This is just a question about how to use the new version of vast-tools/3.1.0 to analyze zebrafish RNA-seq data. I used the original version of vast-tools to analyze human data by calling:
vast-tools align file_1.fastq.gz file_2.fastq.gz --sp Hsa -c 32 --expr
There are three options for --sp Hsa/Mmu/Gga
I downloaded the new version of vast-tools which supports the analysis of zebrafish and sea urchin RNA-seq data. But there are still the original three options for --sp.
I am wondering if there is any other way to write this command for analysis of zebrafish data?
Hi there,
This is just a question about how to use the new version of vast-tools/3.1.0 to analyze zebrafish RNA-seq data. I used the original version of vast-tools to analyze human data by calling: vast-tools align file_1.fastq.gz file_2.fastq.gz --sp Hsa -c 32 --expr There are three options for --sp Hsa/Mmu/Gga I downloaded the new version of vast-tools which supports the analysis of zebrafish and sea urchin RNA-seq data. But there are still the original three options for --sp. I am wondering if there is any other way to write this command for analysis of zebrafish data?
Many thanks!