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A scalable, cost-efficient method for targeted enrichment of long fragments for third-generation sequencing
A scalable, cost-efficient method for targeted enrichment of long fragments for third-generation sequencing
AMP for Novel Fusions
AMP for Novel Fusions
VARIANTPlex Anchored Multiplex PCR Chemistry
VARIANTPlex Anchored Multiplex PCR Chemistry
Comprehensive, reliable answers for heme malignancies with customized Archer™ NGS assays webinar
Comprehensive, reliable answers for heme malignancies with customized Archer™ NGS assays webinar
Overcome challenges in cancer research with IDT’s xGen™ NGS solutions for oncology and MRD research
Overcome challenges in cancer research with IDT’s xGen™ NGS solutions for oncology and MRD research
Unlocking the potential of ultra-low frequency variant identification for cancer research
Unlocking the potential of ultra-low frequency variant identification for cancer research
ctDNA for minimal disease research by hybridization capture in resected cancer samples
ctDNA for minimal disease research by hybridization capture in resected cancer samples
The future of personalized genomics: advancing hematology research with NGS
The future of personalized genomics: advancing hematology research with NGS
Pan-cancer pharmacogenetics: Targeted sequencing panels or exome sequencing?
Pan-cancer pharmacogenetics: Targeted sequencing panels or exome sequencing?
The power of whole exome sequencing to unravel the cause of rare disease
The power of whole exome sequencing to unravel the cause of rare disease
Whole exome sequencing reveals timing and origins of local and distant metastasis in lung cancer
Whole exome sequencing reveals timing and origins of local and distant metastasis in lung cancer
M2GEN’s ORIEN Avatar program accelerates oncology research with a custom xGen Exome Research Panel
M2GEN’s ORIEN Avatar program accelerates oncology research with a custom xGen Exome Research Panel
The history & future of whole exome sequencing at the McDonnell Genome Institute
The history & future of whole exome sequencing at the McDonnell Genome Institute
Overcome cancer research challenges with NGS solutions
Overcome cancer research challenges with NGS solutions
Building one of the nation’s leading COVID-19 surveillance programs
Building one of the nation’s leading COVID-19 surveillance programs
Tackling infectious disease surveillance challenges
Tackling infectious disease surveillance challenges
Comprehensive methylation profiling from low-input samples using the xGen™ Methyl-Seq workflow
Comprehensive methylation profiling from low-input samples using the xGen™ Methyl-Seq workflow
xGen™ NGSꟷmade for virology research.
xGen™ NGSꟷmade for virology research.
Bundled solutions for your research
Bundled solutions for your research
IDT's Virtual Summit | Past, Present, and Future of Whole Exome Sequencing
IDT's Virtual Summit | Past, Present, and Future of Whole Exome Sequencing
Enhanced hybridization capture with the improved xGen™ Custom Hyb Panels design process
Enhanced hybridization capture with the improved xGen™ Custom Hyb Panels design process
Don’t Worry, Bead Happy: Essential Knowledge for Microparticle Use in DNA and RNA Analysis
Don’t Worry, Bead Happy: Essential Knowledge for Microparticle Use in DNA and RNA Analysis
Best practices for data analysis when using UMI adapters to improve variant detection
Best practices for data analysis when using UMI adapters to improve variant detection
Dual index adapters with UMIs resolve index hopping and increase sensitivity of variant detection
Dual index adapters with UMIs resolve index hopping and increase sensitivity of variant detection
Unique, dual-matched adapters mitigate index hopping between NGS samples
Unique, dual-matched adapters mitigate index hopping between NGS samples
rhAmpSeq™ Design Tool tutorial
rhAmpSeq™ Design Tool tutorial