Golden Helix SNP & Variation Suite 7 is offered in several different packages with annual subscription pricing. To request pricing, please complete our Pricing Request Form.
| SVS Viewer | SVS Core Plus | SNP Analysis Package | DNA-Seq Analysis Package | CNV Analysis Package | RNA-Seq Analysis Package | Power Seat | PBAT Analysis |
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| View SVS projects, spreadsheets, and plots | ![]() |
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| Data import/export (70+ file formats) | ![]() |
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| Spreadsheet editor | ![]() |
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| Python scripting | ![]() |
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| Spreadsheet manipulation (subset, merge, append, etc.) | ![]() |
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| General data filtering | ![]() |
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| Column and row statistics | ![]() |
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| General plotting (heat maps, scatter plots, box plots, etc.) | ![]() |
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| Create and merge marker maps, genomes, and annotations | ![]() |
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| Genome browser | ![]() |
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| Numeric regression analysis | ![]() |
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| Numeric PCA analysis | ![]() |
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| Numeric association testing | ![]() |
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| Genotype statistics and filtering (call rate, HWE, MAF, etc.) | ![]() |
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| Genotype data manipulation (recoding, strand flipping, biallelic expansion, etc.) | ![]() |
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| Genotype quality assurance (IBD, autosome heterozygosity, Mendelian error checking, LD pruning, etc.) | ![]() |
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| Genotype principal component analysis | ![]() |
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| Genotype association testing | ![]() |
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| LD and haplotype analysis | ![]() |
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| Runs of homozygosity analysis | ![]() |
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| Filter by Polyphen and SIFT Score | ![]() |
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| Collapsing and association methods | ![]() |
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| Variant binning | ![]() |
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| Variant classification | ![]() |
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| Detect compound heterozygous inheritance | ![]() |
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| Scoring of recessively inherited variants | ![]() |
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| CNV quality assurance (wave detection/correction, DLRS, winsorizing, etc.) | ![]() |
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| CNV optimal segmenting (univariate and multivariate) | ![]() |
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| CNV discretization | ![]() |
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| GPU acceleration for CNV segmentation | ![]() |
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| DE-Seq | ![]() |
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| Pre-study power calculations | ![]() |
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| PBAT family-based QA | ![]() |
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| PBAT genotype analysis | ![]() |
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| PBAT CNV analysis | ![]() |
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