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-   -   Assembly with trimmed FASTQ files fail (http://seqanswers.com/forums/showthread.php?t=89721)

SK-N-BE 06-12-2019 01:58 AM

Assembly with trimmed FASTQ files fail
 
Hello,

spades is working fine when I am using untrimmed fastq files.

I am using Trimmomatic to trim reads (SLIDINGWINDOW:30:20) and used the generated "output_forward_paired.fq.gz" and "output_reverse_paired.fq.gz" for assembly by Spades.

However, when using these files, no scaffolds.fasta file is generated and spades shows the following warnings:

Quote:

======= SPAdes pipeline finished WITH WARNINGS!

=== Error correction and assembling warnings:
* 0:00:38.523 48M / 6G WARN General (kmer_coverage_model.cpp : 218) Too many erroneous kmers, the estimates might be unreliable
* 0:01:00.438 132M / 7G WARN General (pair_info_count.cpp : 342) Unable to estimate insert size for paired library #0
* 0:01:00.438 132M / 7G WARN General (pair_info_count.cpp : 348) None of paired reads aligned properly. Please, check orientation of your read pairs.
* 0:01:00.785 132M / 7G WARN General (repeat_resolving.cpp : 63) Insert size was not estimated for any of the paired libraries, repeat resolution module will not run.
How may I solve this issue? Why do I get these warnings when using trimmed reads?

marieBvr 10-02-2020 02:29 AM

Hi,
I face the same issue.
Were you able to solve these warnings ?

Cheers


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