cnvkit binary package in Ubuntu Focal amd64
A command-line toolkit and Python library for detecting copy number variants
and alterations genome-wide from targeted DNA sequencing. It is designed for
use with hybrid capture, including both whole-exome and custom target panels,
and short-read sequencing platforms such as Illumina and Ion Torrent.
Publishing history
| Date | Status | Target | Component | Section | Priority | Phased updates | Version | ||
|---|---|---|---|---|---|---|---|---|---|
| 2020-01-07 19:48:13 UTC | Published | Ubuntu Focal amd64 | release | universe | science | Optional | 0.9.6-3 | ||
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| Deleted | Ubuntu Focal amd64 | proposed | universe | science | Optional | 0.9.6-3 | |||
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| 2020-01-07 19:48:17 UTC | Superseded | Ubuntu Focal amd64 | release | universe | science | Optional | 0.9.6-2 | ||
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| 2020-01-09 00:10:12 UTC | Deleted | Ubuntu Focal amd64 | proposed | universe | science | Optional | 0.9.6-2 | ||
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| 2019-11-14 02:28:27 UTC | Superseded | Ubuntu Focal amd64 | release | universe | science | Optional | 0.9.6-1 | ||
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| 2019-11-15 06:10:10 UTC | Deleted | Ubuntu Focal amd64 | proposed | universe | science | Optional | 0.9.6-1 | ||
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| 2019-10-30 14:23:30 UTC | Superseded | Ubuntu Focal amd64 | release | universe | science | Optional | 0.9.5-3 | ||
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