The KAPA UDI connector has superior sequencing quality -- the KAPA independent double-terminal labeled connecto
The generation of KAPA independent double- ended labeling connector is derived from solving the problem of mismatching connector labels of different samples when multiple mixes are carried out in high-throughput sequencing. Label mismatch will increase the noise background in the sequencing results, especially the detection of low-frequency mutations, causing great interference and reducing the reliability of the results. The risk of mismatch is mainly caused by the following reasons:
1. Index hopping/switching phenomenon occurs when the sequencer is working
2. Cross contamination between label reagents or samples
3. Template exchange, sequencing reaction error and data analysis error occurred during PCR amplification of mixed samples can be greatly reduced by improving the design and quality control of the joint sequence.
KAPA New products listed
KAPASeparate double-ended marker connector
(Unique Dual-Indexed Adapters,UDI)
With rigorous QC validation, the product offers up to 96 unique designs that effectively reduce label mismatches and meet multiple mixing requirements for a variety of high-throughput DNA and RNA sequencing applications:
High-quality, ready-to-use, full-length, double-ended marker adapters that fit all of Illumina's workflows based on connecting libraries
Unique double-ended labels, Roche's unique design, contain up to 96 non-repetitive combinations of labels to reduce the adverse effects of label mismatches
Multiple mixed-sample sequencing from low (≥2 weights) to high (up to 96 weights) is supported for various Illumina sequencers, and both Patterned and unPatterned Flow cells are supported
It can be used in combination with KAPA HyperPrep, Hyperplus and all KAPA RNA HyperPrep library preparation kits as well as with Roche targeted capture workflow
KAPA The product features
Rigorous functional verification(Based on the quality control process of real sequencing experiments and data analysis), cross-contamination between labels can be effectively blocked
Optimized sequence design,Improve the efficiency of library construction,And significantly reduced joint dimer; At the same time, ensure that different combination tags have a consistent library conversion rate
The 96 sub tag sequences are Roche's unique design can be used alone,Also available with customer existing tag sequencesThe joint application,To meet the needs of more mixed samples
KAPA UDIThe use of the connector effectively reduced the noise background caused by label mismatch during the multi-sample sequencing, and the contamination rate was reduced to less than 0.2% in the experiment as shown in the figure.
Each point in the dataset represents a library of whole human genome samples obtained using the PCR-free database construction process. These libraries were sequenced 8-fold (black dot) or 24-fold (blue dot) mixed samples on Illumina HiSeq X sequencers and calculated by the VeriFybamid process, reflecting the potential risk of cross-contamination of samples based on genotyping. In these contaminations, tag jumping was observed, and the implementation of this non-repeated double-ended labeling strategy significantly reduced the contamination rate of mismatch sequences when the original single-ended joint was replaced with the Kapa UDI joint. In the figure, the green line represents the average pollution rate, while the red line represents the statistical upper and lower limits (JMP analysis). Data provided by The Broad Institute (Cambridge, MA, USA).
Kapa connector reagent ordering information (please order both connector reagent and dilution buffer, such as UDI+ dilution buffer, or DI+ dilution buffer)
* For scientific research only, not for diagnostic purposes
Acadia No. MC-CN-00066 Valid until August 28, 2021

Contact us:Beijing Huaruikang Technology Co., Ltd
The phone:010-69738937
Email:hrky180428@163.com
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