All steps of NGS library prep, including sample DNA Amplification, Fragmentation, and Tagging, are integrated into a single isothermal AFT™  step. As little as 6.6 pg of genomic DNA is sufficient for a perfect whole genome sequencing library. 

         AFT™ technology tolerates inhibitory impurities from raw samples, enables library preparation directly from 0.1 μL of whole blood and environmental microbe pellet.

         Significantly, group of AFT™ amplicons share a common pair-end read, resulting from running-off  amplification of a common mother amplicon, providing a native barcode to link all the daughter amplicons. The unique feature of linked reads facilitates the long scaffolding, de novo assembly, and haploid phasing.

         We invite you for a try of the Whole-Genome, Single-Cell, Raw Blood WGS, and Raw Sample Metagenomics AFT™  Linked-Reads Library Prep kit, free of shipping.

AFT(TM) Linked-Reads Whole-Genome Library Prep Kit

AFT™ Linked-Reads Whole-Genome Library Preparation Kit

AFT(TM) Linked-Reads Single-Cell Whole-Genome Library Preparation Kit

AFT™ Linked-Reads Single-Cell Whole-Genome Library Preparation Kit

AFT(TM) Linked-Reads Single-Cell Whole-Genome Library Preparation Kit

AFT™ Linked-Reads Raw Blood WGS Library Preparation Kit

AFT(TM) Linked-Reads Single-Cell Whole-Genome Library Preparation Kit

AFT™ Linked-Reads Raw Sample Metagenomics Library Preparation Kit