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
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
Comment