Research
Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications
- First Published February 11, 2026
Research
Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T
- First Published March 17, 2025
Research
Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps
- First Published November 1, 2024
Research
SARS-CoV-2 genomic diversity and the implications for qRT-PCR diagnostics and transmission
- First Published February 18, 2021
Research
Complex mosaic structural variations in human fetal brains
- First Published October 29, 2020
Research
Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing
- First Published September 4, 2020
Research
Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line
- First Published June 28, 2018
Research
Adenosine deaminases that act on RNA induce reproducible changes in abundance and sequence of embryonic miRNAs
- First Published February 6, 2012
Research
Deep sequencing reveals distinct patterns of DNA methylation in prostate cancer
- First Published July 1, 2011
Research
Locus co-occupancy, nucleosome positioning, and H3K4me1 regulate the functionality of FOXA2-, HNF4A-, and PDX1-bound loci in islets and liver
- First Published June 15, 2010