79 related articles for article (PubMed ID: 33606251)
1. Common copy number variation detection from multiple sequenced samples.
Duan J; Deng HW; Wang YP
IEEE Trans Biomed Eng; 2014 Mar; 61(3):928-37. PubMed ID: 24557694
[TBL] [Abstract][Full Text] [Related]
2. Inference of Markovian properties of molecular sequences from NGS data and applications to comparative genomics.
Ren J; Song K; Deng M; Reinert G; Cannon CH; Sun F
Bioinformatics; 2016 Apr; 32(7):993-1000. PubMed ID: 26130573
[TBL] [Abstract][Full Text] [Related]
3. CNVpytor: a tool for copy number variation detection and analysis from read depth and allele imbalance in whole-genome sequencing.
Suvakov M; Panda A; Diesh C; Holmes I; Abyzov A
Gigascience; 2021 Nov; 10(11):. PubMed ID: 34817058
[TBL] [Abstract][Full Text] [Related]
4. A method to correct for local alterations in DNA copy number that bias functional genomics assays applied to antibiotic-treated bacteria.
Sullivan GJ; Barquist L; Cain AK
mSystems; 2024 Apr; 9(4):e0066523. PubMed ID: 38470252
[TBL] [Abstract][Full Text] [Related]
5. Modeling the next generation sequencing sample processing pipeline for the purposes of classification.
Ghaffari N; Yousefi MR; Johnson CD; Ivanov I; Dougherty ER
BMC Bioinformatics; 2013 Oct; 14():307. PubMed ID: 24118904
[TBL] [Abstract][Full Text] [Related]
6. Computational characterisation of cancer molecular profiles derived using next generation sequencing.
Oleksiewicz U; Tomczak K; Woropaj J; Markowska M; Stępniak P; Shah PK
Contemp Oncol (Pozn); 2015; 19(1A):A78-91. PubMed ID: 25691827
[TBL] [Abstract][Full Text] [Related]
7. Evaluating statistical approaches to define clonal origin of tumours using bulk DNA sequencing: context is everything.
Kader T; Zethoven M; Gorringe KL
Genome Biol; 2022 Feb; 23(1):43. PubMed ID: 35109903
[TBL] [Abstract][Full Text] [Related]
8. Challenges in the application of NGS in the clinical laboratory.
Yin Y; Butler C; Zhang Q
Hum Immunol; 2021 Nov; 82(11):812-819. PubMed ID: 33892986
[TBL] [Abstract][Full Text] [Related]
9. The emerging roles of NGS in clinical oncology and personalized medicine.
Hussen BM; Abdullah ST; Salihi A; Sabir DK; Sidiq KR; Rasul MF; Hidayat HJ; Ghafouri-Fard S; Taheri M; Jamali E
Pathol Res Pract; 2022 Feb; 230():153760. PubMed ID: 35033746
[TBL] [Abstract][Full Text] [Related]
10. NGS in the clinical microbiology settings.
Pitashny M; Kadry B; Shalaginov R; Gazit L; Zohar Y; Szwarcwort M; Stabholz Y; Paul M
Front Cell Infect Microbiol; 2022; 12():955481. PubMed ID: 36339334
[TBL] [Abstract][Full Text] [Related]
11. FFPE-Based NGS Approaches into Clinical Practice: The Limits of Glory from a Pathologist Viewpoint.
Cappello F; Angerilli V; Munari G; Ceccon C; Sabbadin M; Pagni F; Fusco N; Malapelle U; Fassan M
J Pers Med; 2022 May; 12(5):. PubMed ID: 35629172
[TBL] [Abstract][Full Text] [Related]
12. A Multibreed Genome-Wide Association Study for Cattle Leukocyte Telomere Length.
Igoshin AV; Yudin NS; Romashov GA; Larkin DM
Genes (Basel); 2023 Aug; 14(8):. PubMed ID: 37628647
[TBL] [Abstract][Full Text] [Related]
13. Analysis of Copy Number Variation of DNA Repair/Damage Response Genes in Tumor Tissues.
Izumi T
Methods Mol Biol; 2023; 2701():231-242. PubMed ID: 37574486
[TBL] [Abstract][Full Text] [Related]
14. Statistical Considerations on NGS Data for Inferring Copy Number Variations.
Chen J
Methods Mol Biol; 2021; 2243():27-58. PubMed ID: 33606251
[TBL] [Abstract][Full Text] [Related]
15. CNV-CH: A Convex Hull Based Segmentation Approach to Detect Copy Number Variations (CNV) Using Next-Generation Sequencing Data.
Sinha R; Samaddar S; De RK
PLoS One; 2015; 10(8):e0135895. PubMed ID: 26291322
[TBL] [Abstract][Full Text] [Related]
16. Modeling the next generation sequencing read count data for DNA copy number variant study.
Ji T; Chen J
Stat Appl Genet Mol Biol; 2015 Aug; 14(4):361-74. PubMed ID: 26140731
[TBL] [Abstract][Full Text] [Related]
17. iCopyDAV: Integrated platform for copy number variations-Detection, annotation and visualization.
Dharanipragada P; Vogeti S; Parekh N
PLoS One; 2018; 13(4):e0195334. PubMed ID: 29621297
[TBL] [Abstract][Full Text] [Related]
18. Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges.
Liu B; Morrison CD; Johnson CS; Trump DL; Qin M; Conroy JC; Wang J; Liu S
Oncotarget; 2013 Nov; 4(11):1868-81. PubMed ID: 24240121
[TBL] [Abstract][Full Text] [Related]
19. Statistical challenges associated with detecting copy number variations with next-generation sequencing.
Teo SM; Pawitan Y; Ku CS; Chia KS; Salim A
Bioinformatics; 2012 Nov; 28(21):2711-8. PubMed ID: 22942022
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]