EasySeq™ Human DNA Sample ID Kit 96 rxn - Hereditary Cancer 

The EasySeq™ Human DNA Sample Identification Hereditary Cancer Kit is designed to safeguard sample identity and associated WES/WGS or panel sequencing data integrity within existing NGS workflows (RUO).   The kit is a multiplex NGS library preparation solution for genotyping an optimized panel of 32 exonic SNPs with a high Minor Allele Frequency (MAF) in human genes involved with hereditary cancer. This SNP profile enables verification of sequencing data integrity by matching intrinsic identifiers derived from hereditary cancer panel sequencing data, generating Illumina®-compatible libraries.   The workflow enables one-tube, single reaction NGS library preparation, combining target amplification, indexing and adapter addition in a single reaction to reduce handling steps and decrease the risk of PCR contamination and sample mix-ups. This streamlined workflow is enabled by Reverse Complement PCR technology, which supports multiplex amplification and library construction within the same reaction.   EasySeq™ Human DNA Sample Identification Hereditary Cancer Targets rs3219489 rs1799977 rs2228230 rs1801406 AMEL-X AMEL-Y rs1042522 rs799917 rs357564 rs2071313 rs1800860 rs26279 rs1800392 rs7862221 rs1126417 rs1800935 rs17807673 rs13712 rs4986764 rs13054014 rs866006 rs2736098 rs3744093 rs11528010 rs2066827 rs3852673 rs1801552 rs1126497 rs41737 rs7935 rs709816 rs8556   Compatibility • Illumina® sequencers: iSeq, MiniSeq, MiSeq, NextSeq, NovaSeq    Kit Components • EasySeq™ Human Sample ID Hereditary Cancer Probe Panel• Blood Direct HiFi Master Mix (Hot Start HiFi)• Probe Dilution Buffer Enhanced    Note: This item requires (a) dedicated Index Plate(s).Once you’ve added this RC-PCR kit to your cart, you'll be prompted to select the appropriate Unique Dual Index Primer Plate(s).   Benefits ✓ 32 exonic SNPs with a high Minor Allele Frequency (MAF)✓ Direct DNA amplification from blood samples✓ Detects sample mix-ups and pipetting errors✓ Single-tube reaction for simplified and safe workflow✓ Compatible with multiple short read sequencers