Interested to know how NGS can benefit yur research? Join us on 7th July attend our one day seminar with talks from researchers who have used NGS. Partek Incorporated will also conduct a hands on session on 8th July (limited to 15 participants). Contact us for further details. Online registration link below.
Join our 2 day course to learn the practical aspects of running a NGS bioinformatics experiment. We will proceed with the class when numbers are sufficient.
All in One solution
for Whole Human Exome Sequencing
*Whole Human Exome Analysis by SOLiD 3plus system
*50bp/fragment run
*Approximately 2GB of Data (recommended throughput)
*Includes library construction
*Includes all reagent and Aglient Sure Select Kits necessary
*Bioinformatics: alignment files and list of called SNPs
*30 days free trial and support of Nextgene Bioinformatics software
*Price per Sample: $11,777.00
Multiple Pathogens/bacterial targeted re-sequencing by SOLiD 3-plus system
*50bp/fragment run
*Multiplexing bar-coding of samples
*Includes library construction
*Includes necessary reagents, consumables and kits
*Includes all reagent and Aglient Sure Select Kits necessary
*Includes bioinformatics: alignment files and list of called SNPs
*30 days free trial and support of Nextgene Bioinformatics software
*Throughput: 500MB
*Price: $4,950.00
Serial Analysis of Gene Expression (SAGE) *35bp/run
*35bp/run
*Multiplexing of samples
*Includes library construction
*Includes necessary reagents, consumables and kits
*Primary Analysis for Bioinformatics
*Throughput: 500MB
*Price: $6,000.00