Bumblebee
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Data
- ~ 500B genome
- 7 pairs of data files (paired ends) : lanes 1..3,5..8 (lane 4 wasn't used)
Lane Insert ReadLen #Reads 1 3K(2..6,avg 4K) 124 34,944,099 2 8K(7..9,avg 8K) 124 32,540,640 3 500(450..600) 124 34,745,750 # gDNA 5 500 34,601,239 6 500 34,553,857 7 500 34,682,612 8 500 12,975,839
- Tasks to figure out:
1. Erroneous reads/bases, which we need to correct or discard 2. GC bias, so we can compute a-stats properly 3. Redundancy in the long paired ends, which are lane 1 and lane 2.
- Used the 454 protocol to circularize the DNA for sequencing with the Illumina instrument.
- Some reads will begin in the circularization adaptor and thus will have only one usable read
- Some reads have a few bases of DNA sequence and hit the circularization adaptor right away
- Most reads will have at least 36bp from each end before hitting the adaptor.
- Many reads will not have any adaptor to trim (>125bp of DNA sequence at both ends of the adaptor)
- circularization adaptors
TCGTATAACTTCGTATAATGTATGCTATACGAAGTTATTACG - revcomp -> CGTAATAACTTCGTATAGCATACATTATACGAAGTTATACGA AGCATATTGAAGCATATTACATACGATATGCTTCAATAATGC
- Formatting: keep only the first 100bp (last 24 bp are anyway low qual)
- Location:
/fs/szattic-asmg4/Bees/Bombus_impatiens
Assembly
- Trimming
No OBT adaptors in the seqs
- Kmers
meryl -Dh -s 0-mercounts/asm-C-ms22-cm1 >! 22mers.hist Found 3136399464 mers. Found 379123530 distinct mers. Found 201257394 unique mers. Largest mercount is 12006651; 90 mers are too big for histogram.
countKmers.pl most frequent 42mer : CGTAATAACTTCGTATAGCATACATTATACGAAGTTATACGA ~ 20% of the seqs : circularization adapter
- Unitigger : max utg len=852bp
- Consensus after unitigger : 3 out of 129 jobs failed
- Location
/fs/szdevel/dpuiu/SourceForge/wgs-assembler.030210/Linux-amd64/bin/runCA