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Thread | Thread Starter | Forum | Replies | Last Post |
large sequencing projects | barak | Service Providers | 12 | 11-11-2013 01:55 PM |
large sequencing projects | barak | Bioinformatics | 1 | 11-11-2013 01:47 PM |
detecting deletion in amplicon sequencing of mixed population | Josim | Genomic Resequencing | 0 | 11-10-2011 06:24 AM |
Designing de-novo sequencing projects | isharon | De novo discovery | 0 | 05-25-2010 01:01 AM |
PubMed: Brazilian genome sequencing projects: state of the art. | Newsbot! | Literature Watch | 0 | 12-17-2008 06:03 AM |
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#1 |
Junior Member
Location: cn Join Date: Aug 2008
Posts: 1
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Dear all
We have 3 genomes sequenced of 11, 15 and 23 fold coverage by 454 Sequencer. At least more than 10kb of the gap regions (defined by unsuccessful reference mapping) are coding regions containing little repetitive sequences. Interestingly, these gap regions appear quite concordantly among the 3 genomes. Would anybody know how to utilize the scaffold files or related in order to check whether they are real gaps or not? Automation cannot be done if the process has to be studied by manually comparing the results generated by reference mapper and de novo assembler. _________ ................ ________ |..............|................|..........| |.ATTTCC..|---------->| CGCCC | |_________|................|______| Say, in reference genome, it is: ATTTCCTTAGGAACGCCC can we have a quick way to identify ATTTCCCGCCC (not to do that manually…) so to confirm the genome has deletion of (TTAGGAA) or not? Last edited by watashi; 08-01-2008 at 02:19 PM. |
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