Method
OMKar automates genome karyotyping using optical maps to identify constitutional abnormalities
- First Published November 14, 2025
Research
Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disorders
- First Published September 19, 2024
Resource
Allele-specific transcription factor binding across human brain regions offers mechanistic insight into eQTLs
- First Published August 16, 2024
Method
CoRAL accurately resolves extrachromosomal DNA genome structures with long-read sequencing
- First Published July 9, 2024
Method
Probabilistic association of differentially expressed genes with cis-regulatory elements
- First Published April 17, 2024
Research
Genome-wide strand asymmetry in massively parallel reporter activity favors genic strands
- First Published April 20, 2021
Method
Ancestry-agnostic estimation of DNA sample contamination from sequence reads
- First Published January 24, 2020
Method
Targeted genotyping of variable number tandem repeats with adVNTR
- First Published October 23, 2018
Resource
A genome-wide interactome of DNA-associated proteins in the human liver
- First Published October 11, 2017
Method
HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologies
- First Published December 9, 2016