BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

248 related articles for article (PubMed ID: 20972442)

  • 1. Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing.
    Fujimoto A; Nakagawa H; Hosono N; Nakano K; Abe T; Boroevich KA; Nagasaki M; Yamaguchi R; Shibuya T; Kubo M; Miyano S; Nakamura Y; Tsunoda T
    Nat Genet; 2010 Nov; 42(11):931-6. PubMed ID: 20972442
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly.
    Li Y; Zheng H; Luo R; Wu H; Zhu H; Li R; Cao H; Wu B; Huang S; Shao H; Ma H; Zhang F; Feng S; Zhang W; Du H; Tian G; Li J; Zhang X; Li S; Bolund L; Kristiansen K; de Smith AJ; Blakemore AI; Coin LJ; Yang H; Wang J; Wang J
    Nat Biotechnol; 2011 Jul; 29(8):723-30. PubMed ID: 21785424
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals.
    Nagasaki M; Yasuda J; Katsuoka F; Nariai N; Kojima K; Kawai Y; Yamaguchi-Kabata Y; Yokozawa J; Danjoh I; Saito S; Sato Y; Mimori T; Tsuda K; Saito R; Pan X; Nishikawa S; Ito S; Kuroki Y; Tanabe O; Fuse N; Kuriyama S; Kiyomoto H; Hozawa A; Minegishi N; Douglas Engel J; Kinoshita K; Kure S; Yaegashi N; ; Yamamoto M
    Nat Commun; 2015 Aug; 6():8018. PubMed ID: 26292667
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Whole genome sequence of a Turkish individual.
    Dogan H; Can H; Otu HH
    PLoS One; 2014; 9(1):e85233. PubMed ID: 24416366
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo assembly of a haplotype-resolved human genome.
    Cao H; Wu H; Luo R; Huang S; Sun Y; Tong X; Xie Y; Liu B; Yang H; Zheng H; Li J; Li B; Wang Y; Yang F; Sun P; Liu S; Gao P; Huang H; Sun J; Chen D; He G; Huang W; Huang Z; Li Y; Tellier LC; Liu X; Feng Q; Xu X; Zhang X; Bolund L; Krogh A; Kristiansen K; Drmanac R; Drmanac S; Nielsen R; Li S; Wang J; Yang H; Li Y; Wong GK; Wang J
    Nat Biotechnol; 2015 Jun; 33(6):617-22. PubMed ID: 26006006
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole Genome Analyses of Chinese Population and De Novo Assembly of A Northern Han Genome.
    Du Z; Ma L; Qu H; Chen W; Zhang B; Lu X; Zhai W; Sheng X; Sun Y; Li W; Lei M; Qi Q; Yuan N; Shi S; Zeng J; Wang J; Yang Y; Liu Q; Hong Y; Dong L; Zhang Z; Zou D; Wang Y; Song S; Liu F; Fang X; Chen H; Liu X; Xiao J; Zeng C
    Genomics Proteomics Bioinformatics; 2019 Jun; 17(3):229-247. PubMed ID: 31494266
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole genome sequencing of 35 individuals provides insights into the genetic architecture of Korean population.
    Zhang W; Meehan J; Su Z; Ng HW; Shu M; Luo H; Ge W; Perkins R; Tong W; Hong H
    BMC Bioinformatics; 2014; 15 Suppl 11(Suppl 11):S6. PubMed ID: 25350283
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Precise detection of de novo single nucleotide variants in human genomes.
    Gómez-Romero L; Palacios-Flores K; Reyes J; García D; Boege M; Dávila G; Flores M; Schatz MC; Palacios R
    Proc Natl Acad Sci U S A; 2018 May; 115(21):5516-5521. PubMed ID: 29735690
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Complete genome sequencing and variant analysis of a Pakistani individual.
    Azim MK; Yang C; Yan Z; Choudhary MI; Khan A; Sun X; Li R; Asif H; Sharif S; Zhang Y
    J Hum Genet; 2013 Sep; 58(9):622-6. PubMed ID: 23842039
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Haplotype-resolved genome sequencing of a Gujarati Indian individual.
    Kitzman JO; Mackenzie AP; Adey A; Hiatt JB; Patwardhan RP; Sudmant PH; Ng SB; Alkan C; Qiu R; Eichler EE; Shendure J
    Nat Biotechnol; 2011 Jan; 29(1):59-63. PubMed ID: 21170042
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The diploid genome sequence of an Asian individual.
    Wang J; Wang W; Li R; Li Y; Tian G; Goodman L; Fan W; Zhang J; Li J; Zhang J; Guo Y; Feng B; Li H; Lu Y; Fang X; Liang H; Du Z; Li D; Zhao Y; Hu Y; Yang Z; Zheng H; Hellmann I; Inouye M; Pool J; Yi X; Zhao J; Duan J; Zhou Y; Qin J; Ma L; Li G; Yang Z; Zhang G; Yang B; Yu C; Liang F; Li W; Li S; Li D; Ni P; Ruan J; Li Q; Zhu H; Liu D; Lu Z; Li N; Guo G; Zhang J; Ye J; Fang L; Hao Q; Chen Q; Liang Y; Su Y; San A; Ping C; Yang S; Chen F; Li L; Zhou K; Zheng H; Ren Y; Yang L; Gao Y; Yang G; Li Z; Feng X; Kristiansen K; Wong GK; Nielsen R; Durbin R; Bolund L; Zhang X; Li S; Yang H; Wang J
    Nature; 2008 Nov; 456(7218):60-5. PubMed ID: 18987735
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo assembly and phasing of a Korean human genome.
    Seo JS; Rhie A; Kim J; Lee S; Sohn MH; Kim CU; Hastie A; Cao H; Yun JY; Kim J; Kuk J; Park GH; Kim J; Ryu H; Kim J; Roh M; Baek J; Hunkapiller MW; Korlach J; Shin JY; Kim C
    Nature; 2016 Oct; 538(7624):243-247. PubMed ID: 27706134
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sequencing and analysis of a South Asian-Indian personal genome.
    Gupta R; Ratan A; Rajesh C; Chen R; Kim HL; Burhans R; Miller W; Santhosh S; Davuluri RV; Butte AJ; Schuster SC; Seshagiri S; Thomas G
    BMC Genomics; 2012 Aug; 13():440. PubMed ID: 22938532
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deep whole-genome sequencing of 90 Han Chinese genomes.
    Lan T; Lin H; Zhu W; Laurent TCAM; Yang M; Liu X; Wang J; Wang J; Yang H; Xu X; Guo X
    Gigascience; 2017 Sep; 6(9):1-7. PubMed ID: 28938720
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole-genome sequencing and variant discovery in C. elegans.
    Hillier LW; Marth GT; Quinlan AR; Dooling D; Fewell G; Barnett D; Fox P; Glasscock JI; Hickenbotham M; Huang W; Magrini VJ; Richt RJ; Sander SN; Stewart DA; Stromberg M; Tsung EF; Wylie T; Schedl T; Wilson RK; Mardis ER
    Nat Methods; 2008 Feb; 5(2):183-8. PubMed ID: 18204455
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Misassembly of long reads undermines de novo-assembled ethnicity-specific genomes: validation in a Chinese Han population.
    Mai Z; Liu W; Ding W; Zhang G
    Hum Genet; 2019 Jul; 138(7):757-769. PubMed ID: 31168775
    [TBL] [Abstract][Full Text] [Related]  

  • 17. From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability.
    Lindstrand A; Eisfeldt J; Pettersson M; Carvalho CMB; Kvarnung M; Grigelioniene G; Anderlid BM; Bjerin O; Gustavsson P; Hammarsjö A; Georgii-Hemming P; Iwarsson E; Johansson-Soller M; Lagerstedt-Robinson K; Lieden A; Magnusson M; Martin M; Malmgren H; Nordenskjöld M; Norling A; Sahlin E; Stranneheim H; Tham E; Wincent J; Ygberg S; Wedell A; Wirta V; Nordgren A; Lundin J; Nilsson D
    Genome Med; 2019 Nov; 11(1):68. PubMed ID: 31694722
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comparative analysis of de novo assemblers for variation discovery in personal genomes.
    Tian S; Yan H; Klee EW; Kalmbach M; Slager SL
    Brief Bioinform; 2018 Sep; 19(5):893-904. PubMed ID: 28407084
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole-genome sequencing and genetic variant analysis of a Quarter Horse mare.
    Doan R; Cohen ND; Sawyer J; Ghaffari N; Johnson CD; Dindot SV
    BMC Genomics; 2012 Feb; 13():78. PubMed ID: 22340285
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic variation and the de novo assembly of human genomes.
    Chaisson MJ; Wilson RK; Eichler EE
    Nat Rev Genet; 2015 Nov; 16(11):627-40. PubMed ID: 26442640
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.