DECODING UNCHARTED GENOMIC VARIATIONS IN ACUTE MYELOID LEUKEMIA USING LONG-READ SEQUENCING TECHNOLOGIES

by THAM CHENG YONG
Published 2021

NanoVar : accurate characterization of patients' genomic structural variants using low-depth nanopore sequencing

by Tham, Cheng Yong, Tirado-Magallanes, Roberto, Goh, Yufen, Fullwood, Melissa Jane, Koh, Bryan T. H., Wang, Wilson, Ng, Chin Hin, Chng, Wee Joo, Thiery, Alexandre, Tenen, Daniel G., Benoukraf, Touati
Published 2021

High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform

by Tham, Cheng-Yong, Poon, LaiFong, Yan, TingDong, Koh, Javier Yu Peng, Ramlee, Muhammad Khairul, Teoh, Vania Swee Imm, Zhang, Suihan, Cai, Yi, Hong, Zebin, Lee, Gina SS, Liu, Jin, Song, Hai Wei, Hwang, William Ying Khee, Teh, Bin Tean, Tan, Patrick, Xu, Lifeng, Koh, Angela S, Osato, Motomi, Li, Shang
Published 2024