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Rather than looking at mutation frequency information from the entire pandemic, we're often only interested in recent sequencing (say, within the last 6 months).
## Handler
[Mutations by lineage…
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I am sorry, if I am asking too simple question but after reading read-me file, I am bit confused by the term unpaired data because I am using pair-end data in fastq file and finally after completion o…
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Hello,
I would like to assemble chloroplastic DNA using Fast-Plast.
Unfortunately, the process stops after providing 2-Bowtie_index.
Actually, the process is stopped with this error message :…
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Based on the messy-as-heck workflow sketched out in #356, we want to do a number of partial workflows, with specific stopping and restarting points. The workflow I initially had in mind would require …
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Thanks
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Project UUID: 4e6f083b-5b9a-4393-9890-2a83da8188f1
Project Title: The emergent landscape of the mouse gut endoderm at single-cell resolution
Project Short Name: Mouse Endoderm Project
Submission UU…
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I am working with sequencing data that has short insert sizes but was sequenced with 150 bp paired-end reads, leading to high levels of overlaps within the read pairs. When I visualized the data align…
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Hi,
First of all, thanks for making STARSolo.
Is there any way to get HDF5 as output from STARSolo pipeline after mapping/counting 10x droplet data?
Or any other way to get each individual tran…
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Right now, there's kind of a dead space in between the standard import (which does a ton of qc, sanitizing, linking, etc) and the trusted-importer (which does none of that). As our sequencing partner…
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I believe they belong as part of the treatment of functional programming, which according to [this outline](https://docs.google.com/document/d/1RN9mvAa9c7LMeK1OW6hWNhDBO4mj71TLCevg2cargio/edit#heading…