NanoVar : accurate characterization of patients' genomic structural variants using low-depth nanopore sequencing
The recent advent of third-generation sequencing technologies brings promise for better characterization of genomic structural variants by virtue of having longer reads. However, long-read applications are still constrained by their high sequencing error rates and low sequencing throughput. Here, we...
Saved in:
Main Authors: | 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 |
---|---|
Other Authors: | School of Biological Sciences |
Format: | Article |
Language: | English |
Published: |
2021
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/147971 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
NanoVar: Accurate characterization of patients' genomic structural variants using low-depth nanopore sequencing
by: Tham, C.Y., et al.
Published: (2021) -
204_Những anh chàng Scotland
by: Đoan Trang
Published: (2011) -
SgD-CNV, a database for common and rare copy number variants in three Asian populations
by: Xu, H., et al.
Published: (2014) -
208_Sinh viên làm thêm dịp hè
by: Thu Hằng
Published: (2011) -
Optimization of nano-oxide layer in CIP spin valves
by: Qiu, J., et al.
Published: (2014)