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Thread | Thread Starter | Forum | Replies | Last Post |
de novo assembly using Trinity versus Velvet-Oases | Nol | De novo discovery | 8 | 10-26-2013 12:56 PM |
Denovo RNA-Seq assembly using Velvet/Oases | AdrianP | RNA Sequencing | 5 | 01-03-2013 03:04 AM |
SOAP denovo assembly results | bioinfosm | Bioinformatics | 9 | 06-13-2012 08:22 AM |
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#1 |
Member
Location: Singapore Join Date: Nov 2013
Posts: 36
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Hi,
I used velvet and trinity for denovo assembly for RNA seq of short single end reads of length between 18 to 23. But the results that I got from velvet and trinity are different. In velvet I get contigs of length between 40 and 350 and the no of contigs is more than 20000. In trinity I get only 3 contigs of length more than 1000. Here is the velvet and trinity command that I used. velvet ./velveth directory 17 -sam -short '/home/xxx.fastq' ./velvetg directory -cov_cutoff auto -read_trkg yes Trinity Trinity.pl --seqType fa --JM 10G --single /home/xxx.fasta --CPU 2 Can somebody tell me what parameter am I missing in trinity. Thanks. Vishwesh |
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#2 |
David Eccles (gringer)
Location: Wellington, New Zealand Join Date: May 2011
Posts: 838
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Trinity needs reads of at least ~50 to be effective, because it needs a kmer at each end of the read in order to join -- I think more recent versions have relaxed this requirement a bit, but it's still a reasonable minimum target length. You're not going to get anything much useful out of Trinity with short reads.
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