[ Източник: cnvkit ]
Пакет: cnvkit (0.9.10-2)
Връзки за cnvkit
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Изтегляне на пакет-източник cnvkit.
Отговорници:
- Debian Med Packaging Team (Страница за QA, Пощенски архив)
- Michael R. Crusoe (Страница за QA)
- Steffen Moeller (Страница за QA)
- Olivier Sallou (Страница за QA)
Външни препратки:
- Начална страница [cnvkit.readthedocs.org]
Подобни пакети:
Copy number variant detection from targeted DNA sequencing
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.
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Изтегляне на cnvkit
Архитектура | Големина на пакета | Големина след инсталиране | Файлове |
---|---|---|---|
all | 19 044,6 кБ | 94 731,0 кБ | [списък на файловете] |