Estimating tumor fraction in cell-free DNA from ultra-low-pass whole genome sequencing.
-
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)
Software for Rapid Analyses of Human Copy Number Data
R package: Parent-specific Copy-number Estimation Pipeline using HT-Seq Data
CNprep Package - Pre-process DNA Copy Number (CN) Data for Detection of CN Events
KILDA (KIv2 Length Determined from a kmer Analysis) provides an alignment-free estimation of the number of KIV2 (Kringle IV type 2) repeats from FASTQ files.
Processing DNA Copy Number (CN) Data for Detection of CN Events
Copy number variation detection from WGS/WES using CNVkit
Add a description, image, and links to the copy-number topic page so that developers can more easily learn about it.
To associate your repository with the copy-number topic, visit your repo's landing page and select "manage topics."