BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 26224010)

  • 1. Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing.
    Ji X; Liang D; Sun R; Liu C; Ma D; Wang Y; Hu P; Xu Z
    BMC Med Genet; 2015 Jul; 16():57. PubMed ID: 26224010
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Breakpoints and deleted genes identification of ring chromosome 18 in a Chinese girl by whole-genome low-coverage sequencing: a case report study.
    Yao H; Yang C; Huang X; Yang L; Zhao W; Yin D; Qin Y; Mu F; Liu L; Tian P; Liu Z; Yang Y
    BMC Med Genet; 2016 Jul; 17(1):49. PubMed ID: 27448395
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency and/or congenital malformations.
    Schluth-Bolard C; Labalme A; Cordier MP; Till M; Nadeau G; Tevissen H; Lesca G; Boutry-Kryza N; Rossignol S; Rocas D; Dubruc E; Edery P; Sanlaville D
    J Med Genet; 2013 Mar; 50(3):144-50. PubMed ID: 23315544
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome.
    Korbel JO; Urban AE; Grubert F; Du J; Royce TE; Starr P; Zhong G; Emanuel BS; Weissman SM; Snyder M; Gerstein MB
    Proc Natl Acad Sci U S A; 2007 Jun; 104(24):10110-5. PubMed ID: 17551006
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors.
    Trombetta D; Mertens F; Lonoce A; D'Addabbo P; Rennstam K; Mandahl N; Storlazzi CT
    Genes Chromosomes Cancer; 2009 Nov; 48(11):993-1001. PubMed ID: 19691106
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations.
    Liang D; Wang Y; Ji X; Hu H; Zhang J; Meng L; Lin Y; Ma D; Jiang T; Jiang H; Asan ; Song L; Guo J; Hu P; Xu Z
    Clin Genet; 2017 Apr; 91(4):605-610. PubMed ID: 27491356
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Whole Genome Low-Coverage Sequencing Concurrently Detecting Copy Number Variations and Their Underlying Complex Chromosomal Rearrangements by Systematic Breakpoint Mapping in Intellectual Deficiency/Developmental Delay Patients.
    Xiao B; Ye X; Wang L; Fan Y; Gu X; Ji X; Sun Y; Yu Y
    Front Genet; 2020; 11():616. PubMed ID: 32733533
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints.
    Newman S; Hermetz KE; Weckselblatt B; Rudd MK
    Am J Hum Genet; 2015 Feb; 96(2):208-20. PubMed ID: 25640679
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosomal breakpoints characterization of two supernumerary ring chromosomes 20.
    Guediche N; Brisset S; Benichou JJ; Guérin N; Mabboux P; Maurin ML; Bas C; Laroudie M; Picone O; Goldszmidt D; Prévot S; Labrune P; Tachdjian G
    Am J Med Genet A; 2010 Feb; 152A(2):464-71. PubMed ID: 20101685
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of variations and identifying genomic breakpoints for large deletions in the LDLR by Ion Torrent semiconductor sequencing.
    Faiz F; Allcock RJ; Hooper AJ; van Bockxmeer FM
    Atherosclerosis; 2013 Oct; 230(2):249-55. PubMed ID: 24075752
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes.
    Liang D; Peng Y; Lv W; Deng L; Zhang Y; Li H; Yang P; Zhang J; Song Z; Xu G; Cram DS; Wu L
    J Mol Diagn; 2014 Sep; 16(5):519-526. PubMed ID: 24998187
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exploring the tertiary gene pool of bread wheat: sequence assembly and analysis of chromosome 5M(g) of Aegilops geniculata.
    Tiwari VK; Wang S; Danilova T; Koo DH; Vrána J; Kubaláková M; Hribova E; Rawat N; Kalia B; Singh N; Friebe B; Doležel J; Akhunov E; Poland J; Sabir JS; Gill BS
    Plant J; 2015 Nov; 84(4):733-46. PubMed ID: 26408103
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mapping Breakpoints of Complex Chromosome Rearrangements Involving a Partial Trisomy 15q23.1-q26.2 Revealed by Next Generation Sequencing and Conventional Techniques.
    Pan Q; Hu H; Han L; Jing X; Liu H; Yang C; Zhang F; Hu Y; Yue H; Ning Y
    PLoS One; 2016; 11(5):e0154574. PubMed ID: 27218255
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Next-generation sequencing as a tool for breakpoint analysis in rearrangements of the globin gene clusters.
    Clark BE; Shooter C; Smith F; Brawand D; Thein SL
    Int J Lab Hematol; 2017 May; 39 Suppl 1():111-120. PubMed ID: 28447426
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
    Vincent JB; Choufani S; Horike S; Stachowiak B; Li M; Dill FJ; Marshall C; Hrynchak M; Pewsey E; Ukadike KC; Friedman JM; Srivastava AK; Scherer SW
    Psychiatr Genet; 2008 Jun; 18(3):101-9. PubMed ID: 18496206
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Development of chromosomal markers based on next-generation sequencing: the B chromosome of the cichlid fish Astatotilapia latifasciata as a model.
    Fantinatti BE; Martins C
    BMC Genet; 2016 Aug; 17(1):119. PubMed ID: 27539214
    [TBL] [Abstract][Full Text] [Related]  

  • 17. SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq).
    Johnson SH; Smadbeck JB; Smoley SA; Gaitatzes A; Murphy SJ; Harris FR; Drucker TM; Zenka RM; Pitel BA; Rowsey RA; Hoppman NL; Aypar U; Sukov WR; Jenkins RB; Feldman AL; Kearney HM; Vasmatzis G
    Cancer Genet; 2018 Feb; 221():1-18. PubMed ID: 29405991
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencing.
    Sobreira NL; Gnanakkan V; Walsh M; Marosy B; Wohler E; Thomas G; Hoover-Fong JE; Hamosh A; Wheelan SJ; Valle D
    Genome Res; 2011 Oct; 21(10):1720-7. PubMed ID: 21890680
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Male with mosaicism for supernumerary ring X chromosome: analysis of phenotype and characterization of genotype using array comparative genome hybridization.
    Baker PR; Tsai AC; Springer M; Swisshelm K; March J; Brown K; Bellus G
    J Craniofac Surg; 2010 Sep; 21(5):1369-75. PubMed ID: 20856023
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Analysis of genomic copy number variations in 36 fetuses with heart malformations using next-generation sequencing].
    Gao M; Pang H; Zhao Y; Li-Ling J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):524-527. PubMed ID: 28777851
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.