Difference between revisions of "POC Conf. Call 6-28-11"

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'''POC meeting, Webex Conference Call; Date: Tuesday June 14th, 2011 10am (PDT)'''
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'''POC meeting, Webex Conference Call; Date: Tuesday June 21st, 2011 10am (PDT)'''
  
 
In attendance:  
 
In attendance:  
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Acceptance of the minutes from the [[POC_Conf._Call_6-7-11]]?
 
Acceptance of the minutes from the [[POC_Conf._Call_6-7-11]]?
  
=User requests still open on Source Forge: PSO=
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'''This meeting is postponed until 6-28-11, due to webinar with the Physco group in Germany.'''
  
==[https://sourceforge.net/tracker/?func=detail&aid=3040048&group_id=76834&atid=835555 Legume terms]==
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=New items=
 +
==Report from the[http://www.iplantcollaborative.org/2011/02/09/2011-semantic-web-workshop-june-6-7-santa-fe-nm 2011 Semantic Web Workshop] June 6th and 7th, Santa Fe, NM==
  
submitted by Austin Mast
 
  
Several terms have already been dealt with (Taproot, Stem Hair, Prickles, Anther pore and anther slit)
+
Hosted by Damian Gessler and the iPlant Collaborative, this two-day workshop will focus on biological applications for semantic web services.
  
[https://sourceforge.net/tracker/?func=detail&aid=3165981&group_id=76834&atid=835555 fascicle] The term fascicle can refer to different structures in different taxa. Suggest we use the term '''floral fascicle''' or '''flower fascicle''' in this case, to distinguish it from a "leaf fascicle," which we may want to add for describing gymnosperms.
+
-JE and JP will be attending
  
From Tucker, 2003, Flora:
+
-JE has already worked with Damian to implement a SSWAP web service for PO terms, so further collaboration with him and iPlant will benefit the POC going forward.  
(in the Papilionoideae) "Pseudoracemes (Fig. 5B) differ from racemes in
 
that two to several flowers are initiated in each bract axil rather than
 
just one as in a raceme. '''The cluster of flowers at each node is called a fascicle.''' The order of initiation among flowers at a node (Fig. 5B, Psoralea macrostachys DC) shows
 
'''the fascicle to be a short shoot topped by a second order inflorescence apical meristem'''. This meristem initiates
 
flowers in a bilaterally symmetrical order: a single abaxial flower, then
 
two lateral flowers, another median abaxial, then two more laterals. The
 
number of flowers per fascicle depends on the duration of the axillary
 
inflorescence apex of the short shoot, which ceases activity after
 
initiating the few flowers in the fascicle. No flowers are initiated
 
adaxially (toward the first order axis) on the short shoot (Tucker, 1987b;
 
Tucker and Stirton, 1991). The short shoot in a pseudoraceme can be
 
distinguished from a cyme in that every flower is bract subtended in a
 
pseudoraceme."
 
  
'''Proposed def:''' A second order inflorescence in which the second order inflorescence branch bears two or more flowers but is not elongated. Comment: A fascilce appears to be a cluster of flowers in an axil of a single bract of the main inflorescence. Common in some sections of the Fabaceae.
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For more Workshop details: [http://www.iplantcollaborative.org/Communities/Developers/SemanticWeb Semantic web].
  
 +
=Tech issues=
 +
==New xref in database==
  
[https://sourceforge.net/tracker/?func=detail&aid=3165983&group_id=76834&atid=835555 bristle] (used in key as "Stipules spinose or bristles"; might be thought of as a quality, rather than a structure)
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A stanza for our SF tracker has been added to GO.xrf_abbs (thanks to Becky Foulger):
  
We added the term stipule spine. Could also add the term '''stipule bristle''': A stipule that has a brush-like appearance.
+
abbreviation: OBO_SF_PO
  
Alternative is to suggest bristled to PATO
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database: Source Forge OBO Plant Ontology (PO) term request tracker
  
 +
object: Term request
  
[https://sourceforge.net/tracker/?func=detail&aid=3165984&group_id=76834&atid=835555 phyllode]
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example_id: OBO_SF_PO:3184921
  
'''Proposed def:''' A leaf in which there is no normal lamina development, but instead the petiole or petiole plus rachis is laminar.
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generic_url: http://sourceforge.net/tracker/?func=browse&group_id=76834&atid=835555
  
 +
url_syntax: https://sourceforge.net/tracker/index.php?func=detail&aid=[example_id]&group_id=76834&atid=835555
  
[https://sourceforge.net/tracker/?func=detail&aid=3165994&group_id=76834&atid=835555 banner, wing and keel]
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url_example: https://sourceforge.net/tracker/index.php?func=detail&aid=3184921&group_id=76834&atid=835555
  
'''Banner''' (as in a legume flower) - suggest using name 'banner petal'
 
  
'''Proposed def:''' A petal that is the top-most petal of a corolla in some flowers of the Fabaceae. Comment: The banner is usually larger than the adjacent wing petals.
+
RW also updated the file at http://plantontology.org/docs/dbxref/PO_DBXref.txt.
  
 +
===Action items===
  
'''Wing''' (as in a legume flower) - suggest using name 'wing petal'
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'''Do we need to do anything else to get the new xrefs to link automatically?'''
  
'''Proposed def:''' One of two petals that is adjacent to the banner petal in some flowers of the Fabaceae. Comment: The wing petals are usually much smaller than the banner petal and the corolla keel.
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==Concern from TAIR over how annotations move through relations==
  
 +
Excerpts rom Tanya's message:
  
'''Keel''' (as in a legume flower): The keel consists of two fused petals, and is analogous to the fused collective tepal structure we made for Musa. Maybe name 'corolla keel'
+
We're working on integrating the new relationships that PO is using into our local system and were wondering about handling annotation count propagation over some of these relationships.
  
Suggest three new terms:
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For example,  anther wall endothecium and anther wall middle layer are adjacent.  When you look for annotations to anther wall endothecium, one also retrieves annotations to anther wall middle layer: http://plantontology.org/amigo/go.cgi?view=assoc&search_constraint=terms&query=PO:0020002 Somehow, this does not seem like the expected (or desired) result. 
  
'''fused petal:''' A petal that is fused to another petal.
+
I was wondering '''if you would consider producing a file of the PO that does not contain the 'trickier to count' new relationships?'''
  
Comment: May be fused to two petals (one on either side). This is a phenotype that is a cross-product of PO:0009032 (petal) and PATO:0000642 (fused with).
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===Action items===
  
 +
'''Do we want to create a file without has_part, develops_from, derives_from, and adjacent_to?'''
  
'''fused corolla:''' A corolla in which the petals are fused.
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=Items arising from previous meetings:=
 +
==Children of Leaf- feedback from TAIR:==
 +
The following is a summary from the email correspondence, from Tanya Berardini:
  
Comment: This is a phenotype that is a cross-product of PO:0025023 (collective phyllome structure) and PATO:0000642 (fused with). A corolla may consist of a combination of fused and free petals, in which case fused corolla only refers to those petals that are fused.
+
* TAIR strongly supports creating specific vascular and non-vascular children for leaf apex and similar terms that are part_of leaf, like those describing the leaf apex in rosette leaves and cauline leaves.  
 +
* TAIR proposes we create more specific terms for the is_a children of vascular leaf, like cauline leaf. For example, 'cauline leaf margin' and 'rosette leaf margin'. 
 +
* TAIR suggests creating the terms which already have annotations attached to them, like 'vascular leaf margin' (current Arabidopsis, rice, maize annotations to 'leaf margin') and  adding other terms upon request by annotators or users.
  
 +
Their Reasons:
  
'''corolla keel:''' A fused corolla that consists of the two lowest petals in some flowers of the Fabaceae.  
+
*Much easier for annotators to choose the specific term they need as opposed to having to remember to co-annotate or having a script go in after and clean up
 +
*Benefits for the researcher who is looking for very specific information
 +
*The added granularity of these terms will be a benefit when people want to describe structures such as the leaf apex in rosette leaves and cauline leaves.
 +
*They are not worried about term inflation
 +
*A researcher browsing through the ontology would not know to look at annotations to see that there are combinations of annotations that give the 'same' result ('leaf apex' + 'rosette leaf')
 +
*The current functionality of AmiGO does not allow a search for gene products annotated to Term A AND Term B.
 +
*The the combinatorial solution work will not work if a gene is expressed only in the 'leaf margin of cauline leaves' and in the 'leaf apex of rosette leaves'.  How do we know which 'part' goes with which 'leaf'?
 +
*Unless the co-annotations are captured in a single line in the gaf file (possible with column 16), this could lead to misinformation.
  
Comment: The two petals of the keel may be fused at the apex but free at the base. The remaining three petals (banner and two wings) are free. The keel is boat shaped.
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==Questions and suggestions from last week's meeting:==
  
==TraitNet requests==
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-We could create specific child terms, but at what level should we stop?
  
[https://sourceforge.net/tracker/?func=detail&aid=3080906&group_id=76834&atid=835555 corm]
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-Users could post-compose terms, but then, those terms ultimately would need to go into the PO so that future work could reference the definitions, so it doesn't save much over precomposing the terms (but it does provide a guide for when to stop adding term: you stop at what the users need.
  
proposed def: A short, enlarged storage stem in which the internodes do not elongate. Comment: usually underground.
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-There is an issue of training. Annotators will have to be taught to annotate to the part of the leaf and the type of leaf. The same applies of other types of plant structures as well.  
  
child of stem (PO:0009047).
+
-We could use a script to move annotation from the parts of leaf to the appropriate type of leaf, but this effectively creates another line in the annotation file, and does not solve the problem of how to associate two different annotations (like the annotation to leaf margin with the annotation to rosette leaf). To do this, we need to have the information in the same row of the annotation file.''
  
 +
-Does the GAF format allow us to put the PO id for the type of leaf in column 16? If we put the PO id in column 16, will that create an annotation to that term? Probably we will still have to make a separate line for that annotation.  See: [http://www.geneontology.org/GO.format.gaf-2_0.shtml GO annotation file GAF 2.0 format guide].
  
[https://sourceforge.net/tracker/?func=detail&aid=3080911&group_id=76834&atid=835555 podarium]
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-Rather than setting a strict policy about when to inflate or not, we should probably consider it on a case by case basis. We could start by adding pre-composed terms for those structures that already have annotations associated with them (see below), then asking TAIR and other users to use column 16 to post-compose any other term they might need. They can also use column 16 to associate a structure with a growth or developmental stage. See below for more details.
  
Their comment: is synonym to Tubercle
+
-We should set up a meeting with TAIR to explain to them why we don't want to add all of the specific children, and to work them on a solution. It is important that we have the script for transferring annotation up and running, and that we test out how we can use column 16 for associating leaf types '''before''' we meet with them.
  
podarium (from Beentje 2010): (in cacti or other succulents) a modified leaf base functioning as the photosynthesising organ.
+
-Need to consider how this will affect the processing of the annotation files that happens with each release.
  
tubercle (from Beentje 2010): (in ball- or barrel- shaped cacti), cone-shaped protuberances that are elnarge modified leaf bases fused with adjacent stem tissue (tubercle has two other definitions as well).
 
  
proposed def:
+
===Other related suggestions:===
  
 +
1. Make rosette leaf and cauline leaf is_a children of leaf, rather than is_a children of vascular leaf. Then we could make children vascular rosette leaf and vascular cauline leaf. Do we need these parent terms if rosette leaf and cauline leaf only occur in vascular leaves? (RW: We should create a SF tracker for this.)  Also, we need to work on the definitions of rosette leaf and cauline leaf. Should link them to growth stages, because (at least in Arabidopsis and other Brassicaceae) they are the same leaves at different times.
  
[https://sourceforge.net/tracker/?func=detail&aid=3080913&group_id=76834&atid=835555 pneumatophore]
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2. Move all leaf parts (be they part_of vascular leaf, part_of non-vascular leaf or part_of leaf) to be part_of leaf, so that users could find all of the parts in one place. This might also force them to make the second annotation to the type of leaf. PJ suggested that we could use disjoint_from relation. For example: have leaf vascular system be a part_of leaf (instead of part_of vascular leaf) then make it disjoint_from non-vascular leaf. This would prevent curators form making an association to the wrong type of leaf. Problem with this is that we intentionally omit information that we know to be true (e.g., we would leave out leaf vascular system part_of vascular leaf). That is not necessarily bad, but we need to have a good reason for it.
  
definition from Beentje (2010): erect (breathing) root protruding above the soil, encountered especially in mangroves
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3. Add disjoint_from relations between vascular leaf and non-vascular leaf. In OWL you have to do that, because if you don't assert it, OWL assumes they are not disjoint.''
  
proposed def: A root that is erect and protrudes above the soil, found in trees that live in flooded habitats such as mangroves. Comment: Pneumatophores may provide oxygen to below ground roots growing in flooded soils.
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4. We have both non-vascular leaf meristematic apical cell and vascular leaf meristematic apical cell. We should merge those with leaf apical cell if we are going to be strict about not making any specific part_of children of different leaf types.
  
 +
==Proposed solutions:==
 +
'''All:''' Create specific children for all of the parts of leaf, for each type of leaf. This is pretty much what we did for tuber, although it only has 2 is_a descendents and 8 part_of descendents. There are 15 is_a descendents of leaf (juvenile leaf, transition leaf, adult leaf, transition leaf, non-vascular leaf, vascular leaf, simple leaf, compound leaf, rosette leaf, cauline leaf, cigar leaf, embyro leaf, leaf spine, cotyledon, and flag leaf) and about 30 part_of descendents (not counting those that are only part of vascular or non-vascular leaf), so if we created all of the combinations of child terms it would add about 450 new terms.
  
 +
'''Nothing:''' Do not create any specific part_of children for vascular leaf and other types of leaves. Keep or move all part_of children under leaf, and use column 16 to create cross-products to the correct type of leaf.
  
[https://sourceforge.net/tracker/?func=detail&aid=3080916&group_id=76834&atid=835555 diaspore]
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'''Somewhere in between:''' There are 21 part_of descendents of leaf that currently have annotations associated with them. All of these annotations come from vascular plants. We could create specific part_of vascular leaf children only for these 21 terms, and then add others as annotations for them arise.  
  
definition from Beentje (2010): reproductive portion of a plant, such as a seed, fruit or fragment of fruit, that is dispersed and may give rise to a new plant.
+
We could adopt a policy of only adding specific part_of children for vascular leaf and non-vascular leaf. All other leaf types could be considered phenotypes (e.g. compound or simple leaf, spine leaf) or growth-stage specific forms (e.g., embryo leaf or cotyledon), and we could ask annotators to use column 16 to associate the part of the leaf to the type of leaf in these cases.
  
We could add this term as a kind of upper level bin term (similar to trichome)
 
  
 +
Unless we adopt the "All" strategy (which seems impracticle), we will need a mechanism for associating the annotation that is on the part_of a leaf to the correct type of leaf. Such a mechanism would be very useful for other types of structures, as it would allow users to create new cross-product terms on the fly. It could also be used to more accurately annotate gene expression that occurs in a structures at a specific growth stage (right now, users simply put the annotation on both the structure and the growth stage, without any link between them). Annotation extensions (Column 16) allow us to do this.
  
[https://sourceforge.net/tracker/?func=detail&aid=3080919&group_id=76834&atid=835555 cone]
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See [[PO_Annotation_Extensions_(column_16)]] for a full explanation of how this would work.
  
Should probably be a synonym of strobilus (PO:0025083). Narrow or exact?
+
===Action items===
 +
???
  
 +
==Annotations on terms that are part_of leaf==
  
[https://sourceforge.net/tracker/?func=detail&aid=3080922&group_id=76834&atid=835555 sorus]
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The list below contains all of the terms that are part_of leaf and have annotations associated with them.  
  
from Crum (2001): a cluster of fern sporangia
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In the last round of revisions, we decided that any existing annotation for these terms should also be copied to vascular leaf. Future annotations should go to both the part and to the appropriate leaf type. However, we have not actually transferred any of the annotation yet.
from Beentje (2010): (of pteridophytes) structure bearing or containing groups of sporangia.
 
  
Proposed definition: A cardinal organ part composed of a cluster of two or more adjacent sporagia on the surface of a leaf. Comment: May be enclosed by an indusium.
 
  
Part_of vascular leaf, has_part sporangium
+
term name - (id) - number of annotations (from version 14, not from most recent association files)
  
 +
*leaf aerenchyma (PO:0006215) 1
  
[https://sourceforge.net/tracker/?func=detail&aid=3080925&group_id=76834&atid=835555 tendril]
+
*leaf apex (PO:0020137) 12890
  
Defintion from Beentje (2010): a slender, coiling structure derived from a branch, leaf or inflorescence and used for climbing.
+
*leaf base (PO:0020040) 5
  
tendrils can derived from multiple types of structures. Suggest we make separate terms:  
+
*leaf epidermis (PO:0006016)365, includes:  
  
branch tendril (child of branch): A branch that is slender and coiling. Comment: Aids plant in climbing.
+
**buliform cell (PO:0004001) 1
  
leaf tendril (child of leaf): A leaf that is slender and coiling and lacks a lamina. Comment: Aids plant in climbing.
+
**leaf abaxial epidermis (PO:0006019) 4
  
leaflet tendril (child of leaflet): A leaflet that is slender and coiling and lacks a lamina. Comment: Aids plant in climbing.
+
**leaf adaxial epidermis (PO:0006018) 4
  
leaf apex tendril (child of leaf apex): A leaf apex that is slender and coiling. Comment: Found at the apex of a leaf lamina, but the leaf apex tendril is not laminar. Aids plant in climbing.
+
**leaf lamina epidermis (PO:0000047) 1
  
Can add other types of tendrils if they come up or users need them.
+
**leaf trichome (PO:0006504) 63
  
 +
*leaf intercalary meristem (PO:0006346) 1
  
Alternative is to create a parent 'tendril'(is_a plant structure) with children that are part_of the other structures:
+
*leaf lamina (PO:0020039) 12800, includes:
  
tendril
+
**leaf lamina base (PO:0008019) 12614
  
is_a leaf tendril part_of leaf
+
**leaf lamina vascular system (PO:0000048) 1 (already shows up under vascular leaf)
  
is_a stem tendril part_of stem
+
*leaf margin (PO:0020128) 100
  
is_a branch tendril part_of branch
+
*leaf mesophyll (PO:0005645) 762, includes:
  
==[https://sourceforge.net/tracker/index.php?func=detail&aid=2899934&group_id=76834&atid=835555 root terms]==
+
**palisade mesophyll cell (PO:0006206) 1
  
Submitted by Rich Zobel (Nov 2009).
+
**spongy mesophyll (PO:0005647) 1
  
Still need to work on definitions for these terms.
+
**spongy mesophyll cell (PO:0006205) 2
  
=User requests still open on Source Forge; PGDSO =
+
**leaf prickle (PO:0025175) 0
==[https://sourceforge.net/tracker/index.php?func=detail&aid=3035688&group_id=76834&atid=835555 terms for seed trichome development stages]==
 
  
Open since 07-28-2010
+
*leaf sheath (PO:0020104) 205, includes:
  
===Request===
+
**leaf sheath pulvinus (PO:0008017) 2
 +
  
The following terms have been requested for cotton fiber development (their structure and defintions):
+
If we were to adopt a policy of only creating specific terms when they are needed for annotation, we would have to create a vascular leaf child for each of these 21 terms.
  
seed development stages PO: 0001170
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=Upcoming meetings 2011:=
  
---[part_of]Seed hair development stages
+
'''Botany 2011 Meeting [[http://www.botanyconference.org/ Botany 2011]]'''  St. Louis, MO at the Chase Park Plaza, July 9-13.
  
---[part_of]seed hair initiation stage: The earliest histological
+
Societies participating:  
evidence of seed hair initiation, ie, a change in the orientation of cell
+
Society for Economic Botany, the American Fern Society (AFS), the American Society of Plant Taxonomists (ASPT), and the Botanical Society of America (BSA).
division in the ovule epidermises occurs at or just before anthesis. (Ruan
 
YL, 2003, Plant Cell 15:952-964) [Source:PMID: 12671090].
 
  
---[part_of]seed hair elongation stage: A period of rapid elongation
+
Anybody going??
of hair initials without cell division for 16-25 days. (Lee JJ, 2007,
 
Annals of Botany 100:1391-1401 and Ruan YL, 2003, Plant Cell 15:952-964)
 
[Sources:PMID: 17905721, PMID: 12671090].
 
  
---[part_of] seed hair secondary wall biosynthesis stage: A phase of
 
the massive amounts of secondary cell wall cellulose synthesis. (Lee JJ,
 
2007, Annals of Botany 100:1391-1401 and Ruan YL, 2003, Plant Cell
 
15:952-964) [Sources: PMID:17905721, PMID:12671090].
 
  
---[part_of]seed hair maturation stage: A period of seed hair
+
'''* ICBO 2011  Second International Conference on Biomedical Ontology'''
maturation from 50 to 60 days post-anthesis (DPA).
+
July 26-30, 2011
(Lee JJ, 2007, Annals of Botany 100:1391-1401 and Ruan YL, 2003, Plant
+
Buffalo, New York
Cell 15:952-964) [Sources: PMID:17905721, PMID:12671090].
 
  
===Suggested terms and definitions:===
+
[http://icbo.buffalo.edu ICBO]
  
'''Do we want to use stage or phase throughout PGDSO?'''
+
LC is co-organizing the workshop "From Fins to Limbs to Leaves: Facilitating anatomy ontology interoperability"
 +
along with Melissa Haendel, Chris Mungall, Alan Ruttenberg, David Osumi-Sutherland.
  
'''seed development stages (PO:0001170)'''
+
'''Full-Day Workshops Schedule:'''
  
'''Current definition:''' Stages of seed development, from fertilization to the dry or quiescent state. [source: TAIR:ki]
+
'''July 26 9am-6pm''' The Ontological Representation of Adverse Events: Working with Multiple Biomedical Ontologies
  
'''Proposed name and definition:''' seed development stage: A plant structure development stage that begins with fertilization and ends with seed maturation.
+
'''July 27 8.30am-4pm''' Facilitating Anatomy Ontology Interoperability
  
Comment: Only used for seed plants. Some seeds may enter a period of dormancy after seed development is complete.
+
'''July 26 6.30pm-9pm'''  Evening Workshop: Common Logic
  
is_a plant structure development stage; part_of sporophyte phase; subset for gymnosperms and angiosperms; add relation: seed participates_in seed development stage
+
'''July 27 4pm-8pm''' Evening Workshop: Doctoral and Post-Doctoral Consortium
  
====New terms and proposed definitions:====
+
- LC will attend and represent the PO.  Invite other plant people?
  
'''seed trichome development stage:''' A plant structure development stage that is part of a seed development stage during which one or more seed trichomes develop.
 
  
is_a plant structure development stage; part_of seed development stage; add seed trichome participates_in seed trichome development stage
 
  
synonym: seed hair development stage
+
'''*Plant Biology 2011, Aug 6-10th, Minneapolis, Minn'''
  
 +
[http://my.aspb.org/?page=Meetings_Annual Plant Biology 2011]
  
seed trichome initiation stage: The earliest histological
 
evidence of seed hair initiation, ie, a change in the orientation of cell
 
division in the ovule epidermises occurs at or just before anthesis. (Ruan
 
YL, 2003, Plant Cell 15:952-964) [Source:PMID: 12671090].
 
  
synonym: seed hair initiation stage
+
For inclusion on the program memory stick and in the program book, abstracts must be submitted by '''May 27'''.
  
 +
Gramene will be putting together a workshop again, focusing on pathways.  LC and PJ will present a PO poster.
  
seed trichome elongation stage: A period of rapid elongation
+
TAIR (Kate Dreher) is organizing an Outreach Booth and we are invited to take part.
of hair initials without cell division for 16-25 days. (Lee JJ, 2007,
 
Annals of Botany 100:1391-1401 and Ruan YL, 2003, Plant Cell 15:952-964)
 
[Sources:PMID: 17905721, PMID: 12671090].
 
  
synonym: seed hair elongation stage
 
  
  
seed trichome secondary wall biosynthesis stage: A phase of
 
the massive amounts of secondary cell wall cellulose synthesis. (Lee JJ,
 
2007, Annals of Botany 100:1391-1401 and Ruan YL, 2003, Plant Cell
 
15:952-964) [Sources: PMID:17905721, PMID:12671090].
 
  
synonym: seed hair secondary wall biosynthesis stage
+
'''* International Botanical Congress (IBC2011)'''
  
 +
July 23rd-30th 2011, Melbourne, Australia'''
  
seed trichome maturation stage: A period of seed hair
+
Registration is open  [http://www.ibc2011.com/Dates.htm Important dates]  
maturation from 50 to 60 days post-anthesis (DPA).
 
(Lee JJ, 2007, Annals of Botany 100:1391-1401 and Ruan YL, 2003, Plant
 
Cell 15:952-964) [Sources: PMID:17905721, PMID:12671090].
 
  
synonym: seed hair maturation stage
+
Symposium 'Bio-Ontologies for the Plant Sciences' under the Genetics, Genomics and Bioinformatics theme, wiil be held on Thursday, 27 July, from 13:30 to 15:30.
  
==[http://sourceforge.net/tracker/index.php?func=detail&aid=2812238&group_id=76834&atid=835555 tuber growth and development stages]==
+
Dennis, Alejandra, Pankaj and Ramona are planning to attend.  
  
This item has been open on SF since 6/2009
+
See [[IBC 2011 Bio-Ontologies Symposium]] wiki page for more details
 
 
I have a bunch of potato genes which are expressed in different tuber developmental stages (e.g. the potato pmt gene is expressed in small sprouts only (http://www.ncbi.nlm.nih.gov/pubmed/16088399).
 
 
 
Suggested stages:
 
 
 
-sprout development (does this correspond to tube axillary bud development? Should come after tuber maturation)
 
 
 
-tuber initiation
 
 
 
-tuber growth
 
 
 
-tuber maturation
 
 
 
How we work these in will depend on restructuring of PGDSO
 
 
 
l development in legumes (Plant Physiol, March 2003, Vol. 131, pp. 911-926
 

Revision as of 23:38, 17 June 2011

POC meeting, Webex Conference Call; Date: Tuesday June 21st, 2011 10am (PDT)

In attendance:

POC members:

Absent:

Collaborators:


Acceptance of the minutes from the POC_Conf._Call_6-7-11?

This meeting is postponed until 6-28-11, due to webinar with the Physco group in Germany.

New items

Report from the2011 Semantic Web Workshop June 6th and 7th, Santa Fe, NM

Hosted by Damian Gessler and the iPlant Collaborative, this two-day workshop will focus on biological applications for semantic web services.

-JE and JP will be attending

-JE has already worked with Damian to implement a SSWAP web service for PO terms, so further collaboration with him and iPlant will benefit the POC going forward.

For more Workshop details: Semantic web.

Tech issues

New xref in database

A stanza for our SF tracker has been added to GO.xrf_abbs (thanks to Becky Foulger):

abbreviation: OBO_SF_PO

database: Source Forge OBO Plant Ontology (PO) term request tracker

object: Term request

example_id: OBO_SF_PO:3184921

generic_url: http://sourceforge.net/tracker/?func=browse&group_id=76834&atid=835555

url_syntax: https://sourceforge.net/tracker/index.php?func=detail&aid=[example_id]&group_id=76834&atid=835555

url_example: https://sourceforge.net/tracker/index.php?func=detail&aid=3184921&group_id=76834&atid=835555


RW also updated the file at http://plantontology.org/docs/dbxref/PO_DBXref.txt.

Action items

Do we need to do anything else to get the new xrefs to link automatically?

Concern from TAIR over how annotations move through relations

Excerpts rom Tanya's message:

We're working on integrating the new relationships that PO is using into our local system and were wondering about handling annotation count propagation over some of these relationships.

For example, anther wall endothecium and anther wall middle layer are adjacent. When you look for annotations to anther wall endothecium, one also retrieves annotations to anther wall middle layer: http://plantontology.org/amigo/go.cgi?view=assoc&search_constraint=terms&query=PO:0020002 Somehow, this does not seem like the expected (or desired) result.

I was wondering if you would consider producing a file of the PO that does not contain the 'trickier to count' new relationships?

Action items

Do we want to create a file without has_part, develops_from, derives_from, and adjacent_to?

Items arising from previous meetings:

Children of Leaf- feedback from TAIR:

The following is a summary from the email correspondence, from Tanya Berardini:

  • TAIR strongly supports creating specific vascular and non-vascular children for leaf apex and similar terms that are part_of leaf, like those describing the leaf apex in rosette leaves and cauline leaves.
  • TAIR proposes we create more specific terms for the is_a children of vascular leaf, like cauline leaf. For example, 'cauline leaf margin' and 'rosette leaf margin'.
  • TAIR suggests creating the terms which already have annotations attached to them, like 'vascular leaf margin' (current Arabidopsis, rice, maize annotations to 'leaf margin') and adding other terms upon request by annotators or users.

Their Reasons:

  • Much easier for annotators to choose the specific term they need as opposed to having to remember to co-annotate or having a script go in after and clean up
  • Benefits for the researcher who is looking for very specific information
  • The added granularity of these terms will be a benefit when people want to describe structures such as the leaf apex in rosette leaves and cauline leaves.
  • They are not worried about term inflation
  • A researcher browsing through the ontology would not know to look at annotations to see that there are combinations of annotations that give the 'same' result ('leaf apex' + 'rosette leaf')
  • The current functionality of AmiGO does not allow a search for gene products annotated to Term A AND Term B.
  • The the combinatorial solution work will not work if a gene is expressed only in the 'leaf margin of cauline leaves' and in the 'leaf apex of rosette leaves'. How do we know which 'part' goes with which 'leaf'?
  • Unless the co-annotations are captured in a single line in the gaf file (possible with column 16), this could lead to misinformation.

Questions and suggestions from last week's meeting:

-We could create specific child terms, but at what level should we stop?

-Users could post-compose terms, but then, those terms ultimately would need to go into the PO so that future work could reference the definitions, so it doesn't save much over precomposing the terms (but it does provide a guide for when to stop adding term: you stop at what the users need.

-There is an issue of training. Annotators will have to be taught to annotate to the part of the leaf and the type of leaf. The same applies of other types of plant structures as well.

-We could use a script to move annotation from the parts of leaf to the appropriate type of leaf, but this effectively creates another line in the annotation file, and does not solve the problem of how to associate two different annotations (like the annotation to leaf margin with the annotation to rosette leaf). To do this, we need to have the information in the same row of the annotation file.

-Does the GAF format allow us to put the PO id for the type of leaf in column 16? If we put the PO id in column 16, will that create an annotation to that term? Probably we will still have to make a separate line for that annotation. See: GO annotation file GAF 2.0 format guide.

-Rather than setting a strict policy about when to inflate or not, we should probably consider it on a case by case basis. We could start by adding pre-composed terms for those structures that already have annotations associated with them (see below), then asking TAIR and other users to use column 16 to post-compose any other term they might need. They can also use column 16 to associate a structure with a growth or developmental stage. See below for more details.

-We should set up a meeting with TAIR to explain to them why we don't want to add all of the specific children, and to work them on a solution. It is important that we have the script for transferring annotation up and running, and that we test out how we can use column 16 for associating leaf types before we meet with them.

-Need to consider how this will affect the processing of the annotation files that happens with each release.


Other related suggestions:

1. Make rosette leaf and cauline leaf is_a children of leaf, rather than is_a children of vascular leaf. Then we could make children vascular rosette leaf and vascular cauline leaf. Do we need these parent terms if rosette leaf and cauline leaf only occur in vascular leaves? (RW: We should create a SF tracker for this.) Also, we need to work on the definitions of rosette leaf and cauline leaf. Should link them to growth stages, because (at least in Arabidopsis and other Brassicaceae) they are the same leaves at different times.

2. Move all leaf parts (be they part_of vascular leaf, part_of non-vascular leaf or part_of leaf) to be part_of leaf, so that users could find all of the parts in one place. This might also force them to make the second annotation to the type of leaf. PJ suggested that we could use disjoint_from relation. For example: have leaf vascular system be a part_of leaf (instead of part_of vascular leaf) then make it disjoint_from non-vascular leaf. This would prevent curators form making an association to the wrong type of leaf. Problem with this is that we intentionally omit information that we know to be true (e.g., we would leave out leaf vascular system part_of vascular leaf). That is not necessarily bad, but we need to have a good reason for it.

3. Add disjoint_from relations between vascular leaf and non-vascular leaf. In OWL you have to do that, because if you don't assert it, OWL assumes they are not disjoint.

4. We have both non-vascular leaf meristematic apical cell and vascular leaf meristematic apical cell. We should merge those with leaf apical cell if we are going to be strict about not making any specific part_of children of different leaf types.

Proposed solutions:

All: Create specific children for all of the parts of leaf, for each type of leaf. This is pretty much what we did for tuber, although it only has 2 is_a descendents and 8 part_of descendents. There are 15 is_a descendents of leaf (juvenile leaf, transition leaf, adult leaf, transition leaf, non-vascular leaf, vascular leaf, simple leaf, compound leaf, rosette leaf, cauline leaf, cigar leaf, embyro leaf, leaf spine, cotyledon, and flag leaf) and about 30 part_of descendents (not counting those that are only part of vascular or non-vascular leaf), so if we created all of the combinations of child terms it would add about 450 new terms.

Nothing: Do not create any specific part_of children for vascular leaf and other types of leaves. Keep or move all part_of children under leaf, and use column 16 to create cross-products to the correct type of leaf.

Somewhere in between: There are 21 part_of descendents of leaf that currently have annotations associated with them. All of these annotations come from vascular plants. We could create specific part_of vascular leaf children only for these 21 terms, and then add others as annotations for them arise.

We could adopt a policy of only adding specific part_of children for vascular leaf and non-vascular leaf. All other leaf types could be considered phenotypes (e.g. compound or simple leaf, spine leaf) or growth-stage specific forms (e.g., embryo leaf or cotyledon), and we could ask annotators to use column 16 to associate the part of the leaf to the type of leaf in these cases.


Unless we adopt the "All" strategy (which seems impracticle), we will need a mechanism for associating the annotation that is on the part_of a leaf to the correct type of leaf. Such a mechanism would be very useful for other types of structures, as it would allow users to create new cross-product terms on the fly. It could also be used to more accurately annotate gene expression that occurs in a structures at a specific growth stage (right now, users simply put the annotation on both the structure and the growth stage, without any link between them). Annotation extensions (Column 16) allow us to do this.

See PO_Annotation_Extensions_(column_16) for a full explanation of how this would work.

Action items

???

Annotations on terms that are part_of leaf

The list below contains all of the terms that are part_of leaf and have annotations associated with them.

In the last round of revisions, we decided that any existing annotation for these terms should also be copied to vascular leaf. Future annotations should go to both the part and to the appropriate leaf type. However, we have not actually transferred any of the annotation yet.


term name - (id) - number of annotations (from version 14, not from most recent association files)

  • leaf aerenchyma (PO:0006215) 1
  • leaf apex (PO:0020137) 12890
  • leaf base (PO:0020040) 5
  • leaf epidermis (PO:0006016)365, includes:
    • buliform cell (PO:0004001) 1
    • leaf abaxial epidermis (PO:0006019) 4
    • leaf adaxial epidermis (PO:0006018) 4
    • leaf lamina epidermis (PO:0000047) 1
    • leaf trichome (PO:0006504) 63
  • leaf intercalary meristem (PO:0006346) 1
  • leaf lamina (PO:0020039) 12800, includes:
    • leaf lamina base (PO:0008019) 12614
    • leaf lamina vascular system (PO:0000048) 1 (already shows up under vascular leaf)
  • leaf margin (PO:0020128) 100
  • leaf mesophyll (PO:0005645) 762, includes:
    • palisade mesophyll cell (PO:0006206) 1
    • spongy mesophyll (PO:0005647) 1
    • spongy mesophyll cell (PO:0006205) 2
    • leaf prickle (PO:0025175) 0
  • leaf sheath (PO:0020104) 205, includes:
    • leaf sheath pulvinus (PO:0008017) 2


If we were to adopt a policy of only creating specific terms when they are needed for annotation, we would have to create a vascular leaf child for each of these 21 terms.

Upcoming meetings 2011:

Botany 2011 Meeting [Botany 2011] St. Louis, MO at the Chase Park Plaza, July 9-13.

Societies participating: Society for Economic Botany, the American Fern Society (AFS), the American Society of Plant Taxonomists (ASPT), and the Botanical Society of America (BSA).

Anybody going??


* ICBO 2011 Second International Conference on Biomedical Ontology July 26-30, 2011 Buffalo, New York

ICBO

LC is co-organizing the workshop "From Fins to Limbs to Leaves: Facilitating anatomy ontology interoperability" along with Melissa Haendel, Chris Mungall, Alan Ruttenberg, David Osumi-Sutherland.

Full-Day Workshops Schedule:

July 26 9am-6pm The Ontological Representation of Adverse Events: Working with Multiple Biomedical Ontologies

July 27 8.30am-4pm Facilitating Anatomy Ontology Interoperability

July 26 6.30pm-9pm Evening Workshop: Common Logic

July 27 4pm-8pm Evening Workshop: Doctoral and Post-Doctoral Consortium

- LC will attend and represent the PO. Invite other plant people?


*Plant Biology 2011, Aug 6-10th, Minneapolis, Minn

Plant Biology 2011


For inclusion on the program memory stick and in the program book, abstracts must be submitted by May 27.

Gramene will be putting together a workshop again, focusing on pathways. LC and PJ will present a PO poster.

TAIR (Kate Dreher) is organizing an Outreach Booth and we are invited to take part.



* International Botanical Congress (IBC2011)

July 23rd-30th 2011, Melbourne, Australia

Registration is open Important dates

Symposium 'Bio-Ontologies for the Plant Sciences' under the Genetics, Genomics and Bioinformatics theme, wiil be held on Thursday, 27 July, from 13:30 to 15:30.

Dennis, Alejandra, Pankaj and Ramona are planning to attend.

See IBC 2011 Bio-Ontologies Symposium wiki page for more details