GenDBWiki/WebDocumentation/DialogWindows/SNP-Detector - Revision history

Agoesman at 10:09, 30 November 2011

2011-11-30T10:09:26Z

← Older revision		Revision as of 12:09, 30 November 2011
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	== Starting SNP-Detector and general remarks ==		== Starting SNP-Detector and general remarks ==

	As described above SNP-Detector can be used to list all single nucleotide variations between two strongly related contigs. This is achieved by analyzing blast-results computed for the sequences (CDS or intergenic regions) of one contig (named "source" in the following) against the corresponding sequences of another (strongly related) contig (named "target" in the following). SNP-Detector therefore relies on the results of BLAST-tools from the projects database which already have to be run for the contigs in a former stage as a precondition.		As described above SNP-Detector can be used to list all single nucleotide variations between two strongly related contigs. This is achieved by analyzing blast-results computed for the sequences (CDS or intergenic regions) of one contig (named "source" in the following) against the corresponding sequences of another (strongly related) contig (named "target" in the following). SNP-Detector therefore relies on the results of BLAST-tools from the projects database which already have to be run for the contigs in a former stage as a precondition.
	----		----

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	== Configuring SNP-Detector ==		== Configuring SNP-Detector ==

	[[~~Image~~:~~GenDBWiki$$WebDocumentation$$DialogWindows$$~~SNP-Detector~~$snpconfiguration~~.png]]		[[File:SNP-Detector-Config.png\|Screenshot of the SNP Detector configuration dialog.]]

	----		----
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	'''Selecting a BLAST tool:'''		'''Selecting a BLAST tool:'''

	Here you can select a suitable tool for your purpose. That means, that the tool's predefined database must be related to the "target" contig (see also section [[#StartingSNPDetection\|general remarks]]), since its results where computed for the "source" contig and therefore the combination makes sense.		Here you can select a suitable tool for your purpose. That means, that the tool's predefined database must be related to the "target" contig (see also section [[#StartingSNPDetection\|general remarks]]), since its results where computed for the "source" contig and therefore the combination makes sense.

	When you are ready you can submit the page!		When you are ready you can submit the page!
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	EXAMPLE FOR CORRECT USE:		EXAMPLE FOR CORRECT USE:

	The BLAST-tool "Blast2n_vs_NC_YYYY" with its predefined database "NC_YYYY.cds" was run on contig NC_XXXX!		The BLAST-tool "Blast2n_vs_NC_YYYY" with its predefined database "NC_YYYY.cds" was run on contig NC_XXXX!
	In this case NC_XXXX is the "source" contig, whereas "NC_YYYY" is said to be the "target" contig. Therefore you would select the tool's name from the popup-menue and choose the contig "NC_XXXX" from the popup-menue displaying all contigs in the project!		In this case NC_XXXX is the "source" contig, whereas "NC_YYYY" is said to be the "target" contig. Therefore you would select the tool's name from the popup-menue and choose the contig "NC_XXXX" from the popup-menue displaying all contigs in the project!
	----		----

	'''NOTE THAT THE NAME OF THE SELECTED BLAST-TOOL MUST NOT CONTAIN BLANKS!'''		'''NOTE THAT THE NAME OF THE SELECTED BLAST-TOOL MUST NOT CONTAIN BLANKS!'''
	'''''This is due to the fact, that the processing is made on the cluster and this is a restriction which momentarily has to be made. You ought to keep this in mind, when you create your tools.'''''		'''''This is due to the fact, that the processing is made on the cluster and this is a restriction which momentarily has to be made. You ought to keep this in mind, when you create your tools.'''''

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	Now, go on by clicking on of the links to your results!		Now, go on by clicking on of the links to your results!

	[[~~Image~~:~~GenDBWiki$$WebDocumentation$$DialogWindows$$~~SNP-Detector~~$snpoverview~~.png]]		[[File:SNP-Detector-Results.png\|Screenshot of the SNP Detector result overview.]]
	----		----
	'''''PLEASE NOTE, that you should not close this page unless you want to discard all your results. As long as the overview page is open and your session does not expire your results remain accessible from that overview page.'''''		'''''PLEASE NOTE, that you should not close this page unless you want to discard all your results. As long as the overview page is open and your session does not expire your results remain accessible from that overview page.'''''
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	== Result pages ==		== Result pages ==

	The result page shows the single results for all CDS regions or intergenic regions. The representation of the results differs for CDS regions and intergenic regions. See the appropriate section in this manual to get to know what the entries (single rows) in your result lists mean! To distinguish between "source" (1) and "target" contig (2) numbers were introduced that are appended on the column names as suffixes. Their meaning can be regarded as distinguishing between features related to "region 1" ("source") or "region 2" ("target"), respectively.		The result page shows the single results for all CDS regions or intergenic regions. The representation of the results differs for CDS regions and intergenic regions. See the appropriate section in this manual to get to know what the entries (single rows) in your result lists mean! To distinguish between "source" (1) and "target" contig (2) numbers were introduced that are appended on the column names as suffixes. Their meaning can be regarded as distinguishing between features related to "region 1" ("source") or "region 2" ("target"), respectively.

	----		----
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	If you actually want to see an overview of the detected SNPs you must click on the link named "Show Report". The link "Show Alignment" will direct you to a new window where you can see the alingment of the two sequences.		If you actually want to see an overview of the detected SNPs you must click on the link named "Show Report". The link "Show Alignment" will direct you to a new window where you can see the alingment of the two sequences.
	----		----
	[[~~Image~~:~~GenDBWiki$$WebDocumentation$$DialogWindows$$~~SNP-Detector~~$snpintergenres~~.png]]		[[File:SNP-Detector-List.png\|Screenshot of the SNP Detector result list.]]
	----		----
	It's possible to navigate through the result list. Closing the result page including the result list is no problem, since you can revisit the page from the overview page!		It's possible to navigate through the result list. Closing the result page including the result list is no problem, since you can revisit the page from the overview page!
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	Since SNP-Detector stores its intermediate results in files you will get an information message that these files are deleted. This is normal!		Since SNP-Detector stores its intermediate results in files you will get an information message that these files are deleted. This is normal!
	----		----

	[[Category:Homepage]]		[[Category:Homepage]]

Admin: 23 revisions

2011-10-26T06:16:09Z

23 revisions

← Older revision	Revision as of 08:16, 26 October 2011
(No difference)

imported>SebastianKonietzny at 18:19, 12 April 2006

2006-04-12T18:19:51Z

← Older revision		Revision as of 20:19, 12 April 2006
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	----		----

	'''''NOTE THAT THE NAME OF THE SELECTED BLAST-TOOL MUST NOT CONTAIN BLANKS! This is due to the fact, that the processing is made on the cluster and this is a restriction which momentarily has to be made. You ought to keep this in mind, when you create your tools.'''''		'''NOTE THAT THE NAME OF THE SELECTED BLAST-TOOL MUST NOT CONTAIN BLANKS!'''
			'''''This is due to the fact, that the processing is made on the cluster and this is a restriction which momentarily has to be made. You ought to keep this in mind, when you create your tools.'''''

	'''''The intergenic regions are not region objects in GENDB as for example CDS regions are. They are only computed for the BLAST step and will not be stored in the project's database! That is why you have to use a specific BLAST-tool belonging to the class GENDB::Intergenic_Blast!'''''		'''''The intergenic regions are not region objects in GENDB as for example CDS regions are. They are only computed for the BLAST step and will not be stored in the project's database! That is why you have to use a specific BLAST-tool belonging to the class GENDB::Intergenic_Blast!'''''
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	You will see the names of the determined left and right flanking CDS regions (on "source" and "target" contig) for the intergenic regions that are most likely to be homologous as calculated from the available BLAST results. These names represent links that will direct you to the corresponding objects in GENDB. You also see the PERCENT IDENTITY of the hit and the LENGHT of the hit.		You will see the names of the determined left and right flanking CDS regions (on "source" and "target" contig) for the intergenic regions that are most likely to be homologous as calculated from the available BLAST results. These names represent links that will direct you to the corresponding objects in GENDB. You also see the PERCENT IDENTITY of the hit and the LENGHT of the hit.
	If you actually want to see an overview of the detected SNPs you must click on the link named "Show Report". The link "Show Alignment" will direct you to a new window where you can see the alingment of the two sequences.		If you actually want to see an overview of the detected SNPs you must click on the link named "Show Report". The link "Show Alignment" will direct you to a new window where you can see the alingment of the two sequences.
			----
	[[Image:GenDBWiki$$WebDocumentation$$DialogWindows$$SNP-Detector$snpintergenres.png]]		[[Image:GenDBWiki$$WebDocumentation$$DialogWindows$$SNP-Detector$snpintergenres.png]]
	----		----

imported>SebastianKonietzny at 07:32, 7 April 2006

2006-04-07T07:32:09Z

← Older revision		Revision as of 09:32, 7 April 2006
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	EXAMPLE FOR CORRECT USE:		EXAMPLE FOR CORRECT USE:

	The BLAST-tool "Blast2n_vs_NC_YYYY" with its predefined database "NC_YYYY.cds" was run on contig NC_XXXX! In this case NC_XXXX is the "source" contig, whereas "NC_YYYY" is said to be the "target" contig. Therefore you would select the tool"s name from the popup-menue and choose the contig "NC_XXXX" from the popup-menue ~~displaing~~ all contigs in the project!		The BLAST-tool "Blast2n_vs_NC_YYYY" with its predefined database "NC_YYYY.cds" was run on contig NC_XXXX!
			In this case NC_XXXX is the "source" contig, whereas "NC_YYYY" is said to be the "target" contig. Therefore you would select the tool's name from the popup-menue and choose the contig "NC_XXXX" from the popup-menue displaying all contigs in the project!
			----

	'''''NOTE THAT THE NAME OF THE SELECTED BLAST-TOOL MUST NOT CONTAIN BLANKS! This is due to the fact, that the processing is made on the cluster and this is a restriction which momentarily has to be made. You ought to keep this in mind, when you create your tools.'''''		'''''NOTE THAT THE NAME OF THE SELECTED BLAST-TOOL MUST NOT CONTAIN BLANKS! This is due to the fact, that the processing is made on the cluster and this is a restriction which momentarily has to be made. You ought to keep this in mind, when you create your tools.'''''

imported>SebastianKonietzny at 07:29, 7 April 2006

2006-04-07T07:29:20Z

← Older revision		Revision as of 09:29, 7 April 2006
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	----		----
	EXAMPLE FOR CORRECT USE:~~<br />~~		EXAMPLE FOR CORRECT USE:

	The BLAST-tool "Blast2n_vs_NC_YYYY" with its predefined database "NC_YYYY.cds" was run on contig NC_XXXX! In this case NC_XXXX is the "source" contig, whereas "NC_YYYY" is said to be the "target" contig. Therefore you would select the tool"s name from the popup-menue and choose the contig "NC_XXXX" from the popup-menue displaing all contigs in the project!		The BLAST-tool "Blast2n_vs_NC_YYYY" with its predefined database "NC_YYYY.cds" was run on contig NC_XXXX! In this case NC_XXXX is the "source" contig, whereas "NC_YYYY" is said to be the "target" contig. Therefore you would select the tool"s name from the popup-menue and choose the contig "NC_XXXX" from the popup-menue displaing all contigs in the project!

imported>SebastianKonietzny at 07:28, 7 April 2006

2006-04-07T07:28:38Z

← Older revision		Revision as of 09:28, 7 April 2006
Line 40:		Line 40:

	----		----
	EXAMPLE FOR CORRECT USE:		EXAMPLE FOR CORRECT USE:<br />
	The BLAST-tool "Blast2n_vs_NC_YYYY" with its predefined database "NC_YYYY.cds" was run on contig NC_XXXX! In this case NC_XXXX is the "source" contig, whereas "NC_YYYY" is said to be the "target" contig. Therefore you would select the tool"s name from the popup-menue and choose the contig "NC_XXXX" from the popup-menue displaing all contigs in the project!		The BLAST-tool "Blast2n_vs_NC_YYYY" with its predefined database "NC_YYYY.cds" was run on contig NC_XXXX! In this case NC_XXXX is the "source" contig, whereas "NC_YYYY" is said to be the "target" contig. Therefore you would select the tool"s name from the popup-menue and choose the contig "NC_XXXX" from the popup-menue displaing all contigs in the project!

imported>SebastianKonietzny at 07:24, 7 April 2006

2006-04-07T07:24:29Z

← Older revision		Revision as of 09:24, 7 April 2006
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	'''SNP-Detector detects and lists Single Nucleotide Polymorphisms in genomic data.'''		'''SNP-Detector detects and lists Single Nucleotide Polymorphisms in genomic data.'''

	''Single Nucleotide Polymorphisms'' (abbreviated SNPs,pronounced "snips") are a phenomenon related to homologous sequences. They describe little (regularly only one base is affected) differences between strongly related, homologous sequences. SNPs may fall within coding sequences (CDS) of genes or between genes (intergenic regions). SNPs are due to single nucleotide mutations (substitution, deletion or insertion of a single nucleotide) which may happen independently on the single sequences. Normally, for a variation to be considered a SNP, it must occur in at least 1% of the population. SNP-Detector, though, is not be seen in the context of this statistical approach, but reports all single nucleotide variations between homologous sequences (CDS-regions or intergenic regions) of two contigs belonging to strongly related organisms.		''Single Nucleotide Polymorphisms'' (abbreviated SNPs,pronounced "snips") are a phenomenon related to homologous sequences. They describe little (regularly only one base is affected) differences between strongly related, homologous sequences. SNPs may fall within coding sequences (CDS) of genes or between genes (intergenic regions). SNPs are due to single nucleotide mutations (substitution, deletion or insertion of a single nucleotide) which may happen independently on the single sequences. Normally, for a variation to be considered a SNP, it must occur in at least 1% of the population. SNP-Detector, though, is not to be seen in the context of this statistical approach, but reports all single nucleotide variations between homologous sequences (CDS-regions or intergenic regions) of two contigs belonging to strongly related organisms.

	SNPs are important features of a genomic sequence. Their distributions are normally characteristic for a specific strain. SNPs are often used for rapid classification of an organism. Since SNPs in CDS sequences may change codons they can also differ the function of genes and therefore be responsible for altered phenotypical characteristics of mutants. A convenient method for detecting SNPs is restriction fragment length polymorphism (SNP-RFLP).		SNPs are important features of a genomic sequence. Their distributions are normally characteristic for a specific strain. SNPs are often used for rapid classification of an organism. Since SNPs in CDS sequences may change codons they can also differ the function of genes and therefore be responsible for altered phenotypical characteristics of mutants. A convenient method for detecting SNPs is restriction fragment length polymorphism (SNP-RFLP).

imported>SebastianKonietzny at 13:31, 28 March 2006

2006-03-28T13:31:50Z

← Older revision		Revision as of 15:31, 28 March 2006
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	Now, go on by clicking on of the links to your results!		Now, go on by clicking on of the links to your results!

			[[Image:GenDBWiki$$WebDocumentation$$DialogWindows$$SNP-Detector$snpoverview.png]]
	----		----
	'''''PLEASE NOTE, that you should not close this page unless you want to discard all your results. As long as the overview page is open and your session does not expire your results remain accessible from that overview page.'''''		'''''PLEASE NOTE, that you should not close this page unless you want to discard all your results. As long as the overview page is open and your session does not expire your results remain accessible from that overview page.'''''

	~~[[Image:GenDBWiki$$WebDocumentation$$DialogWindows$$SNP-Detector$snpoverview.png]]~~

	== Result pages ==		== Result pages ==

imported>SebastianKonietzny at 13:30, 28 March 2006

2006-03-28T13:30:34Z

← Older revision		Revision as of 15:30, 28 March 2006
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	----		----
	Options:		Options:
	~~----~~
	'''Mode selection:'''		'''Mode selection:'''
	On the configuration page the user can choose whether he wants SNP-Detector to be run for CDS regions or intergenic regions only, or for both. You simply have to check out the corresponding boxes named "SNPs in CDS" or "SNPs in intergenic regions", respectively.		On the configuration page the user can choose whether he wants SNP-Detector to be run for CDS regions or intergenic regions only, or for both. You simply have to check out the corresponding boxes named "SNPs in CDS" or "SNPs in intergenic regions", respectively.

imported>SebastianKonietzny at 13:29, 28 March 2006

2006-03-28T13:29:59Z

← Older revision		Revision as of 15:29, 28 March 2006
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	-----		-----
	'''Intergenic regions:'''		'''Intergenic regions:'''
	First you see a name for the intergenic region. This name is arbitrary and merely represents a ~~count~~ for the regions. The intergenic regions are not region objects in GENDB as for example CDS regions are. They are only computed for the BLAST step and will not be stored in the project's database! That is why you have to use a specific BLAST-tool belonging to the class GENDB::Intergenic_Blast!		First you see a name for the intergenic region. This name is arbitrary and merely represents a counter for the regions. ''The intergenic regions are not region objects in GENDB as for example CDS regions are. They are only computed for the BLAST step and will not be stored in the project's database! That is why you have to use a specific BLAST-tool belonging to the class GENDB::Intergenic_Blast!''
	~~----~~
	You will see the names of the determined left and right flanking CDS regions (on "source" and "target" contig) for the intergenic regions that are most likely to be homologous as calculated from the available BLAST results. These names represent links that will direct you to the corresponding objects in GENDB. You also see the PERCENT IDENTITY of the hit and the LENGHT of the hit.		You will see the names of the determined left and right flanking CDS regions (on "source" and "target" contig) for the intergenic regions that are most likely to be homologous as calculated from the available BLAST results. These names represent links that will direct you to the corresponding objects in GENDB. You also see the PERCENT IDENTITY of the hit and the LENGHT of the hit.
	If you actually want to see an overview of the detected SNPs you must click on the link named "Show Report". The link "Show Alignment" will direct you to a new window where you can see the alingment of the two sequences.		If you actually want to see an overview of the detected SNPs you must click on the link named "Show Report". The link "Show Alignment" will direct you to a new window where you can see the alingment of the two sequences.

	[[Image:GenDBWiki$$WebDocumentation$$DialogWindows$$SNP-Detector$snpintergenres.png]]		[[Image:GenDBWiki$$WebDocumentation$$DialogWindows$$SNP-Detector$snpintergenres.png]]
			----
	It's possible to navigate through the result list. Closing the result page including the result list is no problem, since you can revisit the page from the overview page!		It's possible to navigate through the result list. Closing the result page including the result list is no problem, since you can revisit the page from the overview page!