BCFtools is a set of utilities that manipulate genomic variant calls in the
Variant Call Format (VCF) and its binary counterpart (BCF). All commands work
transparently with both VCFs and BCFs, both uncompressed and BGZF-compressed.
(This BCFtools includes the polysomy subcommand, which is implemented using
the GNU Scientific Library. Hence this package is licensed according to the
GNU General Public License, rather than the MIT license used when BCFtools
is built without the polysomy subcommand.)
Update Information:
Update to 1.23.1
* Thu Mar 19 2026 Rasmus Ory Nielsen
[ 1 ] Bug #2448857 - CVE-2026-31972 samtools: SAMtools: Information Disclosure and Denial of Service via use-after-free vulnerability in mpileup command
https://bugzilla.redhat.com/show_bug.cgi?id=2448857
[ 2 ] Bug #2448860 - CVE-2026-31973 samtools: SAMtools: Denial of Service due to NULL pointer dereference in cram-size command
https://bugzilla.redhat.com/show_bug.cgi?id=2448860
This update can be installed with the "dnf" update program. Use su -c 'dnf upgrade --advisory FEDORA-2026-cb321bebb5' at the command line. For more information, refer to the dnf documentation available at http://dnf.readthedocs.io/en/latest/command_ref.html#upgrade-command-label
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