Post_Trial#3 » Geneyx

Geneyx Genomex Ltd

Organization name:

Country/Region

Full name and position

Date

Tel

The start date of the trial period:

How many files did you upload ?

Did you analyze the files independently, or did you receive support from Geneyx or PacBio?

Did you upload any short reads files? If yes, how many and what type (Exome, whole genome, panel)?

Did you upload single files or batch?

How many files have you successfully analyzed and resolved?

Did you attempt to analyze non-solved short reads using LRT (Local Realignment Tool)?

Did you perform smart filtering?

Did you follow your own protocols?

Are you working on-premises or on a cloud-based system? Which platform specifically?

For Phenotype-Driven Variant Prioritization, did you use:

free-text HPO (Human Phenotype Ontology)

Is your lab CLIA/CAP accredited?

On a scale of 1 to 10, how would you rate the support you received during the trial period? (10=excellent)

Do you plan to start using the 'Geneyx Analysis' platform?

When do you expect to start?

Do you have any special requirements regarding data privacy and security?

Do you anticipate an increase in sample sequencing? If yes, could you estimate the percentage increase?

Please feel free to provide any additional comments or feedback regarding your trial period experience.