Estimating tumor fraction in cell-free DNA from ultra-low-pass whole genome sequencing.
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Updated
Mar 20, 2024 - R
Estimating tumor fraction in cell-free DNA from ultra-low-pass whole genome sequencing.
Copy number calling and variant classification using targeted short read sequencing
Lifterover copy number segments in whole
High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants
Accucopy is a computational method that infers Allele-Specific Copy Number alterations from low-coverage low-purity tumor sequencing data.
🔬 R package: Analysis of Large Affymetrix Microarray Data Sets
Probabilistic inference of somatic copy number alterations using repeat DNA (FAST-SeqS)
R package: Parent-specific Copy-number Estimation Pipeline using HT-Seq Data
Software for Rapid Analyses of Human Copy Number Data
CNprep Package - Pre-process DNA Copy Number (CN) Data for Detection of CN Events
Processing DNA Copy Number (CN) Data for Detection of CN Events
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