Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data | BMC Genomics | Full Text
Bioinformatics Applications Note Genome Analysis Control-free Calling of Copy Number Alterations in Deep-sequencing Data Using Gc-content Normalization | Semantic Scholar
Frontiers | A shortest path-based approach for copy number variation detection from next-generation sequencing data
WisecondorX: improved copy number detection for routine shallow whole-genome sequencing
Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data
Deep whole-genome sequencing of 3 cancer cell lines on 2 sequencing platforms | Scientific Reports
Replicability and profile comparison. (A) The boxplots of the... | Download Scientific Diagram
BIC-seq2
![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")
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/7-Figure4-1.png "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
G-means of dpGMM, CNVnator, GROM-RD, and BIC-seq2 on simulation1... | Download Scientific Diagram
PDF) Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants
![PDF] dpGMM: A Dirichlet Process Gaussian Mixture Model for Copy Number Variation Detection in Low-Coverage Whole-Genome Sequencing Data | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/67599f97fcb1685769db1734a10ad2519b8ef1c2/10-Table3-1.png "PDF] dpGMM: A Dirichlet Process Gaussian Mixture Model for Copy Number Variation Detection in Low-Coverage Whole-Genome Sequencing Data | Semantic Scholar")
PDF] dpGMM: A Dirichlet Process Gaussian Mixture Model for Copy Number Variation Detection in Low-Coverage Whole-Genome Sequencing Data | Semantic Scholar
Effectiveness of the normalization procedure in BIC-seq2. (A) The... | Download Scientific Diagram
G-means of dpGMM, CNVnator, GROM-RD, and BIC-seq2 on simulation1... | Download Scientific Diagram
WisecondorX: improved copy number detection for routine shallow whole-genome sequencing
![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/10-Table1-1.png "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
GitHub - ding-lab/BICSEQ2: BICSEQ2 pipeline for processing CPTAC3 somatic WGS CNA
Effectiveness of the normalization procedure in BIC-seq2. (A) The... | Download Scientific Diagram
![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/4-Figure1-1.png "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
![PDF] WisecondorX: improved copy number detection for routine shallow whole-genome sequencing | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/7ba883a32a465c6790a2ac06aed46b658db5d38f/6-Figure4-1.png "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
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
