Exploring a large cancer cell line RNA-sequencing dataset with k-mers
Chloé BessièreiD, Haoliang XueiD, Benoit Guibert, Anthony Boureux, Florence RuffléiD, Julien ViotiD, Rayan ChikhiiD, Mikaël SalsoniD, Camille MarchetiD, Thérèse CommesiD, Daniel GautheretiD
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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