of miRXplore Universal Reference (Miltenyi Biotec) RNA using mDOT-seq

Methyltransferase-directed orthogonal tagging and sequencing of miRNAs and bacterial small RNAs in probiotic Lactobacillus casei