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 *

109 related articles for article (PubMed ID: 19949697)

  • 41. Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing.
    Wang W; Shen P; Thiyagarajan S; Lin S; Palm C; Horvath R; Klopstock T; Cutler D; Pique L; Schrijver I; Davis RW; Mindrinos M; Speed TP; Scharfe C
    Nucleic Acids Res; 2011 Jan; 39(1):44-58. PubMed ID: 20843780
    [TBL] [Abstract][Full Text] [Related]  

  • 42. High-throughput resequencing in the diagnosis of BRCA1/2 mutations using oligonucleotide resequencing microarrays.
    Schroeder C; Stutzmann F; Weber BH; Riess O; Bonin M
    Breast Cancer Res Treat; 2010 Jul; 122(1):287-97. PubMed ID: 19941162
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Low density DNA microarray for detection of most frequent TP53 missense point mutations.
    Rangel-López A; Maldonado-Rodríguez R; Salcedo-Vargas M; Espinosa-Lara JM; Méndez-Tenorio A; Beattie KL
    BMC Biotechnol; 2005 Feb; 5():8. PubMed ID: 15713227
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding.
    McKernan KJ; Peckham HE; Costa GL; McLaughlin SF; Fu Y; Tsung EF; Clouser CR; Duncan C; Ichikawa JK; Lee CC; Zhang Z; Ranade SS; Dimalanta ET; Hyland FC; Sokolsky TD; Zhang L; Sheridan A; Fu H; Hendrickson CL; Li B; Kotler L; Stuart JR; Malek JA; Manning JM; Antipova AA; Perez DS; Moore MP; Hayashibara KC; Lyons MR; Beaudoin RE; Coleman BE; Laptewicz MW; Sannicandro AE; Rhodes MD; Gottimukkala RK; Yang S; Bafna V; Bashir A; MacBride A; Alkan C; Kidd JM; Eichler EE; Reese MG; De La Vega FM; Blanchard AP
    Genome Res; 2009 Sep; 19(9):1527-41. PubMed ID: 19546169
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Enabling large-scale pharmacogenetic studies by high-throughput mutation detection and genotyping technologies.
    Shi MM
    Clin Chem; 2001 Feb; 47(2):164-72. PubMed ID: 11159763
    [TBL] [Abstract][Full Text] [Related]  

  • 46. The functional spectrum of low-frequency coding variation.
    Marth GT; Yu F; Indap AR; Garimella K; Gravel S; Leong WF; Tyler-Smith C; Bainbridge M; Blackwell T; Zheng-Bradley X; Chen Y; Challis D; Clarke L; Ball EV; Cibulskis K; Cooper DN; Fulton B; Hartl C; Koboldt D; Muzny D; Smith R; Sougnez C; Stewart C; Ward A; Yu J; Xue Y; Altshuler D; Bustamante CD; Clark AG; Daly M; DePristo M; Flicek P; Gabriel S; Mardis E; Palotie A; Gibbs R;
    Genome Biol; 2011 Sep; 12(9):R84. PubMed ID: 21917140
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Multigene amplification and massively parallel sequencing for cancer mutation discovery.
    Dahl F; Stenberg J; Fredriksson S; Welch K; Zhang M; Nilsson M; Bicknell D; Bodmer WF; Davis RW; Ji H
    Proc Natl Acad Sci U S A; 2007 May; 104(22):9387-92. PubMed ID: 17517648
    [TBL] [Abstract][Full Text] [Related]  

  • 48. SNP and mutation analysis.
    Wang L; Luhm R; Lei M
    Adv Exp Med Biol; 2007; 593():105-16. PubMed ID: 17265721
    [TBL] [Abstract][Full Text] [Related]  

  • 49. SNP discovery in candidate adaptive genes using exon capture in a free-ranging alpine ungulate.
    Roffler GH; Amish SJ; Smith S; Cosart T; Kardos M; Schwartz MK; Luikart G
    Mol Ecol Resour; 2016 Sep; 16(5):1147-64. PubMed ID: 27327375
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Evaluation of oligonucleotide sequence capture arrays and comparison of next-generation sequencing platforms for use in molecular diagnostics.
    Hoppman-Chaney N; Peterson LM; Klee EW; Middha S; Courteau LK; Ferber MJ
    Clin Chem; 2010 Aug; 56(8):1297-306. PubMed ID: 20562348
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A massively parallel strategy for STR marker development, capture, and genotyping.
    Kistler L; Johnson SM; Irwin MT; Louis EE; Ratan A; Perry GH
    Nucleic Acids Res; 2017 Sep; 45(15):e142. PubMed ID: 28666376
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Targeted multiplex next-generation sequencing: advances in techniques of mitochondrial and nuclear DNA sequencing for population genomics.
    Hancock-Hanser BL; Frey A; Leslie MS; Dutton PH; Archer FI; Morin PA
    Mol Ecol Resour; 2013 Mar; 13(2):254-68. PubMed ID: 23351075
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Self-custom-made SFP arrays for nonmodel organisms.
    Ophir R; Sherman A
    Methods Mol Biol; 2012; 815():39-47. PubMed ID: 22130982
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Accurate detection and genotyping of SNPs utilizing population sequencing data.
    Bansal V; Harismendy O; Tewhey R; Murray SS; Schork NJ; Topol EJ; Frazer KA
    Genome Res; 2010 Apr; 20(4):537-45. PubMed ID: 20150320
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Massively parallel sequencing: the next big thing in genetic medicine.
    Tucker T; Marra M; Friedman JM
    Am J Hum Genet; 2009 Aug; 85(2):142-54. PubMed ID: 19679224
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing.
    Summerer D; Wu H; Haase B; Cheng Y; Schracke N; Stähler CF; Chee MS; Stähler PF; Beier M
    Genome Res; 2009 Sep; 19(9):1616-21. PubMed ID: 19638418
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data.
    Carr IM; Morgan J; Watson C; Melnik S; Diggle CP; Logan CV; Harrison SM; Taylor GR; Pena SD; Markham AF; Alkuraya FS; Black GC; Ali M; Bonthron DT
    Hum Mutat; 2013 Jul; 34(7):945-52. PubMed ID: 23554237
    [TBL] [Abstract][Full Text] [Related]  

  • 58. DNA sequence capture and enrichment by microarray followed by next-generation sequencing for targeted resequencing: neurofibromatosis type 1 gene as a model.
    Chou LS; Liu CS; Boese B; Zhang X; Mao R
    Clin Chem; 2010 Jan; 56(1):62-72. PubMed ID: 19910506
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Microarray-based DNA resequencing using 3' blocked primers.
    Sram J; Sommer SS; Liu Q
    Anal Biochem; 2008 Mar; 374(1):41-7. PubMed ID: 18023400
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Array-based genomic resequencing of human leukemia.
    Yamashita Y; Yuan J; Suetake I; Suzuki H; Ishikawa Y; Choi YL; Ueno T; Soda M; Hamada T; Haruta H; Takada S; Miyazaki Y; Kiyoi H; Ito E; Naoe T; Tomonaga M; Toyota M; Tajima S; Iwama A; Mano H
    Oncogene; 2010 Jun; 29(25):3723-31. PubMed ID: 20400977
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.