Target next-generation sequencing efforts on the exonic regions of over
4, 100 medically relevant genes. Choose the optimized hybridization-based
SeqCap EZ Inherited Disease Panel to achieve highly uniform sequencing
coverage for genes classified as pathogenic from OMIM, as well as other
medically relevant content identified by scientific collaborators.
• Use a single 11. 8 Mb panel before NGS to comprehensively replace
many commonly run NGS disease research panels and PCR-based
• Eliminate or decrease the amount of Sanger sequencing necessary
for full gene coverage
• Increase lab efficiency and decrease sequencing costs with uniform
INHERITED DISEASE RESEARCH FOR THE NEXT GENERATION
Number of reads
Number of genes in panel covered 100%
at 20x depth
15M 25M 35M
e s NA12878
Demonstration of the number of coding genes that have 100% base
pair coverage at ≥ 20x depth with 15M, 25M and 35M reads.
Request a free sample today
Evaluate the SeqCap EZ Inherited Disease Panel in your lab with
a complimentary sample* of this optimized panel.
Visit go.roche.com/IDPsample to learn more or request your free
For Research Use Only. Not for use in diagnostic procedures.
*Free sample offer available only to US-based medical researchers
evaluating for commercial use.