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Issues with samblaster when using BISCUIT #38

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KChadwick78 opened this issue Jul 12, 2023 · 3 comments
Closed

Issues with samblaster when using BISCUIT #38

KChadwick78 opened this issue Jul 12, 2023 · 3 comments
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@KChadwick78
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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

@jamorrison
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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 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.

@KChadwick78
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KChadwick78 commented Jul 13, 2023 via email

@jamorrison
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Glad to hear you were able to resolve the issue! Feel free to reopen (or open another) issue if you run into further issues.

jamorrison added a commit that referenced this issue Sep 11, 2023
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.
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