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 *

79 related articles for article (PubMed ID: 29456248)

  • 41. Application of the C4'-alkylated deoxyribose primer system (CAPS) in allele-specific real-time PCR for increased selectivity in discrimination of single nucleotide sequence variants.
    Tews B; Wilhelm J; Summerer D; Strerath M; Marx A; Friedhoff P; Pingoud A; Hahn M
    Biol Chem; 2003; 384(10-11):1533-41. PubMed ID: 14669997
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders.
    Brown R; Lee H; Eskin A; Kichaev G; Lohmueller KE; Reversade B; Nelson SF; Pasaniuc B
    Eur J Hum Genet; 2016 Jan; 24(1):113-9. PubMed ID: 25898925
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The challenge of using SNPs in the understanding and treatment of disease.
    Schifreen RS; Storts DR; Buller AM
    Biotechniques; 2002 Jun; Suppl():14-6, 18, 20-1. PubMed ID: 12083392
    [No Abstract]   [Full Text] [Related]  

  • 44. GeneScreen: a program for high-throughput mutation detection in DNA sequence electropherograms.
    Carr IM; Camm N; Taylor GR; Charlton R; Ellard S; Sheridan EG; Markham AF; Bonthron DT
    J Med Genet; 2011 Feb; 48(2):123-30. PubMed ID: 21037276
    [TBL] [Abstract][Full Text] [Related]  

  • 45. HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations.
    Gu S; Pakstis AJ; Kidd KK
    Bioinformatics; 2005 Oct; 21(20):3938-9. PubMed ID: 16131520
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Allelic variants of human melatonin 1A receptor in patients with familial adolescent idiopathic scoliosis.
    Morcuende JA; Minhas R; Dolan L; Stevens J; Beck J; Wang K; Weinstein SL; Sheffield V
    Spine (Phila Pa 1976); 2003 Sep; 28(17):2025-8; discussion 2029. PubMed ID: 12973153
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Case Report Identification of a novel SLC45A2 mutation in albinism by targeted next-generation sequencing.
    Xue JJ; Xue JF; Xue HQ; Guo YY; Liu Y; Ouyang N
    Genet Mol Res; 2016 Sep; 15(3):. PubMed ID: 27706749
    [TBL] [Abstract][Full Text] [Related]  

  • 48. mtDNA Variation and Analysis Using Mitomap and Mitomaster.
    Lott MT; Leipzig JN; Derbeneva O; Xie HM; Chalkia D; Sarmady M; Procaccio V; Wallace DC
    Curr Protoc Bioinformatics; 2013 Dec; 44(123):1.23.1-26. PubMed ID: 25489354
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Genetic and genomic stability across lymphoblastoid cell line expansions.
    Scheinfeldt LB; Hodges K; Pevsner J; Berlin D; Turan N; Gerry NP
    BMC Res Notes; 2018 Aug; 11(1):558. PubMed ID: 30075799
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Calling known variants and identifying new variants while rapidly aligning sequence data.
    VanRaden PM; Bickhart DM; O'Connell JR
    J Dairy Sci; 2019 Apr; 102(4):3216-3229. PubMed ID: 30772032
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Massively parallel single-nucleotide mutagenesis using reversibly terminated inosine.
    Haller G; Alvarado D; McCall K; Mitra RD; Dobbs MB; Gurnett CA
    Nat Methods; 2016 Nov; 13(11):923-924. PubMed ID: 27694911
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Statistical power for identifying nucleotide markers associated with quantitative traits in genome-wide association analysis using a mixed model.
    Shin J; Lee C
    Genomics; 2015 Jan; 105(1):1-4. PubMed ID: 25451740
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
    Babatz TD; Kumar RA; Sudi J; Dobyns WB; Christian SL
    Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [The human genetic variability map, single nucleotide polymorphisms (SNP's) and some of their applications to medicine].
    Tusié Luna MT
    Rev Invest Clin; 2001; 53(4):308-10. PubMed ID: 11599476
    [No Abstract]   [Full Text] [Related]  

  • 55. [Genetic variation with increased risk of schizophrenia].
    Bakker SC; Kahn RS; Ophoff RA
    Ned Tijdschr Geneeskd; 2010; 154():A1909. PubMed ID: 20977796
    [TBL] [Abstract][Full Text] [Related]  

  • 56. dbSNP-database for single nucleotide polymorphisms and other classes of minor genetic variation.
    Sherry ST; Ward M; Sirotkin K
    Genome Res; 1999 Aug; 9(8):677-9. PubMed ID: 10447503
    [No Abstract]   [Full Text] [Related]  

  • 57. Prevalence of Titin Truncating Variants in General Population.
    Akinrinade O; Koskenvuo JW; Alastalo TP
    PLoS One; 2015; 10(12):e0145284. PubMed ID: 26701604
    [TBL] [Abstract][Full Text] [Related]  

  • 58. What happens if you pose the wrong questions?
    Timmons JA
    J Physiol; 2011 Oct; 589(Pt 19):4799-801; author reply 4803. PubMed ID: 21965633
    [No Abstract]   [Full Text] [Related]  

  • 59. Tales from the crypt(ic).
    Lee JA; Marx CJ
    Science; 2019 Jul; 365(6451):318-319. PubMed ID: 31346051
    [No Abstract]   [Full Text] [Related]  

  • 60. sscNOVA: a semi-supervised convolutional neural network for predicting functional regulatory variants in autoimmune diseases.
    Li H; Yu Z; Du F; Song L; Gao Y; Shi F
    Front Immunol; 2024; 15():1323072. PubMed ID: 38380333
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.