Identification and Interpretation of Clinically Relevant Somatic Variants from Whole-Genome Sequencing Data

被引：0
|
作者：
Maqbool, Khurram [1 ]
Foroughi-Asl, Hassan Hassan [1 ,2 ]
Jeggari, Ashwini Ashwini [1 ]
Ivanchuk, Vadym [1 ]
Eisfeldt, Jesper [2 ]
Renevey, Annick [1 ]
Elhami, Keyvan [1 ]
Rasi, Chiara [1 ]
Nilsson, Daniel [2 ]
Heinaniemi, Merja [3 ]
Lohi, Olli [4 ,5 ]
Wirta, Valtteri [1 ]
机构：
[1] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, Clin Genom Facil, Sci Life Lab, Stockholm, Sweden
[2] Karolinska Inst, Dept Mol Med & Surg, Clin Genet, Stockholm, Sweden
[3] Univ Eastern Finland, Sch Med, Inst Biomed, Kuopio, Finland
[4] Univ Tampere, Tampere Ctr Child, Adolescent & Maternal Hlth Res & Tays Canc Ctr, Tampere, Finland
[5] Tampere Univ Hosp, Tampere, Finland
来源：
BLOOD | 2022年 / 140卷
关键词：
D O I：
10.1182/blood-2022-163295
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：13003 / 13004
页数：2
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