Training materials
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De novo transcriptome reconstruction with RNA-Seq
introduction
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Introduction to Variant analysis
introduction
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Calling very rare variants
introduction
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Mapping and molecular identification of phenotype-causing mutations
model-organisms
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Trio Analysis using Synthetic Datasets from RD-Connect GPAP
cyoa human-genetics-cancer
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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