Package: falcon 0.2

Hao Chen
falcon: Finding Allele-Specific Copy Number in Next-Generation Sequencing Data
This is a method for Allele-specific DNA Copy Number Profiling using Next-Generation Sequencing. Given the allele-specific coverage at the variant loci, this program segments the genome into regions of homogeneous allele-specific copy number. It requires, as input, the read counts for each variant allele in a pair of case and control samples. For detection of somatic mutations, the case and control samples can be the tumor and normal sample from the same individual.
Authors:
falcon_0.2.tar.gz
falcon_0.2.zip(r-4.7-x86_64)falcon_0.2.zip(r-4.7-arm64)falcon_0.2.zip(r-4.6-x86_64)falcon_0.2.zip(r-4.6-arm64)
falcon_0.2.tar.gz(r-4.7-arm64)falcon_0.2.tar.gz(r-4.7-x86_64)falcon_0.2.tar.gz(r-4.6-arm64)falcon_0.2.tar.gz(r-4.6-x86_64)
falcon_0.2.tgz(r-4.6-emscripten)
manual.pdf |manual.html✨
DESCRIPTION
card.svg |card.png
falcon/json (API)
| # Install 'falcon' in R: |
| install.packages('falcon', repos = c('https://cran.r-universe.dev', 'https://cloud.r-project.org')) |
- pos - Position
- readMatrix - An example reads count data
- tauhat - Estimated Break Points
This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.
Last updated from:b12c2b678f. Checks:10 OK. Indexed: yes.
| Target | Result | Time | Files | Syslog |
|---|---|---|---|---|
| linux-devel-arm64 | OK | 96 | ||
| linux-devel-x86_64 | OK | 120 | ||
| source / vignettes | OK | 227 | ||
| linux-release-arm64 | OK | 101 | ||
| linux-release-x86_64 | OK | 130 | ||
| windows-devel-arm64 | OK | 214 | ||
| windows-devel-x86_64 | OK | 98 | ||
| windows-release-arm64 | OK | 178 | ||
| windows-release-x86_64 | OK | 61 | ||
| wasm-release | OK | 92 |
Exports:getASCNgetChangepointsview
Dependencies:
Readme and manuals
Help Manual
| Help page | Topics |
|---|---|
| Finding Allele-Specific Copy Number in Next-Generation Sequencing Data | falcon |
| Getting Allele-specific DNA Copy Number | getASCN |
| Getting Change-points | getChangepoints |
| Position (bp) | pos |
| An example reads count data | readMatrix |
| Estimated Break Points | tauhat |
| Viewing Data with Allele-specific Copy Number | view |