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Issues with samblaster when using BISCUIT #38
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Hi @KChadwick78, Based on a little bit of testing on my end, it looks like the FASTQs you used as input weren't in the working directory you ran I think it's fair to say that Feel free to reach out if you have further hang ups with running BISCUIT. |
Hi Jacob,
I went back to look closely at my directory after you mentioning this might
be the problem, as I was 99% I was running it from where my files are and
realised that I had missed off the '.gz' at the end which is why BISCUIT
couldn't find them as files with just the '.fastq' don't exist!
Getting to grips with this I can't see the wood for the trees sometimes :)
Thanks for your help
Kate
…On Thu, Jul 13, 2023 at 10:18 AM Jacob Morrison ***@***.***> wrote:
Hi @KChadwick78 <https://github.com/KChadwick78>,
Based on a little bit of testing on my end, it looks like the FASTQs you
used as input weren't in the working directory you ran biscuit from.
I think it's fair to say that [gzread] (null) is not a helpful error
message at all for this, so I will fix this to make it more obvious what is
going on.
Feel free to reach out if you have further hang ups with running BISCUIT.
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Addresses Issue #38. If a FASTQ file is missing, biscuit align will now print an error message that the file is unable to be opened.
Hi,
I am working on Compute Canada clusters and getting an output error relating to samblaster when trying to align to me reference genome:
samblaster: Inputting from stdin
samblaster: Outputting to stdout
[M::bwa_idx_load_from_disk] read 0 ALT contigs
[gzread] (null)
samblaster: Loaded 172124 header sequence entries.
samblaster: No reads in input SAM file
This is my code:
module load gcc
module load bowtie2/2.4.1
module load samtools/1.16.1
module load samblaster/0.1.26
module load perl/5.30.2
biscuit align /home/chadders/projects/def-frasiert/methyl_seq/ref_genome/Eubalaena_glacialis_HiC.fasta 1151_B_S11_L001-FP.fastq 1151_B_S11_L001-RP.fastq |
samblaster | samtools sort -o my_output.bam -O BAM -
samtools index my_output.bam
I am super new to this and not sure if I have made a misstep in creating the reference index, but the outputs for this all looked ok. I know the fastq files are ok as they ran fine in bismark.
Thanks
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