SMD Annotating Batch Files: Difference between revisions
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==Using the Batch Creator Script== | |||
If you would like to use the [[Batch_Creator_Script|Batch Creator Script]] to create your batch file visit this [[Using_batch_creator_script|tutorial]]. | |||
==Experiment Description Column in the Batch File== | ==Experiment Description Column in the Batch File== | ||
===Overview=== | ===Overview=== | ||
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**<c-4>Condition -- need to explain | **<c-4>Condition -- need to explain | ||
*An example: | *An example: | ||
K-12 MG1655 rpoS(del)::FRT-kan-FRT, rep. 1<c-anno><c-1>K-12 MG1655</c-1><c-2>rpoS(del)::FRT-kan-FRT</c-2><c-3>LB, 37C, Exponential Phase</c-3><c-4>Mutant vs Wild-type</c-4></c-anno> | |||
===Experiment Description=== | ===Experiment Description=== | ||
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*These description will be copied and pasted in to column L (SINGLE CHANNEL DESCRIPTION) and column M (Experiment Name) ?? | *These description will be copied and pasted in to column L (SINGLE CHANNEL DESCRIPTION) and column M (Experiment Name) ?? | ||
*Here are some examples of experiment descriptions | *Here are some examples of experiment descriptions | ||
** | **UTI89, Aerobic 12h | ||
** | **K-12 MG1655, LB + glucose, rep. 1 | ||
**K-12 MG1655 rpoS(del)::FRT, Biofilm rep. 1 | |||
** | **K-12 BW25113 hha-745(del)::FRT-Kan-FRT, 4 hr Biofilm, LB | ||
**K-12 ATCC 25404 + R1drd19 Plasimd, 24 h biofilm | |||
* Here are some examples of what you DO NOT want to put | |||
** (Don't type WT after the strain name) K-12 BW25113 WT | |||
**You Don't need to put "bio.rep. 1", just put rep. 1 | |||
===Individual Annotation Fields=== | ===Individual Annotation Fields=== | ||
====Conventions for the <c-1> field==== | ====Conventions for the <c-1> field==== | ||
*Put the name of the organism and strain background between the <c-1> and </c-1> tags. | *Put the name of the organism and strain background between the <c-1> and </c-1> tags. | ||
*Do not include mutant alleles or plasmids | *<s>Do not</s> '''Do include''' relevant mutant alleles or plasmids; these will also be added to the <c-2> field.[[User:Siegele|Siegele]] 02:58, 7 June 2011 (UTC) | ||
*Here are some examples: | *Here are some examples: | ||
**<c-1> | **<c-1>K-12 MG155</c-1> | ||
**<c-1> | **<c-1>K-12 MG155 rpoS::Tn10</c-1> | ||
**<c-1> | **<c-1>K-12 BW25113</c-1> | ||
**<c-1> | **<c-1>K-12 W3110</c-1> | ||
*If the experiment uses | **<c-1>O157-H7 EDL933</c-1> | ||
** <c-1>K-12 BW25113 yjgK726(del)::FRT-kan-FRT</c-1> | |||
*If the experiment uses an E. coli strain other than MG1655, BW25113, or W3110, check whether it has a page in EcoliWiki. If it doesn't, make one or ask someone else to make one. | |||
* To find the allele number, go [http://cgsc.biology.yale.edu/MutationQueryForm.php here] and type the gene of interest (yjgK for example) in the field labeled "Mutation of gene." | |||
====Conventions for the <c-2>field==== | ====Conventions for the <c-2>field==== | ||
*Put the name of relevant mutant alleles or plasmids between the <c-2> and </c-2> tags. | *Put the name of relevant <b>mutant alleles or plasmids</b> between the <c-2> and </c-2> tags. | ||
** <c-2>ygjK726(del)::FRT-kan-FRT</c-2> | |||
*Don't use special characters because the database won't accept them. Some of our substitutions are listed below: | *Don't use special characters because the database won't accept them. Some of our substitutions are listed below: | ||
**Instead of ∆ for deletion, put (del) after the gene name and allele number. | **Instead of ∆ for deletion, put (del) after the gene name and allele number. | ||
*If a mutation from the Keio collection was used, look up the allele number at the [http://cgsc.biology.yale.edu Coli Genetics Stock Center]. If the kanamycin resistance gene is still present, describe the strain as yfgA000(del)::FRT-kan-FRT. If the kanR gene was "flipped out", describe the strain as yjgA000(del)::FRT. | *If a mutation from the Keio collection was used, look up the allele number at the [http://cgsc.biology.yale.edu Coli Genetics Stock Center]. If the kanamycin resistance gene is still present, describe the strain as yfgA000(del)::FRT-kan-FRT. If the kanR gene was "flipped out", describe the strain as yjgA000(del)::FRT. | ||
[http://www.pnas.org/content/97/12/6640.long | [http://www.pnas.org/content/97/12/6640.long Paper about how flipase experiments work]: (One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products by Kirill A. Datsenko and Barry L. Wanner) | ||
====Conventions for the <c-3> field==== | ====Conventions for the <c-3> field==== | ||
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**glass wool biofilm | **glass wool biofilm | ||
**time course | **time course | ||
*Use commas to separate conditions listed in the <c-3> field. | |||
**For example, <c-3>LB, 0.3 ug/ml Mecillinam, 60 ug/ml Cefsulodin, 37C, 40 min</c-3> | |||
*Don't use special characters. Use the following substitutions instead. | *Don't use special characters. Use the following substitutions instead. | ||
** 37C for 37°C | ** 37C for 37°C | ||
| Line 49: | Line 62: | ||
*Growth medium information | *Growth medium information | ||
**LB | **LB | ||
**MOPS minimal medium + carbon source (xx) | **MOPS minimal medium + carbon source (0.xx%) (It isn't essential to include the concentration, but DAS usually does because it is information she would want to have.) | ||
**M9 minimal medium + carbon source (0.xx%) (") | |||
**M63 minimal medium + carbon source (0.xx%) (") | |||
*Optical Density | |||
**OD600=0.3 | |||
*List of things you should NOT PUT: | |||
** Do not list the number of grams for glass wool | |||
** Do not list the rpm a solution was shaking at | |||
** | |||
*Other Examples | |||
**LB + glucose (1 g/L), glucose/MgSO4-fed batch culture, OD595=11.5, 50C for 15 min (shifted from 37C) | |||
**K medium (0.64 osmol/kg H2O) + glucose (20 mM) + met (0.5 mM), 0.3 M NaCl, 1 mM glycine betaine, 43C, OD600=04.-0.5 | |||
====Conventions for the <c-4> field==== | ====Conventions for the <c-4> field==== | ||
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| | | | ||
# replace ''carbon source'' with the actual one (ie. glucose, glycerol, acetate, etc.) | # replace ''carbon source'' with the actual one (ie. glucose, glycerol, acetate, etc.) | ||
# use this term ONLY if this is the point | # use this term ONLY if this is the main point! ie. Use mutant vs wild type if it fits better than this. | ||
|- | |- | ||
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|- | |||
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pH | |||
| | |||
"Acidified medium" or "Alkaline medium" | |||
|- class="tableEdit_footer" | |- class="tableEdit_footer" | ||
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|} | |} | ||
<!--box uid=63ce1649aab8b3180235b0af7618f667.170369.H4b5a3bcb7dca8--></protect> | <!--box uid=63ce1649aab8b3180235b0af7618f667.170369.H4b5a3bcb7dca8--></protect> | ||
==Related Tutorials and Resources== | |||
*[[http://ecoliwiki.net/colipedia/index.php/Category:Expression_data Step 1]] List of microarray papers to be annotated. | |||
*[[http://tetramer.tamu.edu/team/wiki/index.php/SMD_Affy_Ecoli_2.0_sets Step 2]] Guide on how to set up a batch file. | |||
*[ Step 3 ] Guide on how to Annotate batch files. | |||
*[[http://tetramer.tamu.edu/team/wiki/index.php/Loading_Microarrays_into_SMD Step 4]] Tutorial on how to load batch files into SMD. | |||
*[[http://tetramer.tamu.edu/team/wiki/index.php/SMD-How_to_Make_a_Publication Step 5]] Guide on how to make a publication. | |||
==Categories== | ==Categories== | ||
[[Category:Expression_data]] | [[Category:Expression_data]] | ||
Latest revision as of 02:23, 31 May 2013
Using the Batch Creator Script
If you would like to use the Batch Creator Script to create your batch file visit this tutorial.
Experiment Description Column in the Batch File
Overview
This column must contain a brief, readable description of the experiment followed by annotation of the samples and conditions, which are entered using the following syntax: <c-anno><c-1></c-1><c-2></c-2><c-3></c-3><c-4></c-4></c-anno>
- The individual annotation fields contain different classes of information, as shown below. Be sure to include the tags for all four annotation fields, even if some of them are empty.
- <c-1> Strain
- <c-2> Mutations (may include plasmids)
- <c-3>Description of Growth Conditions
- <c-4>Condition -- need to explain
- An example:
K-12 MG1655 rpoS(del)::FRT-kan-FRT, rep. 1<c-anno><c-1>K-12 MG1655</c-1><c-2>rpoS(del)::FRT-kan-FRT</c-2><c-3>LB, 37C, Exponential Phase</c-3><c-4>Mutant vs Wild-type</c-4></c-anno>
Experiment Description
- A brief, readable description of the experiment that must be unique (no other column can have the exact same name). You can add rep. 1, rep. 2, etc. if the same experiment was repeated..
- These description will be copied and pasted in to column L (SINGLE CHANNEL DESCRIPTION) and column M (Experiment Name) ??
- Here are some examples of experiment descriptions
- UTI89, Aerobic 12h
- K-12 MG1655, LB + glucose, rep. 1
- K-12 MG1655 rpoS(del)::FRT, Biofilm rep. 1
- K-12 BW25113 hha-745(del)::FRT-Kan-FRT, 4 hr Biofilm, LB
- K-12 ATCC 25404 + R1drd19 Plasimd, 24 h biofilm
- Here are some examples of what you DO NOT want to put
- (Don't type WT after the strain name) K-12 BW25113 WT
- You Don't need to put "bio.rep. 1", just put rep. 1
Individual Annotation Fields
Conventions for the <c-1> field
- Put the name of the organism and strain background between the <c-1> and </c-1> tags.
Do notDo include relevant mutant alleles or plasmids; these will also be added to the <c-2> field.Siegele 02:58, 7 June 2011 (UTC)- Here are some examples:
- <c-1>K-12 MG155</c-1>
- <c-1>K-12 MG155 rpoS::Tn10</c-1>
- <c-1>K-12 BW25113</c-1>
- <c-1>K-12 W3110</c-1>
- <c-1>O157-H7 EDL933</c-1>
- <c-1>K-12 BW25113 yjgK726(del)::FRT-kan-FRT</c-1>
- If the experiment uses an E. coli strain other than MG1655, BW25113, or W3110, check whether it has a page in EcoliWiki. If it doesn't, make one or ask someone else to make one.
- To find the allele number, go here and type the gene of interest (yjgK for example) in the field labeled "Mutation of gene."
Conventions for the <c-2>field
- Put the name of relevant mutant alleles or plasmids between the <c-2> and </c-2> tags.
- <c-2>ygjK726(del)::FRT-kan-FRT</c-2>
- Don't use special characters because the database won't accept them. Some of our substitutions are listed below:
- Instead of ∆ for deletion, put (del) after the gene name and allele number.
- If a mutation from the Keio collection was used, look up the allele number at the Coli Genetics Stock Center. If the kanamycin resistance gene is still present, describe the strain as yfgA000(del)::FRT-kan-FRT. If the kanR gene was "flipped out", describe the strain as yjgA000(del)::FRT.
Paper about how flipase experiments work: (One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products by Kirill A. Datsenko and Barry L. Wanner)
Conventions for the <c-3> field
- Put information about the experimental conditions between the <c-3> and </c-3> tags. This includes information about the growth medium, growth temperature, growth phase, chemicals added, time points, etc. Here are some examples:
- biofilm
- planktonic
- glass wool biofilm
- time course
- Use commas to separate conditions listed in the <c-3> field.
- For example, <c-3>LB, 0.3 ug/ml Mecillinam, 60 ug/ml Cefsulodin, 37C, 40 min</c-3>
- Don't use special characters. Use the following substitutions instead.
- 37C for 37°C
- uM for micromolar
- ug for microgram
- Growth medium information
- LB
- MOPS minimal medium + carbon source (0.xx%) (It isn't essential to include the concentration, but DAS usually does because it is information she would want to have.)
- M9 minimal medium + carbon source (0.xx%) (")
- M63 minimal medium + carbon source (0.xx%) (")
- Optical Density
- OD600=0.3
- List of things you should NOT PUT:
- Do not list the number of grams for glass wool
- Do not list the rpm a solution was shaking at
- Other Examples
- LB + glucose (1 g/L), glucose/MgSO4-fed batch culture, OD595=11.5, 50C for 15 min (shifted from 37C)
- K medium (0.64 osmol/kg H2O) + glucose (20 mM) + met (0.5 mM), 0.3 M NaCl, 1 mM glycine betaine, 43C, OD600=04.-0.5
Conventions for the <c-4> field
- The most important thing is KEY word! Pick the term that BEST suits the sample.
- The term chosen may vary accordingly in the set, but each sample will be given a term.
- Limit the <c-4> field to a small number of terms, preferably 1 or 2. Examples where you might want to use 2 terms: Parental strain + Autoinducer-2 (AI-2); Parental strain + Aerobic growth; Mutant + Aerobic growth
- The table below contains a list of potential keywords for the <c-4> field that DAS and BDM chose on 1/22/2010. This table can be updated or modified.
| Potential c-4 terms | Example or brief explanation |
|---|---|
|
Biofilm vs planktonic |
|
|
Biofilm + chemical |
Put the actual chemical name in. |
|
Chemical |
Again, put the chemical name here. |
|
Control |
ie. if sample is replicate 1 vs replicate 2 of same strain and same growth conditions |
|
Ultraviolet (UV) light |
|
|
Wild type vs mutant |
|
|
Wild type vs complemented null mutant |
|
|
Wild type vs overexpression |
|
|
Null mutant vs complemented null mutant |
|
|
Strain comparison |
ie. E. coli K-12 MG1655 compared to E. coli B REL606 |
|
Stationary phase |
This includes starvation. |
|
Heat shock |
|
|
Cold shock |
|
|
Minimal medium + carbon source |
|
|
Mutant |
|
|
Growth curve |
Following expression changes as a function of cell density. |
|
Parental strain |
|
|
Aerobic growth |
|
|
Anaerobic growth |
|
|
No treatment |
|
|
pH |
"Acidified medium" or "Alkaline medium" |
| edit table |
Related Tutorials and Resources
- [Step 1] List of microarray papers to be annotated.
- [Step 2] Guide on how to set up a batch file.
- [ Step 3 ] Guide on how to Annotate batch files.
- [Step 4] Tutorial on how to load batch files into SMD.
- [Step 5] Guide on how to make a publication.