Description Usage Arguments Details Value Author(s) Examples
Creates an instance of S4 class SGVariants
for storing
splice variants.
1 | SGVariants(x)
|
x |
|
SGVariants
includes columns as described below.
from
and to
indicate the variant start and end,
respectively. from
nodes are splice donors (“D”)
or transcript starts (“S”). to
nodes are splice
acceptors (“A”) or transcript ends (“E”).
type
and featureID
describe the variant in
terms of the splice graph features that make up the variant.
segmentID
specifies unique identifiers labelling
unbranched segments of the splice graph.
closed5p
indicates whether nodes in the variant can be
reached from nodes outside of the variant exclusively through the
from
node.
closed3p
indicates whether nodes in the variant can reach
nodes outside of the variant exclusively through the to
node.
closed5pEvent
indicates whether nodes in the event can
be reached from nodes outside of the event exclusively through the
from
node.
closed3pEvent
indicates whether nodes in the event can
reach nodes outside of the event exclusively through the to
node.
geneID
has the same interpretation as for
SGFeatures
.
eventID
and variantID
are unique identifiers for
each event and variant, respectively.
featureID5p
and featureID3p
indicate representative
features used for variant quantification at the start and end of the
variant, respectively.
featureID5pEvent
and featureID3pEvent
indicate the
ensemble of representative features at the start and end of the event,
respectively.
txName
indicates structurally compatible transcripts.
geneName
behaves as for SGFeatures
.
variantType
indicates whether a splice variant is
consistent with a canonical splice event (for a list of possible
values, see the manual page for annotateSGVariants
).
variantName
provides a unique name for each splice variant
(for details, see the manual page for makeVariantNames
).
SGVariants
object
Leonard Goldstein
1 | sgv <- SGVariants()
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