-- dump date   	20140619_234449
-- class       	Genbank::Contig
-- table       	contig_comment
-- id	comment
NC_022533.1	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 AP012552.PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filledPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding regionPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the correspondingPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosomePROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library.PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers,PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and anPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems).PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqManPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI,PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA).PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START##PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5xPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5x Sequencing Technology :: 454 GS20PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5x Sequencing Technology :: 454 GS20 ##Genome-Assembly-Data-END##PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012552. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5x Sequencing Technology :: 454 GS20 ##Genome-Assembly-Data-END## COMPLETENESS: full length.
NC_022534.1	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 AP012553.PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filledPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding regionPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the correspondingPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosomePROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library.PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers,PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and anPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems).PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqManPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI,PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA).PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START##PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5xPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5x Sequencing Technology :: 454 GS20PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5x Sequencing Technology :: 454 GS20 ##Genome-Assembly-Data-END##PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012553. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5x Sequencing Technology :: 454 GS20 ##Genome-Assembly-Data-END## COMPLETENESS: full length.
NC_022546.1	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 AP012551.PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filledPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding regionPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the correspondingPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosomePROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library.PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers,PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and anPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems).PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqManPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI,PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA).PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START##PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5xPROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5x Sequencing Technology :: 454 GS20PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5x Sequencing Technology :: 454 GS20 ##Genome-Assembly-Data-END##PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence is identical to AP012551. Sequencing gaps between the contigs obtained by GS20 were filled either by sequencing the PCR products of the corresponding region amplified by appropriate primers or by sequencing the corresponding clones from a shotgun library and a bacterial artificial chromosome library. Sequencings were performed using appropriate sequencing primers, ABI Prism BigDye Terminator v3.1 Cycle Sequencing Kits and an ABI3700 genetic analyzer (Applied Biosystems). Assembling the sequences and the contigs were done using SeqMan program in the Lasergene software package (DNAstar, Madison, WI, USA). ##Genome-Assembly-Data-START## Assembly Method       :: Newbler v. 1.0.52.06 Genome Coverage       :: 20.5x Sequencing Technology :: 454 GS20 ##Genome-Assembly-Data-END## COMPLETENESS: full length.