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Thread | Thread Starter | Forum | Replies | Last Post |
De Novo Assembly of a transcriptome | Neil | De novo discovery | 82 | 02-28-2012 10:44 AM |
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De Novo Transcriptome Assembly QC | Noremac | General | 0 | 05-19-2011 12:02 PM |
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de novo transcriptome assembly | chenjy | RNA Sequencing | 4 | 12-07-2010 12:54 AM |
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#1 |
Junior Member
Location: Bangladesh Join Date: Nov 2013
Posts: 4
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Hi all,
We performed a plant whole transcriptome sequencing in Ion PROTON. We have about 10 Gbp data of 74 million reads in a single run using v2 proton kits. Average read length is 129 bp. Which assembler will give us better output for de nove assembly. Could anyone suggest me? Thanks Rasel |
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#2 |
Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 7,080
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Have a look at this thread: http://seqanswers.com/forums/showthread.php?t=1610
There are several other threads available (look at the top panel in "similar threads"). Short answer may be that you may have to try a few assemblers out. If you have a similar species for which a transcriptome/genome is available then you can use that as a rough reference to do some comparisons to the assembly that you build. |
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#3 |
Junior Member
Location: Bangladesh Join Date: Nov 2013
Posts: 4
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Thanks GenoMax for your suggestion.
We tried newbler but it was failed to assemble the data. Now MIRA is running for 13 days but still not completed. We don;t know why it is taking too much time although we only took 5 Gbp data for MIRA assembly running now. Last time in case of 2 Gbp PROTON transcriptome data MIRA took 12 days to complete and the metrics were not good. Actually I am worried about the data type of PROTON which may cause problem in assembler. Unfortunately there is no sufficient past example or I couldn't find specific post related to PROTON transcriptome (plant) data de novo assembly. Thanks again! Rasel |
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#4 |
Senior Member
Location: Germany Join Date: Oct 2008
Posts: 415
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Soapdenovo or in your case the -trans version has been pretty capable or at least quick in my hands.
CLC assembly cell (commercial) or CLC genomics workbench might also be worth a look. Velvet might be an option too. |
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#5 |
Junior Member
Location: Bangladesh Join Date: Nov 2013
Posts: 4
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Thanks colindaven for your suggestion
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#6 |
Member
Location: Rockville, MD Join Date: Apr 2011
Posts: 23
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CLC's assembler is quite good (and very fast) - so I would second that suggestion. Also, you may want to try IDBA's transcriptome assembler: http://i.cs.hku.hk/~alse/hkubrg/proj...ran/index.html
That being said -- 129 bp reads are not going to give you great assemblies - no matter what assembler you choose. Proton RNA-seq data is going to be much better for read mapping and mutation/SNP mapping. For de novo assembly of transcriptomes, you would do much better using PE reads. |
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#7 |
Senior Member
Location: UK Join Date: Feb 2014
Posts: 206
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Hi rasel@barj ,
I have similar issue , average reads length is 114 bp at Proton , 28 M reads per run. Proton use MIRA as their GUI plugin, but it seems that it is very slow from your post. So which assembler did you use eventually ?! |
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#8 | |
Senior Member
Location: UK Join Date: Feb 2014
Posts: 206
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![]() Quote:
(1)Why do you say that? (i.e. 129 bp reads are not going to give you great assemblies) (2)Why do you say you would prefer use PE reads ? (3) Is the IDBA's transcriptome assembler suitable for Proton data as well? how does it compare with Abyss, Velvet or Soapdenovo? Last edited by super0925; 07-22-2015 at 06:55 AM. |
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#9 |
Senior Member
Location: UK Join Date: Feb 2014
Posts: 206
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How about Trinity?
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#10 |
Junior Member
Location: Bangladesh Join Date: Nov 2013
Posts: 4
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Hi super0925
We tried several assemblers but no one can build high quality assembly. Among all the assemblers Trinity gives much better metrics than others. |
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