Originally posted by Rachelly
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Thanks to Wallysb01!
As you mean the mapping mechanism is different from the ones used by bwa or bowtie, then what parameters should be changed in the bwa/bowtie softwares? It is hard for me to give an equivalent parameterset, because I do not know any rules for mapping by SOAPdenovo.
Thanks!
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So, the contig file will be different from the final scafSeq file, but only because you've done scaffolding, some error correction, and probably gap filling as well. So, all else equal, you should see more or at least similar numbers of reads map to your genome in the final SOAPdenovo output than in the contig file. However, your after assembly mapping might not use the same mechanism as the SOAP map. When using bwa or bowtie, you may need to loosen the alignment parameters to obtain the same level of mapping.
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I am going to this soon! Is it possible that the contig sequences are different in the log file and the real output(.contig) ?
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I also have this problem.
From the SOAPdenovo log, it seems about 90% reads align to the contig.
However, when I use the bowtie trying to align the raw reads to the contig file, it is also just about 1/3 reads align to the contig.
I also don't understand why there is so much difference between SOAPdenovo log and after-assembly-mapping?
Thanks!
Jingjing
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Thanks for your reply tonybloger.
SOAPdenovo doesn't supply useful data from the "map" step, there is no way to know what reads the indices refer to..
So I did remapping of the reads to the assembly, but got a totaly different amount of reads mapped back to the assembly, than what SOAPdenovo states in the log file.. It seems that only about 1/3 of the reads were able to re-map to the assembly when using BWA or Bowtie, while SOAPdenovo showed over 94% mapping!
SOAPdenovo states:
Code:15646393 out of 16551980 (94.5)% reads mapped to contigs
Code:# reads processed: 8275990 # reads with at least one reported alignment: 862689 (10.42%) # reads that failed to align: 7413301 (89.58%) Reported 862689 paired-end alignments to 1 output stream(s)
Code:16551980 + 0 in total (QC-passed reads + QC-failed reads) 0 + 0 duplicates 6108971 + 0 mapped (36.91%:nan%) 16551980 + 0 paired in sequencing 8275990 + 0 read1 8275990 + 0 read2 3906364 + 0 properly paired (23.60%:nan%) 4618869 + 0 with itself and mate mapped 1490102 + 0 singletons (9.00%:nan%) 1192368 + 0 with mate mapped to a different chr 1188458 + 0 with mate mapped to a different chr (mapQ>=5)
Does anyone know why is there such a big difference between the mapping of SOAPdenovo and after-assembly-mapping?
Thanks!
Rachelly.
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Originally posted by Rachelly View PostDoes anyone know a better way of getting the unused reads?
Unmapped reads from the re-mapping is your best bet - i think there is such an output already from the soap 'map' step.
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Unused reads in SOAPdenovo
Hi all,
I want to extract the reads that were not used in the assembly process of SOAPdenovo.
I did not find a straight forward way of doing so. I thought about mapping the reads back to the assembly and taking the unmapped reads. But it seems like a simple output SOAPdenovo could give, and I'm not sure the unmapped reads from re-mapping are the same as the reads that were not used for the assembly.
Does anyone know a better way of getting the unused reads?
Thanks,
Rachelly.Tags: None
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