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For analyzing, comparing, and visualizing next-generation sequencing data
For identifying disease-causing variants from human whole genome, exome, and gene panel next-generation sequencing studies
For basic analysis of NGS data using the GeneRead DNAseq panels V2; acceptable file formats include FASTQ or BAM
EpiTect Methyl II 96-Well Complete Data Analysis Spreadsheet
EpiTect Methyl II 384-Well Complete Data Analysis Spreadsheet
EpiTect Methyl II qPCR Primers Data Analysis Spreadsheet
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