en to unknown language translation catalogue (130 entries)

[ctx: AppSettingsDialog]
en: AppSettingsDialog
target: Application Settings

[ctx: AuthenticationDialog]
en: Authetication
target: Authentification

[ctx: BlastAllSupportDialog]
en: Multiple Hits window size
target: Multiple Hits Window Size

[ctx: BlastDBCmdDialog]
en: Entery query ID:
target: Enter query ID:

[ctx: DotPlotDialog]
en: Search direct repeats
target: Search for direct repeats

[ctx: DotPlotDialog]
en: Search inverted repeats
target: Search for inverted repeats

[ctx: EDSetupRecBoundDlg]
en: Setup Recognition Bound
target: м

[ctx: ETSSettingsWidget]
en: Check lastest version of external tools package
target: Check latest version of external tools package

[ctx: EditSequenceDialog]
en: To change the regsion select it on a sequence
target: To change the region select it on a sequence

[ctx: ExpertDiscoverySearchDialog]
en: strand_complement_wit
target: Complement

[ctx: ExpertDiscoverySearchDialog]
en: strand_direct_wit
target: Direct

[ctx: ExportHighlightedDialog]
en: Exported area:  from
target: Exported area: from

[ctx: GenomeAlignerSettings]
en: Chech this box if mismatches between the reference sequence and the reads are allowed.
target: Check this box if mismatches between the reference sequence and the reads are allowed.

[ctx: HMMBuildDialog]
en: 
                 By default, the model is configured to find one or more nonoverlapping alignments to the complete model:
                 multiple global alignments with respect to the model, and local with respect to the sequence
target: By default, the model is configured to find one or more nonoverlapping alignments to the complete model:
    multiple global alignments with respect to the model, and local with respect to the sequence

[ctx: HMMBuildDialog]
en: 
                 Configure the model for finding a single global alignment to a target sequence,
                 analogous to the old hmms program of HMMER 1.
target: Configure the model for finding a single global alignment to a target sequence,
    analogous to the old hmms program of HMMER 1.

[ctx: HMMBuildDialog]
en: 
                 Configure the model for finding a single local alignment per target sequence.
                 This is analogous to the standard Smith/Waterman algorithm or the hmmsw program of HMMER 1.
target: Configure the model for finding a single local alignment per target sequence.
    This is analogous to the standard Smith/Waterman algorithm or the hmmsw program of HMMER 1.

[ctx: HMMBuildDialog]
en: 
                 Configure the model for finding multiple domains per sequence, where each domain can be a local (fragmentary) alignment.
                 This is analogous to the old hmmfs program of HMMER 1.
target: Configure the model for finding multiple domains per sequence, where each domain can be a local (fragmentary) alignment.
    This is analogous to the old hmmfs program of HMMER 1.

[ctx: HMMBuildWorker]
en: Fix the length of the random sequences to <n>, where <n> is a positive (and reasonably sized) integer. <p>The default is instead to generate sequences with a variety of different lengths, controlled by a Gaussian (normal) distribution.
target: Fix the length of the random sequences to <n>, where <n> is a positive (and reasonably sized) integer. 
    The default is instead to generate sequences with a variety of different lengths, controlled by a Gaussian (normal) distribution.

[ctx: HMMBuildWorker]
en: Number of synthetic sequences. If <n> is less than about 1000, the fit to the EVD may fail. <p>Higher numbers of <n> will give better determined EVD parameters. <p>The default is 5000; it was empirically chosen as a tradeoff between accuracy and computation time.
target: Number of synthetic sequences. If <n> is less than about 1000, the fit to the EVD may fail. 
    Higher numbers of <n> will give better determined EVD parameters. 
    The default is 5000; it was empirically chosen as a tradeoff between accuracy and computation time.

[ctx: HMMBuildWorker]
en: The random seed, where <n> is a positive integer. <p>The default is to use time() to generate a different seed for each run, <p>which means that two different runs of hmmcalibrate on the same HMM will give slightly different results. <p>You can use this option to generate reproducible results for different hmmcalibrate runs on the same HMM.
target: The random seed, where <n> is a positive integer. The default is to use time() to generate a different seed for each run, 
    which means that two different runs of hmmcalibrate on the same HMM will give slightly different results. 
    You can use this option to generate reproducible results for different hmmcalibrate runs on the same HMM.

[ctx: HMMCalibrateDialog]
en: 
                 Fix the length of the random sequences to n
                     , where n is a positive (and reasonably sized) integer. 
    The default is instead to generate sequences with a variety of different lengths, controlled by a Gaussian (normal) distribution.
target: Fix the length of the random sequences to n, where n is a positive (and reasonably sized) integer. 
    The default is instead to generate sequences with a variety of different lengths, controlled by a Gaussian (normal) distribution.

[ctx: HMMCalibrateDialog]
en: 
                 Number of synthetic sequences.
                 If n is less than about 1000, the fit to the EVD may fail
                 Higher numbers of n will give better determined EVD parameters. 
                 The default is 5000; it was empirically chosen as a tradeoff between accuracy and computation time.
target: Number of synthetic sequences.
    If n is less than about 1000, the fit to the EVD may fail
    Higher numbers of n will give better determined EVD parameters. 
    The default is 5000; it was empirically chosen as a tradeoff between accuracy and computation time.

[ctx: HMMCalibrateDialog]
en: 
                 Standard deviation of the synthetic sequence length.
                 A positive number. The default is 200.
                 Note that the Gaussian is left-truncated so that no sequences have lengths less or equal 0.
target: Standard deviation of the synthetic sequence length.
    A positive number. The default is 200.
    Note that the Gaussian is left-truncated so that no sequences have lengths less or equal 0.

[ctx: HMMCalibrateDialog]
en: 
                 The random seed, where n is a positive integer. 
                 The default is to use time() to generate a different seed for each run, 
                 which means that two different runs of hmmcalibrate on the same HMM will give slightly different results. 
                 You can use this option to generate reproducible results for different hmmcalibrate runs on the same HMM.
target: The random seed, where n is a positive integer. 
    The default is to use time() to generate a different seed for each run, 
    which means that two different runs of hmmcalibrate on the same HMM will give slightly different results. 
    You can use this option to generate reproducible results for different hmmcalibrate runs on the same HMM.

[ctx: HMMSearchDialog]
en: 1E
target: 1e

[ctx: HMMSearchDialog]
en: Calculate the E-value scores as if we had seen a sequence database of &lt;n&gt; sequences.
target: Calculate the E-value scores as if we had seen a sequence database of <n> sequences.

[ctx: ImageExportForm]
en:  export settings
target: Export settings

[ctx: ImportOptionsWidget]
en: <!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0//EN" "http://www.w3.org/TR/REC-html40/strict.dtd">
    <html><head><meta name="qrichtext" content="1" /><style type="text/css">
    p, li { white-space: pre-wrap; }
    </style></head><body style=" font-family:'MS Shell Dlg 2'; font-size:8.25pt; font-weight:400; font-style:normal;">
    <p style=" margin-top:0px; margin-bottom:0px; margin-left:0px; margin-right:0px; -qt-block-indent:0; text-indent:0px;"><span style=" font-size:10pt;">Number of 'unknown' symbols </span><span style=" font-size:10pt; font-style:italic;">('N 'for nucleic or 'X' for amino)</span><span style=" font-size:10pt;"> between parts:</span></p></body></html>
target: <!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0//EN" "http://www.w3.org/TR/REC-html40/strict.dtd">
    <html><head><meta name="qrichtext" content="1" /><style type="text/css">
    p, li { white-space: pre-wrap; }
    </style></head><body style=" font-family:'MS Shell Dlg 2'; font-size:8.25pt; font-weight:400; font-style:normal;">
    <p style=" margin-top:0px; margin-bottom:0px; margin-left:0px; margin-right:0px; -qt-block-indent:0; text-indent:0px;"><span style=" font-size:8pt;">Number of 'unknown' symbols </span><span style=" font-size:8pt; font-style:italic;">('N 'for nucleic or 'X' for amino)</span><span style=" font-size:8pt;"> between parts:</span></p></body></html> {3C?} {4.0/?} {3.?} {40/?} {1"?} {2'?} {8.25p?} {400;?} {0p?} {0p?} {0p?} {0p?} {0;?} {0p?} {10p?} {10p?} {10p?}

[ctx: LogSettingsWidget]
en: LogSettingsWidget
target: Logger settings

[ctx: MarkerEditorWidget]
en: Edit
target: Add

[ctx: Primer3Dialog]
en: #N's
target: N

[ctx: Primer3Dialog]
en: <!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0//EN" "http://www.w3.org/TR/REC-html40/strict.dtd">
    <html><head><meta name="qrichtext" content="1" /><style type="text/css">
    p, li { white-space: pre-wrap; }
    </style></head><body style=" font-family:'MS Shell Dlg 2'; font-size:7.8pt; font-weight:400; font-style:normal;">
    <p style=" margin-top:0px; margin-bottom:0px; margin-left:0px; margin-right:0px; -qt-block-indent:0; text-indent:0px;"><span style=" font-size:8pt;">Equivalent parameter of primer DNA concentration for the internal oligo. </span></p></body></html>
target: <!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0//EN" "http://www.w3.org/TR/REC-html40/strict.dtd">
    <html><head><meta name="qrichtext" content="1" /><style type="text/css">
    p, li { white-space: pre-wrap; }
    </style></head><body style=" font-family:'MS Shell Dlg 2'; font-size:7.8pt; font-weight:400; font-style:normal;">
    <p style=" margin-top:0px; margin-bottom:0px; margin-left:0px; margin-right:0px; -qt-block-indent:0; text-indent:0px;"><span style=" font-size:8pt;">ДНК концентрация гибридизации олиго. </span></p></body></html>

[ctx: Primer3Dialog]
en: <!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0//EN" "http://www.w3.org/TR/REC-html40/strict.dtd">
    <html><head><meta name="qrichtext" content="1" /><style type="text/css">
    p, li { white-space: pre-wrap; }
    </style></head><body style=" font-family:'MS Shell Dlg 2'; font-size:7.8pt; font-weight:400; font-style:normal;">
    <p style=" margin-top:0px; margin-bottom:0px; margin-left:0px; margin-right:0px; -qt-block-indent:0; text-indent:0px;"><span style=" font-size:8pt;">Equivalent parameter of primer concentration of the dNTPs for the internal oligo. </span></p></body></html>
target: <!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0//EN" "http://www.w3.org/TR/REC-html40/strict.dtd">
    <html><head><meta name="qrichtext" content="1" /><style type="text/css">
    p, li { white-space: pre-wrap; }
    </style></head><body style=" font-family:'MS Shell Dlg 2'; font-size:7.8pt; font-weight:400; font-style:normal;">
    <p style=" margin-top:0px; margin-bottom:0px; margin-left:0px; margin-right:0px; -qt-block-indent:0; text-indent:0px;"><span style=" font-size:8pt;">Гибридизация олиго [dNTP]. </span></p></body></html>

[ctx: Primer3Dialog]
en: <!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0//EN" "http://www.w3.org/TR/REC-html40/strict.dtd">
    <html><head><meta name="qrichtext" content="1" /><style type="text/css">
    p, li { white-space: pre-wrap; }
    </style></head><body style=" font-family:'Sans Serif'; font-size:9pt; font-weight:400; font-style:normal;">
    <p style=" margin-top:0px; margin-bottom:0px; margin-left:0px; margin-right:0px; -qt-block-indent:0; text-indent:0px;"><span style=" font-family:'MS Shell Dlg 2'; font-size:8pt;">In this section user can specify if primer product must overlap exon-exon junction or span intron. This only applies when designing primers for a cDNA (mRNA) sequence with annotated exons. </span></p></body></html>
target: <!DOCTYPE HTML PUBLIC "-//W3C//DTD HTML 4.0//EN" "http://www.w3.org/TR/REC-html40/strict.dtd">
    <html><head><meta name="qrichtext" content="1" /><style type="text/css">
    p, li { white-space: pre-wrap; }
    </style></head><body style=" font-family:'Sans Serif'; font-size:9pt; font-weight:400; font-style:normal;">
    <p style=" margin-top:0px; margin-bottom:0px; margin-left:0px; margin-right:0px; -qt-block-indent:0; text-indent:0px;"><span style=" font-family:'MS Shell Dlg 2'; font-size:8pt;">RT-PCR. </span></p></body></html>

[ctx: ProjectViewWidget]
en: Form
target: Project View

[ctx: QObject]
en: HMM reader error occurred:
target: HMM reader error:

[ctx: QObject]
en: Tubes
target: Model

[ctx: SecStructPredictTask]
en: psipred: sequence is too long, max seq size is 10000
target: Sequence is too long: maximum allowed length is 10000

[ctx: SecStructPredictTask]
en: psipred: sequence is too short, min seq size is 5
target: Sequence is too short: minimum allowed length is 5

[ctx: SecStructPredictTask]
en: seq database not found
target: Sequence database not found

[ctx: SecStructPredictTask]
en: sequence is too long, max seq size is 10000
target: Too long input sequence: maximum allowed length is 10000

[ctx: TmpDirChangeDialog]
en: Dialog
target: Create New Project

[ctx: U2::AssemblySettingsWidget]
en: You should add a refrence first for correct displaying of selected highlighting
target: You should add a reference first for correct displaying of selected highlighting

[ctx: U2::AssemblySettingsWidget]
en: You should add refrence  first for correct dispalying of this highlighting
target: You should add reference first for correct dispalying of this highlighting

[ctx: U2::BlastAllSupportMultiTask]
en: Used databse
target: Used database

[ctx: U2::BlastPlusSupportMultiTask]
en: Used databse
target: Used database

[ctx: U2::BuildIndexDialog]
en: DNA Assembly
target: DNA assembly

[ctx: U2::ClustalOWithExtFileSpecifySupportRunDialog]
en: Kalign with Align
target: Align with Kalign

[ctx: U2::ClustalWWithExtFileSpecifySupportRunDialog]
en: Kalign with Align
target: Align with Kalign

[ctx: U2::ConvertAssemblyToSamDialog]
en: Data base file url is not set!
target: Database file url is not set!

[ctx: U2::ConvertAssemblyToSamDialog]
en: Data base to SAM converter
target: Database to SAM converter

[ctx: U2::CreateDocumentFromTextDialogController]
en: Filename is empty
target: File name is empty

[ctx: U2::DnaAssemblySupport]
en: DNA Assembly
target: DNA assembly

[ctx: U2::DotPlotViewAction]
en: Show dot plot
target: Show dotplot

[ctx: U2::DotPlotWidget]
en: Save dot-plot
target: Save dotplot

[ctx: U2::DotPlotWidget]
en: Save dot-plot data before closing?
target: Save dotplot data before closing?

[ctx: U2::EditSequenceDialogController]
en: Filename is empty
target: File name is empty

[ctx: U2::ExpertDiscoveryPlugin]
en: Expert Discovery plugin
target: ExpertDiscovery is a system for analysis and recognition of gene regulatory regions using hierarchical approach. It implements a powerful machine learning method "Discovery" (http://math.nsc.ru/AP/ScientificDiscovery/)

[ctx: U2::ExpertDiscoverySetupRecBoundDialog]
en: Minimal bound must not be grater then maximal bound
target: Minimal bound must not be less then maximal bound

[ctx: U2::ExportSequencesDialog]
en: Translate to amino alphabet
target: Save both strands

[ctx: U2::ExternalToolSupportPlugin]
en: Blast format database...
target: BLAST format database...

[ctx: U2::ExternalToolSupportSettingsPageWidget]
en: <i>Cistrome</i> is a UGENE version of Cistrome pipeline which also includes some tools useful for ChIP-seq analysisThis pipeline is aimed to provide the following analysis steps: peak calling and annotating, motif search and gene ontology.
target: <i>Cistrome</i> is a UGENE version of Cistrome pipeline which also includes some tools useful for ChIP-seq analysis. This pipeline is aimed to provide the following analysis steps: peak calling and annotating, motif search and gene ontology.

[ctx: U2::FindEnzymesTask]
en: Found %1 restriction sites
target: Number of results exceed %1, stopping

[ctx: U2::FindTandemsDialog]
en: No annotations found: %1
target: "No annotations found: %1

[ctx: U2::GTest_uHMMERCalibrate]
en: uhmmer-calibrate-subtask
target: HMM Calibrate

[ctx: U2::KalignAlignWithExtFileSpecifyDialogController]
en: Kalign with Align
target: Align with Kalign

[ctx: U2::LoadDasFeaturesTask]
en: Can not receive response from the server "
target: Can not receive response from the server

[ctx: U2::LoadDotPlotTask]
en: DotPlot loading
target: Dotplot loading

[ctx: U2::LocalWorkflow::BowtieWorker]
en: Maximum permitted total of quality values at all mismatched read positions throughout the entire alignment,                              not just in the seed. The default is 70. Like Maq, bowtie rounds quality values to the nearest 10 and saturates at 30;                              rounding can be disabled with --nomaqround.
target: Maximum permitted total of quality values at all mismatched read positions throughout the entire alignment, not just in the seed. The default is 70. Like Maq, bowtie rounds quality values to the nearest 10 and saturates at 30; rounding can be disabled with --nomaqround.

[ctx: U2::LocalWorkflow::BowtieWorker]
en: The number of megabytes of memory a given thread is given to store path descriptors in --best mode. Best-first                                search must keep track of many paths at once to ensure it is always extending the path with the lowest cumulative cost.                                Bowtie tries to minimize the memory impact of the descriptors, but they can still grow very large in some cases.                                If you receive an error message saying that chunk memory has been exhausted in --best mode,                                try adjusting this parameter up to dedicate more memory to the descriptors. Default: 64.
target: The number of megabytes of memory a given thread is given to store path descriptors in --best mode. 
    Best-first search must keep track of many paths at once to ensure it is always extending the path with the lowest cumulative cost. 
    Bowtie tries to minimize the memory impact of the descriptors, but they can still grow very large in some cases. 
    If you receive an error message saying that chunk memory has been exhausted in --best mode, 
    try adjusting this parameter up to dedicate more memory to the descriptors. 
    Default: 64.

[ctx: U2::LocalWorkflow::BowtieWorker]
en: When the -n option is specified (which is the default), bowtie determines which alignments                               are valid according to the following policy, which is similar to Maq's default policy.                               In -v mode, alignments may have no more than V mismatches, where V may be a number from 0                               through 3 set using the -v option. Quality values are ignored. The -v option is mutually exclusive with the -n option.
target: When the -n option is specified (which is the default), bowtie determines which alignments are valid according to the following policy, which is similar to Maq's default policy. In -v mode, alignments may have no more than V mismatches, where V may be a number from 0 through 3 set using the -v option. Quality values are ignored. The -v option is mutually exclusive with the -n option.

[ctx: U2::LocalWorkflow::BwaWorker]
en: Quolity threshold
target: Quality threshold

[ctx: U2::LocalWorkflow::BwaWorker]
en: Quolity threshold (-q).
target: Quality threshold (-q).

[ctx: U2::LocalWorkflow::CallVariantsWorker]
en: A site is considered to be a variant if P(ref|D)<FLOAT (bcf view)(-p).
target: A site is considered to be a variant if P(ref|D) less than FLOAT (bcf view)(-p).

[ctx: U2::LocalWorkflow::CallVariantsWorker]
en: Enable pair/trio calling. For trio calling, option -s is usually needed to be applied to configure the trio members and their ordering. In the file supplied to the option -s, the first sample must be the child, the second the father and the third the mother. The valid values of STR are 'pair', 'trioauto', 'trioxd' and 'trioxs', where 'pair' calls differences between two input samples, and 'trioxd' ('trioxs')specifies that the input is from the X chromosome non-PAR regions and the child is a female (male) (bcf view)(-T).
target: Enable pair/trio calling. For trio calling, option -s is usually needed to be applied to configure the trio members and their ordering. In the file supplied to the option -s, the first sample must be the child, the second the father and the third the mother. The valid values of STR are 'ÂpairÂ', 'ÂtrioautoÂ', 'ÂtrioxdÂ' and 'ÂtrioxsÂ', where 'ÂpairÂ' calls differences between two input samples, and 'ÂtrioxdÂ' ('ÂtrioxsÂ')specifies that the input is from the X chromosome non-PAR regions and the child is a female (male) (bcf view)(-T).

[ctx: U2::LocalWorkflow::GenomecovWorker]
en: Calculate coverage of 3’ positions (instead of entire interval). (-3)
target: Calculate coverage of 3' positions (instead of entire interval). (-3)

[ctx: U2::LocalWorkflow::GenomecovWorker]
en: Calculate coverage of 5’ positions (instead of entire interval). (-5)
target: Calculate coverage of 5' positions (instead of entire interval). (-5)

[ctx: U2::LocalWorkflow::GenomecovWorker]
en: Treat “split” BAM or BED12 entries as distinct BED intervals when computing coverage. For BAM files, this uses the CIGAR “N” and “D” operations to infer the blocks for computing coverage. For BED12 files, this uses the BlockCount, BlockStarts, and BlockEnds fields (i.e., columns 10,11,12). (-split)
target: Treat  BAM or BED12 entries as distinct BED intervals when computing coverage. For BAM files, this uses the CIGAR  and  operations to infer the blocks for computing coverage. For BED12 files, this uses the BlockCount, BlockStarts, and BlockEnds fields (i.e., columns 10,11,12). (-split)

[ctx: U2::LocalWorkflow::MACSWorker]
en: Cutoff for broad region. This option is not available unless “Broad” is set.If “P-value” is set, this is a pvalue cutoff, otherwise, it's a qvalue cutoff.
target: Cutoff for broad region. This option is not available unless Broad is set.If P-value is set, this is a pvalue cutoff, otherwise, it's a qvalue cutoff.

[ctx: U2::LocalWorkflow::MACSWorker]
en: If set, MACS will try to call broad peaks by linking nearby highly enriched regions.The linking region is controlled by another cutoff through “Broad cutoff”.The maximum linking region length is 4 times of d from MACS.
target: If set, MACS will try to call broad peaks by linking nearby highly enriched regions.The linking region is controlled by another cutoff through Broad cutoff. The maximum linking region length is 4 times of d from MACS.

[ctx: U2::LocalWorkflow::MACSWorker]
en: Whether turn on the auto pair model process.If set, when MACS failed to build paired model, it will use the nomodelsettings, the “Shift size” parameter to shift and extend each tags (--on-auto).
target: Whether turn on the auto pair model process.If set, when MACS failed to build paired model, it will use the nomodelsettings, the Shift size parameter to shift and extend each tags (--on-auto).

[ctx: U2::LocalWorkflow::SWWorker]
en: smith_waterman_task
target: Smith waterman task

[ctx: U2::LocalWorkflow::SiteconBuildWorker]
en: Window size, bp
target: Window size

[ctx: U2::LocalWorkflow::SlopbedWorker]
en: Define -l and -r as a fraction of the feature’s length. E.g. if used on a 1000bp feature, -l 0.50, will add 500 bp “upstream”. (-pct)
target: Define -l and -r as a fraction of the featureâs length. E.g. if used on a 1000bp feature, -l 0.50, will add 500 bp âupstreamâ. (-pct)

[ctx: U2::LocalWorkflow::TCoffeeWorker]
en: Directory for temporary file.s
target: Directory for temporary files

[ctx: U2::LogViewWidget]
en: logview_set_case
target: Set case

[ctx: U2::LogViewWidget]
en: logview_use_regexp
target: Use regexp

[ctx: U2::MAFFTWithExtFileSpecifySupportRunDialog]
en: Kalign with Align
target: Align with Kalign

[ctx: U2::MuscleAlignWithExtFileSpecifyDialogController]
en: Kalign with Align
target: Align with Kalign

[ctx: U2::Primer3Task]
en: Pick primers task
target: Pick primers

[ctx: U2::QDSWActor]
en: smith_waterman_task
target: Smith-Waterman task

[ctx: U2::QDSiteconActor]
en: Sitecon
target: SITECON

[ctx: U2::QDSiteconTask]
en: Sitecon Query
target: SITECON Query

[ctx: U2::RetrieveRemoteMachineInfoTask]
en: Retrieving remomote machine info...
target: Retrieving remote machine info...

[ctx: U2::SAMFormat]
en: The Sequence Alignment/Map (SAM) format is a generic alignment format forstoring read alignments against reference sequence
target: The Sequence Alignment/Map (SAM) format is a generic alignment format for storing read alignments against reference sequence

[ctx: U2::SaveDotPlotTask]
en: DotPlot saving
target: Dotplot saving

[ctx: U2::SiteconPlugin]
en: Build SITECON model...
target: Build SITECON Model...

[ctx: U2::TCoffeeWithExtFileSpecifySupportRunDialog]
en: Kalign with Align
target: Align with Kalign

[ctx: U2::TaskViewDockWidget]
en: finished
target: Finished

[ctx: U2::UHMM3ADVContext]
en: error
target: Error

[ctx: U2::UHMM3BuildDialogImpl]
en: Select hmm file to create
target: Select HMM file to create

[ctx: U2::UHMM3BuildDialogImpl]
en: input file is empty
target: Input file is empty

[ctx: U2::UHMM3BuildDialogImpl]
en: output hmm file is empty
target: Output HMM profile file is empty

[ctx: U2::UHMM3BuildToFileTask]
en: adjust effective sequence number to achieve relative entropy target
target: Adjust effective sequence number to achieve relative entropy target

[ctx: U2::UHMM3BuildToFileTask]
en: effective sequence number is number of single linkage clusters
target: Effective sequence number is number of single linkage clusters

[ctx: U2::UHMM3BuildToFileTask]
en: no effective sequence number weighting: just use number of sequences
target: No effective sequence number weighting: just use number of sequences

[ctx: U2::UHMM3BuildToFileTask]
en: set effective sequence number for all models to: %1
target: Set effective sequence number for all models to: %1

[ctx: U2::UHMM3PhmmerTask]
en: HMM Phmmer search %1 sequence in %2 database
target: HMM Phmmer search %1 sequence in %2 databas

[ctx: U2::UHMM3PhmmerToAnnotationsTask]
en: HMM Phmmer search %1 sequence with %2 database
target: Phmmer search %1 sequence with %2 database

[ctx: U2::UHMM3PhmmerToAnnotationsTask]
en: annotation group
target: Annotation group

[ctx: U2::UHMM3PhmmerToAnnotationsTask]
en: annotation name
target: Annotation name

[ctx: U2::UHMM3PhmmerToAnnotationsTask]
en: annotation object
target: Annotation object

[ctx: U2::UHMM3PhmmerToAnnotationsTask]
en: db sequence
target: Database sequence

[ctx: U2::UHMM3Plugin]
en: Target sequence not selected: no opened annotated dna view
target: No target sequence

[ctx: U2::UHMM3SWPhmmerTask]
en: HMM Phmmer search %1 sequence in %2 database
target: HMM Phmmer search %1 sequence in %2 databas

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: Annotation object removed
target: Choosed annotation object removed

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: HMMER3 search task
target: HMM3 search task

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: No sequence objects loaded
target: No sequence objects found in document

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: Sequence file
target: Sequence file path

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: Unknown sequence type loaded
target: No sequence objects found in document

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: annotation object
target: Annotation object

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: annotations group name
target: Annotations group name

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: annotations name
target: Annotations name

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: dna sequence
target: Sequence to search in

[ctx: U2::UHMM3SWSearchToAnnotationsTask]
en: hmm profile filename
target: Profile HMM file path

[ctx: UHMM3BuildDialog]
en: fast
target: Fast

[ctx: UHMM3SearchDialog]
en: Query HMM file:
target: Query profile HMM file:

[ctx: UserApplicationsSettingsWidget]
en: LangBoxTitle
target: Language of User Interface (applied after restart)

[ctx: WelcomePageWidget]
en: Form
target: Project View

[ctx: getSequenceByIdDialog]
en: The sequences from selected BLAST results will be downloaded from
     NCBI Genbank by their GI identifier
target: The sequences from selected BLAST results will be downloaded from
     NCBI Genbank by their GI identifie
