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©The Author(s) 2025.
World J Gastrointest Oncol. Jun 15, 2025; 17(6): 107382
Published online Jun 15, 2025. doi: 10.4251/wjgo.v17.i6.107382
Published online Jun 15, 2025. doi: 10.4251/wjgo.v17.i6.107382
Table 1 Comparison of performance and application of common single-cell sequencing platforms
Platform | Technical features | Data quality | Application scenarios | Comparative advantage |
10× genomics | A system based on liquid droplets | High | High-throughput sequencing of cells | High-throughput, easy to operate, and large-scale cell atlas construction |
BD rhapsody | A technology based on micropores | Medium | High unique molecular identifier detection sensitivity | Using imaging systems, populations with lower cell viability can be detected |
Fluidigm C1 | Isolation of single cells in a size and shape-dependent manner based on an automated microfluidic platform | High | High gene detection rate (> 10000) | Single-cell full-length transcripts were analyzed and complete cDNA libraries were prepared |
ICELL8 | Nanopore-based cell trapping and relying on cell and transcript specific barcodes to obtain individual cell transcript counts | High | High-throughput single-cell RNA sequencing | Ease of use and fast turnaround time allow experiments on a variety of biological samples |
Illumina | Sequencing was performed based on the captured mtDNA | Medium | High-throughput sequencing of single cells | High throughput and high precision |
- Citation: Zhang Z, Wang HM, Xu ZX, Luan WY, Lin SX, Miao YD. Application of single-cell sequencing in the study of immune cell infiltration in inflammatory bowel disease and colorectal cancer. World J Gastrointest Oncol 2025; 17(6): 107382
- URL: https://www.wjgnet.com/1948-5204/full/v17/i6/107382.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v17.i6.107382