Method
Fast and accurate out-of-core PCA framework for large scale biobank data
- First Published August 24, 2023
Method
Haplotype and population structure inference using neural networks in whole-genome sequencing data
- First Published July 6, 2022
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
Estimating inbreeding coefficients from NGS data: Impact on genotype calling and allele frequency estimation
- First Published August 15, 2013
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