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Thread | Thread Starter | Forum | Replies | Last Post |
csfasta --> fasta conversion | doxologist | SOLiD | 35 | 05-15-2012 10:27 AM |
FASTA to ACE | Farhat | Bioinformatics | 1 | 07-08-2011 05:58 AM |
454 .ace to .bam conversion issue | pmiguel | Bioinformatics | 14 | 06-24-2011 12:30 AM |
EMBL like file to FASTA conversion.. | empyrean | Bioinformatics | 1 | 05-14-2011 01:49 AM |
fastq to fasta conversion | kwtennis311 | Bioinformatics | 4 | 06-11-2010 12:06 PM |
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#1 |
Member
Location: Pune, India Join Date: Apr 2008
Posts: 21
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Is there a program to convert a Fasta file to an Ace assembly file? While googling I came across references to fasta2ace.pl but no program itself.
Thanks. |
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#2 |
Senior Member
Location: USA Join Date: Jan 2008
Posts: 482
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I am looking for the exact same tool ... fasta to ace, but have not succeeded yet.
If it can use quality values, even better... the ace file can then be used by eagleView to visualize reads on reference |
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#3 |
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Location: Pune, India Join Date: Apr 2008
Posts: 21
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I am looking for it for Eagleview as well.
-Farhat |
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#4 |
Senior Member
Location: The University of Melbourne, AUSTRALIA Join Date: Apr 2008
Posts: 275
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#5 |
Senior Member
Location: USA, Midwest Join Date: May 2008
Posts: 1,178
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Farhat,
I don't think it is possible to do what you are asking. FASTA files only contain ID/definition line(s) followed by sequence line(s). You may also have an accompanying quality score file. An ACE file contains much more information than this. For each contig (an ACE file may include more than one contig) it will contain the gapped sequence and quality scores, the gapped sequences of the constituent reads as well as offset information indicating where each of the constituent reads is located on the contig (reference). This information does not exist in the FASTA files so it would be impossible to construct a meaningful ACE file. |
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#6 |
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Location: Pune, India Join Date: Apr 2008
Posts: 21
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Thanks for the replies. Yes, I realize the Fasta File by itself doesn't have enough information to construct the ACE file. I wrote my own script to take in a FASTA file, a FASTQ quality file and the output from a SOAP or ELAND aligner and convert that to ACE which does work with EagleView.
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#7 | |
Senior Member
Location: USA Join Date: Jan 2008
Posts: 482
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I started writing a script of my own, but then got on to other things Farhat - is it possible for you to share the script for format conversion? |
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#8 | |
Member
Location: Pune, India Join Date: Apr 2008
Posts: 21
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-F |
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#9 |
Junior Member
Location: Florida Join Date: Aug 2008
Posts: 1
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I'm looking for exactly the same thing for eagleview too!!
Would you mind sharing your script with me? I'll send you a message shortly. Thanks! Jia |
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#10 |
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Location: France Join Date: Jan 2010
Posts: 23
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Can I ave a look to your script ?
Thanks ![]() nico l'allias |
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#11 |
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Location: Cambridge, UK Join Date: Jul 2008
Posts: 146
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This still makes no sense.
ACE is an assembly output, while fasta is just a bunch of sequences with no assembly information. Are you asking for advice on what assembler to use? This will obviously depend a lot on the type of data and whether you want a denovo or mapped assembly. James PS. Contrary to above, I don't believe ACE supports quality values. At least I've never seen any - instead the authors of ace preferred to store qualities in "phd" files (in possibly the most inefficient format known to man). I'd love to be wrong on this though as it'll make my life easier. :-) |
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#12 | |
Peter (Biopython etc)
Location: Dundee, Scotland, UK Join Date: Jul 2009
Posts: 1,543
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P.S. The MIRA assembly format (MAF, which is a bit like ACE), stores both - using FASTQ like encoding which is much more space efficient: http://mira-assembler.sourceforge.ne.../mira_maf.html |
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#13 |
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Location: Cambridge, UK Join Date: Jul 2008
Posts: 146
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Getting off-topic, sorry.
However MAF looks like a nice format. The problems of random ordering of data in CAF and the complete lack of sequence quality in ACE is one reason why I produced BAF, although it never really went anywhere and I only use it locally as an interchange format. Certainly it's true that ACE and CAF are very cumbersome for next-gen data, while SAM/BAM have other major issues when it comes to mixed technologies (such as not supporting older capillary style assemblies with potentially more than two sequences per template). A good find. :-) |
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#14 | ||
Peter (Biopython etc)
Location: Dundee, Scotland, UK Join Date: Jul 2009
Posts: 1,543
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#15 | |
Peter (Biopython etc)
Location: Dundee, Scotland, UK Join Date: Jul 2009
Posts: 1,543
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#16 | |
Junior Member
Location: india Join Date: May 2010
Posts: 7
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I wanna know ,how to extract contig file ,I am running velvet algorithm , i got .afg format, that i have viewed in hawkeye .,and i wanna extract specific contig .can you help me on that, ??? it would be wonder if i get the positive reply from you thanks |
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#17 |
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Location: india Join Date: May 2010
Posts: 7
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#18 |
Senior Member
Location: The University of Melbourne, AUSTRALIA Join Date: Apr 2008
Posts: 275
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Velvet produces a file called "contigs.fa" with all the contigs. Just cut+paste the contig you want out of that file.
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#19 |
Junior Member
Location: india Join Date: May 2010
Posts: 7
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Hi all, i can extract the best contig file by using a perl program .but i wanna view the extracted contig file.
Need help |
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#20 |
Senior Member
Location: The University of Melbourne, AUSTRALIA Join Date: Apr 2008
Posts: 275
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