GitHub - tgac-vumc/ACE: Absolute Copy Number Estimation using low-coverage whole genome sequencing data
By A Mystery Man Writer
Description
Absolute Copy Number Estimation using low-coverage whole genome sequencing data - tgac-vumc/ACE
Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue, Genome Medicine
CNAplot — Software for visual inspection of chromosomal copy number alteration in cancer using juxtaposed sequencing read depth ratios and variant allele frequencies - SoftwareX
Diagnostics, Free Full-Text
Accurate quantification of copy-number aberrations and whole-genome duplications in multi-sample tumor sequencing data
GitHub - Nealelab/whole_genome_analysis_pipeline
Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion
Low-Pass Whole Genome Sequencing
PDF) HBOS-CNV: A New Approach to Detect Copy Number Variations From Next-Generation Sequencing Data
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data
Detection of Copy Number Variation using Shallow Whole Genome Sequencing Data to replace Array-Comparative Genomic Hybridization Analysis
GitHub - immunogenomics/SCENT: Single-Cell ENhancer Target gene mapping using multimodal data with ATAC + RNA
Absolute copy number fitting from shallow whole genome sequencing data
DNA copy number profiling: from bulk tissue to single cells
GATK-gCNV: A Rare Copy Number Variant Discovery Algorithm and Its Application to Exome Sequencing in the UK Biobank
PDF) WAVECNV: A New Approach for Detecting Copy Number Variation by Wavelet Clustering
from
per adult (price varies by group size)