Apps tagged with 'Genomics'

VE3 Genomix is the platform purpose-built to unify NHS-grade clinical genomics, flexible bioinformatics research, and AI-powered analysis. All delivered through a flexible, compliant, and scalable cloud architecture.

Pathomx is a workflow-based tool for the analysis and visualisation of experimental data. Initially created as a tool for metabolomic data analysis is has been extended and can now be used for any scientific and non-scientific data analysis.

Aimosti re-analyses the raw DNA file you already have (23andMe, AncestryDNA, MyHeritage, or whole-genome sequencing) into a report on medication response, carrier status, health, traits, and ancestry.

QIAGEN CLC Main Workbench is ideal for DNA, RNA, & protein sequence data analysis with a wide variety of features, no advanced computer skills required! The workbench is available for Windows, Mac OS X, and Linux platforms.

Folklore is Helena Bioinformatics' clinical variant interpretation platform for supported GRCh38 germline SNVs and simple indels. It combines variant resolution, annotation, automated ACMG/AMP classification, evidence, phenotype context, prioritisation and source-linked...

The DNASTAR Lasergene package is the most robust of our software offerings, and includes all of the applications from our genomics, structural biology, molecular biology, and cloning suites.

GeneStudio Pro is a modern suite of molecular biology applications for the Windows platform built on our sequence format conversion engine, SeqVerter. All manipulations with sequences of different formats are thus seamless and transparent for the user.

DecodeMyBio is a web-based pharmacogenomics tool that interprets the raw genotyping files exported from consumer DNA tests (23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, Living DNA). It reports how a user's genetic variants relate to medication response, drawing on CPIC...

Complete bioinformatics toolkit for a wide range of genomics analysis needs, including transcriptomics, variant calling, epigenomics, metagenomics, comparative genomics and many more.

Reads your existing 23andMe, AncestryDNA or MyHeritage raw DNA file into reports on traits, medication response and carrier status.