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 *

313 related articles for article (PubMed ID: 22353194)

  • 21. Large-scale detection of rare variants via pooled multiplexed next-generation sequencing: towards next-generation Ecotilling.
    Marroni F; Pinosio S; Di Centa E; Jurman I; Boerjan W; Felice N; Cattonaro F; Morgante M
    Plant J; 2011 Aug; 67(4):736-45. PubMed ID: 21554453
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The complete genome of an individual by massively parallel DNA sequencing.
    Wheeler DA; Srinivasan M; Egholm M; Shen Y; Chen L; McGuire A; He W; Chen YJ; Makhijani V; Roth GT; Gomes X; Tartaro K; Niazi F; Turcotte CL; Irzyk GP; Lupski JR; Chinault C; Song XZ; Liu Y; Yuan Y; Nazareth L; Qin X; Muzny DM; Margulies M; Weinstock GM; Gibbs RA; Rothberg JM
    Nature; 2008 Apr; 452(7189):872-6. PubMed ID: 18421352
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Exome Sequencing of Familial Bipolar Disorder.
    Goes FS; Pirooznia M; Parla JS; Kramer M; Ghiban E; Mavruk S; Chen YC; Monson ET; Willour VL; Karchin R; Flickinger M; Locke AE; Levy SE; Scott LJ; Boehnke M; Stahl E; Moran JL; Hultman CM; Landén M; Purcell SM; Sklar P; Zandi PP; McCombie WR; Potash JB
    JAMA Psychiatry; 2016 Jun; 73(6):590-7. PubMed ID: 27120077
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Effective variant detection by targeted deep sequencing of DNA pools: an example from Parkinson's disease.
    Pihlstrøm L; Rengmark A; Bjørnarå KA; Toft M
    Ann Hum Genet; 2014 May; 78(3):243-52. PubMed ID: 24660942
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Analysis of pathogenic variants from the ClinVar database in healthy people using next-generation sequencing.
    Rančelis T; Arasimavičius J; Ambrozaitytė L; Kavaliauskienė I; Domarkienė I; Karčiauskaitė D; Kučinskienė ZA; Kučinskas V
    Genet Res (Camb); 2017 Aug; 99():e6. PubMed ID: 28851476
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Targeted capture and massively parallel sequencing of 12 human exomes.
    Ng SB; Turner EH; Robertson PD; Flygare SD; Bigham AW; Lee C; Shaffer T; Wong M; Bhattacharjee A; Eichler EE; Bamshad M; Nickerson DA; Shendure J
    Nature; 2009 Sep; 461(7261):272-6. PubMed ID: 19684571
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study.
    Hawi Z; Cummins TD; Tong J; Arcos-Burgos M; Zhao Q; Matthews N; Newman DP; Johnson B; Vance A; Heussler HS; Levy F; Easteal S; Wray NR; Kenny E; Morris D; Kent L; Gill M; Bellgrove MA
    Mol Psychiatry; 2017 Apr; 22(4):580-584. PubMed ID: 27457811
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing.
    Ramos E; Levinson BT; Chasnoff S; Hughes A; Young AL; Thornton K; Li A; Vallania FL; Province M; Druley TE
    BMC Genomics; 2012 Dec; 13():683. PubMed ID: 23216810
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverage.
    Jansen S; Aigner B; Pausch H; Wysocki M; Eck S; Benet-Pagès A; Graf E; Wieland T; Strom TM; Meitinger T; Fries R
    BMC Genomics; 2013 Jul; 14():446. PubMed ID: 23826801
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Validation of OncoPanel: A Targeted Next-Generation Sequencing Assay for the Detection of Somatic Variants in Cancer.
    Garcia EP; Minkovsky A; Jia Y; Ducar MD; Shivdasani P; Gong X; Ligon AH; Sholl LM; Kuo FC; MacConaill LE; Lindeman NI; Dong F
    Arch Pathol Lab Med; 2017 Jun; 141(6):751-758. PubMed ID: 28557599
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
    Waldmüller S; Schroeder C; Sturm M; Scheffold T; Imbrich K; Junker S; Frische C; Hofbeck M; Bauer P; Bonin M; Gawaz M; Gramlich M
    Mol Cell Probes; 2015 Oct; 29(5):308-14. PubMed ID: 25979592
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Preparing a re-sequencing DNA library of 2 cancer candidate genes using the ligation-by-amplification protocol by two PCR reactions.
    Su Y; Lin L; Tian G; Chen C; Liu T; Xu X; Qi X; Zhang X; Yang H
    Sci China C Life Sci; 2009 May; 52(5):483-91. PubMed ID: 19471873
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders.
    Cheung YH; Wang G; Leal SM; Wang S
    Genet Epidemiol; 2012 Nov; 36(7):675-85. PubMed ID: 22865616
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Detection of rare genomic variants from pooled sequencing using SPLINTER.
    Vallania F; Ramos E; Cresci S; Mitra RD; Druley TE
    J Vis Exp; 2012 Jun; (64):. PubMed ID: 22760212
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma.
    Campbell CD; Mohajeri K; Malig M; Hormozdiari F; Nelson B; Du G; Patterson KM; Eng C; Torgerson DG; Hu D; Herman C; Chong JX; Ko A; O'Roak BJ; Krumm N; Vives L; Lee C; Roth LA; Rodriguez-Cintron W; Rodriguez-Santana J; Brigino-Buenaventura E; Davis A; Meade K; LeNoir MA; Thyne S; Jackson DJ; Gern JE; Lemanske RF; Shendure J; Abney M; Burchard EG; Ober C; Eichler EE
    PLoS One; 2014; 9(8):e104396. PubMed ID: 25116239
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Introduction to deep sequencing and its application to drug addiction research with a focus on rare variants.
    Wang S; Yang Z; Ma JZ; Payne TJ; Li MD
    Mol Neurobiol; 2014 Feb; 49(1):601-14. PubMed ID: 23990377
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Characterization of ADME gene variation in 21 populations by exome sequencing.
    Hovelson DH; Xue Z; Zawistowski M; Ehm MG; Harris EC; Stocker SL; Gross AS; Jang IJ; Ieiri I; Lee JE; Cardon LR; Chissoe SL; Abecasis G; Nelson MR
    Pharmacogenet Genomics; 2017 Mar; 27(3):89-100. PubMed ID: 27984508
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A statistical method for the detection of variants from next-generation resequencing of DNA pools.
    Bansal V
    Bioinformatics; 2010 Jun; 26(12):i318-24. PubMed ID: 20529923
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.