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 *

241 related articles for article (PubMed ID: 25827348)

  • 21. Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation.
    Hayes JL; Tzika A; Thygesen H; Berri S; Wood HM; Hewitt S; Pendlebury M; Coates A; Willoughby L; Watson CM; Rabbitts P; Roberts P; Taylor GR
    Genomics; 2013 Sep; 102(3):174-81. PubMed ID: 23598253
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Exploiting sequence similarity to validate the sensitivity of SNP arrays in detecting fine-scaled copy number variations.
    Wong G; Leckie C; Gorringe KL; Haviv I; Campbell IG; Kowalczyk A
    Bioinformatics; 2010 Apr; 26(8):1007-14. PubMed ID: 20189937
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Chromosomal Microarray Detection of Constitutional Copy Number Variation Using Saliva DNA.
    Reiner J; Karger L; Cohen N; Mehta L; Edelmann L; Scott SA
    J Mol Diagn; 2017 May; 19(3):397-403. PubMed ID: 28315673
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genes.
    Villacis RA; Miranda PM; Gomy I; Santos EM; Carraro DM; Achatz MI; Rossi BM; Rogatto SR
    Int J Cancer; 2016 Apr; 138(8):1928-35. PubMed ID: 26620301
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?
    Ganesamoorthy D; Bruno DL; McGillivray G; Norris F; White SM; Adroub S; Amor DJ; Yeung A; Oertel R; Pertile MD; Ngo C; Arvaj AR; Walker S; Charan P; Palma-Dias R; Woodrow N; Slater HR
    BJOG; 2013 Apr; 120(5):594-606. PubMed ID: 23332022
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Single-nucleotide polymorphism-based chromosomal microarray analysis provides clues and insights into disease mechanisms.
    Daum H; Meiner V; Hacohen N; Zvi N; Eilat A; Drai-Hasid R; Yagel S; Zenvirt S; Frumkin A
    Ultrasound Obstet Gynecol; 2019 Nov; 54(5):655-660. PubMed ID: 30693591
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A genome-wide analysis of loss of heterozygosity and chromosomal copy number variation in Proteus syndrome using high-density SNP microarrays.
    Yilmaz A; Hamel N; Schwartz CE; Houlston RS; Harper JI; Foulkes WD
    J Hum Genet; 2010 Sep; 55(9):627-30. PubMed ID: 20555334
    [TBL] [Abstract][Full Text] [Related]  

  • 28. High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?
    Bernardini L; Alesi V; Loddo S; Novelli A; Bottillo I; Battaglia A; Digilio MC; Zampino G; Ertel A; Fortina P; Surrey S; Dallapiccola B
    Eur J Hum Genet; 2010 Feb; 18(2):178-85. PubMed ID: 19809473
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The pitfalls of platform comparison: DNA copy number array technologies assessed.
    Curtis C; Lynch AG; Dunning MJ; Spiteri I; Marioni JC; Hadfield J; Chin SF; Brenton JD; Tavaré S; Caldas C
    BMC Genomics; 2009 Dec; 10():588. PubMed ID: 19995423
    [TBL] [Abstract][Full Text] [Related]  

  • 30. High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.
    Carr J; Bown NP; Case MC; Hall AG; Lunec J; Tweddle DA
    Cancer Genet Cytogenet; 2007 Jan; 172(2):127-38. PubMed ID: 17213021
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Algorithm implementation for CNV discovery using Affymetrix and Illumina SNP array data.
    Winchester L; Ragoussis J
    Methods Mol Biol; 2012; 838():291-310. PubMed ID: 22228018
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Single nucleotide polymorphism microarray analysis of genetic alterations in cancer.
    Mullighan CG
    Methods Mol Biol; 2011; 730():235-58. PubMed ID: 21431646
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Estimation of copy number aberrations: Comparison of exome sequencing data with SNP microarrays identifies homozygous deletions of 19q13.2 and CIC in neuroblastoma.
    Fransson S; Östensson M; Djos A; Javanmardi N; Kogner P; Martinsson T
    Int J Oncol; 2016 Mar; 48(3):1103-16. PubMed ID: 26794043
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chromosome microarrays in diagnostic testing: interpreting the genomic data.
    Peters GB; Pertile MD
    Methods Mol Biol; 2014; 1168():117-55. PubMed ID: 24870134
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Using expression arrays for copy number detection: an example from E. coli.
    Skvortsov D; Abdueva D; Stitzer ME; Finkel SE; Tavaré S
    BMC Bioinformatics; 2007 Jun; 8():203. PubMed ID: 17570850
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
    Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
    Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genome-wide copy number analysis on GeneChip platform using copy number analyzer for affymetrix GeneChip 2.0 software.
    Ogawa S; Nanya Y; Yamamoto G
    Methods Mol Biol; 2007; 396():185-206. PubMed ID: 18025694
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Performance assessment of copy number microarray platforms using a spike-in experiment.
    Halper-Stromberg E; Frelin L; Ruczinski I; Scharpf R; Jie C; Carvalho B; Hao H; Hetrick K; Jedlicka A; Dziedzic A; Doheny K; Scott AF; Baylin S; Pevsner J; Spencer F; Irizarry RA
    Bioinformatics; 2011 Apr; 27(8):1052-60. PubMed ID: 21478196
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A multicenter, cross-platform clinical validation study of cancer cytogenomic arrays.
    Li MM; Monzon FA; Biegel JA; Jobanputra V; Laffin JJ; Levy B; Leon A; Miron P; Rossi MR; Toruner G; Alvarez K; Doho G; Dougherty MJ; Hu X; Kash S; Streck D; Znoyko I; Hagenkord JM; Wolff DJ
    Cancer Genet; 2015 Nov; 208(11):525-36. PubMed ID: 26454669
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data.
    Baross A; Delaney AD; Li HI; Nayar T; Flibotte S; Qian H; Chan SY; Asano J; Ally A; Cao M; Birch P; Brown-John M; Fernandes N; Go A; Kennedy G; Langlois S; Eydoux P; Friedman JM; Marra MA
    BMC Bioinformatics; 2007 Oct; 8():368. PubMed ID: 17910767
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.