Method
Graph-based deep reinforcement learning for haplotype assembly with Ralphi
- First Published November 14, 2025
Method
Accurate fusion transcript identification from long- and short-read isoform sequencing at bulk or single-cell resolution
- First Published March 14, 2025
Method
Secure discovery of genetic relatives across large-scale and distributed genomic data sets
- First Published August 7, 2024
Resource
Precision environmental health monitoring by longitudinal exposome and multi-omics profiling
- First Published June 6, 2022
Method
Microfluidic isoform sequencing shows widespread splicing coordination in the human transcriptome
- First Published December 1, 2017
Method
Linking disease associations with regulatory information in the human genome
- First Published September 5, 2012
Resource
Annotation of functional variation in personal genomes using RegulomeDB
- First Published September 5, 2012
Resource
Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors
- First Published September 5, 2012
Resource
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia
- First Published September 5, 2012
Research
Deep sequencing of subcellular RNA fractions shows splicing to be predominantly co-transcriptional in the human genome but inefficient for lncRNAs
- First Published September 5, 2012