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Thread | Thread Starter | Forum | Replies | Last Post |
How to Improve Newbler Assembly | shuang | Bioinformatics | 2 | 09-13-2011 10:45 PM |
newbler assembly ... padding and SNPs | jnfass | De novo discovery | 12 | 06-09-2011 04:58 AM |
Newbler de novo assembly | moinul | De novo discovery | 3 | 05-27-2011 06:13 PM |
newbler assembly of mated reads (FASTA format) | dpuiu | De novo discovery | 1 | 01-22-2010 12:27 AM |
Filtering and excluding reads | dawe | Bioinformatics | 3 | 09-09-2009 09:47 AM |
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#1 |
Member
Location: Norway Join Date: Jan 2010
Posts: 83
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Hi,
I have sequenced genomic DNA from a eukaryote and have ran a newbler assembly of the sff file from the 454 lab. Some of the contigs are clearly belonging together, but are not assembled into one. This seems to be caused by a few reads that looks like artefacts from the genomic amplification. (These reads are split into two and the two halves match each end of the contig, like a circle.) I wonder if it is possible to run newbler and to specify that these reads (i have the names) should not be considered? Thanks! Jon |
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#2 |
Senior Member
Location: USA, Midwest Join Date: May 2008
Posts: 1,178
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Jon,
Yes, you can exclude specific reads from the assembly. Create a text file with the read names you wish to exclude, one name per line, nothing else. When you run newbler use the parameter '-fe <filename>' where filename is the file described above. |
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Tags |
454, assembly, exclude, newbler, reads |
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