Pseudodomonas syringae

Pseudodomonas syringae strain DC 3000

Originally sequenced and finished at TIGR

 AA: no assembly
 TA: ftp://ftp.ncbi.nih.gov/pub/TraceDB/pseudomonas_syringae_pv_tomato_str_dc3000/ : 80,959 reads

UNC:

New sequence:

 * Solexa 3 lanes; 
 * 454 shotgun 1/4 Plate (250bp read); 
 * 454 paired ends 1/4 Plate.	

Download:

 http://biology622.dhcp.unc.edu/~labweb/DCData/

UNC assembly:

 * Theoretical minimum number of contigs we can obtain is 268 (our reads fail to cover 269 nucleotides). 
 * Our de novo assembly spans the genome in 853 contigs totaling 6,313,026 bp. 
 * 98.7% of the genome is covered by a contig; 
 * 84% of the genome is covered by contigs 10,000 bp or greater. 
 * The average gap size between contigs is 98 bp; 
 * average contig size 7401 bp. 
 * The N50 = 37,444 bp. 
 * Our largest BAMBUS "scaffold" is 2,565,761 bp,

Data stats

 .                               #elem           min     median  max     sum             mean    stdev   n50
 DC3000.format.454Reads.fna      123992          38      86      329     15623908        126.01  58.89   142     DC3000 Paired End Reads
 DC3000.TCA.454reads.format.fna  77466           35      244     371     18627363        240.46  26.85   245     DC3000 454 Reads
 DC3000.reads.filtered.fasta     6340136         32      32      32      202884352       32      0       32      DC3000 Solexa Reads
 DC3000Plasmids.fa               2               67473   73661   73661   141134          70567   3094    73661   Pseudomonas syringae pv. tomato DC3000 Plasmids
 Psudomonas_syringae.fa          1               6397126 6397126 6397126 6397126         6397126 0       6397126 Pseudomonas syringae pv. tomato DC3000 reference

Files location:

 /fs/szasmg2/Bacteria/Pseudodomonas_syringae/Data
 /fs/szasmg2/Bacteria/Pseudodomonas_syringae/Assembly

Best CBCB assembly:

 /fs/szasmg2/Bacteria/Pseudodomonas_syringae/Assembly/Solexa-454/2007_1009_AMOSCmp-relaxed
 142 contigs (37 negative gaps)
 based on the mix of 454 single reads + Solexa reads (no 454 paired ends) 
 AMOScmp used the following parameters:
   nucmer -c  20
   casm-layout -t 20 -o 5
 No read trimming was done. "casm-layout -t 20" allows for 20 bp long  dirty sequence ends which seem to solve the "low quality" problem.