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We (VIDRL) are moving from sanger sequencing to HTS sequencing using a custom hybridisation probe panel which will be sequenced on either iSeq or NextSeq. I've looked at a few pipelines, with MiCall being the (IMO) the one which ticks all the boxes. I had a few questions if you had sometime to answer:
Can MiCall be used on different illumina platforms?
From reading the code, the pipeline isn't tied to your internal systems (eg on Kive) and it can be deployed on any system?
I want to confirm MiCall is doing the resistance interpretation locally and not using the Sierra API to transmit data to stanford?
Thanks!
Ammar
The text was updated successfully, but these errors were encountered:
We've only used it on MiSeq data, but its only critical dependency is on the FASTQ file format. You should be able to work around differences in any other dependencies, like the Interop folder data. MiCall doesn't need to run under Kive, you can run it under docker, run it under Singularity, run it on BaseSpace, or install the dependencies and run it directly on your system.
We're happy to give guidance if you have any questions as you try to run it on your own data.
Hi CFE-Lab,
We (VIDRL) are moving from sanger sequencing to HTS sequencing using a custom hybridisation probe panel which will be sequenced on either iSeq or NextSeq. I've looked at a few pipelines, with MiCall being the (IMO) the one which ticks all the boxes. I had a few questions if you had sometime to answer:
Thanks!
Ammar
The text was updated successfully, but these errors were encountered: