Training materials
6675 materials found
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Identification of somatic and germline variants from tumor and normal sample pairs
human-genetics-cancer
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Calling variants in diploid systems
introduction
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Somatic Variant Discovery from WES Data Using Control-FREEC
human-genetics-cancer
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Calling variants in non-diploid systems
introduction microgalaxy prokaryote
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Exome sequencing data analysis for diagnosing a genetic disease
human-genetics-cancer
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Deciphering Virus Populations - Single Nucleotide Variants (SNVs) and Specificities in Baculovirus Isolates
one-health
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Querying the University of Bradford GDC Beacon Database for Copy Number Variants (CNVs)
data-management
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Working with Beacon V2: A Comprehensive Guide to Creating, Uploading, and Searching for Variants with Beacons
data-management
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Visualisation with Circos
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Ploting a Microbial Genome with Circos