Whole Genome Sequencing of Bacterial or Eukaryotic Single Cells

QIAseq FX Library Kit MCF
Unravel the complexity of single cells – powered by QIAseq
Somatic genome variations occur during normal development and ageing, contribute to pathogenesis and are the cause of diseases such as cancer, as well as autoimmune, brain and other disorders. Single-cell next-generation sequencing enables cell-by-cell analysis of the genomic sequence, the detection of single nucleotide variants, copy number variations and structural variants for tumor or cell profiling and cell evolution analysis. Our streamlined PCR-free workflow takes you from one single cell (mammalian cell or microbial cell) to a high-quality NGS library with exceptional fidelity and superior accuracy in about 3.5 hours. Gain meaningful biological insights from the NGS data with our bioinformatics solutions for data analysis and interpretation.
For accessible, affordable and reliable recovery of viable single cells
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Single-cell whole genome libraries with comprehensive coverage and high sequence fidelity
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用于二代测序数据的分析、对比和可视化
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适用于从人全基因组、外显子组和基因检测板二代测序研究中鉴定致病性变异
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