Entering edit mode
9.5 years ago
mafireyi
▴
80
I am trying to use Soap Denovo for my assembly. I first trimmed my reads with trimmomate and used Flash to merge reads. Flash outputs 4 output files. Which ones would I use as inputs for Soap denovo. Should I use the out.extendedFrags.fastq or should I include the out.notCombined ones too?
Thanks
Thanks, will it be possible to get a complete assembly if i just use the graph assembly with asm_flags = 3. below is my config file for the pair end library
max_rd_len=100
[LIB]
name = Hiseq14
avg_ins=200
reverse_seq=0
asm_flags=3
rd_len_cutoff=100
rank=1
pair_num_cutoff=3
map_len=32
q1=/scratch/sysusers/godwin/GuavaGenome/Hiseq_Run14_150313/Sample_Guava_IT2_350/out.extendedFrags.fastq
Will that work? Sorry, I am quite new to Soap
Yes, that should be enough. However, I'm not entirely sure, what SOAP will do about scaffolding with only a single end library. My guess: not a lot ;).
I might be a good idea to add the trimmed but not flashed libraries as scaffold-only libraries (asm_flags = 2) to your config.