-- dump date   	20120504_153432
-- class       	Genbank::Contig
-- table       	contig_comment
-- id	comment
NC_016807.1	PROVISIONAL REFSEQ: This record has not yet been subject to finalPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303.PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer andPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. ThePROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 largePROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencingPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencing of PCR products. The sites suspected to have sequencing errorsPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencing of PCR products. The sites suspected to have sequencing errors caused by 454 sequencing were inspected by Sanger sequencing of PCRPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencing of PCR products. The sites suspected to have sequencing errors caused by 454 sequencing were inspected by Sanger sequencing of PCR products and were corrected.PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencing of PCR products. The sites suspected to have sequencing errors caused by 454 sequencing were inspected by Sanger sequencing of PCR products and were corrected. ##Genome-Assembly-Data-START##PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencing of PCR products. The sites suspected to have sequencing errors caused by 454 sequencing were inspected by Sanger sequencing of PCR products and were corrected. ##Genome-Assembly-Data-START## Assembly Method       :: GS de-novo assembler v. 2.5p1PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencing of PCR products. The sites suspected to have sequencing errors caused by 454 sequencing were inspected by Sanger sequencing of PCR products and were corrected. ##Genome-Assembly-Data-START## Assembly Method       :: GS de-novo assembler v. 2.5p1 Genome Coverage       :: 90xPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencing of PCR products. The sites suspected to have sequencing errors caused by 454 sequencing were inspected by Sanger sequencing of PCR products and were corrected. ##Genome-Assembly-Data-START## Assembly Method       :: GS de-novo assembler v. 2.5p1 Genome Coverage       :: 90x Sequencing Technology :: Roche 454 GS junior; ABI 3130xlPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencing of PCR products. The sites suspected to have sequencing errors caused by 454 sequencing were inspected by Sanger sequencing of PCR products and were corrected. ##Genome-Assembly-Data-START## Assembly Method       :: GS de-novo assembler v. 2.5p1 Genome Coverage       :: 90x Sequencing Technology :: Roche 454 GS junior; ABI 3130xl ##Genome-Assembly-Data-END##PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012303. The genome was sequenced using Roche 454 GS junior sequencer and assembled by GS de-novo assembler software version 2.5p1. The complete genome sequence was generated by connecting 8 large contains. The order of contigs were confirmed by Sanger sequencing of PCR products. The sites suspected to have sequencing errors caused by 454 sequencing were inspected by Sanger sequencing of PCR products and were corrected. ##Genome-Assembly-Data-START## Assembly Method       :: GS de-novo assembler v. 2.5p1 Genome Coverage       :: 90x Sequencing Technology :: Roche 454 GS junior; ABI 3130xl ##Genome-Assembly-Data-END## COMPLETENESS: full length.