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Exploring a large cancer cell line RNA-sequencing dataset with k-mers

Bessiere, C.; Xue, H.; Guibert, B.; Boureux, A.; Ruffle, F.; Viot, J.; Chikhi, R.; Salson, M.; Marchet, C.; Commes, T.; Gautheret, D.

2024-03-01 bioinformatics
10.1101/2024.02.27.581927 bioRxiv
Show abstract

Analyzing the immense diversity of RNA isoforms in large RNA-seq repositories requires laborious data processing using specialized tools. Indexing techniques based on k-mers have previously been effective at searching for RNA sequences across thousands of RNA-seq libraries but falling short of enabling direct RNA quantification. We show here that RNAs queried in the form of k-mer sets can be quantified in seconds, with a precision akin to that of conventional RNA quantification methods. We showcase several applications by exploring an index of the Cancer Cell Line Encyclopedia (CCLE) collection consisting of 1019 RNA-seq samples. Non-reference RNA sequences such as RNAs harboring driver mutations and fusions, splicing isoforms or RNAs derived from repetitive elements, can be retrieved with high accuracy. Moreover, we show that k-mer indexing offers a powerful means to reveal variant RNAs induced by specific gene alterations, for instance in splicing factors. A web server allows public queries in CCLE and other indexes: https://transipedia.fr. Code is provided to allow users to set up their own server from any RNA-seq dataset.

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