inferCNV¶
InferCNV is used to explore tumor single cell RNA-Seq data to identify evidence for somatic large-scale chromosomal copy number alterations, such as gains or deletions of entire chromosomes or large segments of chromosomes.
homepage: https://github.com/broadinstitute/inferCNV/wiki
| version | versionsuffix | toolchain |
|---|---|---|
1.0.4 |
-Python-3.7.2-R-3.6.0 |
foss/2019a |
1.10.1 |
-R-4.1.2 |
foss/2021b |
1.12.0 |
-R-4.2.1 |
foss/2022a |
1.14.2 |
-R-4.2.2 |
foss/2022b |
1.2.1 |
-Python-3.7.4 |
foss/2019b |
1.21.0 |
-R-4.3.2 |
foss/2023a |
1.3.3 |
-Python-3.8.2 |
foss/2020a |
1.3.3 |
foss/2020b |
|
1.3.3 |
foss/2021a |
(quick links: (all) - 0 - a - b - c - d - e - f - g - h - i - j - k - l - m - n - o - p - q - r - s - t - u - v - w - x - y - z)