230 related articles for article (PubMed ID: 37674481)
1. Resolving complex structural variants via nanopore sequencing.
Romagnoli S; Bartalucci N; Vannucchi AM
Front Genet; 2023; 14():1213917. PubMed ID: 37674481
[TBL] [Abstract][Full Text] [Related]
2. Evaluation of Germline Structural Variant Calling Methods for Nanopore Sequencing Data.
Bolognini D; Magi A
Front Genet; 2021; 12():761791. PubMed ID: 34868242
[TBL] [Abstract][Full Text] [Related]
3. Combined use of Oxford Nanopore and Illumina sequencing yields insights into soybean structural variation biology.
Lemay MA; Sibbesen JA; Torkamaneh D; Hamel J; Levesque RC; Belzile F
BMC Biol; 2022 Feb; 20(1):53. PubMed ID: 35197050
[TBL] [Abstract][Full Text] [Related]
4. MetaSVs: A pipeline combining long and short reads for analysis and visualization of structural variants in metagenomes.
Li Y; Cao J; Wang J
Imeta; 2023 Nov; 2(4):e139. PubMed ID: 38868213
[TBL] [Abstract][Full Text] [Related]
5. Oxford Nanopore and Bionano Genomics technologies evaluation for plant structural variation detection.
Canaguier A; Guilbaud R; Denis E; Magdelenat G; Belser C; Istace B; Cruaud C; Wincker P; Le Paslier MC; Faivre-Rampant P; Barbe V
BMC Genomics; 2022 Apr; 23(1):317. PubMed ID: 35448948
[TBL] [Abstract][Full Text] [Related]
6. Targeted long-read sequencing identifies and characterizes structural variants in cases of inherited platelet disorders.
Zamora-Cánovas A; de la Morena-Barrio B; Marín-Quilez A; Sierra-Aisa C; Male C; Fernández-Mosteirin N; Trapero-Marugán M; Padilla J; Garrido-Rodriguez P; Sánchez-Fuentes A; Rodríguez-Alen A; Gómez-González PL; Revilla N; de la Morena-Barrio ME; Bastida JM; Corral J; Rivera J; Lozano ML
J Thromb Haemost; 2024 Mar; 22(3):851-859. PubMed ID: 38007062
[TBL] [Abstract][Full Text] [Related]
7. Applications and potentials of nanopore sequencing in the (epi)genome and (epi)transcriptome era.
Xie S; Leung AW; Zheng Z; Zhang D; Xiao C; Luo R; Luo M; Zhang S
Innovation (Camb); 2021 Nov; 2(4):100153. PubMed ID: 34901902
[TBL] [Abstract][Full Text] [Related]
8. Application of long-read sequencing to the detection of structural variants in human cancer genomes.
Sakamoto Y; Zaha S; Suzuki Y; Seki M; Suzuki A
Comput Struct Biotechnol J; 2021; 19():4207-4216. PubMed ID: 34527193
[TBL] [Abstract][Full Text] [Related]
9. Adaptation of Oxford Nanopore technology for hepatitis C whole genome sequencing and identification of within-host viral variants.
Riaz N; Leung P; Barton K; Smith MA; Carswell S; Bull R; Lloyd AR; Rodrigo C
BMC Genomics; 2021 Mar; 22(1):148. PubMed ID: 33653280
[TBL] [Abstract][Full Text] [Related]
10. ONT long-read WGS for variant discovery and orthogonal confirmation of short read WGS derived genetic variants in clinical genetic testing.
Kaplun L; Krautz-Peterson G; Neerman N; Stanley C; Hussey S; Folwick M; McGarry A; Weiss S; Kaplun A
Front Genet; 2023; 14():1145285. PubMed ID: 37152986
[TBL] [Abstract][Full Text] [Related]
11. Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing.
Thibodeau ML; O'Neill K; Dixon K; Reisle C; Mungall KL; Krzywinski M; Shen Y; Lim HJ; Cheng D; Tse K; Wong T; Chuah E; Fok A; Sun S; Renouf D; Schaeffer DF; Cremin C; Chia S; Young S; Pandoh P; Pleasance S; Pleasance E; Mungall AJ; Moore R; Yip S; Karsan A; Laskin J; Marra MA; Schrader KA; Jones SJM
Genet Med; 2020 Nov; 22(11):1892-1897. PubMed ID: 32624572
[TBL] [Abstract][Full Text] [Related]
12. SVJedi: genotyping structural variations with long reads.
Lecompte L; Peterlongo P; Lavenier D; Lemaitre C
Bioinformatics; 2020 Nov; 36(17):4568-4575. PubMed ID: 32437523
[TBL] [Abstract][Full Text] [Related]
13. Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome.
Begum G; Albanna A; Bankapur A; Nassir N; Tambi R; Berdiev BK; Akter H; Karuvantevida N; Kellam B; Alhashmi D; Sung WWL; Thiruvahindrapuram B; Alsheikh-Ali A; Scherer SW; Uddin M
Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33669700
[TBL] [Abstract][Full Text] [Related]
14. Benchmarking Oxford Nanopore read alignment-based insertion and deletion detection in crop plant genomes.
Yildiz G; Zanini SF; Afsharyan NP; Obermeier C; Snowdon RJ; Golicz AA
Plant Genome; 2023 Jun; 16(2):e20314. PubMed ID: 36988043
[TBL] [Abstract][Full Text] [Related]
15. Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologies.
Talsania K; Shen TW; Chen X; Jaeger E; Li Z; Chen Z; Chen W; Tran B; Kusko R; Wang L; Pang AWC; Yang Z; Choudhari S; Colgan M; Fang LT; Carroll A; Shetty J; Kriga Y; German O; Smirnova T; Liu T; Li J; Kellman B; Hong K; Hastie AR; Natarajan A; Moshrefi A; Granat A; Truong T; Bombardi R; Mankinen V; Meerzaman D; Mason CE; Collins J; Stahlberg E; Xiao C; Wang C; Xiao W; Zhao Y
Genome Biol; 2022 Dec; 23(1):255. PubMed ID: 36514120
[TBL] [Abstract][Full Text] [Related]
16. Comparison of multiple algorithms to reliably detect structural variants in pears.
Liu Y; Zhang M; Sun J; Chang W; Sun M; Zhang S; Wu J
BMC Genomics; 2020 Jan; 21(1):61. PubMed ID: 31959124
[TBL] [Abstract][Full Text] [Related]
17. Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing.
Tsuiko O; El Ayeb Y; Jatsenko T; Allemeersch J; Melotte C; Ding J; Debrock S; Peeraer K; Vanhie A; De Leener A; Pirard C; Kluyskens C; Denayer E; Legius E; Vermeesch JR; Brems H; Dimitriadou E
Hum Reprod; 2023 Mar; 38(3):511-519. PubMed ID: 36625546
[TBL] [Abstract][Full Text] [Related]
18. Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human Genomes.
Fatima N; Petri A; Gyllensten U; Feuk L; Ameur A
Genes (Basel); 2020 Nov; 11(12):. PubMed ID: 33266238
[TBL] [Abstract][Full Text] [Related]
19. Resolving Genotype-Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore Sequencing.
Gueuning M; Thun GA; Trost N; Schneider L; Sigurdardottir S; Engström C; Larbes N; Merki Y; Frey BM; Gassner C; Meyer S; Mattle-Greminger MP
Biomedicines; 2024 Jan; 12(1):. PubMed ID: 38275395
[TBL] [Abstract][Full Text] [Related]
20. Nanopore sequencing detects structural variants in cancer.
Norris AL; Workman RE; Fan Y; Eshleman JR; Timp W
Cancer Biol Ther; 2016; 17(3):246-53. PubMed ID: 26787508
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]