Nature Genetics · Nov 9, 2023

Massive effort to understand how efficient short read sequencing is in capturing large SVs in cancer.

Nature · Aug 16, 2023

Structural variant remnants caused by different backup DNA repair pathways in BRCA1-null and BRCA2-null HRD tumors.

Nature Communications · Jul 8, 2022

Our work showing recurrent mutation analyses informing biomarkers in cancer.

Nature Biotechnology · May 30, 2022

New assay to understand the complexities of 3D chromatin conformation.

PNAS · Apr 13, 2021

Integrated whole genome, whole exome and RNA-seq analyses of uterine leiomyosarcomas.

Cell Reports · Feb 2, 2021

A glimpse in the genomic alterations in RTK/RAS/RAF negative lung cancers using whole genome sequencing.

Cell · Oct 1, 2020

Lab's massive effort to shed new light on complex SV in cancer.

Gynecologic Oncology · Sep 5, 2018

My masters collaborative work on assessing the molecular heterogeneity in bi-phasic uterine carcinosarcomas.

BMC Bioinformatics · Jan 5, 2018

My masters work on exploring optimal mutation calling workflow for Ion Torrent targeted sequencing platform