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**Bug Description**
I have recently installed an Illumina iSeq-100 benchtop sequencer in my lab, and it was announced allready in 2018, that there will be a 2x 250 bp sequencing cartrige available so…
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Sometimes I just want to trim "from xx bases onward" or "take just the first xx bases". In trimmomatic (considerably slower than atropos) this is obtained with the `HEADCROP` and `CROP` commands, resp…
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I just came across the preprint and got curious to try out burst.
I need to assigning the taxonomy for Illumina short-reads (MiSeq, up to ~450bp) from an amplicon sequencing run (COI & 16S). Are t…
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What steps will reproduce the problem?
1.MosaikBuild -q 0019.fq -out 19.bin -st illumina
2.MosaikBuild -assignQual 10 -q 0019.fq -out 19.bin -st illumina
3.
What is the expected output?
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Dear rMATs team,
I used rMATS-turbo using FASTQ files for the detection of differential alternative splicing. The FASTQ file had the standard Illumina adaptor for paired-end sequencing. I did not t…
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### Project short name:
PathogenicVariantsCardiomyopathies
### Primary Wrangler:
Ida
### Secondary Wrangler:
### Associated files
* Google Drive: [folder](https://drive.google.com/drive/folders/…
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The reason multiple insert libraries are used is to strike a balance between long and short range information. Long-insert mate pair libraries are great at telling you two contigs are linked but doesn…
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We need to do a 'true' power analysis for readcomb - we know it detects phase changes, but how often do we expect it to actually catch them in real data?
We've looked into [ART](https://academic.o…
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```
What steps will reproduce the problem?
1.MosaikBuild -q 0019.fq -out 19.bin -st illumina
2.MosaikBuild -assignQual 10 -q 0019.fq -out 19.bin -st illumina
3.
What is the expected output?
---…