Skip site navigation (1)Skip section navigation (2)
Date:      Sun, 29 Jul 2018 23:18:21 +0000
From:      bugzilla-noreply@freebsd.org
To:        ports-bugs@FreeBSD.org
Subject:   [Bug 230169] biology/bcftools: Update 1.9
Message-ID:  <bug-230169-7788@https.bugs.freebsd.org/bugzilla/>

next in thread | raw e-mail | index | archive | help
https://bugs.freebsd.org/bugzilla/show_bug.cgi?id=3D230169

            Bug ID: 230169
           Summary: biology/bcftools: Update 1.9
           Product: Ports & Packages
           Version: Latest
          Hardware: Any
                OS: Any
            Status: New
          Severity: Affects Only Me
          Priority: ---
         Component: Individual Port(s)
          Assignee: ports-bugs@FreeBSD.org
          Reporter: ndowens.fbsd@yandex.com
                CC: cartwright@asu.edu
             Flags: maintainer-feedback?(cartwright@asu.edu)
                CC: cartwright@asu.edu

Created attachment 195614
  --> https://bugs.freebsd.org/bugzilla/attachment.cgi?id=3D195614&action=
=3Dedit
Update

Release Notes:

    annotate

        REF and ALT columns can be now transferred from the annotation file.

        fixed bug when setting vector_end values.

    consensus

        new -M option to control output at missing genotypes

        variants immediately following insersions should not be skipped. No=
te
however, that the current fix requires normalized VCF and may still falsely
skip variants adjacent to multiallelic indels.

        bug fixed in -H selection handling

    convert

        the --tsv2vcf option now makes the missing genotypes diploid, "./."
instead of "."

        the behavior of -i/-e with --gvcf2vcf changed. Previously only sites
with FILTER set to "PASS" or "." were expanded and the -i/-e options dropped
sites completely. The new behavior is to let the -i/-e options control which
records will be expanded. In order to drop records completely, one can stre=
am
through "bcftools view" first.

    csq

        since the real consequence of start/splice events are not known, the
aminoacid positions at subsequent variants should stay unchanged

        add --force option to skip malformatted transcripts in GFFs with
out-of-phase CDS exons.

    +dosage: output all alleles and all their dosages at multiallelic sites

    +fixref: fix serious bug in -m top conversion

    -i/-e filtering expressions:

        add two-tailed binomial test

        add functions N_PASS() and F_PASS()

        add support for lists of samples in filtering expressions, with many
samples it was impractical to list them all on the command line. Samples ca=
n be
now in a file as, e.g., GT[@samples.txt]=3D"het"

        allow multiple perl functions in the expressions and some bug fixes

        fix a parsing problem, @ was not removed from @filename expressions

    mpileup: fixed bug where, if samples were renamed using the -G
(--read-groups) option, some samples could be omitted from the output file.

    norm: update INFO/END when normalizing indels

    +split: new -S option to subset samples and to use custom file names
instead of the defaults

    +smpl-stats: new plugin

    +trio-stats: new plugin

    Fixed build problems with non-functional configure script produced on s=
ome
platforms

--=20
You are receiving this mail because:
You are the assignee for the bug.=



Want to link to this message? Use this URL: <https://mail-archive.FreeBSD.org/cgi/mid.cgi?bug-230169-7788>