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{{ infobox Application
{{ infobox Application
| title = '''MotifView - A motif viewing tool'''
| title = '''MotifView - A motif viewing tool'''
| screenshot = [[Image:GEvo_Screenshot.png|200px|thumb]]
| screenshot = [[Image:motifview_image.png|200px|thumb]]
| caption = Not yet a motif view image
| caption = MotifView at work
| developer = CoGe Team
| developer = CoGe Team
| analysis = Compare multiple genomic regions for motifs
| analysis = Compare multiple genomic regions for motifs
| working_state = Released
| working_state = Testing
| tools = blastn, tblastx, blastz, CHAOS, LAGAN, DiAlign 2
| tools = blastn, LAGAN
| website = http://synteny.cnr.berkeley.edu/CoGe/MotifView.pl
}}  
}}  


MotifView is a tool using GEvo to visualize motifs in compared genomic regions.
MotifView is a tool that visualizes motifs in compared genomic regions.




= Introduction =
= Introduction =
MotifView uses the same tools employed in GEvo to visualize motifs within multiple genomic regions. As in GEvo, we it's possible to compare sequences from any number of organisms using a variety of different sequence comparison algorithms.
MotifView uses visual and algorithmic tools to visualize motifs within multiple genomic regions. Sharing many functional similarities to GEvo, it's possible to compare sequences from any number of organisms using a variety of different sequence comparison algorithms.


On this page we provide only a brief description of options that are shared with GEvo. If descriptions and directions are ambiguous, please follow the links to specific sections to the [[GEvo#GEvo|GEvo]] instructions on that section.
On this page we provide only a brief description of options that are shared with GEvo. If descriptions and directions are ambiguous, please follow the links to specific sections to the [[GEvo#GEvo|GEvo]] instructions on that section.
There's also the option to use the embedded videos to view demos of the sections following. One can either follow the text along with the video or choose to use either exclusively.


=MotifView basics=
=MotifView basics=
[[Image:GEvo-setup.png|thumb|right|500px|Screen-shot of where a GEvo analysis is configured.  Two genomic regions have been specified by gene name and the amount of additional upstream/downstream sequence]]
[[Image:Motifview-setup.png|thumb|right|400px|Screen-shot of where a MotifView analysis is configured.  Four genomic regions have been specified by gene name, dataset and the amount of additional upstream/downstream sequence]]


# Select genomic regions to analyze
# Select genomic regions to analyze
# Select a sequence alignment algorithm appropriate for the sequences and questions in mind
# Select a sequence alignment algorithm appropriate for the sequences and area of interest
#Select motifs to visualize and how to visualize them
# Select motifs to visualize
# Press "Find Motifs!" button
# Press "Find Motifs!" button
To alternate between areas to configure an analysis, select the appropriate tab.
To alternate between these options to configure an analysis, select the appropriate tab.


=Sequence Submission=
=Sequence Submission=
Select the "Sequence Submission" tab to open these options.  Here, you can specify sequence submission boxes for each sequence that will be submitted for a GEvo anlaysis.  This is also were you can adjust the amount of sequence analyzed, select which sequences are analyzed, reverse complement a sequence, mask a sequence according the the genomic features it contains, and change the display order of sequences.
===Manual Submission===
Select the "Sequence Submission" tab to open these options.  Here, you can specify sequence submission boxes for each sequence that will be submitted for a MotifView anlaysis.  This is also were you can adjust the amount of sequence analyzed, select which sequences are analyzed, reverse complement a sequence, mask a sequence according the the genomic features it contains, and change the display order of sequences.
 
===Merge analysis===
Frequently users have links from previous GEvo analyses that they wish to screen for motifs. Pasting the link into the "Merge Previous GEvo Analysis" window allows panels created in GEvo to be analyzed in MotifView.


The different options for submitting and modifying sequences to be visualized can be found [[GEvo#Adding_a_sequence|here]].
The different options for submitting and modifying sequences to be visualized can be found [[GEvo#Adding_a_sequence|here]].


= Alignment Algorithms =
= Alignment Algorithms =
While the default alignment algorithm will be useful for most queries, we've provided many major algorithms for use in alignment. The options and suitability of available algorithms is discussed [[GEvo#Alignment_Algorithms|here]].
While many major algorithms exist for alignment, not all are suitable for the analysis available in MotifView. As such, MotifView compares genes at a scale that makes BlastN and LAGAN the most ideal algorithm choices. The options and suitability of available algorithms is discussed [[GEvo#Alignment_Algorithms|here]].


= Select Motifs =
= Select Motifs =
This tab allows the user to define how and which motifs will be found and analyzed.
This tab allows the user to define how and which motifs will be found and analyzed. The "Select Motifs" tab contains four pull down options when choosing motifs for analysis.
 
[[Image:Select-motifs.png|thumb|right|400px]]
 
===Choose TFBS Motif===
Users can manually enter a motif in the section "Search for User-Defined Motifs". Also, while colors are automatically provided to motifs, users can define their own color separated from the motif by a colon. For example:
 
CACGTG:Red
 
===Select from Comprehensive List of Motifs===
It's also possible to browse the full list of motifs in our database and add them to be analyzed. In the window presenting the full list, motifs appear by name, then sequence. Information on highlighted motifs will pop up on pressing the "Get Motif Info" button.
 
Once selected, the motif will appear in the "Selected Motifs" window where they can be additionally deselected or the list cleared entirely for a new list.
 
===Select Motifs from Categories===
Additionally, there is a choice of provided motif categories: Stress and Families. Toggling any category will pull a down list of motifs linked to that stress or transcription factor family. If desired, a range of motifs not confined to categories is available below the categories. In addition, users can select or deselect all options in a category if needed.
 
Once motifs are chosen, press the "Find Motifs!" button above the tabs to begin analysis.
 
=Demo MotifView Analysis=


First, determine how you'd like to see the motifs represented visually (as a diamond or flag) then choose whether or not you'd like to see motifs present in CNSs or anywhere in the window of sequence.
Below is a demo basic MotifView analysis. In it we illustrate how to submit a region to be analyzed, how to choose an algorithm, relevant changes to the graphics, and how to choose motifs.


[[Image:Demo-sequence-submission5.png|thumb|500px|right|Fig. 1 Sequence submission]]


===Sequence Submission (Fig. 1)===


= Regenerating/Saving a GEvo Analysis =
Enter the genomic region:
#Enter a gene accession number in the box labeled "Name:". In this case, we've chosen AT3G11580 and AT5G06250, two homeologs with annotations that will be seen later. A list that identifies which datasets contain what annotations can be found [[Extra Annotations|here]].
#Choose datasets to be analyzed. When you enter the accession number, pull down menus will be populated with datasets that contain that gene, including genomic datasets, type of DNA, etc. This example requires that we use Arabidopsis TAIR V8 that has been masked for repeats.


[[Image:GEvo-links.png|thumb|right|500px]]
Additionally, you may define how many base pairs flank each genomic region. This will become more relevant when refining an analysis.


=== GEvo Links ===
===Algorithm (Fig. 2)===


After results are generated by GEvo, a URL will be created that will be a hyperlink to GEvo with your analysis pre-configured. To regenerated the results, all you need to do is press the "Run GEvo Analysis!" button and wait for the analysis to run. This link is stored in two places:
[[Image:Demo-algorithm3.png|thumb|500px|left|Fig. 2 Algorithm]]


#At the bottom of the results under "GEvo Links" (see example image.) This link has been condensed using the tinyurl redirecting service.
#Next, the alignment algorithm must be chosen from the pulldown menu next to "Alignment Algorithm:". While many alignment algorithms exist, MotifView analyzes DNA within a very small defined region. As such, this example uses "BlastN" for this analysis since it works best when analyzing small regions.
#At the bottom of the log file. The link to the log file can also be found at the bottom of the results (see example image.)


=== GEvo Direct ===
===Results Parameters (Fig. 3)===
There are many options available for ease of use when viewing the analysis. In this example the most relevant options address annotations.


GEvo Direct is a tool for quickly viewing the results of a previously run analysis without having to re-run the analysis.  <font color=red>Please Note: </font> CoGe saves all the files from a GEvo analysis for ~24 hours.  After that time, the data-files are deleted and the GEvo Direct link will no longer work.
# The gene pair we've selected includes annotations for CNSs, gene spaces, and PIL5 sites. As such, we definitely want to see said annotations in the final results so all three boxes are checked.
# Further, it's possible to be overwhelmed by the number of motifs present in the imaging panel if a wide selection of motifs is chosen so we chose the option to only view motifs that overlap our annotations.


===Save Work History===
[[Image:Demo-results-parameters5.png|thumb|450px|center|Fig. 3 Results Parameters]]


Registered CoGe users can save a link to a GEvo analysis for later retrieval from their work history.  This permits a GEvo analysis to also be names and annotated for future reference.
===Select Motifs (Fig. 4)===


=Modifying result graphics=
[[Image:Demo-motif-select-stress2.png|thumb|300px|right|Fig. 4 Select Motifs]]
 
Though users can define their own motifs or select from our full list of motifs as shown above, we're illustrating how categories of motifs can be analyzed.
 
# Toggle "Select Motifs from Stress Categories". The expanding window allows the user to choose from stresses associated with motifs including Chemical/Oxidative/Pathogen, Cold, Drought/Heat, Hypoxia, Light, Nutrient, Salt, Water, and Unspecified stresses.
# In this case, toggle the Cold Stress category.
# To illustrate how one can search for a range of motifs, Select All motifs in the Cold Stress category.


===MotifView Panel (Fig. 5)===


===Showing Contigs===
Below is the image of the analysis performed. Show in the panel are:
[[Image:GEvo-with-labels.png|thumb|right|500px|Example GEvo result with contigs, hsp labels, and genomic feature labels drawn.]]
[[Image:GEvo-contigs-and-labels.png|thumb|right|500px|Where to find GEvo's options for viewing contigs, HSP labels, and genomic feature labels.]]


Some genomes have contig assembly information. To view this in GEvo's results:
# HSPs: A high-scoring segment pair, or HSP, is a subsegment of a pair of sequences. In this case, the HSPs have been toggled to show the regions of similarity between the gene pair.
#Select the "Results Parameters" tab from GEvo's configuration box
# Genomic features: The gene is shown with exons painted gold, the introns painted grey and non coding regions painted blue. Notice that that gene space is also highlighted by the yellow background underlying the gene and other annotations
#Select "yes" for the option "Color contigs <font color=red>red</font>".
# Motifs: These annotations are painted on as diamonds. It's important to realize that the diamonds don't represent the real size of the motifs. Rather, the motifs must be artificially represented or, because of their small size, they won't be visible at all. Notice how the green motif appears to have an HSP associated with a PIL5 site on its homeolog.
# CNSs: Conserved non-coding sequences are very prevalent in this gene pair and can be differentiated from the PIL5 sites by being colored half purple.
# PIL5 sites: One type of annotation, PIL5 sites are transcription factor binding sites. Notice how some sites have HSPs associated with that denote sequence similarity with sites on the homeolog.


===Turning on labels for HSPs (blast hits) in GEvo's results===
[[Image:Demo-panel3.png|thumb|1000px|center|Fig. 5 MotifView Panel]]
If you want to have the HSP number drawn on the HSP:
#Select the "Results Parameters" tab from GEvo's configuration box
#Select "yes" for the option "Label HSPs".
*You can have the labels drawn linearly, so each label is at the same vertical position for a track, or staggered, where they are drawn top, middle, bottom alternating.


===Turning on labels for Genomic Features (e.g. genes) in GEvo's results===
=Modifying result graphics=
If you want to have the feature names drawn on the feature:
#Select the "Results Parameters" tab from GEvo's configuration box
#Select "yes" for the option "Label Genomic Features".
*You can have the labels drawn linearly, so each label is at the same vertical position for a track, or staggered, where they are drawn top, middle, bottom alternating.


===Expanding Overlapping Features and Regions of Sequence Similarity===
===Show preloaded annotations===
[[Image:GEvo-show-overlapping.png|thumb|500px|right|Where to find GEvo's options for viewing overlapping genomic features and regions of sequence similarlity.]]
An important feature when using MotifView is the ability to view other features such as CNSs. In the "Results Parameters" section there is the option to show preloaded annotations in the panel, including CNSs, genespace and PIL5 sites.


[[Image:GEvo-local-dup-no-show-overlap.png|thumb|500px|right|Example of GEvo result with local duplications that are obfuscated by not showing separating overlapping HSPs. Comparison is between orthologous regions of Arabidopsis thaliana and Arabidopsis lyrata. (A) No wedges drawn connecting regions of sequence similarity. (B) Wedges drawn connecting regions of sequence similarity. Note the "messy" regions where the local duplication is. Results can be regenerated at http://tinyurl.com/mokdnn .]]
Further, one can restrict viewing motifs anywhere except when overlapping with any preloaded annotations. This is especially important because motifs are painted larger in the panel than they would actually appear. Not painting the motifs larger would result in invisible motifs but this representation can appear to make motifs overlap with other features when they do not. Restricting visible motifs to those that overlap with annotations eliminates any such error.


[[Image:GEvo-local-dup-show-overlap.png|thumb|500px|right|vo results with "auto adjust" HSP and Genomic Features turned on. This causes GEvo to find genomic features and blast-hits that overlap at the same position, and drawn them such that they are separated in order to identify local duplications in a genomic region, repeat sequences, and alternatively spliced transcripts. This is a comparison between orthologous regions of Arabidopsis thaliana and Arabidopsis lyrata, and can be regenerated at http://tinyurl.com/mokdnn. Wedges have been drawn connection regions of sequence similarity between one gene in the bottom panel. This shows that this one gene has sequence similar to four regions in the orthologous genomic region, which is indicative of a local gene duplication. Also, there is a "stack" of HSPs which is caused by repeated sequences. Note that two genes have annotations for being alternatively spliced, which is visualized by separating the drawing of overlapping genomic features. ]]
===Other useful graphics modifications===
[[Image:Demo-panel2.png|thumb|right|500px|Example MotifView result with hsps, genomic feature, CNSs, PIL5 sites, genespace, and motifs drawn. Note that motifs are also only restricted to viewing those that overlap with genespace and PIL5 sites]]
[[Image:Demo-results-parameters4.png|thumb|500px|right|Other useful graphic modifications in the Results Parameters tab]]


By default GEvo will drawn overlapping genomic features and regions of sequence similarity on top of one another.  However, this sometimes hides some of the interesting complexities in a genomic region such as local duplications or regions containing repeated sequences.  To view these, select the "Results Parameters" tab and select "Yes" for "Auto adjust overlapping features" and/or "Auto adjust overlapping HSPs".  These options are set to "No" by default because finding and drawing overlapping features can take a long time to process, and are not always useful.
[[GEvo#Showing_Contigs|Showing contigs]].


=Merging Analyses=
[[GEvo#Turning_on_labels_for_HSPs_(blast_hits)_in_GEvo's_results | Turning on labels for HSPs]].
Often, there are times when you will want to merge together two or more separate GEvo anlayses.  To do this, copy a [[GEvo#GEvo_Links | GEvo link]] into the text-box next the text: "Merge Previous GEvo Analysis (paste in URL)" located at the top of the sequence submission tab.  Then press the "Merge" button".  The sequences as specified in the pasted URL will appear as new sequence submission boxes configured as specified in the link (extra up/downstream sequence, reverse complement, masked, etc.)


=Refining an analysis=
[[GEvo#Turning on labels for Genomic Features (e.g. genes) in GEvo's results|Drawing feature names on features]]
Once a GEvo analysis has run, you can change any of the analysis parameters and re-run the analysis by pressing the "Run GEvo analysis" button again.
The common parameters changed are:
*The extent of the genomic region analyzed.  [[Gobe#Changing_the_extent_of_a_genomic_region | The interactive results ]] make this easy with slider bars.
*The algorithm used in the analysis
*Masking sequences
*Skipping sequences
*Reverse complementing sequences
*The coloration and information displayed in the result's graphics


=Hints and Tricks=
[[GEvo#Expanding_Overlapping_Features_and_Regions_of_Sequence_Similarity | Expanding Overlapping Features and Regions of Sequence Similarity]]
===Sequences with many common sub-sequences===
Comparing sequences with lots of common sub-sequences usually causes GEvo to take a very long time processing the analysis (both in terms of identifying the common sequences and generating the final results).  Also, if many regions are identified, it is often difficult to make sense of the results.  This kind of problem will surface in many large genomes, such as mammal and plant genomes.  For example human and maize are both riddled with large amounts of repetitive sequences derived from retroviruses and transposons.  This makes the comparison of large genome regions in these genomes difficult, if not impossible.  To circumvent this problem, mask all sequence that does not code for protein.  You can select this option under the "Sequence options" menu and selecting "non-CDS" for the row "Mask Sequence".


=Example Analyses=
=Refining an analysis=
[[GEvo-4at-cp-vv|Analysis of syntenic regions from Arabidopsis thaliana, Carica papaya, and Vitis vinifera]]
Once a MotifView analysis has run, any of the analysis parameters can be changed and re-run after pressing the "Clear all previous analysis" button. Some existing parameters will remain and other will have to be selected again.


The common parameters changed are:
*The extent of the genomic region analyzed. The amount to which the panel extends beyond the gene in question can be changed in the "Left sequence" and "Right sequence" boxes on the "Sequence Submission" tab. Changes to these boxes will remain in new analysis.
*Reverse complementing sequences. This change will remain after previous analysis is cleared.
*Also reset when previous analysis is cleared are the datasets for the sequence submissions, algorithm, and motifs selected. This means that this information will have to defined again after the user clears previous analysis


=Linking to GEvo=
=Linking to GEvo=
Line 119: Line 142:
=Tutorials =
=Tutorials =


=References=
=References/Downloads=
{{reflist}}
For a list of all datasets with annotations, click [[Extra Annotations|here]]
 
For a list of all TFBS motifs used in Spangler et al., New Phytologist (2011) Evidence for Conserved Noncoding Sequence Functions in Arabidopsis thaliana. , click [http://coge.iplantcollaborative.org/CoGe/tmp/MotifView/MotifsUsedInSpanglerPaper.txt here]
 
For a list of all TFBS motifs used in this site, click [http://coge.iplantcollaborative.org/CoGe/tmp/MotifView/Motiflist.txt here]
 
=Frequently Asked Questions=
 
=Bug Report=
 
Progress on bugs can be found [[Motifview bugs|here]].

Latest revision as of 20:02, 20 November 2013

MotifView - A motif viewing tool

MotifView at work
Software companyCoGe Team
Analysis TypeCompare multiple genomic regions for motifs
Working stateTesting
Tools Utilizedblastn, LAGAN

MotifView is a tool that visualizes motifs in compared genomic regions.


Introduction

MotifView uses visual and algorithmic tools to visualize motifs within multiple genomic regions. Sharing many functional similarities to GEvo, it's possible to compare sequences from any number of organisms using a variety of different sequence comparison algorithms.

On this page we provide only a brief description of options that are shared with GEvo. If descriptions and directions are ambiguous, please follow the links to specific sections to the GEvo instructions on that section.

There's also the option to use the embedded videos to view demos of the sections following. One can either follow the text along with the video or choose to use either exclusively.

MotifView basics

Screen-shot of where a MotifView analysis is configured. Four genomic regions have been specified by gene name, dataset and the amount of additional upstream/downstream sequence
  1. Select genomic regions to analyze
  2. Select a sequence alignment algorithm appropriate for the sequences and area of interest
  3. Select motifs to visualize
  4. Press "Find Motifs!" button

To alternate between these options to configure an analysis, select the appropriate tab.

Sequence Submission

Manual Submission

Select the "Sequence Submission" tab to open these options. Here, you can specify sequence submission boxes for each sequence that will be submitted for a MotifView anlaysis. This is also were you can adjust the amount of sequence analyzed, select which sequences are analyzed, reverse complement a sequence, mask a sequence according the the genomic features it contains, and change the display order of sequences.

Merge analysis

Frequently users have links from previous GEvo analyses that they wish to screen for motifs. Pasting the link into the "Merge Previous GEvo Analysis" window allows panels created in GEvo to be analyzed in MotifView.

The different options for submitting and modifying sequences to be visualized can be found here.

Alignment Algorithms

While many major algorithms exist for alignment, not all are suitable for the analysis available in MotifView. As such, MotifView compares genes at a scale that makes BlastN and LAGAN the most ideal algorithm choices. The options and suitability of available algorithms is discussed here.

Select Motifs

This tab allows the user to define how and which motifs will be found and analyzed. The "Select Motifs" tab contains four pull down options when choosing motifs for analysis.

Choose TFBS Motif

Users can manually enter a motif in the section "Search for User-Defined Motifs". Also, while colors are automatically provided to motifs, users can define their own color separated from the motif by a colon. For example:

CACGTG:Red

Select from Comprehensive List of Motifs

It's also possible to browse the full list of motifs in our database and add them to be analyzed. In the window presenting the full list, motifs appear by name, then sequence. Information on highlighted motifs will pop up on pressing the "Get Motif Info" button.

Once selected, the motif will appear in the "Selected Motifs" window where they can be additionally deselected or the list cleared entirely for a new list.

Select Motifs from Categories

Additionally, there is a choice of provided motif categories: Stress and Families. Toggling any category will pull a down list of motifs linked to that stress or transcription factor family. If desired, a range of motifs not confined to categories is available below the categories. In addition, users can select or deselect all options in a category if needed.

Once motifs are chosen, press the "Find Motifs!" button above the tabs to begin analysis.

Demo MotifView Analysis

Below is a demo basic MotifView analysis. In it we illustrate how to submit a region to be analyzed, how to choose an algorithm, relevant changes to the graphics, and how to choose motifs.

Fig. 1 Sequence submission

Sequence Submission (Fig. 1)

Enter the genomic region:

  1. Enter a gene accession number in the box labeled "Name:". In this case, we've chosen AT3G11580 and AT5G06250, two homeologs with annotations that will be seen later. A list that identifies which datasets contain what annotations can be found here.
  2. Choose datasets to be analyzed. When you enter the accession number, pull down menus will be populated with datasets that contain that gene, including genomic datasets, type of DNA, etc. This example requires that we use Arabidopsis TAIR V8 that has been masked for repeats.

Additionally, you may define how many base pairs flank each genomic region. This will become more relevant when refining an analysis.

Algorithm (Fig. 2)

Fig. 2 Algorithm
  1. Next, the alignment algorithm must be chosen from the pulldown menu next to "Alignment Algorithm:". While many alignment algorithms exist, MotifView analyzes DNA within a very small defined region. As such, this example uses "BlastN" for this analysis since it works best when analyzing small regions.

Results Parameters (Fig. 3)

There are many options available for ease of use when viewing the analysis. In this example the most relevant options address annotations.

  1. The gene pair we've selected includes annotations for CNSs, gene spaces, and PIL5 sites. As such, we definitely want to see said annotations in the final results so all three boxes are checked.
  2. Further, it's possible to be overwhelmed by the number of motifs present in the imaging panel if a wide selection of motifs is chosen so we chose the option to only view motifs that overlap our annotations.
Fig. 3 Results Parameters

Select Motifs (Fig. 4)

Fig. 4 Select Motifs

Though users can define their own motifs or select from our full list of motifs as shown above, we're illustrating how categories of motifs can be analyzed.

  1. Toggle "Select Motifs from Stress Categories". The expanding window allows the user to choose from stresses associated with motifs including Chemical/Oxidative/Pathogen, Cold, Drought/Heat, Hypoxia, Light, Nutrient, Salt, Water, and Unspecified stresses.
  2. In this case, toggle the Cold Stress category.
  3. To illustrate how one can search for a range of motifs, Select All motifs in the Cold Stress category.

MotifView Panel (Fig. 5)

Below is the image of the analysis performed. Show in the panel are:

  1. HSPs: A high-scoring segment pair, or HSP, is a subsegment of a pair of sequences. In this case, the HSPs have been toggled to show the regions of similarity between the gene pair.
  2. Genomic features: The gene is shown with exons painted gold, the introns painted grey and non coding regions painted blue. Notice that that gene space is also highlighted by the yellow background underlying the gene and other annotations
  3. Motifs: These annotations are painted on as diamonds. It's important to realize that the diamonds don't represent the real size of the motifs. Rather, the motifs must be artificially represented or, because of their small size, they won't be visible at all. Notice how the green motif appears to have an HSP associated with a PIL5 site on its homeolog.
  4. CNSs: Conserved non-coding sequences are very prevalent in this gene pair and can be differentiated from the PIL5 sites by being colored half purple.
  5. PIL5 sites: One type of annotation, PIL5 sites are transcription factor binding sites. Notice how some sites have HSPs associated with that denote sequence similarity with sites on the homeolog.
Fig. 5 MotifView Panel

Modifying result graphics

Show preloaded annotations

An important feature when using MotifView is the ability to view other features such as CNSs. In the "Results Parameters" section there is the option to show preloaded annotations in the panel, including CNSs, genespace and PIL5 sites.

Further, one can restrict viewing motifs anywhere except when overlapping with any preloaded annotations. This is especially important because motifs are painted larger in the panel than they would actually appear. Not painting the motifs larger would result in invisible motifs but this representation can appear to make motifs overlap with other features when they do not. Restricting visible motifs to those that overlap with annotations eliminates any such error.

Other useful graphics modifications

Example MotifView result with hsps, genomic feature, CNSs, PIL5 sites, genespace, and motifs drawn. Note that motifs are also only restricted to viewing those that overlap with genespace and PIL5 sites
Other useful graphic modifications in the Results Parameters tab

Showing contigs.

Turning on labels for HSPs.

Drawing feature names on features

Expanding Overlapping Features and Regions of Sequence Similarity

Refining an analysis

Once a MotifView analysis has run, any of the analysis parameters can be changed and re-run after pressing the "Clear all previous analysis" button. Some existing parameters will remain and other will have to be selected again.

The common parameters changed are:

  • The extent of the genomic region analyzed. The amount to which the panel extends beyond the gene in question can be changed in the "Left sequence" and "Right sequence" boxes on the "Sequence Submission" tab. Changes to these boxes will remain in new analysis.
  • Reverse complementing sequences. This change will remain after previous analysis is cleared.
  • Also reset when previous analysis is cleared are the datasets for the sequence submissions, algorithm, and motifs selected. This means that this information will have to defined again after the user clears previous analysis

Linking to GEvo

Linking to GEvo is easy! Please see this page on how.

Tutorials

References/Downloads

For a list of all datasets with annotations, click here

For a list of all TFBS motifs used in Spangler et al., New Phytologist (2011) Evidence for Conserved Noncoding Sequence Functions in Arabidopsis thaliana. , click here

For a list of all TFBS motifs used in this site, click here

Frequently Asked Questions

Bug Report

Progress on bugs can be found here.