Title | ||
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Preprocessing Sequence Coverage Data for Precise Detection of Copy Number Variations. |
Abstract | ||
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Copy number variation (CNV) is a type of genomic/genetic variation that plays an important role in phenotypic diversity, evolution, and disease susceptibility. Next generation sequencing (NGS) technologies have created an opportunity for more accurate detection of CNVs with higher resolution. However, efficient and precise detection of CNVs remains challenging due to high levels of noise and biase... |
Year | DOI | Venue |
---|---|---|
2020 | 10.1109/TCBB.2018.2869738 | IEEE/ACM Transactions on Computational Biology and Bioinformatics |
Keywords | DocType | Volume |
Microsoft Windows,Bioinformatics,Genomics,Tumors,Sequential analysis,Cancer,Pipelines | Journal | 17 |
Issue | ISSN | Citations |
3 | 1545-5963 | 0 |
PageRank | References | Authors |
0.34 | 0 | 4 |
Name | Order | Citations | PageRank |
---|---|---|---|
Fatima Zare | 1 | 0 | 2.37 |
Sardar Ansari | 2 | 12 | 7.05 |
Kayvan Najarian | 3 | 262 | 59.53 |
Sheida Nabavi | 4 | 18 | 8.68 |