Teredinibacter turnerae T7902
Seq. Project name:
Teredinibacter turnerae T7902 ( Project ID: 403887 )
Product:
Standard Draft
Proposal Name:
Marine microbial communities from multiple species of wood-boring bivalves (shipworm isolates) (Proposal ID: 920)
Project PI:
User Program:
CSP
Program Year:
2011
Scientific Program:
Microbial
Genome Portal:
Related Projects:
FD 1078654; SP 403887; AP 1377988
Release Date:
2012-05-10
Organism
Genus/species/strain/isolate: Teredinibacter / Teredinibacter turnerae / T7902 /
GOLD ID: Gp0012860
Data Submission
NCBI BioProject ID: 163003
NCBI Tax ID: 1056820
SRA accession:
  • SRP079020 (2016-07-20)
Contacts
JGI: IMG [email protected]
Request DNA:
Daniel L Distel <[email protected]>
General Information
QD/SAG JGI ISOLATE QC AND ASSEMBLY REPORT - 4094038 Teredinibacter turnerae T7902 1) RAW DATA: LibraryName NumReads ReadType FileName ICZC 29983482 2x150 /house/groupdirs/pi/project/4094038/ill_dir/ICZC.2108.1.1763.GATCAG.fastq QC Dir:/house/groupdirs/pi/project/4094038/ill.qd 2) READ FILTERING STATS: Pairs of matching reads were removed from the dataset. Total input reads: 29983482 (100%) Artifact reads removed: 215614 (0.7%) Trimmed reads removed: 1487426 (5.0%) Total reads removed: 1703040 (5.7%) Total reads remaining: 28280442 (94.3%) 3) ASSEMBLY STATS: b) Velvet assembly: Assembly stats of the Velvet assembly created by the velvet optimizer. The input reads have been . Avg GC Content: 50.38 +/- 6.53% Largest Contig: 312.1 KB Main genome scaffold total: 262 Main genome contig total: 262 Main genome scaffold sequence total: 5.3 MB Main genome contig sequence total: 5.3 MB (-> 0.0% gap) Main genome scaffold N/L50: 17/94.6 KB Main genome contig N/L50: 17/94.6 KB Number of scaffolds > 50 KB: 38 % main genome in scaffolds > 50 KB: 81.3% Minimum Number Number Total Total Scaffold Scaffold of of Scaffold Contig Contig Length Scaffolds Contigs Length Length Coverage -------- --------- ------- ----------- ----------- -------- All 262 262 5,269,991 5,269,991 100.00% 1 kb 100 100 5,234,133 5,234,133 100.00% 2.5 kb 86 86 5,210,510 5,210,510 100.00% 5 kb 81 81 5,192,244 5,192,244 100.00% 10 kb 68 68 5,097,975 5,097,975 100.00% 25 kb 55 55 4,883,860 4,883,860 100.00% 50 kb 38 38 4,286,070 4,286,070 100.00% 100 kb 12 12 2,211,687 2,211,687 100.00% 250 kb 1 1 312,063 312,063 100.00% c) Allpaths + Velvet simulated read pairs: Assembly stats of the ALLPATHS assembly. The input contains simulated 1-3 kb read pairs created from the Velvet assembly and reads that have been . Avg GC Content: 48.92 +/- 4.09% Largest Contig: 353.6 KB Main genome scaffold total: 79 Main genome contig total: 79 Main genome scaffold sequence total: 5.4 MB Main genome contig sequence total: 5.4 MB (-> 0.0% gap) Main genome scaffold N/L50: 11/176.4 KB Main genome contig N/L50: 11/176.4 KB Number of scaffolds > 50 KB: 33 % main genome in scaffolds > 50 KB: 86.5% Minimum Number Number Total Total Scaffold Scaffold of of Scaffold Contig Contig Length Scaffolds Contigs Length Length Coverage -------- --------- ------- ----------- ----------- -------- All 79 79 5,383,522 5,383,520 100.00% 1 kb 79 79 5,383,522 5,383,520 100.00% 2.5 kb 68 68 5,367,721 5,367,719 100.00% 5 kb 65 65 5,356,022 5,356,020 100.00% 10 kb 57 57 5,293,243 5,293,241 100.00% 25 kb 47 47 5,133,006 5,133,004 100.00% 50 kb 33 33 4,658,932 4,658,930 100.00% 100 kb 16 16 3,422,996 3,422,996 100.00% 250 kb 4 4 1,248,888 1,248,888 100.00% 4) KEY PIPELINE CMDS: a) Velvet assembly step for creating simulated read pairs: Velvet version: Velvet optimizer version: 2.1.7 Velvet optimizer params: --v --s 51 --e 71 --i 4 --t 1 --f "-shortPaired -fastq $FASTQ" --o "-ins_length 250 -min_contig_lgth 500" b) Simulated read pairing creation step: Wgsim version: 0.3.0 Wgsim params: -e 0 -1 76 -2 76 -r 0 -R 0 -X 0 c) ALLPATHS assembly step: ALLPATHS version: r40295 Contents of in_libs.csv: library_name, project_name, organism_name, type, paired, frag_size, frag_stddev, insert_size, insert_stddev, read_orientation, genomic_start, genomic_end STD_1,project,assembly,fragment,1,200,35,,,inward,0,0 SIMREADS,project,assembly,jumping,1,,,3000,300,inward,0,0 5) WORKFLOW STEPS: 1. Removed illumina artifacts (synthetic oligos used in the laboratory). 2. Created velvet assembly of the artifact filtered data (using velvet optimiser). 3. Created simulated 1-3 kb read pairs using velvet contigs from step 2. 4. Created allpaths assembly using velvet simulated read pairs (step 3) and the artifact filtered data.6) RELEASE DATE: Wed Feb 15 14:45:51 PST 2012 By Andrew Tritt- [email protected] Wed Feb 15 14:53:37 PST 2012 By Kecia Duffy- [email protected] Wed Feb 15 16:39:04 PST 2012 By Kecia Duffy- [email protected] 7) AUTHORS: For additional information, please contact: Kecia Duffy - [email protected] Stephan Trong - [email protected] James Han - [email protected] This file was automatically generated by the single cell pipeline software (version 1.1.8).
Funding
The work conducted by the U.S. Department of Energy Joint Genome Institute, a DOE Office of Science User Facility, is supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231.
Groups
This portal belongs to the following groups
## Name Type
1 Gammaproteobacteria
2 Host Associated
3 Proteobacteria