Comparing 10x Genomics single-cell 3' and 5' assay in short-and long-read sequencing

Hsu, J.; Jarroux, J.; Joglekar, A.; Romero, J. P.; Nemec, C.; Reyes, D.; Royall, A.; He, Y.; Belchikov, N.; Leo, K.; Taylor, S. E. B.; Tilgner, H. U.

doi:10.1101/2022.10.27.514084

bioRxiv · 10.1101/2022.10.27.514084

Comparing 10x Genomics single-cell 3' and 5' assay in short-and long-read sequencing

Hsu, J.·Jarroux, J.·Joglekar, A.·Romero, J. P.·Nemec, C.·Reyes, D.·Royall, A.·He, Y.·Belchikov, N.·Leo, K.·Taylor, S. E. B.·Tilgner, H. U.

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Abstract

Barcoding strategies are fundamental to droplet-based single-cell sequencing, and understanding the biases and caveats between approaches is essential. Here, we comprehensively evaluated both short and long reads of the cDNA obtained through the two marketed approaches from 10x Genomics, the "3 assay" and the "5 assay", which attach barcodes at different ends of the mRNA molecule. Although the barcode detection, cell-type identification, and gene expression profile are similar in both assays, the 5 assay captured more exonic molecules and fewer intronic molecules compared to the 3 assay. We found that 13.7% of genes sequenced have longer average read lengths and are more complete (spanning both polyA-site and TSS) in the long reads from the 5 assay compared to the 3 assay. These genes are characterized by long average transcript length, high intron number, and low expression overall. Despite these differences, cell-type-specific isoform profiles observed from the two assays remain highly correlated. This study provides a benchmark for choosing the single-cell assay for the intended research question, and insights regarding platform-specific biases to be mindful of when analyzing data, particularly across samples and technologies.

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Hsu, J., Jarroux, J., Joglekar, A., Romero, J. P., Nemec, C., Reyes, D., Royall, A., He, Y., Belchikov, N., Leo, K., Taylor, S. E. B., Tilgner, H. U.. 2022-10-28. Comparing 10x Genomics single-cell 3' and 5' assay in short-and long-read sequencing. https://doi.org/10.1101/2022.10.27.514084

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