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NadPrep Library
Library Preparation
NadPrep DNA Library Preparation Module v2
New
NadPrep EZ DNA Library Preparation Kit v2
NadPrep Methyl Library Preparation Kit v2
New
NadPrep DNA Methyl Bisulfite Conversion Module
NadPrep rRNA Blocking Reagent
New
NadPrep Total RNA-To-DNA Module
NadPrep RNA & DNA Library Co-Preparation Module
New
NadPrep Universal Circularization Kit v2
NadInstrument
NadAuto-96
NadAuto-96 Automatic Sample System
NadAuto-16
NadAuto-16R Fully-automated NGS Workstation
New
μCaler (Ultra-sensitive Probes)
μCaler Hybrid System
μCaler DNA Full Screen System Comprehensive Solution
New
μCaler Total Solution for Methylation
New
μCaler Total Solution for AML
μCaler Total Solution for SARS-CoV-2
μCaler MRD Solution
μCaler Panel
μCaler EMS Panel v1.0
New
μCaler HotSpot Panel v1.0
NadHyb
NadPrep NanoBlockers(for MGI)
NadPrep NanoBlockers(for MGI)
NadPrep NanoBlockers (for Illumina)
NadPrep NanoBlockers (for Illumina®, NXT)
NadPrep NanoBlockers (for Illumina®)
Reagents
NadPrep ES Hybrid Capture Reagents
NadPrep Hybrid Capture Reagents
NadProbe
NAD Probes
XCapert Online Design Platform
Beta
NAD Probes
NadPanel (Conventional Probes)
Extended
NEXome Mini Panel v1.0
New
NEXome XP Panel v1.0
NEXome Plus Panel v1.0
NEXome Core Panel
Solid Tumor
NanOnco Plus Panel v3.0
OncoFu Elite (for RNA) Panel v1.0
HRR Panel
HiSNP-series Panel
NanOnCT Panel
LungCancer Panel
Hematologic Disorders
NanoHema Research Panel
MetaCap
NEX-t Panel v1.0
HPVisual Panel
NanoRV Panel-Tech Access
Others
HGBP Panel v1.0
HLAtyping Panel v2.0
IGTR Panel v1.0
Ext-RNA Control Panel
Solutions
AutoCap
Target Capture Solution for Pan-Cancer Solid Tumor Based on NadAuto-96 Automatic Sample System
DNA Cap
Sequencing single library on different platform--Universal Stubby Adapter (UDI)
HRD score Analysis
Unique Dual Index for MGI platforms
Total Solution for MGI Platforms
Whole Exome Sequencing
Low-frequency Mutation Analysis
RNA Cap
RNA-Cap Sequencing of Human Respiratory Viruses Including SARS-CoV-2
Total Solution for RNA-Cap Sequencing
MethylCap
Methyl Library Preparation Total Solution
Customization
Probe Design
Wet Labs
FAQs
Product Sheet
Product Catalog
Poster
Technical Note
Bed File
Demo Data
Application Note
DNACap
RNACap
MethylCap
COA
MSDS
Universal module
Library Preparation (for MGI)
Library Preparation (for Illumina®)
Hybridization Reagents
Panel
μCaler
Video
NadPrep Library
NadInstrument
μCaler (Ultra-sensitive Probes)
NadHyb
NadPanel (Conventional Probes)
NadProbe
Solutions
AutoCap
Target Capture Solution for Pan-Cancer Solid Tumor Based on NadAuto-96 Automatic Sample System
DNA Cap
Sequencing single library on different platform--Universal Stubby Adapter (UDI)
HRD score Analysis
Unique Dual Index for MGI platforms
Total Solution for MGI Platforms
Whole Exome Sequencing
Low-frequency Mutation Analysis
RNA Cap
RNA-Cap Sequencing of Human Respiratory Viruses Including SARS-CoV-2
Total Solution for RNA-Cap Sequencing
MethylCap
Methyl Library Preparation Total Solution
Customization
Probe Design
Wet Labs
FAQs
Sequencing single library on different platform--Universal Stubby Adapter (UDI)
2022-03-02
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HRD score Analysis
Homologous recombination repair (HRR) is an important pathway for normal cells to repair DNA damage. The loss-of-function variants in BRCA1/B...
2021-06-18
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Unique Dual Index for MGI platforms
Recently, MDI adapters have been expanded to 768 varieties!
2021-06-15
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RNA-Cap Sequencing of Human Respiratory Viruses Including SARS-CoV-2
Nanodigmbio provides a reliable solution for RNA-Cap Sequencing of RNA viruses such as SARS-CoV-2.
2021-01-28
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Total Solution for RNA-Cap Sequencing
Nanodigmbio Technology provides a total solution for RNA-Cap sequencing on both MGI platforms and Illumina® platforms.
2021-01-07
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Total Solution for MGI Platforms
Nanodigmbio provides NGS total solution on MGI platforms, including library preparation and hybridization capture.
2019-11-01
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Whole Exome Sequencing
WES provides insight into multiple variants, including single nucleotide variants (SNVs), insertions and deletions (Indels) and copy number variants var...
2019-10-14
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Low-frequency Mutation Analysis
Next generation sequencing (NGS) has enabled assessment of variants in numerous genes in a single assay. However, when it comes to low-frequency vari...
2019-09-30
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