NEXome Mini Panel focuses on the exome associated with clinical inherited diseases,
with probe coverage spanning a 16.1 Mb genomic region involving 5650 clinically
significant genes and encompassing over 4000 genetic disorders. In comparison
to the whole exome panel, the NEXome Mini Panel can be used to rapidly and
efficiently detect pathogenic genetic variations within target genes in the
human genome. This not only reduces sequencing costs but also significantly
shortens data analysis time.
Capture Performance
Figure 1. Capture performance of NEXome mini Panel v1.0. Cell Line gDNA Standard (Coriell, NA12878) were used to prepare library with the NadPrep DNA Library Preparation Kit (for Illumina®). NEXome Mini Panel v1.0 were used to complete hybridization capture. The BWA was used for alignment of raw reads to the reference genome (hg38). A. Mappability, On-target rate, and target coverage; B. GC Bias.
Note: Sequencing platform: Illumina Novaseq 6000,PE150.
High Confidence Variant Calls
Figure 2. Sensitivity and positive predictive value (PPV) of NEXome Mini Panel for NA12878 mutation identification.
More Efficient and Cost-effective
Figure 3. The NEXome Mini Panel reduces sequencing raw data to minimize costs. A. Minimum amount of raw data required for the NEXome Mini Panel and NEXome Core Panel to achieve a specific depth; B. Coverage region and relationship between the NEXome Mini Panel and NEXome Core Panel.
Catalog# |
Color of Tube Cap |
Product |
Volume |
Package/Storage |
1001881 |
|
NEXome Mini Panel v1.0, 96 rxn |
415 μL |
-25 ~ -15℃ |
1001882 |
|
NEXome MIni Panel v1.0, 16 rxn |
70 μL |
-25 ~ -15℃ |
Product | Catalog# |
NEXome Mini Panel v1.0, 16 rxn | 1001882 |
NEXome Mini Panel v1.0, 96 rxn | 1001881 |
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