EMBLGenbankAbstractDocument The file contains features of another remote GenBank file. These features have been skipped. The file contains features of another remote GenBank file. These features have been skipped. The file contains joined annotations with regions, located on different strands. All such joined parts will be stored on the same strand. The file contains joined annotations with regions, located on different strands. All such joined parts will be stored on the same strand. Location parsing error. Location parsing error. The number of valid sequence characters does not coincide with the declared size in the sequence header. The number of valid sequence characters does not coincide with the declared size in the sequence header. LocationParser Ignoring remote entry Ignoring remote entry Ignoring different strands in JOIN Ignoring different strands in JOIN QObject Fail to open "%1" for reading Fail to open "%1" for reading Fail to read the header from the file: "%1" Fail to read the header from the file: "%1" Can not build the fasta index for the file: "%1" Can not build the fasta index for the file: "%1" Error parsing the reads from the file: "%1" Error parsing the reads from the file: "%1" Truncated file: "%1" Truncated file: "%1" Can't open file with given url: %1. Can't open file with given url: %1. Invalid database user permissions set, so UGENE unable to use this database. Connect to your system administrator to fix the issue. Invalid database user permissions set, so UGENE unable to use this database. Connect to your system administrator to fix the issue. Can not read data. The database is closed or the data were changed. Can not read data. The database is closed or the data were changed. Can not write data. The database is closed or the data were changed. Can not write data. The database is closed or the data were changed. BED BED FPKM Tracking Format FPKM Tracking Format GTF GTF Unexpected number of modified objects. Expected: 1, actual: %1 Unexpected number of modified objects. Expected: 1, actual: %1 U2::ABIFormat ABIF ABIF A chromatogram file format A chromatogram file format Not a valid ABIF file: %1 Not a valid ABIF file: %1 Failed to load sequence from ABI file %1 Failed to load sequence from ABI file %1 U2::ACEFormat ACE ACE Line is too long Line is too long A name is not match with AF names A name is not match with AF names First line is not an ace header First line is not an ace header No contig count tag in the header line No contig count tag in the header line Must be CO keyword Must be CO keyword Unexpected end of file Unexpected end of file There is no note about reads count There is no note about reads count There is no AF note There is no AF note ACE is a format used for storing information about genomic confgurations ACE is a format used for storing information about genomic confgurations A name is duplicated A name is duplicated No consensus No consensus BQ keyword hasn't been found BQ keyword hasn't been found Bad consensus data Bad consensus data Bad AF note Bad AF note There is no read note There is no read note No sequence No sequence QA keyword hasn't been found QA keyword hasn't been found QA error no clear range QA error no clear range QA error bad range QA error bad range Bad sequence data Bad sequence data Alphabet unknown Alphabet unknown File doesn't contain any msa objects File doesn't contain any msa objects U2::ASNFormat MMDB MMDB ASN is a format used my the Molecular Modeling Database (MMDB) ASN is a format used my the Molecular Modeling Database (MMDB) Standard residue dictionary not found Standard residue dictionary not found Unknown error occurred Unknown error occurred no root element no root element states stack is not empty states stack is not empty First line is too long First line is too long read error occurred read error occurred biostruct3d obj loading error: %1 biostruct3d obj loading error: %1 U2::AbstractVariationFormat SNP formats are used to store single-nucleotide polymorphism data SNP formats are used to store single-nucleotide polymorphism data Line %1: There are too few columns in this line. The line was skipped. Line %1: There are too few columns in this line. The line was skipped. U2::AceImporter ACE file importer ACE file importer ACE files importer is used to convert conventional ACE files into UGENE database format.Having ACE file converted into UGENE DB format you get an fast and efficient interface to your data with an option to change the content ACE files importer is used to convert conventional ACE files into UGENE database format.Having ACE file converted into UGENE DB format you get an fast and efficient interface to your data with an option to change the content U2::AceImporterTask ACE file import: %1 ACE file import: %1 Dbi ref is invalid Dbi ref is invalid Can't create a temporary database Can't create a temporary database Failed to get load task for : %1 Failed to get load task for : %1 U2::AprFormat Unexpected end of file Unexpected end of file There is no sequences in alignment Attemt to find any number in the string failed Vector NTI/AlignX Vector NTI/AlignX is a Vector NTI format for multiple alignment Open in read-only mode File doesn't contain any msa objects File doesn't contain any msa objects Illegal header line Illegal header line Sequences not found Alphabet is unknown Alphabet is unknown U2::AprImporter Vector NTI/AlignX file importer Vector NTI/AlignX files importer is used to convert conventional APR files to a multiple sequence alignment formats Convert to another format: U2::AprImporterTask APR file import: %1 Empty destination url Invalid I/O environment! U2::BAMUtils There is no header in the SAM file "%1". The header information will be generated automatically. There is no header in the SAM file "%1". The header information will be generated automatically. Sort bam file: "%1" using %2 Mb of memory. Result sorted file is: "%3" Sort bam file: "%1" using %2 Mb of memory. Result sorted file is: "%3" Merging BAM files: "%1". Resulting merged file is: "%2" Merging BAM files: "%1". Resulting merged file is: "%2" Remove PCR duplicate in BAM file: "%1". Resulting file is: "%2" Remove PCR duplicate in BAM file: "%1". Resulting file is: "%2" Build index for bam file: "%1" Build index for bam file: "%1" Wrong line in a SAM file. Wrong line in a SAM file. U2::BedFormat The BED (Browser Extensible Data) format was developed by UCSC for displaying transcript structures in the genome browser. The BED (Browser Extensible Data) format was developed by UCSC for displaying transcript structures in the genome browser. File "%1" contains too many annotation tables to be displayed. However, you can process these data using pipelines built with Workflow Designer. File "%1" contains too many annotation tables to be displayed. However, you can process these data using pipelines built with Workflow Designer. BED parsing error: incorrect format of the 'track' header line! BED parsing error: incorrect format of the 'track' header line! BED parsing error: unexpected number of fields in the first annotations line! BED parsing error: unexpected number of fields in the first annotations line! The file does not contain valid annotations! The file does not contain valid annotations! BED parsing error: incorrect number of fields at line %1! BED parsing error: incorrect number of fields at line %1! BED parsing error: a field at line %1 is empty! BED parsing error: a field at line %1 is empty! BED parsing error: incorrect coordinates at line %1! BED parsing error: incorrect coordinates at line %1! BED parsing error: incorrect score value '%1' at line %2! BED parsing error: incorrect score value '%1' at line %2! BED parsing error: incorrect strand value '%1' at line %2! BED parsing error: incorrect strand value '%1' at line %2! BED parsing error: incorrect thick coordinates at line %1! BED parsing error: incorrect thick coordinates at line %1! BED parsing error: incorrect itemRgb value '%1' at line %2! BED parsing error: incorrect itemRgb value '%1' at line %2! BED parsing error: incorrect value of the block parameters at line %1! BED parsing error: incorrect value of the block parameters at line %1! Starting BED saving: '%1' Starting BED saving: '%1' Can not convert GObject to AnnotationTableObject Can not convert GObject to AnnotationTableObject Can not detect chromosome name. 'Chr' name will be used. Can not detect chromosome name. 'Chr' name will be used. You are trying to save joined annotation to BED format! The joining will be lost You are trying to save joined annotation to BED format! The joining will be lost BED saving error: incorrect thick coordinates in the first annotation! BED saving error: incorrect thick coordinates in the first annotation! BED saving error: incorrect block fields in the first annotation! BED saving error: incorrect block fields in the first annotation! BED saving: detected %1 fields per line for file '%2' BED saving: detected %1 fields per line for file '%2' BED saving error: an annotation is expected to have '%1' qualifier, but it is absent! Skipping the annotation. BED saving error: an annotation is expected to have '%1' qualifier, but it is absent! Skipping the annotation. BED saving error: an annotation is expected to have the block qualifiers! Skipping the annotation. BED saving error: an annotation is expected to have the block qualifiers! Skipping the annotation. Finished BED saving: '%1' Finished BED saving: '%1' U2::BgzipTask Bgzip Compression task Bgzip Compression task Start bgzip compression '%1' Start bgzip compression '%1' IOAdapterRegistry is NULL! IOAdapterRegistry is NULL! IOAdapterFactory is NULL! IOAdapterFactory is NULL! Can not create IOAdapter! Can not create IOAdapter! Can not open input file '%1' Can not open input file '%1' Can not open output file '%2' Can not open output file '%2' Error reading file Error reading file Error writing to file Error writing to file Bgzip compression finished Bgzip compression finished Bgzip compression task was finished with an error: %1 Bgzip compression task was finished with an error: %1 Bgzip compression task was finished. A new bgzf file is: <a href="%1">%2</a> Bgzip compression task was finished. A new bgzf file is: <a href="%1">%2</a> U2::CloneAssemblyWithReferenceToDbiTask Clone assembly object to the destination database Clone assembly object to the destination database Invalid assembly ID Invalid assembly ID Invalid source database reference Invalid source database reference Invalid destination database reference Invalid destination database reference Can't get the cloned object Can't get the cloned object Unexpected result object: expect AssemblyObject, got %1 object Unexpected result object: expect AssemblyObject, got %1 object Unexpected result object: expect U2SequenceObject, got %1 object Unexpected result object: expect U2SequenceObject, got %1 object U2::ClustalWAlnFormat CLUSTALW CLUSTALW Clustalw is a format for storing multiple sequence alignments Clustalw is a format for storing multiple sequence alignments Illegal header line Illegal header line Error parsing file Error parsing file Invalid alignment format Invalid alignment format Incorrect number of sequences in block Incorrect number of sequences in block Sequence names are not matched Sequence names are not matched Alphabet is unknown Alphabet is unknown U2::ConvertAceToSqliteTask Convert ACE to UGENE database (%1) Convert ACE to UGENE database (%1) Converting assembly from %1 to %2 started Converting assembly from %1 to %2 started IOAdapterFactory is NULL IOAdapterFactory is NULL Can't open file '%1' Can't open file '%1' DBI is NULL DBI is NULL Object DBI is NULL Object DBI is NULL Importing Importing Assembly DBI is NULL Assembly DBI is NULL Sequence DBI is NULL Sequence DBI is NULL Invalid source file Invalid source file Packing reads for assembly '%1' (%2 of %3) Packing reads for assembly '%1' (%2 of %3) Attribute DBI is NULL Attribute DBI is NULL Warning: incorrect maxProw == %1, probably packing was not done! Attribute was not set Warning: incorrect maxProw == %1, probably packing was not done! Attribute was not set U2::ConvertAssemblyToSamTask Given file is not valid UGENE database file Given file is not valid UGENE database file U2::ConvertSnpeffVariationsToAnnotationsTask Convert SnpEff variations to annotations task Convert SnpEff variations to annotations task U2::DNAQualityIOUtils No IO adapter found for URL: %1 No IO adapter found for URL: %1 U2::Database Not a valid S3-database file: %1 Not a valid S3-database file: %1 File already exists: %1 File already exists: %1 U2::DefaultConvertFileTask The formats are not compatible: %1 and %2 The formats are not compatible: %1 and %2 U2::DifferentialFormat Differential Differential Differential format is a text-based format for representing Cuffdiff differential output files: expression, splicing, promoters and cds. Differential format is a text-based format for representing Cuffdiff differential output files: expression, splicing, promoters and cds. Required column is missed: %1 Required column is missed: %1 U2::Document Document is empty. Document is empty. U2::DocumentFormat Database connection Database connection A fake format that was added to implement shared database connection within existing document model. A fake format that was added to implement shared database connection within existing document model. You have no permissions to modify the content of this database You have no permissions to modify the content of this database Empty object name Empty object name U2::DocumentFormatUtils Undefined sequence alphabet Undefined sequence alphabet First line is not an ace header First line is not an ace header There is no assemblies in input file There is no assemblies in input file There are not enough assemblies There are not enough assemblies Unexpected end of file Unexpected end of file Line is too long Line is too long No contig count tag in the header line No contig count tag in the header line Not enough parameters in current line Not enough parameters in current line Parameter is not a digit Parameter is not a digit There is no note about reads count There is no note about reads count A name is duplicated A name is duplicated No consensus No consensus BQ keyword hasn't been found BQ keyword hasn't been found Unexpected symbols in consensus data Unexpected symbols in consensus data Can't find a sequence name in current line Can't find a sequence name in current line An empty sequence name An empty sequence name Invalid AF tag Invalid AF tag A name is duplicated: %1 A name is duplicated: %1 Not all reads were found Not all reads were found Bad AF note Bad AF note There is no read note There is no read note Invalid RD part Invalid RD part Can't find the RD tag Can't find the RD tag QA keyword hasn't been found QA keyword hasn't been found QA error bad range QA error bad range Unexpected symbols in sequence data Unexpected symbols in sequence data A name is not match with AF names A name is not match with AF names Can't find clear range start in current line Can't find clear range start in current line Clear range start is invalid Clear range start is invalid Can't find clear range end in current line Can't find clear range end in current line Clear range end is invalid Clear range end is invalid There is no next element There is no next element Conversion file from %1 to %2 Conversion file from %1 to %2 Merge BAM files with SAMTools merge Merge BAM files with SAMTools merge U2::EMBLGenbankAbstractDocument File "%1" contains too many sequences to be displayed. However, you can process these data using instruments from the menu <i>Tools -> NGS data analysis</i> or pipelines built with Workflow Designer. File "%1" contains too many sequences to be displayed. However, you can process these data using instruments from the menu <i>Tools -> NGS data analysis</i> or pipelines built with Workflow Designer. Reading entry header Reading entry header Merge error: found annotations without sequence Merge error: found annotations without sequence The file contains an incorrect data that describes a qualifier value. The file contains an incorrect data that describes a qualifier value. The value cannot contain a single quote character. The qualifier is '%1' The value cannot contain a single quote character. The qualifier is '%1' Annotation name is empty Annotation name is empty Error parsing location Error parsing location Unexpected line format Unexpected line format Reading sequence %1 Reading sequence %1 Error parsing sequence: unexpected empty line Error parsing sequence: unexpected empty line Sequence is truncated Sequence is truncated Reading annotations %1 Reading annotations %1 Invalid format of feature table Invalid format of feature table Line is too long. Line is too long. IO error. IO error. Record is truncated. Record is truncated. Annotation start position is empty Annotation start position is empty Annotation end position is empty Annotation end position is empty U2::EMBLPlainTextFormat EMBL EMBL EMBL Flat File Format is a rich format for storing sequences and associated annotations EMBL Flat File Format is a rich format for storing sequences and associated annotations ID is not the first line ID is not the first line Error parsing ID line Error parsing ID line U2::FastaFormat FASTA FASTA FASTA format is a text-based format for representing either nucleotide sequences or peptide sequences, in which base pairs or amino acids are represented using single-letter codes. The format also allows for sequence names and comments to precede the sequences. FASTA format is a text-based format for representing either nucleotide sequences or peptide sequences, in which base pairs or amino acids are represented using single-letter codes. The format also allows for sequence names and comments to precede the sequences. Line is too long Line is too long First line is not a FASTA header First line is not a FASTA header File "%1" contains too many sequences to be displayed. However, you can process these data using instruments from the menu <i>Tools -> NGS data analysis</i> or pipelines built with Workflow Designer. File "%1" contains too many sequences to be displayed. However, you can process these data using instruments from the menu <i>Tools -> NGS data analysis</i> or pipelines built with Workflow Designer. Loaded sequences: %1. Loaded sequences: %1. Skipped sequences: %1. Skipped sequences: %1. The following sequences are empty: %1 The following sequences are empty: %1 Unreferenced sequence in the beginning of patterns: %1 Unreferenced sequence in the beginning of patterns: %1 U2::FastqFormat FASTQ FASTQ FASTQ format is a text-based format for storing both a biological sequence (usually nucleotide sequence) and its corresponding quality scores. Both the sequence letter and quality score are encoded with a single ASCII character for brevity. It was originally developed at the Wellcome Trust Sanger Institute to bundle a FASTA sequence and its quality data, but has recently become the de facto standard for storing the output of high throughput sequencing instruments. FASTQ format is a text-based format for storing both a biological sequence (usually nucleotide sequence) and its corresponding quality scores. Both the sequence letter and quality score are encoded with a single ASCII character for brevity. It was originally developed at the Wellcome Trust Sanger Institute to bundle a FASTA sequence and its quality data, but has recently become the de facto standard for storing the output of high throughput sequencing instruments. Error while trying to find sequence name start Error while trying to find sequence name start Error while reading sequence Error while reading sequence Sequence name differs from quality scores name: %1 and %2 Sequence name differs from quality scores name: %1 and %2 Bad quality scores: inconsistent size. Bad quality scores: inconsistent size. File "%1" contains too many sequences to be displayed. However, you can process these data using instruments from the menu <i>Tools -> NGS data analysis</i> or pipelines built with Workflow Designer. File "%1" contains too many sequences to be displayed. However, you can process these data using instruments from the menu <i>Tools -> NGS data analysis</i> or pipelines built with Workflow Designer. Not a valid FASTQ file, sequence name differs from quality scores name Not a valid FASTQ file, sequence name differs from quality scores name Not a valid FASTQ file. Bad quality scores: inconsistent size. Not a valid FASTQ file. Bad quality scores: inconsistent size. U2::FpkmTrackingFormat The FPKM (fragments per kilobase of exon model per million mapped fragments) Tracking Format is a native Cufflinks format to output estimated expression values. The FPKM (fragments per kilobase of exon model per million mapped fragments) Tracking Format is a native Cufflinks format to output estimated expression values. Internal error: qualifier with name '%1' and '%2' can't be added Internal error: qualifier with name '%1' and '%2' can't be added FPKM Tracking Format parsing error: incorrect number of fields at line %1! FPKM Tracking Format parsing error: incorrect number of fields at line %1! FPKM Tracking Format parsing error: a field at line %1 is empty! FPKM Tracking Format parsing error: a field at line %1 is empty! FPKM Tracking Format parsing error: incorrect coordinates at line %1! FPKM Tracking Format parsing error: incorrect coordinates at line %1! FPKM Tracking Format parsing error: different sequence names were detected in an input file. Sequence name '%1' is used. FPKM Tracking Format parsing error: different sequence names were detected in an input file. Sequence name '%1' is used. FPKM Tracking Format parsing error: tracking ID value is empty at line %1! FPKM Tracking Format parsing error: tracking ID value is empty at line %1! FPKM Tracking Format parsing error: incorrect length value at line %1! FPKM Tracking Format parsing error: incorrect length value at line %1! FPKM Tracking Format parsing error: incorrect coverage value at line %1! FPKM Tracking Format parsing error: incorrect coverage value at line %1! Skipped qualifier '%1' while saving a FPKM header. Skipped qualifier '%1' while saving a FPKM header. FPKM Tracking Format saving error: tracking ID shouldn't be empty! FPKM Tracking Format saving error: tracking ID shouldn't be empty! FPKM Tracking Format saving error: failed to parse locus qualifier '%1', writing it to the output file anyway! FPKM Tracking Format saving error: failed to parse locus qualifier '%1', writing it to the output file anyway! FPKM Tracking Format saving error: an annotation region (%1, %2) differs from the information stored in the 'locus' qualifier (%3, %4). Writing the 'locus' qualifier to output! FPKM Tracking Format saving error: an annotation region (%1, %2) differs from the information stored in the 'locus' qualifier (%3, %4). Writing the 'locus' qualifier to output! FPKM Tracking Format saving error: one or more errors occurred while saving a file, see TRACE log for details! FPKM Tracking Format saving error: one or more errors occurred while saving a file, see TRACE log for details! U2::GFFFormat GFF GFF GFF is a format used for storing features and annotations GFF is a format used for storing features and annotations Parsing error: invalid header Parsing error: invalid header Parsing error: file does not contain version header Parsing error: file does not contain version header Parsing error: format version is not an integer Parsing error: format version is not an integer Parsing error: GFF version %1 is not supported Parsing error: GFF version %1 is not supported File "%1" contains too many sequences to be displayed. However, you can process these data using instruments from the menu <i>Tools -> NGS data analysis</i> or pipelines built with Workflow Designer. File "%1" contains too many sequences to be displayed. However, you can process these data using instruments from the menu <i>Tools -> NGS data analysis</i> or pipelines built with Workflow Designer. Parsing error: file contains empty line %1, line skipped Parsing error: file contains empty line %1, line skipped Parsing error: sequence in FASTA sequence has whitespaces at line %1 Parsing error: sequence in FASTA sequence has whitespaces at line %1 Parsing error: too few fields at line %1 Parsing error: too few fields at line %1 Parsing error: start position at line %1 is not integer Parsing error: start position at line %1 is not integer Parsing error: end position at line %1 is not integer Parsing error: end position at line %1 is not integer Parsing error: incorrect annotation region at line %1 Parsing error: incorrect annotation region at line %1 Parsing error: incorrect attributes field %1 at line %2 Parsing error: incorrect attributes field %1 at line %2 Parsing error: incorrect score parameter at line %1. Score can be a float number or '.' symbol Parsing error: incorrect score parameter at line %1. Score can be a float number or '.' symbol Parsing error: incorrect frame parameter at line %1. Frame can be a number between 0-2 or '.' symbol Parsing error: incorrect frame parameter at line %1. Frame can be a number between 0-2 or '.' symbol Parsing error: incorrect strand patameter at line %1. Strand can be '+','-' or '.' Parsing error: incorrect strand patameter at line %1. Strand can be '+','-' or '.' One or more sequences in this file don't have names. Their names are generated automatically. One or more sequences in this file don't have names. Their names are generated automatically. Can not detect chromosome name. 'Chr' name will be used. Can not detect chromosome name. 'Chr' name will be used. Wrong location for joined annotation at line %1. Line was skipped. Wrong location for joined annotation at line %1. Line was skipped. U2::GTFFormat The Gene transfer format (GTF) is a file format used to hold information about gene structure. The Gene transfer format (GTF) is a file format used to hold information about gene structure. GTF parsing error: incorrect number of fields at line %1! GTF parsing error: incorrect number of fields at line %1! GTF parsing error: a field at line %1 is empty! GTF parsing error: a field at line %1 is empty! GTF parsing error: incorrect coordinates at line %1! GTF parsing error: incorrect coordinates at line %1! GTF parsing error: unexpected value of the "feature" value "%1" at line %2! GTF parsing error: unexpected value of the "feature" value "%1" at line %2! GTF parsing error: incorrect score value "%1" at line %2! GTF parsing error: incorrect score value "%1" at line %2! GTF parsing error: incorrect frame value "%1" at line %2! GTF parsing error: incorrect frame value "%1" at line %2! GTF parsing error: invalid attributes format at line %1! GTF parsing error: invalid attributes format at line %1! GTF parsing error: mandatory attribute ' GTF parsing error: mandatory attribute ' ' is absent at line %1! ' is absent at line %1! GTF parsing error: incorrect strand value "%1" at line %2! GTF parsing error: incorrect strand value "%1" at line %2! File "%1" contains too many annotation tables to be displayed. However, you can process these data using pipelines built with Workflow Designer. File "%1" contains too many annotation tables to be displayed. However, you can process these data using pipelines built with Workflow Designer. Can't save an annotation to a GTF file - the annotation doesn't have the '%1' qualifier! Can't save an annotation to a GTF file - the annotation doesn't have the '%1' qualifier! GTF saving error: one or more errors occurred while saving a file, see TRACE log for details! GTF saving error: one or more errors occurred while saving a file, see TRACE log for details! U2::Genbank::LocationParser 'a single base from a range' in combination with 'sequence span' is not supported 'a single base from a range' in combination with 'sequence span' is not supported Ignoring '<' at start position Ignoring '<' at start position Ignoring '>' at end position Ignoring '>' at end position Wrong token after JOIN %1 Wrong token after JOIN %1 Wrong token after JOIN - order %1 Wrong token after JOIN - order %1 Can't parse location on JOIN Can't parse location on JOIN Must be RIGHT_PARENTHESIS instead of %1 Must be RIGHT_PARENTHESIS instead of %1 Wrong token after ORDER %1 Wrong token after ORDER %1 Wrong token after ORDER - join %1 Wrong token after ORDER - join %1 Can't parse location on ORDER Can't parse location on ORDER Wrong token after BOND %1 Wrong token after BOND %1 Can't parse location on BONDs Can't parse location on BONDs Must be LEFT_PARENTHESIS instead of %1 Must be LEFT_PARENTHESIS instead of %1 Can't parse location on COMPLEMENT Can't parse location on COMPLEMENT U2::GenbankPlainTextFormat Genbank Genbank GenBank GenBank Flat File Format is a rich format for storing sequences and associated annotations GenBank Flat File Format is a rich format for storing sequences and associated annotations LOCUS is not the first line LOCUS is not the first line Error parsing LOCUS line Error parsing LOCUS line incomplete SOURCE record incomplete SOURCE record Error writing document Error writing document There is no IOAdapter registry yet There is no IOAdapter registry yet IOAdapterFactory is NULL IOAdapterFactory is NULL IOAdapter is NULL IOAdapter is NULL Invalid annotation table! Invalid annotation table! U2::GzipDecompressTask Decompression task Decompression task '%1' is not zipped file '%1' is not zipped file Start decompression '%1' Start decompression '%1' IOAdapterRegistry is NULL! IOAdapterRegistry is NULL! IOAdapterFactory is NULL! IOAdapterFactory is NULL! Can not create IOAdapter! Can not create IOAdapter! Can not open output file '%1' Can not open output file '%1' Can not open input file '%1' Can not open input file '%1' Error reading file Error reading file Error writing to file Error writing to file Decompression finished Decompression finished Decompression task was finished with an error: %1 Decompression task was finished with an error: %1 Decompression task was finished. A new decompressed file is: <a href="%1">%1</a> Decompression task was finished. A new decompressed file is: <a href="%1">%1</a> U2::InfoPartParser Too few values in the entry: '%1'. Expected at least %2 values. Too few values in the entry: '%1'. Expected at least %2 values. Too many values in the entry '%1', extra entries are ignored Too many values in the entry '%1', extra entries are ignored U2::LoadConvertAndSaveSnpeffVariationsToAnnotationsTask Load file and convert SnpEff variations to annotations task Load file and convert SnpEff variations to annotations task '%1' load failed, the result document is NULL '%1' load failed, the result document is NULL File '%1' doesn't contain variation tracks File '%1' doesn't contain variation tracks U2::MSFFormat MSF MSF MSF format is used to store multiple aligned sequences. Files include the sequence name and the sequence itself, which is usually aligned with other sequences in the file. MSF format is used to store multiple aligned sequences. Files include the sequence name and the sequence itself, which is usually aligned with other sequences in the file. Incorrect format Incorrect format Unexpected end of file Unexpected end of file Check sum test failed Check sum test failed Alphabet unknown Alphabet unknown U2::MegaFormat Mega Mega Mega is a file format of native MEGA program Mega is a file format of native MEGA program Found sequences of different sizes Found sequences of different sizes Bad name of sequence Bad name of sequence Unexpected # in comments Unexpected # in comments A comment has not end A comment has not end Unexpected symbol between comments Unexpected symbol between comments Incorrect format Incorrect format Identical symbol at the first sequence Identical symbol at the first sequence Incorrect order of sequences' names Incorrect order of sequences' names Incorrect sequence Incorrect sequence Alphabet is unknown Alphabet is unknown No header No header No # before header No # before header Not MEGA-header Not MEGA-header No data in file No data in file Incorrect title Incorrect title Sequence has empty part Sequence has empty part Bad symbols in a sequence Bad symbols in a sequence U2::MysqlUpgradeTask Upgrade mysql database Upgrade mysql database U2::NEXUSFormat NEXUS NEXUS Nexus is a multiple alignment and phylogenetic trees file format Nexus is a multiple alignment and phylogenetic trees file format #NEXUS header missing #NEXUS header missing U2::NewickFormat Newick Standard Newick Standard Newick is a simple format used to write out trees in a text file Newick is a simple format used to write out trees in a text file U2::PDBFormat PDB PDB The Protein Data Bank (PDB) format provides a standard representation for macromolecular structure data derived from X-ray diffraction and NMR studies. The Protein Data Bank (PDB) format provides a standard representation for macromolecular structure data derived from X-ray diffraction and NMR studies. Line is too long Line is too long Some mandatory records are absent Some mandatory records are absent PDB warning: unknown residue name: %1 PDB warning: unknown residue name: %1 Invalid secondary structure record Invalid secondary structure record Invalid SEQRES: less then 24 charachters Invalid SEQRES: less then 24 charachters U2::PDWFormat pDRAW pDRAW pDRAW is a sequence file format used by pDRAW software pDRAW is a sequence file format used by pDRAW software Line is too long Line is too long U2::PairedFastqComparator Too much reads without a pair (>%1). Check the input data is set correctly. Too much reads without a pair (>%1). Check the input data is set correctly. The list doesn't contains the item The list doesn't contains the item Invalid sequence info Invalid sequence info U2::PhylipFormat PHYLIP multiple alignment format for phylogenetic applications. PHYLIP multiple alignment format for phylogenetic applications. Alphabet is unknown Alphabet is unknown Error parsing file Error parsing file U2::PhylipInterleavedFormat PHYLIP Interleaved PHYLIP Interleaved Illegal line Illegal line Wrong header Wrong header Block is incomplete Block is incomplete Block is incomlete Block is incomlete Number of characters does not correspond to the stated number Number of characters does not correspond to the stated number U2::PhylipSequentialFormat PHYLIP Sequential PHYLIP Sequential Illegal line Illegal line Wrong header Wrong header There is not enough data There is not enough data Error parsing file Error parsing file Number of characters does not correspond to the stated number Number of characters does not correspond to the stated number U2::PlainTextFormat Plain text Plain text A simple plain text file. A simple plain text file. U2::RawDNASequenceFormat Raw sequence Raw sequence Raw sequence file - a whole content of the file is treated either as a single/multiple nucleotide or peptide sequence(s). UGENE will remove all non-alphabetic chars from the result sequence. By default the characters in the file are considered a single sequence. Raw sequence file - a whole content of the file is treated either as a single/multiple nucleotide or peptide sequence(s). UGENE will remove all non-alphabetic chars from the result sequence. By default the characters in the file are considered a single sequence. Sequence is empty Sequence is empty U2::SAMFormat Field "%1" not matched pattern "%2", expected pattern "%3" Field "%1" not matched pattern "%2", expected pattern "%3" SAM SAM The Sequence Alignment/Map (SAM) format is a generic alignment format forstoring read alignments against reference sequence The Sequence Alignment/Map (SAM) format is a generic alignment format for storing read alignments against reference sequence U2::SCFFormat SCF SCF It is Standard Chromatogram Format It is Standard Chromatogram Format Failed to parse SCF file: %1 Failed to parse SCF file: %1 Failed to load sequence from SCF file %1 Failed to load sequence from SCF file %1 U2::SnpeffInfoParser Can't parse the next INFO part: '%1' Can't parse the next INFO part: '%1' U2::StockholmFormat invalid file: bad header line invalid file: bad header line invalid file: empty sequence name invalid file: empty sequence name invalid file: equal sequence names in one block invalid file: equal sequence names in one block invalid file: sequence names are not equal in blocks invalid file: sequence names are not equal in blocks invalid file: sequences in block are not of equal size invalid file: sequences in block are not of equal size invalid file: empty sequence alignment invalid file: empty sequence alignment invalid file: unknown alphabet invalid file: unknown alphabet Stockholm Stockholm A multiple sequence alignments file format A multiple sequence alignments file format unknown error occurred unknown error occurred U2::SwissProtPlainTextFormat Swiss-Prot Swiss-Prot SwissProt is a format of the UniProtKB/Swiss-prot database used for storing annotated protein sequence SwissProt is a format of the UniProtKB/Swiss-prot database used for storing annotated protein sequence ID is not the first line ID is not the first line Error parsing ID line Error parsing ID line Error parsing ID line. Not found sequence length Error parsing ID line. Not found sequence length Reading sequence %1 Reading sequence %1 Error parsing sequence: unexpected empty line Error parsing sequence: unexpected empty line Error reading sequence: memory allocation failed Error reading sequence: memory allocation failed Sequence is truncated Sequence is truncated Reading annotations %1 Reading annotations %1 Invalid format of feature table Invalid format of feature table U2::U2DbiL10n There is no assembly object with the specified id. There is no assembly object with the specified id. Unsupported attribute type: %1 Unsupported attribute type: %1 Required attribute is not found Required attribute is not found Database url is incorrect Database url is incorrect User login is not specified User login is not specified Host is not specified Host is not specified Database name is not specified Database name is not specified Error opening MySQL database: %1 Error opening MySQL database: %1 Not a %1 MySQL database: %2, %3 Not a %1 MySQL database: %2, %3 Warning! The database was created with a newer %1 version: %2. Not all database features may be supported! Current %1 version: %3. Warning! The database was created with a newer %1 version: %2. Not all database features may be supported! Current %1 version: %3. Illegal database state: %1 Illegal database state: %1 Can't synchronize database state Can't synchronize database state Annotation table object is not found. Annotation table object is not found. Feature is not found. Feature is not found. An object single modification step not found An object single modification step not found Failed to find user step ID Failed to find user step ID Not main thread Not main thread Can't create a common user modifications step, previous one is not complete Can't create a common user modifications step, previous one is not complete Can't create a common multiple modifications step, previous one is not complete Can't create a common multiple modifications step, previous one is not complete Failed to create a common user modifications step Failed to create a common user modifications step Failed to create a common multiple modifications step Failed to create a common multiple modifications step Msa object not found Msa object not found Msa row not found Msa row not found Unexpected modification type '%1' Unexpected modification type '%1' Invalid row position: %1 Invalid row position: %1 An error occurred during updating an alignment alphabet An error occurred during updating an alignment alphabet An error occurred during reverting adding of rows An error occurred during reverting adding of rows An error occurred during reverting addition of a row An error occurred during reverting addition of a row An error occurred during reverting removing of rows An error occurred during reverting removing of rows An error occurred during reverting removing of a row An error occurred during reverting removing of a row An error occurred during updating an alignment gaps An error occurred during updating an alignment gaps An error occurred during updating an alignment row order An error occurred during updating an alignment row order An error occurred during updating a row info An error occurred during updating a row info An error occurred during updating an msa length An error occurred during updating an msa length An error occurred during addition of a row An error occurred during addition of a row Can't undo an operation for the object Can't undo an operation for the object Can't redo an operation for the object Can't redo an operation for the object Object not found Object not found Folder not found: %1 (canonical: %2) Folder not found: %1 (canonical: %2) Not an object, id: %1, type: %2 Not an object, id: %1, type: %2 Unknown object type! Id: %1, type: %2 Unknown object type! Id: %1, type: %2 Can't undo an unknown operation: '%1' Can't undo an unknown operation: '%1' Can't redo an unknown operation: '%1' Can't redo an unknown operation: '%1' An error occurred during updating an object name An error occurred during updating an object name An error occurred during updating an object name! An error occurred during updating an object name! Sequence object not found Sequence object not found Internal error occurred during the sequence processing Internal error occurred during the sequence processing An exception was thrown during reading sequence data from dbi An exception was thrown during reading sequence data from dbi An error occurred during reverting replacing sequence data An error occurred during reverting replacing sequence data An error occurred during replacing sequence data An error occurred during replacing sequence data Invalid variant track type: %1 Invalid variant track type: %1 Sequence name is not set Sequence name is not set New variant public ID is empty New variant public ID is empty New variant track ID is empty New variant track ID is empty Packed data is empty Packed data is empty Packing method prefix is not supported: %1 Packing method prefix is not supported: %1 Data is corrupted, no name end marker found: %1 Data is corrupted, no name end marker found: %1 Data is corrupted, no sequence end marker found: %1 Data is corrupted, no sequence end marker found: %1 Data is corrupted, no CIGAR end marker found: %1 Data is corrupted, no CIGAR end marker found: %1 Data is corrupted, no rnext end marker found: %1 Data is corrupted, no rnext end marker found: %1 Can not convert pnext to a number: %1 Can not convert pnext to a number: %1 Bound values: Bound values: Cannot start a transaction Cannot start a transaction Failed to detect assembly storage format: %1 Failed to detect assembly storage format: %1 Failed to parse range: %1, full: %2 Failed to parse range: %1, full: %2 Failed to parse packed row range info %1 Failed to parse packed row range info %1 Unsupported reads storage type: %1 Unsupported reads storage type: %1 Packing method is not supported: %1 Packing method is not supported: %1 Packed data is empty! Packed data is empty! Error checking SQLite database: %1! Error checking SQLite database: %1! Error creating table: %1, error: %2 Error creating table: %1, error: %2 Not a %1 SQLite database: %2 Not a %1 SQLite database: %2 Database is already opened! Database is already opened! URL is not specified URL is not specified Error opening SQLite database: %1! Error opening SQLite database: %1! Database is already closed! Database is already closed! Illegal database state %1! Illegal database state %1! Failed to close database: %1, err: %2 Failed to close database: %1, err: %2 Annotation table object not found. Annotation table object not found. An object single modification step not found! An object single modification step not found! Msa object not found! Msa object not found! Msa row not found! Msa row not found! Not an object! Id: %1, type: %2 Not an object! Id: %1, type: %2 Can't undo an operation for the object! Can't undo an operation for the object! Can't redo an operation for the object! Can't redo an operation for the object! Object not found! Object not found! Unexpected row count. Query: '%1', rows: %2 Object not found. Object not found. Folder not found: %1 Folder not found: %1 Sequence object not found. Sequence object not found. Sequence name is not set! Sequence name is not set! Error during RTree index creation: %1! Check if SQLite library has RTree index support! Error during RTree index creation: %1! Check if SQLite library has RTree index support! An error occurred during updating UDR U2::VectorNtiSequenceFormat Vector NTI sequence Vector NTI sequence Vector NTI sequence format is a rich format based on NCBI GenBank format for storing sequences and associated annotations Vector NTI sequence format is a rich format based on NCBI GenBank format for storing sequences and associated annotations Error writing document Error writing document