Presented March 23, 2016. This webinar is for those who have experience with RNA-Seq analysis, variant calling or metagenomic data and want to work with large genomic datasets, use cloud computing for analyzing genomic datasets and perform parallel work on genomic datasets. You will learn how to call variants from SRA and dbGaP with GATK, realign reads with HISAT2, view expression levels and variants, search SRA data rapidly, integrate with Spark and mount dbGaP to an EBS volume.
Get video updates, subscribe to the NCBI YouTube channel:
www.youtube.com/ncbinlm
Find other NCBI webinars:
www.ncbi.nlm.nih.gov/home/coursesandwebi
Related Posts
Presented March 23, 2016. This webinar is for those who have experience with RNA-Seq analysis, variant calling or metagenomic data and want to work with large genomic datasets, use cloud computing for analyzing genomic datasets and perform parallel work on genomic datasets. You will learn how to call variants from SRA and dbGaP with GATK, realign reads with HISAT2, view expression levels and variants, search SRA data rapidly, integrate with Spark and mount dbGaP to an EBS volume.
Get video updates, subscribe to the NCBI YouTube channel:
www.youtube.com/ncbinlm
Find other NCBI webinars:
www.ncbi.nlm.nih.gov/home/coursesandwebi
Related Posts
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