147 related articles for article (PubMed ID: 34202028)
1. CIRCNV: Detection of CNVs Based on a Circular Profile of Read Depth from Sequencing Data.
Zhao HY; Li Q; Tian Y; Chen YH; Alvi HAK; Yuan XG
Biology (Basel); 2021 Jun; 10(7):. PubMed ID: 34202028
[TBL] [Abstract][Full Text] [Related]
2. HBOS-CNV: A New Approach to Detect Copy Number Variations From Next-Generation Sequencing Data.
Guo Y; Wang S; Yuan X
Front Genet; 2021; 12():642473. PubMed ID: 34163521
[TBL] [Abstract][Full Text] [Related]
3. A Local Outlier Factor-Based Detection of Copy Number Variations From NGS Data.
Yuan X; Li J; Bai J; Xi J
IEEE/ACM Trans Comput Biol Bioinform; 2021; 18(5):1811-1820. PubMed ID: 31880558
[TBL] [Abstract][Full Text] [Related]
4. MFCNV: A New Method to Detect Copy Number Variations From Next-Generation Sequencing Data.
Zhao H; Huang T; Li J; Liu G; Yuan X
Front Genet; 2020; 11():434. PubMed ID: 32499814
[TBL] [Abstract][Full Text] [Related]
5. A shortest path-based approach for copy number variation detection from next-generation sequencing data.
Liu G; Yang H; Yuan X
Front Genet; 2022; 13():1084974. PubMed ID: 36733945
[TBL] [Abstract][Full Text] [Related]
6. A Density Peak-Based Method to Detect Copy Number Variations From Next-Generation Sequencing Data.
Xie K; Tian Y; Yuan X
Front Genet; 2020; 11():632311. PubMed ID: 33519925
[TBL] [Abstract][Full Text] [Related]
7. Noise cancellation using total variation for copy number variation detection.
Zare F; Hosny A; Nabavi S
BMC Bioinformatics; 2018 Oct; 19(Suppl 11):361. PubMed ID: 30343665
[TBL] [Abstract][Full Text] [Related]
8. A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data.
Liu G; Zhang J
Front Genet; 2021; 12():699510. PubMed ID: 34262604
[TBL] [Abstract][Full Text] [Related]
9. CNV-PCC: An efficient method for detecting copy number variations from next-generation sequencing data.
Zhang T; Dong J; Jiang H; Zhao Z; Zhou M; Yuan T
Front Bioeng Biotechnol; 2022; 10():1000638. PubMed ID: 36532569
[TBL] [Abstract][Full Text] [Related]
10. Detection of copy number variations based on a local distance using next-generation sequencing data.
Liu G; Yang H; He Z
Front Genet; 2023; 14():1147761. PubMed ID: 37811148
[TBL] [Abstract][Full Text] [Related]
11. RKDOSCNV: A Local Kernel Density-Based Approach to the Detection of Copy Number Variations by Using Next-Generation Sequencing Data.
Liu G; Zhang J; Yuan X; Wei C
Front Genet; 2020; 11():569227. PubMed ID: 33329705
[TBL] [Abstract][Full Text] [Related]
12. CNV_IFTV: An Isolation Forest and Total Variation-Based Detection of CNVs from Short-Read Sequencing Data.
Yuan X; Yu J; Xi J; Yang L; Shang J; Li Z; Duan J
IEEE/ACM Trans Comput Biol Bioinform; 2021; 18(2):539-549. PubMed ID: 31180897
[TBL] [Abstract][Full Text] [Related]
13. Copy Number Variation Detection Using Total Variation.
Zare F; Nabavi S
ACM BCB; 2019 Sep; 2019():423-428. PubMed ID: 32515750
[TBL] [Abstract][Full Text] [Related]
14. CNV-MEANN: A Neural Network and Mind Evolutionary Algorithm-Based Detection of Copy Number Variations From Next-Generation Sequencing Data.
Huang T; Li J; Jia B; Sang H
Front Genet; 2021; 12():700874. PubMed ID: 34484298
[TBL] [Abstract][Full Text] [Related]
15. KNNCNV: A K-Nearest Neighbor Based Method for Detection of Copy Number Variations Using NGS Data.
Xie K; Liu K; Alvi HAK; Chen Y; Wang S; Yuan X
Front Cell Dev Biol; 2021; 9():796249. PubMed ID: 35004691
[TBL] [Abstract][Full Text] [Related]
16. Copy number variation analysis based on AluScan sequences.
Yang JF; Ding XF; Chen L; Mat WK; Xu MZ; Chen JF; Wang JM; Xu L; Poon WS; Kwong A; Leung GK; Tan TC; Yu CH; Ke YB; Xu XY; Ke XY; Ma RC; Chan JC; Wan WQ; Zhang LW; Kumar Y; Tsang SY; Li S; Wang HY; Xue H
J Clin Bioinforma; 2014; 4(1):15. PubMed ID: 25558350
[TBL] [Abstract][Full Text] [Related]
17. GROM-RD: resolving genomic biases to improve read depth detection of copy number variants.
Smith SD; Kawash JK; Grigoriev A
PeerJ; 2015; 3():e836. PubMed ID: 25802807
[TBL] [Abstract][Full Text] [Related]
18. DeviCNV: detection and visualization of exon-level copy number variants in targeted next-generation sequencing data.
Kang Y; Nam SH; Park KS; Kim Y; Kim JW; Lee E; Ko JM; Lee KA; Park I
BMC Bioinformatics; 2018 Oct; 19(1):381. PubMed ID: 30326846
[TBL] [Abstract][Full Text] [Related]
19. Whole-Genome Shotgun Sequence CNV Detection Using Read Depth.
Kahveci F; Alkan C
Methods Mol Biol; 2018; 1833():61-72. PubMed ID: 30039363
[TBL] [Abstract][Full Text] [Related]
20. Shape-based retrieval of CNV regions in read coverage data.
Hong S; Yoon J; Hong D; Lee U; Kim B; Park S
Int J Data Min Bioinform; 2014; 9(3):254-76. PubMed ID: 25163168
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
