These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 29112749)

  • 1. PGG.Population: a database for understanding the genomic diversity and genetic ancestry of human populations.
    Zhang C; Gao Y; Liu J; Xue Z; Lu Y; Deng L; Tian L; Feng Q; Xu S
    Nucleic Acids Res; 2018 Jan; 46(D1):D984-D993. PubMed ID: 29112749
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PGG.Han: the Han Chinese genome database and analysis platform.
    Gao Y; Zhang C; Yuan L; Ling Y; Wang X; Liu C; Pan Y; Zhang X; Ma X; Wang Y; Lu Y; Yuan K; Ye W; Qian J; Chang H; Cao R; Yang X; Ma L; Ju Y; Dai L; Tang Y; ; Zhang G; Xu S
    Nucleic Acids Res; 2020 Jan; 48(D1):D971-D976. PubMed ID: 31584086
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.
    Zhang C; Gao Y; Ning Z; Lu Y; Zhang X; Liu J; Xie B; Xue Z; Wang X; Yuan K; Ge X; Pan Y; Liu C; Tian L; Wang Y; Lu D; Hoh BP; Xu S
    Genome Biol; 2019 Oct; 20(1):215. PubMed ID: 31640808
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PGG.SV: a whole-genome-sequencing-based structural variant resource and data analysis platform.
    Wang Y; Ling Y; Gong J; Zhao X; Zhou H; Xie B; Lou H; Zhuang X; Jin L; ; Fan S; Zhang G; Xu S
    Nucleic Acids Res; 2023 Jan; 51(D1):D1109-D1116. PubMed ID: 36243989
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Human genetic variation database, a reference database of genetic variations in the Japanese population.
    Higasa K; Miyake N; Yoshimura J; Okamura K; Niihori T; Saitsu H; Doi K; Shimizu M; Nakabayashi K; Aoki Y; Tsurusaki Y; Morishita S; Kawaguchi T; Migita O; Nakayama K; Nakashima M; Mitsui J; Narahara M; Hayashi K; Funayama R; Yamaguchi D; Ishiura H; Ko WY; Hata K; Nagashima T; Yamada R; Matsubara Y; Umezawa A; Tsuji S; Matsumoto N; Matsuda F
    J Hum Genet; 2016 Jun; 61(6):547-53. PubMed ID: 26911352
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome Variation Map: a data repository of genome variations in BIG Data Center.
    Song S; Tian D; Li C; Tang B; Dong L; Xiao J; Bao Y; Zhao W; He H; Zhang Z
    Nucleic Acids Res; 2018 Jan; 46(D1):D944-D949. PubMed ID: 29069473
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Iranome: A catalog of genomic variations in the Iranian population.
    Fattahi Z; Beheshtian M; Mohseni M; Poustchi H; Sellars E; Nezhadi SH; Amini A; Arzhangi S; Jalalvand K; Jamali P; Mohammadi Z; Davarnia B; Nikuei P; Oladnabi M; Mohammadzadeh A; Zohrehvand E; Nejatizadeh A; Shekari M; Bagherzadeh M; Shamsi-Gooshki E; Börno S; Timmermann B; Haghdoost A; Najafipour R; Khorram Khorshid HR; Kahrizi K; Malekzadeh R; Akbari MR; Najmabadi H
    Hum Mutat; 2019 Nov; 40(11):1968-1984. PubMed ID: 31343797
    [TBL] [Abstract][Full Text] [Related]  

  • 8. India Allele Finder: a web-based annotation tool for identifying common alleles in next-generation sequencing data of Indian origin.
    Zhang JF; James F; Shukla A; Girisha KM; Paciorkowski AR
    BMC Res Notes; 2017 Jun; 10(1):233. PubMed ID: 28655339
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PopHuman: the human population genomics browser.
    Casillas S; Mulet R; Villegas-Mirón P; Hervas S; Sanz E; Velasco D; Bertranpetit J; Laayouni H; Barbadilla A
    Nucleic Acids Res; 2018 Jan; 46(D1):D1003-D1010. PubMed ID: 29059408
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The humankind genome: from genetic diversity to the origin of human diseases.
    Belizário JE
    Genome; 2013 Dec; 56(12):705-16. PubMed ID: 24433206
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Progress in the detection of human genome structural variations.
    WU X; XIAO H
    Sci China C Life Sci; 2009 Jun; 52(6):560-7. PubMed ID: 19557334
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Demographic history and biologically relevant genetic variation of Native Mexicans inferred from whole-genome sequencing.
    Romero-Hidalgo S; Ochoa-Leyva A; Garcíarrubio A; Acuña-Alonzo V; Antúnez-Argüelles E; Balcazar-Quintero M; Barquera-Lozano R; Carnevale A; Cornejo-Granados F; Fernández-López JC; García-Herrera R; García-Ortíz H; Granados-Silvestre Á; Granados J; Guerrero-Romero F; Hernández-Lemus E; León-Mimila P; Macín-Pérez G; Martínez-Hernández A; Menjivar M; Morett E; Orozco L; Ortíz-López G; Pérez-Villatoro F; Rivera-Morales J; Riveros-McKay F; Villalobos-Comparán M; Villamil-Ramírez H; Villarreal-Molina T; Canizales-Quinteros S; Soberón X
    Nat Commun; 2017 Oct; 8(1):1005. PubMed ID: 29044207
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Increasing the reference populations for the 55 AISNP panel: the need and benefits.
    Pakstis AJ; Kang L; Liu L; Zhang Z; Jin T; Grigorenko EL; Wendt FR; Budowle B; Hadi S; Al Qahtani MS; Morling N; Mogensen HS; Themudo GE; Soundararajan U; Rajeevan H; Kidd JR; Kidd KK
    Int J Legal Med; 2017 Jul; 131(4):913-917. PubMed ID: 28070634
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Massively parallel sequencing of 165 ancestry informative SNPs in two Chinese Tibetan-Burmese minority ethnicities.
    Wang Z; He G; Luo T; Zhao X; Liu J; Wang M; Zhou D; Chen X; Li C; Hou Y
    Forensic Sci Int Genet; 2018 May; 34():141-147. PubMed ID: 29477877
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Population-ethnic group specific genome variation allele frequency data: a querying and visualization journey.
    Viennas E; Gkantouna V; Ioannou M; Georgitsi M; Rigou M; Poulas K; Patrinos GP; Tzimas G
    Genomics; 2012 Aug; 100(2):93-101. PubMed ID: 22659238
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ancestry patterns inferred from massive RNA-seq data.
    Barral-Arca R; Pardo-Seco J; Bello X; Martinón-Torres F; Salas A
    RNA; 2019 Jul; 25(7):857-868. PubMed ID: 31010885
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Finnish disease heritage database (FinDis) update-a database for the genes mutated in the Finnish disease heritage brought to the next-generation sequencing era.
    Polvi A; Linturi H; Varilo T; Anttonen AK; Byrne M; Fokkema IF; Almusa H; Metzidis A; Avela K; Aula P; Kestilä M; Muilu J
    Hum Mutat; 2013 Nov; 34(11):1458-66. PubMed ID: 23904198
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genomic resources and their influence on the detection of the signal of positive selection in genome scans.
    Manel S; Perrier C; Pratlong M; Abi-Rached L; Paganini J; Pontarotti P; Aurelle D
    Mol Ecol; 2016 Jan; 25(1):170-84. PubMed ID: 26562485
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.
    Patrinos GP; Giardine B; Riemer C; Miller W; Chui DH; Anagnou NP; Wajcman H; Hardison RC
    Nucleic Acids Res; 2004 Jan; 32(Database issue):D537-41. PubMed ID: 14681476
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.