VSClinical
VSClinical streamlines genomics data analysis by guiding users through the American College of Medical Genetics (ACMG) guidelines for variant classification. Its tailored workflow facilitates efficient scoring of variants, integrating bioinformatic evidence and clinical literature, while minimizing subjectivity. This software is essential for accurately diagnosing inherited diseases and cancer predispositions.
Top VSClinical Alternatives
VarSeq
VarSeq is an integrated genomics data analysis software designed for researchers needing efficient tertiary analysis of gene panels, exomes, and whole genomes.
CZ CELLxGENE Discover
CZ CELLxGENE Discover revolutionizes spatial transcriptomics analysis by enabling visualization of datasets through the Visium and Slide-seqV2 assays.
GenomeBrowse
GenomeBrowse is a powerful genomics data analysis software that offers exceptional visualizations of genomic data at the base pair level.
Cufflinks
Cufflinks assembles RNA-Seq transcripts, estimates their relative abundances, and tests for differential expression in aligned samples.
SnapGene
SnapGene revolutionizes molecular biology with its intuitive interface, enabling scientists to visualize and design cloning procedures effortlessly.
Parse Biosciences Evercode
Parse Biosciences Evercode revolutionizes single-cell research by enabling the profiling of up to 5 million cells in a single experiment without specialized instruments.
MEGA
The integration with DrPhylo streamlines fragile species relationship analysis, while an intuitive Tree Explorer toolbar...
BioTuring Browser
It enables users to import diverse data types, perform cell type prediction, and execute custom...
Galaxy
It facilitates analysis of deep sequencing data, phylogenetic tree construction, and gene essentiality score estimation...
ROSALIND
It offers instant results, extensive collaboration features, and rich visualizations that enhance data interpretation...
GeoMx Digital Spatial Profiler (DSP)
This advanced platform allows for precise profiling of distinct tissue compartments and cell populations, integrating...
Microsoft Genomics
With ISO and HIPAA compliance, users benefit from a scalable, secure infrastructure, paying only for...
Loupe Browser
With the ability to convert Seurat objects into Loupe files via the LoupeR package, users...
Alissa Interpret
It enhances productivity by streamlining CGH and NGS tertiary analysis, supporting various variant types...
Bioconductor
With over 2,000 R packages and robust support resources, it enhances bioinformatics workflows through annual...
Top VSClinical Features
- ACMG guideline adherence
- Auto-computed variant classification
- Guided workflow for consistency
- Integration with clinical knowledgebases
- Historical context for classifications
- Support for AMP guidelines
- Monthly curated cancer trial updates
- Germline variant interpretation catalog
- Somatic auto-classifier for oncogenic potential
- Customizable reporting templates
- Comprehensive annotation sources
- Variant scientist training resources
- Cloud deployment flexibility
- Minimal internet connectivity requirements
- Rapid processing of novel variants
- Automated re-evaluation flagging
- Standardized scoring questions
- Efficient rare disease diagnosis
- Integration with additional products
- Support for CNV analysis
