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科研机构
北京大学 [3]
中国医学科学院 北京... [2]
内容类型
期刊论文 [5]
发表日期
2017 [3]
2014 [2]
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Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations
期刊论文
HUMAN MUTATION, 2017
Dou, Yanmei
;
Yang, Xiaoxu
;
Li, Ziyi
;
Wang, Sheng
;
Zhang, Zheng
;
Ye, Adam Yongxin
;
Yan, Linlin
;
Yang, Changhong
;
Wu, Qixi
;
Li, Jiarui
;
Zhao, Boxun
;
Huang, August Yue
;
Wei, Liping
收藏
  |  
浏览/下载:121/0
  |  
提交时间:2017/12/03
autism spectrum disorder
autistic traits
parental mosaicism
single-nucleotide mosaicism
DE-NOVO MUTATIONS
INTERACTION NETWORKS
SOMATIC MOSAICISM
DRAVET SYNDROME
HUMAN-DISEASE
GENETIC RISK
HUMAN BRAIN
EVOLUTION
PATTERNS
GENOME
MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples
期刊论文
NUCLEIC ACIDS RESEARCH, 2017
Huang, August Yue
;
Zhang, Zheng
;
Ye, Adam Yongxin
;
Dou, Yanmei
;
Yan, Linlin
;
Yang, Xiaoxu
;
Zhang, Yuehua
;
Wei, Liping
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2017/12/03
MONOZYGOTIC TWINS DISCORDANT
SOMATIC POINT MUTATIONS
HUMAN CANCER GENOMES
DE-NOVO MUTATIONS
WHOLE-GENOME
COPY NUMBER
CLONAL HEMATOPOIESIS
HUMAN TISSUES
VARIANT
IDENTIFICATION
Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations
期刊论文
2017, 卷号: 38, 期号: 8, 页码: 1002-1013
作者:
Dou, Yanmei
;
Yang, Xiaoxu
;
Li, Ziyi
;
Wang, Sheng
;
Zhang, Zheng
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2020/01/04
autism spectrum disorder
autistic traits
parental mosaicism
single-nucleotide mosaicism
Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals
期刊论文
细胞研究英文版, 2014
Huang, August Y.
;
Xu, Xiaojing
;
Ye, Adam Y.
;
Wu, Qixi
;
Yan, Linlin
;
Zhao, Boxun
;
Yang, Xiaoxu
;
He, Yao
;
Wang, Sheng
;
Zhang, Zheng
;
Gu, Bowen
;
Zhao, Han-Qing
;
Wang, Meng
;
Gao, Hua
;
Gao, Ge
;
Zhang, Zhichao
;
Yang, Xiaoling
;
Wu, Xiru
;
Zhang, Yuehua
;
Wei, Liping
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2015/11/11
single-nucleotide mutation
postzygotic mosaicism
Dravet syndrome
next-generation sequencing
Bayesian model
DETECTABLE CLONAL MOSAICISM
SOMATIC MUTATIONS
DRAVET SYNDROME
MATERNAL MICROCHIMERISM
SENSITIVE DETECTION
HUMAN TISSUES
PIK3CA CAUSE
HUMAN BRAIN
CANCER
DISEASE
Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals
期刊论文
2014, 卷号: 24, 期号: 11, 页码: 1311-1327
作者:
Huang, August Y.
;
Xu, Xiaojing
;
Ye, Adam Y.
;
Wu, Qixi
;
Yan, Linlin
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2020/01/13
single-nucleotide mutation
postzygotic mosaicism
Dravet syndrome
next-generation sequencing
Bayesian model
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