BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

6346 related articles for article (PubMed ID: 23128226)

  • 1. An integrated map of genetic variation from 1,092 human genomes.
    ; Abecasis GR; Auton A; Brooks LD; DePristo MA; Durbin RM; Handsaker RE; Kang HM; Marth GT; McVean GA
    Nature; 2012 Nov; 491(7422):56-65. PubMed ID: 23128226
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A map of human genome variation from population-scale sequencing.
    ; Abecasis GR; Altshuler D; Auton A; Brooks LD; Durbin RM; Gibbs RA; Hurles ME; McVean GA
    Nature; 2010 Oct; 467(7319):1061-73. PubMed ID: 20981092
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A global reference for human genetic variation.
    ; Auton A; Brooks LD; Durbin RM; Garrison EP; Kang HM; Korbel JO; Marchini JL; McCarthy S; McVean GA; Abecasis GR
    Nature; 2015 Oct; 526(7571):68-74. PubMed ID: 26432245
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An integrated map of structural variation in 2,504 human genomes.
    Sudmant PH; Rausch T; Gardner EJ; Handsaker RE; Abyzov A; Huddleston J; Zhang Y; Ye K; Jun G; Fritz MH; Konkel MK; Malhotra A; Stütz AM; Shi X; Casale FP; Chen J; Hormozdiari F; Dayama G; Chen K; Malig M; Chaisson MJP; Walter K; Meiers S; Kashin S; Garrison E; Auton A; Lam HYK; Mu XJ; Alkan C; Antaki D; Bae T; Cerveira E; Chines P; Chong Z; Clarke L; Dal E; Ding L; Emery S; Fan X; Gujral M; Kahveci F; Kidd JM; Kong Y; Lameijer EW; McCarthy S; Flicek P; Gibbs RA; Marth G; Mason CE; Menelaou A; Muzny DM; Nelson BJ; Noor A; Parrish NF; Pendleton M; Quitadamo A; Raeder B; Schadt EE; Romanovitch M; Schlattl A; Sebra R; Shabalin AA; Untergasser A; Walker JA; Wang M; Yu F; Zhang C; Zhang J; Zheng-Bradley X; Zhou W; Zichner T; Sebat J; Batzer MA; McCarroll SA; ; Mills RE; Gerstein MB; Bashir A; Stegle O; Devine SE; Lee C; Eichler EE; Korbel JO
    Nature; 2015 Oct; 526(7571):75-81. PubMed ID: 26432246
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The analysis of APOL1 genetic variation and haplotype diversity provided by 1000 Genomes project.
    Peng T; Wang L; Li G
    BMC Nephrol; 2017 Aug; 18(1):267. PubMed ID: 28800731
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping and characterization of structural variation in 17,795 human genomes.
    Abel HJ; Larson DE; Regier AA; Chiang C; Das I; Kanchi KL; Layer RM; Neale BM; Salerno WJ; Reeves C; Buyske S; ; Matise TC; Muzny DM; Zody MC; Lander ES; Dutcher SK; Stitziel NO; Hall IM
    Nature; 2020 Jul; 583(7814):83-89. PubMed ID: 32460305
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole-genome sequence variation, population structure and demographic history of the Dutch population.
    Genome of the Netherlands Consortium
    Nat Genet; 2014 Aug; 46(8):818-25. PubMed ID: 24974849
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A structural variation reference for medical and population genetics.
    Collins RL; Brand H; Karczewski KJ; Zhao X; Alföldi J; Francioli LC; Khera AV; Lowther C; Gauthier LD; Wang H; Watts NA; Solomonson M; O'Donnell-Luria A; Baumann A; Munshi R; Walker M; Whelan CW; Huang Y; Brookings T; Sharpe T; Stone MR; Valkanas E; Fu J; Tiao G; Laricchia KM; Ruano-Rubio V; Stevens C; Gupta N; Cusick C; Margolin L; ; ; Taylor KD; Lin HJ; Rich SS; Post WS; Chen YI; Rotter JI; Nusbaum C; Philippakis A; Lander E; Gabriel S; Neale BM; Kathiresan S; Daly MJ; Banks E; MacArthur DG; Talkowski ME
    Nature; 2020 May; 581(7809):444-451. PubMed ID: 32461652
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Small insertions and deletions (INDELs) in human genomes.
    Mullaney JM; Mills RE; Pittard WS; Devine SE
    Hum Mol Genet; 2010 Oct; 19(R2):R131-6. PubMed ID: 20858594
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mapping and sequencing of structural variation from eight human genomes.
    Kidd JM; Cooper GM; Donahue WF; Hayden HS; Sampas N; Graves T; Hansen N; Teague B; Alkan C; Antonacci F; Haugen E; Zerr T; Yamada NA; Tsang P; Newman TL; Tüzün E; Cheng Z; Ebling HM; Tusneem N; David R; Gillett W; Phelps KA; Weaver M; Saranga D; Brand A; Tao W; Gustafson E; McKernan K; Chen L; Malig M; Smith JD; Korn JM; McCarroll SA; Altshuler DA; Peiffer DA; Dorschner M; Stamatoyannopoulos J; Schwartz D; Nickerson DA; Mullikin JC; Wilson RK; Bruhn L; Olson MV; Kaul R; Smith DR; Eichler EE
    Nature; 2008 May; 453(7191):56-64. PubMed ID: 18451855
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations.
    Teo YY; Sim X; Ong RT; Tan AK; Chen J; Tantoso E; Small KS; Ku CS; Lee EJ; Seielstad M; Chia KS
    Genome Res; 2009 Nov; 19(11):2154-62. PubMed ID: 19700652
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The sequences of 150,119 genomes in the UK Biobank.
    Halldorsson BV; Eggertsson HP; Moore KHS; Hauswedell H; Eiriksson O; Ulfarsson MO; Palsson G; Hardarson MT; Oddsson A; Jensson BO; Kristmundsdottir S; Sigurpalsdottir BD; Stefansson OA; Beyter D; Holley G; Tragante V; Gylfason A; Olason PI; Zink F; Asgeirsdottir M; Sverrisson ST; Sigurdsson B; Gudjonsson SA; Sigurdsson GT; Halldorsson GH; Sveinbjornsson G; Norland K; Styrkarsdottir U; Magnusdottir DN; Snorradottir S; Kristinsson K; Sobech E; Jonsson H; Geirsson AJ; Olafsson I; Jonsson P; Pedersen OB; Erikstrup C; Brunak S; Ostrowski SR; ; Thorleifsson G; Jonsson F; Melsted P; Jonsdottir I; Rafnar T; Holm H; Stefansson H; Saemundsdottir J; Gudbjartsson DF; Magnusson OT; Masson G; Thorsteinsdottir U; Helgason A; Jonsson H; Sulem P; Stefansson K
    Nature; 2022 Jul; 607(7920):732-740. PubMed ID: 35859178
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of genomic variation in non-coding elements using population-scale sequencing data from the 1000 Genomes Project.
    Mu XJ; Lu ZJ; Kong Y; Lam HY; Gerstein MB
    Nucleic Acids Res; 2011 Sep; 39(16):7058-76. PubMed ID: 21596777
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The UK10K project identifies rare variants in health and disease.
    ; Walter K; Min JL; Huang J; Crooks L; Memari Y; McCarthy S; Perry JR; Xu C; Futema M; Lawson D; Iotchkova V; Schiffels S; Hendricks AE; Danecek P; Li R; Floyd J; Wain LV; Barroso I; Humphries SE; Hurles ME; Zeggini E; Barrett JC; Plagnol V; Richards JB; Greenwood CM; Timpson NJ; Durbin R; Soranzo N
    Nature; 2015 Oct; 526(7571):82-90. PubMed ID: 26367797
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Natural Selection and Functional Potentials of Human Noncoding Elements Revealed by Analysis of Next Generation Sequencing Data.
    Jha P; Lu D; Xu S
    PLoS One; 2015; 10(6):e0129023. PubMed ID: 26053627
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The genetic structure of the Turkish population reveals high levels of variation and admixture.
    Kars ME; Başak AN; Onat OE; Bilguvar K; Choi J; Itan Y; Çağlar C; Palvadeau R; Casanova JL; Cooper DN; Stenson PD; Yavuz A; Buluş H; Günel M; Friedman JM; Özçelik T
    Proc Natl Acad Sci U S A; 2021 Sep; 118(36):. PubMed ID: 34426522
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prioritizing sequence variants in conserved non-coding elements in the chicken genome using chCADD.
    Groß C; Bortoluzzi C; de Ridder D; Megens HJ; Groenen MAM; Reinders M; Bosse M
    PLoS Genet; 2020 Sep; 16(9):e1009027. PubMed ID: 32966296
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype, haplotype and copy-number variation in worldwide human populations.
    Jakobsson M; Scholz SW; Scheet P; Gibbs JR; VanLiere JM; Fung HC; Szpiech ZA; Degnan JH; Wang K; Guerreiro R; Bras JM; Schymick JC; Hernandez DG; Traynor BJ; Simon-Sanchez J; Matarin M; Britton A; van de Leemput J; Rafferty I; Bucan M; Cann HM; Hardy JA; Rosenberg NA; Singleton AB
    Nature; 2008 Feb; 451(7181):998-1003. PubMed ID: 18288195
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CYP3A variation and the evolution of salt-sensitivity variants.
    Thompson EE; Kuttab-Boulos H; Witonsky D; Yang L; Roe BA; Di Rienzo A
    Am J Hum Genet; 2004 Dec; 75(6):1059-69. PubMed ID: 15492926
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians.
    Shen H; Li J; Zhang J; Xu C; Jiang Y; Wu Z; Zhao F; Liao L; Chen J; Lin Y; Tian Q; Papasian CJ; Deng HW
    PLoS One; 2013; 8(4):e59494. PubMed ID: 23577066
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 318.