[Bioc-devel] InteractionSet for structural variants

[Kasper Daniel Hansen]

I know little about SV and the associated software, but it is clear to me
that we will see a lot of "personal" genomes in the future and having the
ability to move between different reference genomes (coordinate systems)
will be something I think we should think about having good/great support
for.

On Tue, May 21, 2019 at 9:37 AM Michael Lawrence via Bioc-devel <
bioc-devel using r-project.org> wrote:

> The new package StructuralVariantAnnotation is worth mentioning. It
> operates on the general "breakend" notation so should be able to represent
> any type of structural variant.
>
> On Tue, May 21, 2019 at 3:22 AM Sean Davis <seandavi using gmail.com> wrote:
>
> > On Tue, May 21, 2019 at 2:54 AM Aaron Lun <
> > infinite.monkeys.with.keyboards using gmail.com> wrote:
> >
> > > > Thanks for your response. So far my intention is to to plot them and
> I
> > > > do not intend on performing any other operation. The first step would
> > be
> > > > read in the VCF file and transform it into a meaningful object and I
> > was
> > > > hoping there was a core package already taking care of that, but I
> get
> > > > from your answer that there's no such functionality implemented.
> > >
> > > Not to my knowledge... but if you're planning on writing some relevant
> > > functions, I'm sure we could find a home for it somewhere.
> > >
> >
> > I do have a couple of simple functions in VCFWrenchR (not in Bioc), but
> > like much VCF code, it probably misses a bunch of edge cases. The
> functions
> > target VRanges, not interactionsets.
> >
> > https://github.com/seandavi/VCFWrenchR
> >
> > Sean
> >
> >
> > > -A
> > >
> > > > El 5/18/19 a las 4:47 AM, Aaron Lun escribió:
> > > >> I would say that it depends on what operations you intend to perform
> > > >> on them. You can _store_ things any way you like, but the trick is
> to
> > > >> ensure that operations and manipulations on those things are
> > > >> consistent and meaningful. It is not obvious that there are
> meaningful
> > > >> common operations that one might want to apply to all structural
> > > >> variants.
> > > >>
> > > >> For example, translocations involve two genomic regions (i.e., the
> two
> > > >> bits that get stuck together) and so are inherently
> two-dimensional. A
> > > >> lot of useful operations will be truly translocation-specific, e.g.,
> > > >> calculation of distances between anchor regions, identification of
> > > >> bounding boxes in two-dimensional space. These operations will be
> > > >> meaningless to 1-dimensional variants on the linear genome, e.g.,
> > > >> CNVs, inversions. The converse also applies where operations on the
> > > >> linear genome have no single equivalent in the two-dimensional case.
> > > >>
> > > >> So, I would be inclined to store them separately. If you must keep
> > > >> them in one object, just lump them into a List with "translocation"
> > > >> (GInteractions), "cnv" (GRanges) and "inversion" (another GRanges)
> > > >> elements, and people/programs can pull out bits and pieces as
> needed.
> > > >>
> > > >> -A
> > > >>
> > > >>
> > > >> On 5/17/19 4:38 AM, Bernat Gel Moreno wrote:
> > > >>> Hi all,
> > > >>>
> > > >>> Is there any standard recommended container for genomic structural
> > > >>> variants? I think InteractionSet would work fine for translocation
> > and
> > > >>> GRanges for inversions and copy number changes, but I don't know
> what
> > > >>> would be the recommended way to store them all together using
> > standard
> > > >>> Bioconductor objects.
> > > >>>
> > > >>> And actually, is there any package that would load a SV VCF by
> lumpy
> > or
> > > >>> delly and build that object?
> > > >>>
> > > >>> Thanks!
> > > >>>
> > > >>> Bernat
> > >
> >
> >         [[alternative HTML version deleted]]
> >
> > _______________________________________________
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> >
>
>
> --
>
> Michael Lawrence
>
> Scientist, Bioinformatics and Computational Biology
>
> Genentech <https://www.gene.com/>, A Member of the Roche Group
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