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Beijing Annoroad Medical Inspection Laboratory
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Fertility Reproduction
Non-invasive Prenatal DNA Screening
Non-invasive Prenatal Screening Version 1.0
Non-invasive Prenatal Screening Version 2.0
Copy Number Variation Sequencing
[Kaiyun’an] Carrier Screening for Monogenic Disease
Whole Exome Sequencing for Genetic Disease
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Gene Detection for Hematonosis
Gene Detection for Lung Cancer
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Gene Detection for Colorectal Cancer
Gene Detection for Pan-cancer
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PRODUCTS & SERVICES
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PRODUCTS & SERVICES
Fertility Reproduction
Cancer Treatment
Scientific Research Services
PRODUCTS & SERVICES
LncRNA Sequencing
Whole Transcriptome Sequencing
Hi-C sequencing
10x Genomics Single-cell Immunolibrary Sequencing
10x Genomics Single-cell Transcriptome Sequencing
10x Genomics Visium Spatial Transcriptome Sequencing
Single-cell Transcriptome Sequencing
10x Genomics ATAC Sequencing
Full-length Transcriptome Sequencing
Third-generation Metagenomic Sequencing
Third-generation Animal and Plant De Novo Sequencing
Non-invasive Prenatal DNA Testing
a non-invasive, convenient, accurate, and rapid technology for detecting fetal chromosome abnormalities, such as trisomy 21 (Down's syndrome), trisomy 18 (Edward's syndrome) and trisomy 13 (Patau's syndrome).
Non-invasive Prenatal Testing Version 1.0
[Kaiyun’an] Carrier Screening for Monogenic Disease
Whole Exome Sequencing for Genetic Disease
Gene Detection for Lung Cancer
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LncRNA Sequencing
Whole Transcriptome Sequencing
Hi-C sequencing
10x Genomics Single-cell Immunolibrary Sequencing
10x Genomics Single-cell Transcriptome Sequencing
10x Genomics Visium Spatial Transcriptome Sequencing
Single-cell Transcriptome Sequencing
10x Genomics ATAC Sequencing
Full-length Transcriptome Sequencing
Third-generation Metagenomic Sequencing
Third-generation Animal and Plant De Novo Sequencing
Non-invasive Prenatal DNA Testing
a non-invasive, convenient, accurate, and rapid technology for detecting fetal chromosome abnormalities, such as trisomy 21 (Down's syndrome), trisomy 18 (Edward's syndrome) and trisomy 13 (Patau's syndrome).
Non-invasive Prenatal Testing Version 1.0
[Kaiyun’an] Carrier Screening for Monogenic Disease
Whole Exome Sequencing for Genetic Disease
Gene Detection for Lung Cancer
1
2
3
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尊龙凯时
