(cache)Overview - Xbio 2.0

Project information

Project Code

F25A420000338_PHYrijoR

Species

Physcomitrium_patens

Sample Size

sample_num：9

Average Data Size

data_base：6.64G

Average Genome Mapping Rate

genome_rate：98.05%

Expressed Transcript Number

transcript_num：24,197

Platform Advantage

Using sequencers and cloud computing platforms with independent intellectual property rights, we provide scientific researchers with highly accurate, most cost-effective genome sequencing services and one-stop scientific research solutions, supporting large-scale cohort research and helping precision medicine.

Using sequencers and cloud computing platforms with independent intellectual property rights, we provide high-accuracy, most cost-effective genome sequencing services and one-stop scientific research solutions for scientific researchers, support large-scale cohort research, and help precision Medicine, the most cost-effective genome sequencing service

Stable output of high-quality sequencing data

Statistical analysis of 1000+ randomly selected lane DNBSEQ platform WGS data quality values, the average value of Raw data Q20 offline is 96.16%, and the average value of Raw data Q30 is 87.86%.

Low duplicates, more effective data and higher coverage

Duplicates are low, use less data to get more high-accuracy and high-coverage comparison data, you can find more mutation sites, help to mine low-frequency and rare mutations of diseases, and obtain More comprehensive genome mutation information

The detection rate of rare mutations and the consistent rate of microarray typing are high

The evaluation of the mutation results of the DNBSEQ platform and the Illumina Human Omni genotyping chip shows that the detection rate of rare mutations is high, and the detected rare mutations are highly consistent with the chip typing results.

Meet the needs of multiple sample types

DNBSEQ platform data source samples are diverse, including formalin-fixed paraffin-embedded samples, single-cell samples, blood samples, genomic DNA samples, saliva samples, fresh tissue samples conventionally cryopreserved, etc. Conventional The sequencing success rate of gene library construction is 99%. For degraded samples such as FFPE, the sequencing success rate of library construction is also over 90%.