DNA 염기서열 분석
낮은 빈도의 변이체 확실하게 검출
디지털 DNA 염기서열 분석(DNA-seq) 응용 분야에서 신뢰할 수 있는 결과를 얻기 위해서는 균일한 적용 범위와 분석에서 발생하는 방대한 양의 데이터와 다양한 변형을 처리할 수 있는 능력이 필요합니다. 이러한 과제를 해결하려면 염기서열 분석과 생물정보학 인프라 및 역량에 대한 과감한 투자가 필요합니다. 또한 대체 방식(전체 엑솜, 표적 패널)과 비교하여 얻은 실행 가능한 데이터는 비용 증가를 정당화하기에 충분하지 않을 수 있습니다.
표적 디지털 DNA 염기서열 분석을 위한 당사의 전용 DNA 염기서열 분석 키트를 사용하면 빈도가 낮은 변이체를 확실하게 검출할 수 있습니다. 통합 표적 DNA 및 RNA 염기서열 분석의 경우, 워크플로우를 간소화하고 DNA 변이체, RNA 융합 및 유전자 발현 수준의 농축 및 프로파일링을 가능하게 하는 다중 모드 제품을 제공합니다.
검색 DNA 염기서열 분석
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QIAseq xHYB CGP Panels
For comprehensive genomic profiling of DNA and RNA variants from a single nucleic acid sample
QIAseq Targeted DNA Pro Panels
For unprecedented ease-of-use and biological insights using targeted DNA sequencing
QIAseq Targeted DNA Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq Targeted DNA Pro Custom Panels
For unprecedented ease-of-use and biological insights using targeted DNA sequencing.
QIAseq Targeted DNA Custom Panels
用于在NGS实验前，对与某一通路相关的基因进行靶向扩增
REPLI-g Single Cell Kit
For highly uniform whole genome amplification (WGA) from single cells or limited sample material
QIAseq Index Kits
Indices for QIAseq Targeted NGS now available in unique dual bar-coded format
QIAseq FX DNA Library Kit
For all-enzymatic whole genome and hybrid capture library preparation for Illumina instruments with minimal bias
QIAseq Multimodal Custom Panels
A single day sample to sequencing workflow for simultaneous enrichment and profiling of DNA variants, RNA fusions and gene expression levels from one sample input, as low as 10 ng
REPLI-G Kits
For highly uniform whole genome amplification from 10ng of genomic DNA
QIAseq Human Exome Kits
Reduce exome sequencing costs by up to 50%, improve scalability with a single-day, automation-compatible sample to sequencing workflow and accelerate time to insights
QIAseq 1-Step Amplicon Library Kit
For fast and efficient preparation of DNA libraries for use in NGS applications
QIAseq Ultralow Input Library Kit
Highly flexible DNA library preparation for sequencing with Illumina instruments
REPLI-g Cell WGA & WTA Kit
For parallel whole genome and whole transcriptome amplification from cells and limited samples
QIAseq Targeted DNA Booster Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq FX Single Cell DNA Library Kit
Single-cell whole genome libraries with comprehensive coverage and high sequence fidelity
REPLI-g FFPE Kit
Formalin-fixed, paraffin-embedded (FFPE) tissue로 부터 얻어진 DNA를 이용하여 곧바로 whole genome amplification할 수 있습니다
REPLI-g Mitochondrial DNA Kit
Total DNA샘플에 포함된 human mitochondrial DNA로 부터 신뢰성있는 whole genome amplification이 가능합니다
QIAseq Targeted DNA Extended Panels
Digital DNA sequencing to confidently detect low-frequency variants
QIAseq Multimodal Pan-Cancer Panel
The only one-day, low-input sample to sequencing workflow for simultaneous and comprehensive genomic profiling of DNA variants, RNA fusions and assessing TMB/MSI in solid tumors and heme malignancies
QIAseq Targeted Methyl Custom Panels
A liquid biopsy-compatible solution for targeting methylation status of DNA, from as low as 1 ng input DNA from cells and tissues, or 10 ng from FFPE samples and liquid biopsies
QIAseq Targeted Methyl Panels
A liquid biopsy-compatible solution for targeting methylation status of DNA, from as low as 1 ng input DNA from cells and tissues, or 10 ng from FFPE samples and liquid biopsies
QIAseq Single Cell DNA Library Kits UDI
For PCR-free, single-cell whole genome libraries with comprehensive coverage and high sequence fidelity
QIAseq xHYB Human Hybrid Capture Panels
Curated genome-wide content for a single-day, automation-compatible sample to sequencing workflow that accelerates time to insights
QIAseq xHYB Custom Human Panels
Customizable genome-wide content for a single-day, automation-compatible sample-to-sequencing workflow that accelerates time to insights
QIAseq UPX Single Cell DNA Lib Kit
For ultraplex pooling of Repli-g amplified samples starting from 1 cell or 1 ng of total DNA
QIAseq Targeted cfDNA Ultra Panels
For ultrasensitive targeted next-generation sequencing of cfDNA on Illumina platforms
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