For Research Use Only. Not for use in diagnostic procedures. Others KAPA HyperExome V2 Probes RUO KAPA HyperExome V2 Probes PID00000515 09 718 630 001 9 718 630 001 09718630001 9718630001 09718630001 KAPA HyperExome V2 Probes, 12 rxn KAPA HyperExome V2 Probes, 12 rxn 07613336215968 Reagents, kits 12 reactions Not Available 09 718 664 001 9 718 664 001 09718664001 9718664001 09718664001 KAPA HyperExome V2 Probes, 96 rxn KAPA HyperExome V2 Probes, 96 rxn 07613336215999 Reagents, kits 96 reactions Not Available 09 718 656 001 9 718 656 001 09718656001 9718656001 09718656001 KAPA HyperExome V2 Probes, 48 rxn KAPA HyperExome V2 Probes, 48 rxn 07613336215982 Reagents, kits 48 reactions Not Available 09 718 699 001 9 718 699 001 09718699001 9718699001 09718699001 KAPA HyperExome V2 Probes, 384 rxn KAPA HyperExome V2 Probes, 384 rxn 07613336216019 Reagents, kits 384 reactions Not Available 09 718 648 001 9 718 648 001 09718648001 9718648001 09718648001 KAPA HyperExome V2 Probes, 24 rxn KAPA HyperExome V2 Probes, 24 rxn 07613336215975 Reagents, kits 24 reactions Not Available 09 718 672 001 9 718 672 001 09718672001 9718672001 09718672001 KAPA HyperExome V2 Probes, 192 rxn KAPA HyperExome V2 Probes, 192 rxn 07613336216002 Reagents, kits 192 reactions Not Available Superior uniformity and low duplication Reduced sequencing costs Renowned probe design and selection algorithm Achieve broad database coverage in an efficient compact design More uniform coverage across the GC % range Confidence in variants calling High precision (99.49%) and recall (98.95%) for SNP detection Intrinsically targeted sample tracking SNPs eliminate the need to spike-in external controls Optimized with the KAPA HyperCap Workflow v3.4 Streamlined and easily automatable enables high sample throughput en The KAPA HyperExome V2 Probes deliver exceptional coverage of the recent versions of ACMGv3.1, RefSeq (June 29, 2022), CCDS, ClinVar (June 29, 2022), Ensembl v106 and COSMIC genomic databases across 20626 genes within a compact capture target of 43.2 Mb and with low sequencing requirements. The new T2T (telomere-to-telomere) genome assembly was utilized as part of the design process to identify potentially problematic regions not apparent in the GRCh38 genome assembly. The number of sample tracking SNPs has increased to 529. en

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