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Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data

WisecondorX: improved copy number detection for routine shallow whole-genome sequencing

PDF] WisecondorX: improved copy number detection for routine shallow whole-genome sequencing | Semantic Scholar

Flowchart showing the main steps of our comparison, including... | Download Scientific Diagram

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

True CNVs in a simulated genome and detected by BIC-seq2. a Forty CNVs... | Download Scientific Diagram

PDF] dpGMM: A Dirichlet Process Gaussian Mixture Model for Copy Number Variation Detection in Low-Coverage Whole-Genome Sequencing Data | Semantic Scholar

WisecondorX: improved copy number detection for routine shallow whole-genome sequencing. - Abstract - Europe PMC

Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data | BMC Genomics | Full Text

PDF] Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants | Semantic Scholar

Bioinformatics Applications Note Genome Analysis Control-free Calling of Copy Number Alterations in Deep-sequencing Data Using Gc-content Normalization | Semantic Scholar

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

Frontiers | A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data

Deep whole-genome sequencing of 3 cancer cell lines on 2 sequencing platforms | Scientific Reports

True CNVs in a simulated genome and detected by BIC-seq2. a Forty CNVs... | Download Scientific Diagram

Frontiers | A shortest path-based approach for copy number variation detection 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

PDF] WisecondorX: improved copy number detection for routine shallow whole-genome sequencing | Semantic Scholar

Replicability and profile comparison. (A) The boxplots of the... | Download Scientific Diagram

Frontiers | Detection of copy number variations based on a local distance using next-generation sequencing data

Analytical Validation of Clinical Whole-Genome and Transcriptome Sequencing of Patient-Derived Tumors for Reporting Targetable Variants in Cancer - ScienceDirect

Deep whole-genome sequencing of 3 cancer cell lines on 2 sequencing platforms | Scientific Reports