Correspondence on NanoVar’s performance outlined by Jiang T. et al. in “Long-read sequencing settings for efficient structural variation detection based on comprehensive evaluation...

por Tham, Cheng Yong, Benoukraf, Touati
Publicado 2023

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

por Tham, Cheng Yong, Tirado-Magallanes, Roberto, Goh, Yufen, Fullwood, Melissa J., Koh, Bryan T.H., Wang, Wilson, Ng, Chin Hin, Chng, Wee Joo, Thiery, Alexandre, Tenen, Daniel G., Benoukraf, Touati
Publicado 2020

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

por 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 S., Liu, Jin, Song, Hai Wei, Hwang, William Ying Khee, Teh, Bin Tean, Tan, Patrick, Xu, Lifeng, Koh, Angela S., Osato, Motomi, Li, Shang
Publicado 2023