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Combine NGS power with PCR simplicity for your next amplicon sequencing project
Lotus™ DNA Library Prep Kit: A single flexible workflow with endless applications
Precise genome editing with A.s. Cas12a (Cpf1) Ultra: A mutant protein with the reliability of S.p. Cas9
A CRISPR Q&A with our experts: You ask, we answer
Design considerations for qPCR assays
Increasing genome editing efficiency and specificity with optimized CRISPR-Cas9 guide RNAs
Overcoming the challenges of CRISPR guide RNA design
Best practices for data analysis when using UMI adapters to improve variant detection
Tips for working with gBlocks Gene Fragments
The quest for high confidence mutations in plasma: searching for a needle in a haystack
SNP genotyping on qPCR platforms: Troubleshooting for amplification and cluster separation
Optimized methods for using Cas9 nickases in genome editing
Dual index adapters with UMIs resolve index hopping and increase sensitivity of variant detection
Characterizing Alzheimer's disease candidate genes and transcripts with targeted, long-read, single-molecule sequencing
rhAmp™ SNP genotyping: A novel approach for improving PCR-based SNP genotyping
Unique, dual-matched adapters mitigate index hopping between NGS samples
Ordering rhAmp™ SNP Assays and ADME SNP Assays in plates
Target capture of DNA from FFPE samples–recommendations for generating robust sequencing data
High efficiency qPCR with PrimeTime™ Gene Expression Master Mix
Tips for effective use of BLAST and other NCBI tools
High-throughput qPCR: Tips for analysis across multiple plates
gBlocks Gene Fragments Design Tool—highlighting complexities (2017)
Building an NGS-based platform for clinical cancer care
IDT Codon Optimization Tool Tutorial
IDT Codon Optimization Tool
rhAmpSeq™ Design Tool tutorial
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