Detecting Functional Rare Variants Relating to Type 2 Diabetes Using Deep Whole Genome Sequencing

被引:0
|
作者
Jun, Goo
Almeida, Marcio
Cingolani, Pablo
Wood, Andrew R.
Fuchsberger, Christian
Teslovich, Tanya M.
Dyer, Thomas D.
Curran, Joanne
Grunstad, Jason
Blackwell, Thomas W.
Lehman, Donna M.
Grossman, Robert
Lincoln, Stephen E.
Laramie, Jason
Boehnke, Michael
Mccarthy, Mark
Frayling, Timothy M.
Sladek, Robert
Duggirala, Ravindranath
Blangero, John
Abecasis, Goncalo
机构
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
140-OR
引用
收藏
页码:A37 / A37
页数:1
相关论文
共 50 条
  • [41] Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability
    Kierczak, Marcin
    Rafati, Nima
    Hoglund, Julia
    Gourle, Hadrien
    Lo Faro, Valeria
    Schmitz, Daniel
    Ek, Weronica E.
    Gyllensten, Ulf
    Enroth, Stefan
    Ekman, Diana
    Nystedt, Bjorn
    Karlsson, Torgny
    Johansson, Asa
    NATURE COMMUNICATIONS, 2022, 13 (01)
  • [42] Copy number variants in clinical whole genome sequencing: deployment and interpretation for rare and undiagnosed disease
    Gross, Andrew M.
    CANCER GENETICS, 2018, 224 : 71 - 71
  • [43] Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability
    Marcin Kierczak
    Nima Rafati
    Julia Höglund
    Hadrien Gourlé
    Valeria Lo Faro
    Daniel Schmitz
    Weronica E. Ek
    Ulf Gyllensten
    Stefan Enroth
    Diana Ekman
    Björn Nystedt
    Torgny Karlsson
    Åsa Johansson
    Nature Communications, 13
  • [44] Identification of New Variants Associated with Type 2 Diabetes in Maya Families by Whole- Exome Sequencing
    Sanchez-Pozos, Katy
    Cesar Lara-Riegos, Julio
    Guadalupe Ortiz-Lopez, Maria
    Verleyen, Jerome
    Jimenez-Jacinto, Veronica
    Angeles Granados-Silvestre, Maria De Los
    Sanchez-Flores, Alejandro
    Menjivar, Marta
    DIABETES, 2015, 64 : A704 - A704
  • [45] Whole genome sequencing analysis on coronary artery disease in type 1 diabetes
    Antikainen, A. A. V.
    Sandholm, N.
    Haukka, J.
    Valo, E.
    Groop, P. -H.
    DIABETOLOGIA, 2019, 62 : S149 - S149
  • [46] Rare germline variants identified using genome sequencing in patients with hereditary cancer
    Wright, Carter
    Cooper, Sara
    GENETICS IN MEDICINE, 2022, 24 (03) : S42 - S43
  • [47] Rare variants analysis using penalization methods for whole genome sequence data
    Akram Yazdani
    Azam Yazdani
    Eric Boerwinkle
    BMC Bioinformatics, 16
  • [48] Rare variants analysis using penalization methods for whole genome sequence data
    Yazdani, Akram
    Yazdani, Azam
    Boerwinkle, Eric
    BMC BIOINFORMATICS, 2015, 16
  • [49] Scalable approaches for functional analyses of whole-genome sequencing non-coding variants
    Kuksa, Pavel P.
    Greenfest-Allen, Emily
    Cifello, Jeffrey
    Ionita, Matei
    Wang, Hui
    Issen, Heather
    Cheng, Po-Liang
    Lee, Wan-Ping
    Wang, Li-San
    Leung, Yuk Yee
    HUMAN MOLECULAR GENETICS, 2022, 31 (R1) : R62 - R72
  • [50] Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites
    Tao Long
    Michael Hicks
    Hung-Chun Yu
    William H Biggs
    Ewen F Kirkness
    Cristina Menni
    Jonas Zierer
    Kerrin S Small
    Massimo Mangino
    Helen Messier
    Suzanne Brewerton
    Yaron Turpaz
    Brad A Perkins
    Anne M Evans
    Luke A D Miller
    Lining Guo
    C Thomas Caskey
    Nicholas J Schork
    Chad Garner
    Tim D Spector
    J Craig Venter
    Amalio Telenti
    Nature Genetics, 2017, 49 : 568 - 578