Difference between revisions of "Francisella tularensis"
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Line 30: | Line 30: | ||
OSU18 : BCM complete | OSU18 : BCM complete | ||
− | + | Final assembly steps: | |
1. Reads were downloaded from TA and formatted using tarchive2ca | 1. Reads were downloaded from TA and formatted using tarchive2ca | ||
2. There are 2 Sanger libraries for this project | 2. There are 2 Sanger libraries for this project | ||
− | BFTBP:58051 | + | BFTBP: #reads=58051 , insert_mean=2000, insert_stdev=666 |
− | BFTDP:10409 | + | BFTDP: #reads=10409 , insert_mean=2000, insert_stdev=666 |
3. The reads have been retrimmed using veraTrim (-T 10 -M 100 -E 500) | 3. The reads have been retrimmed using veraTrim (-T 10 -M 100 -E 500) | ||
4. runCA-OBT.pl has been used to assemble all the reads | 4. runCA-OBT.pl has been used to assemble all the reads | ||
5. The library sizes were updates using the WGA estimates | 5. The library sizes were updates using the WGA estimates | ||
+ | BFTBP: insert_mean=2690.042, insert_stdev=643.126 | ||
+ | BFTDP: insert_mean=3675.914, insert_stdev=1225 | ||
6. The WGA was aligned to the reference using nucmer; one rearrangement, one | 6. The WGA was aligned to the reference using nucmer; one rearrangement, one | ||
deletion and several SNP's were noticed | deletion and several SNP's were noticed | ||
+ | 7. The reads were assembled using AMOScmp (default parameters); 2 missoriented | ||
+ | read pile regions were noticed | ||
+ | 8. The assembly was aligned to itself; 950 bp inverted repeats were identified as | ||
+ | flanking the problem regions | ||
+ | 9. The 2 regions were flipped | ||
− | |||
− | |||
Final assembly location: | Final assembly location: | ||
/fs/szasmg/Bacteria/F_tularensis_holarctica_OSU18/best | /fs/szasmg/Bacteria/F_tularensis_holarctica_OSU18/best | ||
+ | |||
+ | Assembly locations: | ||
+ | /fs/szasmg/Bacteria/F_tularensis_holarctica_OSU18/ | ||
== Novicida == | == Novicida == | ||
== Mediasiatica == | == Mediasiatica == |
Revision as of 19:36, 8 August 2007
Data sources:
NCBI:
Broad:
Baylor:
Type A:
FSC033 : Broad assembly (15 contigs)
Assemblies location:
/fs/szasmg/Bacteria/F_tularensis_tularensis_FSC033/
Type B:
OSU18 : BCM complete
Final assembly steps:
1. Reads were downloaded from TA and formatted using tarchive2ca 2. There are 2 Sanger libraries for this project BFTBP: #reads=58051 , insert_mean=2000, insert_stdev=666 BFTDP: #reads=10409 , insert_mean=2000, insert_stdev=666 3. The reads have been retrimmed using veraTrim (-T 10 -M 100 -E 500) 4. runCA-OBT.pl has been used to assemble all the reads 5. The library sizes were updates using the WGA estimates BFTBP: insert_mean=2690.042, insert_stdev=643.126 BFTDP: insert_mean=3675.914, insert_stdev=1225 6. The WGA was aligned to the reference using nucmer; one rearrangement, one deletion and several SNP's were noticed 7. The reads were assembled using AMOScmp (default parameters); 2 missoriented read pile regions were noticed 8. The assembly was aligned to itself; 950 bp inverted repeats were identified as flanking the problem regions 9. The 2 regions were flipped
Final assembly location:
/fs/szasmg/Bacteria/F_tularensis_holarctica_OSU18/best
Assembly locations:
/fs/szasmg/Bacteria/F_tularensis_holarctica_OSU18/