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 #2448750 - CVE-2026-31962 htslib: htslib: Heap buffer overflow leading to arbitrary code execution via crafted CRAM file
https://bugzilla.redhat.com/show_bug.cgi?id=2448750
[ 2 ] Bug #2448751 - CVE-2026-31965 htslib: HTSlib: Information disclosure or denial of service via out-of-bounds read in CRAM record processing
https://bugzilla.redhat.com/show_bug.cgi?id=2448751
[ 3 ] Bug #2448755 - CVE-2026-31963 htslib: HTSlib: Arbitrary code execution via crafted CRAM file
https://bugzilla.redhat.com/show_bug.cgi?id=2448755
[ 4 ] Bug #2448756 - CVE-2026-31964 htslib: HTSlib: Denial of Service via NULL pointer dereference in CRAM decoding
https://bugzilla.redhat.com/show_bug.cgi?id=2448756
This update can be installed with the "dnf" update program. Use su -c 'dnf upgrade --advisory FEDORA-2026-3b06345bf2' 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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