DECODING UNCHARTED GENOMIC VARIATIONS IN ACUTE MYELOID LEUKEMIA USING LONG-READ SEQUENCING TECHNOLOGIES
Ph.D
Saved in:
Main Author: | THAM CHENG YONG |
---|---|
Other Authors: | CANCER SCIENCE INSTITUTE OF SINGAPORE |
Format: | Theses and Dissertations |
Language: | English |
Published: |
2021
|
Subjects: | |
Online Access: | https://scholarbank.nus.edu.sg/handle/10635/191712 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
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) -
Detection of CEBPA Mutation Gene in Acute Myeloid Leukemia Patients
by: Takol Chareonsirisuthigul, et al.
Published: (2022) -
Improved outcome in childhood acute myeloid leukemia in Singapore with the MRC AML 10 protocol
by: Tan, R.M., et al.
Published: (2011) -
ONTbarcoder and MinION barcodes aid biodiversity discovery and identification by everyone, for everyone
by: Srivathsan, Amrita, et al.
Published: (2022) -
MinION-in-ARMS: Nanopore Sequencing to Expedite Barcoding of Specimen-Rich Macrofaunal Samples From Autonomous Reef Monitoring Structures
by: Chang, J.J.M., et al.
Published: (2021)