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PDF) Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants
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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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Bioinformatics Applications Note Genome Analysis Control-free Calling of Copy Number Alterations in Deep-sequencing Data Using Gc-content Normalization | Semantic Scholar
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Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data
GitHub - d3b-center/d3b_bic-seq2: CWL Implementation based on this tool http://compbio.med.harvard.edu/BIC-seq/ and this cluster implementation : https://github.com/ding-lab/BICSEQ2
![Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer - ScienceDirect Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1525157817306219-gr5.jpg)
Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer - ScienceDirect
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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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PDF] dpGMM: A Dirichlet Process Gaussian Mixture Model for Copy Number Variation Detection in Low-Coverage Whole-Genome Sequencing Data | Semantic Scholar
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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
Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data
![True CNVs in a simulated genome and detected by BIC-seq2. a Forty CNVs... | Download Scientific Diagram True CNVs in a simulated genome and detected by BIC-seq2. a Forty CNVs... | Download Scientific Diagram](https://www.researchgate.net/publication/315062499/figure/fig4/AS:962449238925313@1606477188214/True-CNVs-in-a-simulated-genome-and-detected-by-BIC-seq2-a-Forty-CNVs-were-introduced-in.gif)
True CNVs in a simulated genome and detected by BIC-seq2. a Forty CNVs... | Download Scientific Diagram
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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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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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PDF] WisecondorX: improved copy number detection for routine shallow whole-genome sequencing | Semantic Scholar
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