-- dump date   	20140619_094119
-- class       	Genbank::Contig
-- table       	contig_comment
-- id	comment
NC_009613.3	REVIEWED REFSEQ: This record has been curated by NCBI staff. TheREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681.REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733.REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference GenomeREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt GenomeREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger readsREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA libraryREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additionalREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clonesREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in termsREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copyREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copy   numbers and maybe impossible to solve :REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copy   numbers and maybe impossible to solve :   The first region is between nucleotide positions 400,740 andREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copy   numbers and maybe impossible to solve :   The first region is between nucleotide positions 400,740 and 408,701.REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copy   numbers and maybe impossible to solve :   The first region is between nucleotide positions 400,740 and 408,701.   The second region is between nucleotide positions 2,274,300 andREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copy   numbers and maybe impossible to solve :   The first region is between nucleotide positions 400,740 and 408,701.   The second region is between nucleotide positions 2,274,300 and 2,280,580.REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copy   numbers and maybe impossible to solve :   The first region is between nucleotide positions 400,740 and 408,701.   The second region is between nucleotide positions 2,274,300 and 2,280,580.   However, the overal organization of these two regions wasREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copy   numbers and maybe impossible to solve :   The first region is between nucleotide positions 400,740 and 408,701.   The second region is between nucleotide positions 2,274,300 and 2,280,580.   However, the overal organization of these two regions was confirmed using SouthernREVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copy   numbers and maybe impossible to solve :   The first region is between nucleotide positions 400,740 and 408,701.   The second region is between nucleotide positions 2,274,300 and 2,280,580.   However, the overal organization of these two regions was confirmed using Southern   blots.REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence is identical to AM398681. On Jun 11, 2013 this sequence version replaced gi:511344733. RefSeq Category: Reference Genome             UPR: UniProt Genome   Comment on the second version of the assembly:   We noticed that the previous genome version was mis-assembled.   In order to correct the mistakes we added 10,000 Sanger reads from a gDNA library   (vector pCNS, 12 kb insert size). We also performed additional walks on clones   covering repeats.   Two regions encoding large size adhesins remain doubtful in terms of repeat copy   numbers and maybe impossible to solve :   The first region is between nucleotide positions 400,740 and 408,701.   The second region is between nucleotide positions 2,274,300 and 2,280,580.   However, the overal organization of these two regions was confirmed using Southern   blots. COMPLETENESS: full length.