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Frontiers | Detection of copy number variations based on a local distance using next-generation sequencing data
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PDF] Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants | Semantic Scholar
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True CNVs in a simulated genome and detected by BIC-seq2. a Forty CNVs... | Download Scientific Diagram
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Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data
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WisecondorX: improved copy number detection for routine shallow whole-genome sequencing. - Abstract - Europe PMC
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PDF] Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants | Semantic Scholar
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Frontiers | A shortest path-based approach for copy number variation detection from next-generation sequencing data
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Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer - ScienceDirect
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Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data | BMC Genomics | Full Text
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Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data
Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants
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True CNVs in a simulated genome and detected by BIC-seq2. a Forty CNVs... | Download Scientific Diagram
![PDF] WisecondorX: improved copy number detection for routine shallow whole-genome sequencing | Semantic Scholar PDF] WisecondorX: improved copy number detection for routine shallow whole-genome sequencing | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/7ba883a32a465c6790a2ac06aed46b658db5d38f/6-Figure3-1.png)
PDF] WisecondorX: improved copy number detection for routine shallow whole-genome sequencing | Semantic Scholar
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Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data
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Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data
![PDF] Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants | Semantic Scholar PDF] Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/aa261b192f8eef42d0724a397ee0515e738b588d/6-Figure3-1.png)
PDF] Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants | Semantic Scholar
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PDF] WisecondorX: improved copy number detection for routine shallow whole-genome sequencing | Semantic Scholar
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PDF] WisecondorX: improved copy number detection for routine shallow whole-genome sequencing | Semantic Scholar
![Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data](https://www.frontiersin.org/files/Articles/699510/fgene-12-699510-HTML-r1/image_m/fgene-12-699510-g004.jpg)
Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data
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