What is it?
These are our full applications ready for use. Improvements? New Features? New Apps?
a web app for investigating potential disease-causing variants
a web app for generating list of genes based on suspected conditions and phenotypes.
an alignment data inspector tool that quickly samples bam files and visualizes a series of metrics
an variant data inspector tool that quickly samples vcf files and visualizes a series of metrics
Here are some ideas we have explored but haven't turned into full polished apps.
Clusters 1000G data based on variants while showing the region and population of origin. Also allows realtime re-analysis by changing the minor allele frequence filter threshold
Variant Caller Comparer
Real-time variant calling, comparing two callers. Also allows changing parameters and seeing how it affects results
Developed in the
Marth Lab by