98 related articles for article (PubMed ID: 35714795)
1. CNV assessments associated with outcome distinctions for adult and pediatric cancers: Loss of BRCA1 in neuroblastoma associates with a lower survival probability.
Varkhedi M; Barker VR; Eakins RA; Blanck G
Gene; 2022 Aug; 836():146673. PubMed ID: 35714795
[TBL] [Abstract][Full Text] [Related]
2. Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia.
Boujemaa M; Hamdi Y; Mejri N; Romdhane L; Ghedira K; Bouaziz H; El Benna H; Labidi S; Dallali H; Jaidane O; Ben Nasr S; Haddaoui A; Rahal K; Abdelhak S; Boussen H; Boubaker MS
PLoS One; 2021; 16(1):e0245362. PubMed ID: 33503040
[TBL] [Abstract][Full Text] [Related]
3. Germline copy number variations in BRCA1-associated ovarian cancer patients.
Yoshihara K; Tajima A; Adachi S; Quan J; Sekine M; Kase H; Yahata T; Inoue I; Tanaka K
Genes Chromosomes Cancer; 2011 Mar; 50(3):167-77. PubMed ID: 21213370
[TBL] [Abstract][Full Text] [Related]
4. Next-Generation Sequencing-Based Detection of Germline Copy Number Variations in BRCA1/BRCA2: Validation of a One-Step Diagnostic Workflow.
Schmidt AY; Hansen TVO; Ahlborn LB; Jønson L; Yde CW; Nielsen FC
J Mol Diagn; 2017 Nov; 19(6):809-816. PubMed ID: 28822785
[TBL] [Abstract][Full Text] [Related]
5. Evaluation of somatic copy number estimation tools for whole-exome sequencing data.
Nam JY; Kim NK; Kim SC; Joung JG; Xi R; Lee S; Park PJ; Park WY
Brief Bioinform; 2016 Mar; 17(2):185-92. PubMed ID: 26210357
[TBL] [Abstract][Full Text] [Related]
6. Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample.
Wenric S; Sticca T; Caberg JH; Josse C; Fasquelle C; Herens C; Jamar M; Max S; Gothot A; Caers J; Bours V
Genet Epidemiol; 2017 Jan; 41(1):35-40. PubMed ID: 27862228
[TBL] [Abstract][Full Text] [Related]
7. Combinatorial approach to estimate copy number genotype using whole-exome sequencing data.
Hwang MY; Moon S; Heo L; Kim YJ; Oh JH; Kim YJ; Kim YK; Lee J; Han BG; Kim BJ
Genomics; 2015 Mar; 105(3):145-9. PubMed ID: 25535679
[TBL] [Abstract][Full Text] [Related]
8. Assessing the reproducibility of exome copy number variations predictions.
Hong CS; Singh LN; Mullikin JC; Biesecker LG
Genome Med; 2016 Aug; 8(1):82. PubMed ID: 27503473
[TBL] [Abstract][Full Text] [Related]
9. Systematic computational identification of prognostic cytogenetic markers in neuroblastoma.
Qin C; He X; Zhao Y; Tong CY; Zhu KY; Sun Y; Cheng C
BMC Med Genomics; 2019 Dec; 12(1):192. PubMed ID: 31831008
[TBL] [Abstract][Full Text] [Related]
10. Exome sequence read depth methods for identifying copy number changes.
Kadalayil L; Rafiq S; Rose-Zerilli MJ; Pengelly RJ; Parker H; Oscier D; Strefford JC; Tapper WJ; Gibson J; Ennis S; Collins A
Brief Bioinform; 2015 May; 16(3):380-92. PubMed ID: 25169955
[TBL] [Abstract][Full Text] [Related]
11. Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
Glessner JT; Bick AG; Ito K; Homsy J; Rodriguez-Murillo L; Fromer M; Mazaika E; Vardarajan B; Italia M; Leipzig J; DePalma SR; Golhar R; Sanders SJ; Yamrom B; Ronemus M; Iossifov I; Willsey AJ; State MW; Kaltman JR; White PS; Shen Y; Warburton D; Brueckner M; Seidman C; Goldmuntz E; Gelb BD; Lifton R; Seidman J; Hakonarson H; Chung WK
Circ Res; 2014 Oct; 115(10):884-896. PubMed ID: 25205790
[TBL] [Abstract][Full Text] [Related]
12. CNV Radar: an improved method for somatic copy number alteration characterization in oncology.
Soong D; Stratford J; Avet-Loiseau H; Bahlis N; Davies F; Dispenzieri A; Sasser AK; Schecter JM; Qi M; Brown C; Jones W; Keats JJ; Auclair D; Chiu C; Powers J; Schaffer M
BMC Bioinformatics; 2020 Mar; 21(1):98. PubMed ID: 32143562
[TBL] [Abstract][Full Text] [Related]
13. An evaluation of copy number variation detection tools for cancer using whole exome sequencing data.
Zare F; Dow M; Monteleone N; Hosny A; Nabavi S
BMC Bioinformatics; 2017 May; 18(1):286. PubMed ID: 28569140
[TBL] [Abstract][Full Text] [Related]
14. Loss of Heterozygosity in BRCA1 and BRCA2 Genes in Patients with Ovarian Cancer and Probability of Its Use for Clinical Classification of Variations.
Kechin AA; Boyarskikh UA; Ermolenko NA; Tyulyandina AS; Lazareva DG; Avdalyan AM; Tyulyandin SA; Kushlinskii NE; Filipenko ML
Bull Exp Biol Med; 2018 May; 165(1):94-100. PubMed ID: 29797126
[TBL] [Abstract][Full Text] [Related]
15. Copy number loss or silencing of apoptosis-effector genes in cancer.
Mauro JA; Butler SN; Ramsamooj M; Blanck G
Gene; 2015 Jan; 554(1):50-7. PubMed ID: 25307873
[TBL] [Abstract][Full Text] [Related]
16. Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.
Szatkiewicz JP; Neale BM; O'Dushlaine C; Fromer M; Goldstein JI; Moran JL; Chambert K; Kähler A; Magnusson PK; Hultman CM; Sklar P; Purcell S; McCarroll SA; Sullivan PF
Mol Psychiatry; 2013 Nov; 18(11):1178-84. PubMed ID: 23938935
[TBL] [Abstract][Full Text] [Related]
17. [Detecting Large Germline Rearrangements of BRCA1 by Next Generation Tumor Sequencing].
Minucci A; Mazzuccato G; Marchetti C; Pietragalla A; Scambia G; Fagotti A; Urbani A
Mol Biol (Mosk); 2020; 54(4):688-698. PubMed ID: 32840490
[TBL] [Abstract][Full Text] [Related]
18. Clinical evaluation of integrated panel testing by next-generation sequencing for somatic mutations in neuroblastomas with MYCN unamplification.
Cao Y; Jin Y; Yu J; Wang J; Qiu Y; Duan X; Ye Y; Cheng Y; Dong L; Feng X; Wang D; Li Z; Tian X; Wang H; Yan J; Zhao Q
Oncotarget; 2017 Jul; 8(30):49689-49701. PubMed ID: 28591696
[TBL] [Abstract][Full Text] [Related]
19. Inter- and intra-breed genome-wide copy number diversity in a large cohort of European equine breeds.
Solé M; Ablondi M; Binzer-Panchal A; Velie BD; Hollfelder N; Buys N; Ducro BJ; François L; Janssens S; Schurink A; Viklund Å; Eriksson S; Isaksson A; Kultima H; Mikko S; Lindgren G
BMC Genomics; 2019 Oct; 20(1):759. PubMed ID: 31640551
[TBL] [Abstract][Full Text] [Related]
20. Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohort.
Retterer K; Scuffins J; Schmidt D; Lewis R; Pineda-Alvarez D; Stafford A; Schmidt L; Warren S; Gibellini F; Kondakova A; Blair A; Bale S; Matyakhina L; Meck J; Aradhya S; Haverfield E
Genet Med; 2015 Aug; 17(8):623-9. PubMed ID: 25356966
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
