Ubuntu
snpsift package

snpsift 5.1+dfsg2-2 source package in Ubuntu

snpsift (5.1+dfsg2-2) unstable; urgency=medium

  * Source-only upload

 -- Pierre Gruet <email address hidden>  Sun, 27 Feb 2022 14:17:09 +0100

Series	Pocket	Published	Component	Section
Noble	release	on 2023-10-23	universe	misc
Mantic	release	on 2023-04-25	universe	misc
Lunar	release	on 2022-10-27	universe	misc

File	Size	SHA-256 Checksum
snpsift_5.1+dfsg2-2.dsc	2.4 KiB	0385efb8c9358e42d346aa8bc5f611a2b1b42969c11d931a7de82f697b7c84b3
snpsift_5.1+dfsg2.orig.tar.xz	6.2 MiB	ac6d61b9e4656d3f2134ffdd08f497741622d14aa41767c117cf1d6d60b01556
snpsift_5.1+dfsg2-2.debian.tar.xz	6.9 KiB	2a7168509b64ab6d9bbd4a590c8243dfa863be7df3c87b2226bd2f0d700b307e

No changes file available.

libsnpsift-java: tool to annotate and manipulate genome variants - lib: SnpSift is a toolbox that allows one to filter and manipulate annotated files.
Once the genomic variants have been annotated, one needs to filter them out in
order to find the "interesting / relevant variants". Given the large data
files, this is not a trivial task (e.g. one cannot load all the variants into
XLS spreadsheet). SnpSift helps to perform this VCF file manipulation and
filtering required at this stage in data processing pipelines.
.
This package contains the library.

libsnpsift-java-doc: No summary available for libsnpsift-java-doc in ubuntu kinetic.: No description available for libsnpsift-java-doc in ubuntu kinetic.

snpsift: tool to annotate and manipulate genome variants - tool: SnpSift is a toolbox that allows one to filter and manipulate annotated files.
Once the genomic variants have been annotated, one needs to filter them out in
order to find the "interesting / relevant variants". Given the large data
files, this is not a trivial task (e.g. one cannot load all the variants into
XLS spreadsheet). SnpSift helps to perform this VCF file manipulation and
filtering required at this stage in data processing pipelines.
.
This package contains the command line tool.