Publications:

DeteX: A highly accurate software for detecting SNV and InDel in single and paired NGS data in cancer research.

Frontiers In Genetics

Cui, Yunlong Y; Li, Hongfeng H; Liu, Pengfei P; Wang, Hailong H; Zhang, Zhenzhen Z; Qu, Hongzhu H; Tian, Caijuan C; Fang, Xiangdong X

Publication Date: 2022

Variant appearance in text: TET2: 3885del; Tyr1295fs

PubMed Link: 36685970

Variant Present in the following documents:

• Table4.xlsx, sheet 1

View BVdb publication page

A sex-informed approach to improve the personalised decision making process in myelodysplastic syndromes: a multicentre, observational cohort study.

The Lancet. Haematology

,

Publication Date: 2022-11-24

Variant appearance in text: TET2: 3885del; Y1295*

PubMed Link: 36436542

Variant Present in the following documents:

• mmc2.xlsx, sheet 1

View BVdb publication page

The significance of genetic mutations and their prognostic impact on patients with incidental finding of isolated del(20q) in bone marrow without morphologic evidence of a myeloid neoplasm.

Blood Cancer Journal

Ravindran, Aishwarya A; He, Rong R; Ketterling, Rhett P RP; Jawad, Majd D MD; Chen, Dong D; Oliveira, Jennifer L JL; Nguyen, Phuong L PL; Viswanatha, David S DS; Reichard, Kaaren K KK; Hoyer, James D JD; Go, Ronald S RS; Shi, Min M

Publication Date: 2020-01-23

Variant appearance in text: TET2: 3885del; Tyr1295*

PubMed Link: 31974359

Variant Present in the following documents:

• Main text
• 41408_2020_Article_275.pdf

View BVdb publication page