Hi, I have been running velveth and velvetg for mapping on a reference file (Columbus extension) but I am getting the following error:
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Velvet Columbus (No roadmap)
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How to set cutoff coverage and expected coverage
Hi all,
I am new to mitochondrial genome assembly using whole genome sequencing. I tried to assemble with velvet with different k-mers, expected...
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velvetg coverage parameter
Hi everyone, I am new with Velvet and I have some questions regarding velvetg parameters.
I am doing the de novo assembly for my Illumia...
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why I have a velvetg blank script?
Hey there,
I came across this really odd situation and have no idea about what to do. I’ve just installed Velvet-1.2.10 and realized that...Last edited by leonardo_ca; 04-05-2018, 12:44 PM.
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Reconstructing a de Bruijn Graph from Velvet's LastGraph
Hi,
I was wondering if someone can explain/ give hints to me about how to regain a de Bruijn Graph from Velvet's LastGraph representation...Last edited by Splinter479; 07-12-2017, 11:26 PM.
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Metavelvet not producing "meta-velvetg.contigs.fa"
Hi everyone
I'm having problems running Metavelvet on my Ubuntu 14/Biolinux 8 (64GB RAM)
I follow the tutorial step by...
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can't export complete coverage image from Tablet
Hi everyone
I'm using Tablet to visualize contigs built from velvet but in one case i have a big coverage image that i can't export complete...
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Velvet referenced assembly
Hello all,
I see that Velvet has a Columbus module to assemble genomes using a reference as a template. Although it also says this is best...
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Velvet usage
Hi everyone!
I'm trying to use velvet to work with unmapped_reads of a rna-seq experiment, to make a kind of quantification of the contaminants...
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Choosing MAXKMERLENGTH in Velvet
Hi everyone,
I am a newbie in genome sequencing and assembly and I need some help.
I had to sequence several bacterial genomes (the...
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why are sRNA output reads longer than siRNA?
Hi,
this is possibly a dumb question, but if my goal is to find siRNA (20-25 nt long) why are the Illumina reads 36 nt long, at least before...
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MUMmer plot full of dots and no diagonal lines
I know from the MUMmer manual that a perfect alignment should, ideally, show a red diagonal line going from the bottom to up in the plot. However, I used...