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Thread | Thread Starter | Forum | Replies | Last Post |
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How to extract paired-end reads from .sff 454? | pmiguel | Bioinformatics | 8 | 02-22-2010 08:17 AM |
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#1 |
Senior Member
Location: oceania Join Date: Feb 2014
Posts: 115
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Hi,
I'm new here, thanks in advance for any help. I have a 454 dataset of 'allcontigs.ace'. The reads consist of paired and unpaired. If I use a viewer like Tablet, which I find very good.. I can see the paired reads in the contigs and which other contigs they are paired to etc. but I cannot see the corresponding orientation of those contigs.. I should say, I am trying to examine a 'chain' of contigs out from one of interest, none of which have been included in the scaffold (because they originate from a 16S sequence). So my question is.. is there a viewer I can use which will show the contigs and their relative orientation, based on the paired reads they share? I have tried several so far with no luck. Thanks very much, S. |
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#2 |
Senior Member
Location: uk Join Date: Mar 2009
Posts: 666
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What viewers have you tried?
Have you tried Hawkeye, it is part of the Amos package? |
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#3 |
Senior Member
Location: oceania Join Date: Feb 2014
Posts: 115
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Hi,
I tried Eagle, Consed (couldn't install), Tablet, Magicviewer. Tablet does show the orietation of each paired read.. The more I think about it, that should be enough, but it would be nice to view the 'joined' contigs together. I will try amos. Thanks, S. |
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#4 |
Senior Member
Location: Berlin, DE Join Date: May 2008
Posts: 628
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If you want to edit the assembly (e.g. move contigs around etc.) I'd recommend consed. Installation is not really complicated and very well documented. Newbler, gsAssembler, is able to produce a complete consed folder. This has to be checked before the actual (denovo) assembly.
If it is just for viewing the paired reads information / contig layout, Hawkeye is the way to go :-) my 2p, Sven |
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#5 |
Senior Member
Location: oceania Join Date: Feb 2014
Posts: 115
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Thanks Sven, I followed the consed docs on installation and wasted a day in the attempt.. error after error.. so don't have time for it. Need results. I'll try the other progs.
Thx again. S. |
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#6 | |
Peter (Biopython etc)
Location: Dundee, Scotland, UK Join Date: Jul 2009
Posts: 1,543
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Also Newbler had some experimental BAM output support - I'm not sure if it was ever properly finished and working though. |
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#7 | |
Senior Member
Location: oceania Join Date: Feb 2014
Posts: 115
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Thanks for the advice. ![]() S. |
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#8 |
Peter (Biopython etc)
Location: Dundee, Scotland, UK Join Date: Jul 2009
Posts: 1,543
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You could also try 454 assembly with MIRA4 which has SAM output (or you can convert MIRA's own output into SAM).
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#9 | |
Senior Member
Location: Berlin, DE Join Date: May 2008
Posts: 628
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But I agree, .. with MIRA4 you gain more flexibilty. E.g. Staden's gap4/5 :-) |
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#10 |
Peter (Biopython etc)
Location: Dundee, Scotland, UK Join Date: Jul 2009
Posts: 1,543
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The other option is to hunt for a working ACE to SAM/BAM converter which handles the paired information - people have tried this before but I'm not sure if there is a complete solution.
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Tags |
454, assembly, contigs, paired reads, scaffolds |
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