saasCNV
Somatic Copy Number Alteration Analysis Using Sequencing and SNP Array Data
Perform joint segmentation on two signal dimensions derived from total read depth (intensity) and allele specific read depth (intensity) for whole genome sequencing (WGS), whole exome sequencing (WES) and SNP array data.
Versions across snapshots
| Version | Repository | File | Size |
|---|---|---|---|
0.3.4 |
rolling linux/jammy R-4.5 | saasCNV_0.3.4.tar.gz |
823.8 KiB |
0.3.4 |
rolling linux/noble R-4.5 | saasCNV_0.3.4.tar.gz |
823.8 KiB |
0.3.4 |
rolling source/ R- | saasCNV_0.3.4.tar.gz |
823.8 KiB |
0.3.4 |
latest linux/jammy R-4.5 | saasCNV_0.3.4.tar.gz |
823.8 KiB |
0.3.4 |
latest linux/noble R-4.5 | saasCNV_0.3.4.tar.gz |
823.8 KiB |
0.3.4 |
latest source/ R- | saasCNV_0.3.4.tar.gz |
823.8 KiB |
0.3.4 |
2026-04-26 source/ R- | saasCNV_0.3.4.tar.gz |
823.8 KiB |
0.3.4 |
2026-04-23 source/ R- | saasCNV_0.3.4.tar.gz |
823.8 KiB |
0.3.4 |
2025-04-20 source/ R- | saasCNV_0.3.4.tar.gz |
823.8 KiB |