2/8 Our colleague @markusriester developed & validated PureCN for allele-specific copy number analysis of clinical whole-exome sequencing at Novartis and published the software in @Bioconductor, but it needed public validation. https://t.co/hvwGVDuXBw
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RT @ExomeAnalysis: PureCN: copy number calling and SNV classification using targeted short read sequencing https://t.co/0Ox5OCqTzv #scfbm h…
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RT @ExomeAnalysis: PureCN: copy number calling and SNV classification using targeted short read sequencing https://t.co/0Ox5OCqTzv #scfbm h…
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RT @ExomeAnalysis: PureCN: copy number calling and SNV classification using targeted short read sequencing https://t.co/0Ox5OCqTzv #scfbm h…