109 related articles for article (PubMed ID: 21934286)
1. SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control.
de Leeuw N; Hehir-Kwa JY; Simons A; Geurts van Kessel A; Smeets DF; Faas BH; Pfundt R
Cytogenet Genome Res; 2011; 135(3-4):212-21. PubMed ID: 21934286
[TBL] [Abstract][Full Text] [Related]
2. Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis.
Kooper AJ; Faas BH; Feenstra I; de Leeuw N; Smeets DF
Mol Cytogenet; 2014 Jan; 7(1):6. PubMed ID: 24428858
[TBL] [Abstract][Full Text] [Related]
3. Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays.
Hoyer J; Dreweke A; Becker C; Göhring I; Thiel CT; Peippo MM; Rauch R; Hofbeck M; Trautmann U; Zweier C; Zenker M; Hüffmeier U; Kraus C; Ekici AB; Rüschendorf F; Nürnberg P; Reis A; Rauch A
J Med Genet; 2007 Oct; 44(10):629-36. PubMed ID: 17601928
[TBL] [Abstract][Full Text] [Related]
4. Statistical issues in the analysis of DNA Copy Number Variations.
Wineinger NE; Kennedy RE; Erickson SW; Wojczynski MK; Bruder CE; Tiwari HK
Int J Comput Biol Drug Des; 2008; 1(4):368-95. PubMed ID: 19774103
[TBL] [Abstract][Full Text] [Related]
5. Reference alignment of SNP microarray signals for copy number analysis of tumors.
Pounds S; Cheng C; Mullighan C; Raimondi SC; Shurtleff S; Downing JR
Bioinformatics; 2009 Feb; 25(3):315-21. PubMed ID: 19052058
[TBL] [Abstract][Full Text] [Related]
6. Array-Based Comparative Genomic Hybridization for the Detection of Copy Number Alterations in Single Cells.
Feliciello G; Czyz ZT; Polzer BM
Methods Mol Biol; 2024; 2752():167-187. PubMed ID: 38194034
[TBL] [Abstract][Full Text] [Related]
7. Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses.
Treff NR; Su J; Tao X; Northrop LE; Scott RT
Mol Hum Reprod; 2011 Jun; 17(6):335-43. PubMed ID: 21177337
[TBL] [Abstract][Full Text] [Related]
8. Copy Number Variation and Risk of Stroke.
Grond-Ginsbach C; Erhart P; Chen B; Kloss M; Engelter ST; Cole JW
Stroke; 2018 Oct; 49(10):2549-2554. PubMed ID: 30355123
[No Abstract] [Full Text] [Related]
9. SNP array profiling of mouse cell lines identifies their strains of origin and reveals cross-contamination and widespread aneuploidy.
Didion JP; Buus RJ; Naghashfar Z; Threadgill DW; Morse HC; de Villena FP
BMC Genomics; 2014 Oct; 15(1):847. PubMed ID: 25277546
[TBL] [Abstract][Full Text] [Related]
10. A genomic random interval model for statistical analysis of genomic lesion data.
Pounds S; Cheng C; Li S; Liu Z; Zhang J; Mullighan C
Bioinformatics; 2013 Sep; 29(17):2088-95. PubMed ID: 23842812
[TBL] [Abstract][Full Text] [Related]
11. Homology Identification and Cross-Contamination Analysis: A Method for Evaluating the Quality of Biological Samples Stored in a Biobank Using the Advanta Sample ID Genotyping Panel.
Wang C; Hu Z; Zhang X; Xu M; Shen W; Du L; Sun M; Gao H
Biopreserv Biobank; 2024 Apr; 22(2):115-122. PubMed ID: 37889987
[TBL] [Abstract][Full Text] [Related]
12. Detection of Constitutional Structural Variants by Optical Genome Mapping: A Multisite Study of Postnatal Samples.
Broeckel U; Iqbal MA; Levy B; Sahajpal N; Nagy PL; Scharer G; Rodriguez V; Bossler A; Stence A; Skinner C; Skinner SA; Kolhe R; Stevenson R
J Mol Diagn; 2024 Mar; 26(3):213-226. PubMed ID: 38211722
[TBL] [Abstract][Full Text] [Related]
13. SNP array technology: an array of hope in breast cancer research.
Ho CC; Mun KS; Naidu R
Malays J Pathol; 2013 Jun; 35(1):33-43. PubMed ID: 23817393
[TBL] [Abstract][Full Text] [Related]
14. Significance of genome-wide analysis of copy number alterations and UPD in myelodysplastic syndromes using combined CGH - SNP arrays.
Ahmad A; Iqbal MA
Curr Med Chem; 2012; 19(22):3739-47. PubMed ID: 22680919
[TBL] [Abstract][Full Text] [Related]
15. Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how?
Sato-Otsubo A; Sanada M; Ogawa S
Semin Oncol; 2012 Feb; 39(1):13-25. PubMed ID: 22289488
[TBL] [Abstract][Full Text] [Related]
16. Novel applications of array comparative genomic hybridization in molecular diagnostics.
Cheung SW; Bi W
Expert Rev Mol Diagn; 2018 Jun; 18(6):531-542. PubMed ID: 29848116
[TBL] [Abstract][Full Text] [Related]
17. Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rate.
Catusi I; Recalcati MP; Bestetti I; Garzo M; Valtorta C; Alfonsi M; Alghisi A; Cappellani S; Casalone R; Caselli R; Ceccarini C; Ceglia C; Ciaschini AM; Coviello D; Crosti F; D'Aprile A; Fabretto A; Genesio R; Giagnacovo M; Granata P; Longo I; Malacarne M; Marseglia G; Montaldi A; Nardone AM; Palka C; Pecile V; Pessina C; Postorivo D; Redaelli S; Renieri A; Rigon C; Tiberi F; Tonelli M; Villa N; Zilio A; Zuccarello D; Novelli A; Larizza L; Giardino D
Mol Genet Genomic Med; 2020 Jan; 8(1):e1056. PubMed ID: 31851782
[TBL] [Abstract][Full Text] [Related]
18. European guidelines for constitutional cytogenomic analysis.
Silva M; de Leeuw N; Mann K; Schuring-Blom H; Morgan S; Giardino D; Rack K; Hastings R
Eur J Hum Genet; 2019 Jan; 27(1):1-16. PubMed ID: 30275486
[TBL] [Abstract][Full Text] [Related]
19. Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors.
Fox AJ; Hiemenz MC; Lieberman DB; Sukhadia S; Li B; Grubb J; Candrea P; Ganapathy K; Zhao J; Roth D; Alley E; Loren A; Morrissette JJ
J Vis Exp; 2016 Sep; (115):. PubMed ID: 27684276
[TBL] [Abstract][Full Text] [Related]
20. Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies.
Vazharova R; Vragaleva S; Dimitrova V; Ivanov S; Balabanski L; Malinov M; Toncheva D
Case Rep Obstet Gynecol; 2016; 2016():1462818. PubMed ID: 27642530
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
