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  • image/svg+xml art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos Open Access logo, converted into svg, designed by PLoS. This version with transparent background. http://commons.wikimedia.org/wiki/File:Open_Access_logo_PLoS_white.svg art designer at PLoS, modified by Wikipedia users Nina, Beao, JakobVoss, and AnonMoos http://www.plos.org/
    Authors: HAMMEL, M.; Touchard, F.; Burioli, E. A. V.; Paradis, L.; +9 Authors

    This document contains all raw data, environemental data sources, primers sequences, PCR results and statistical results. Each table is referred in the main document.

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    Dataset . 2024
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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Table S6: List of genes clustered by Gene Ontology (GO) terms comprised in enriched biological processes (p.adj<0.05).

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Table S1: Transcript annotation

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Figure S1: Validation of the results obtained from RNAseq data by RT-qPCR quantification on 10 additional samples (cancerous: CAN7-11, healthy: EDU7-11). A) Normalised Ct values (mean of three replicates) of 17 selected genes with contrasting expression levels and oncogenic relevance. Normalisation was performed on the mean of the Ct of three constitutively expressed genes (GAPDH, RPS28 and UBE2D3) within each sample; B) Comparison of Log2FC values between the two quantification methods (RT-qPCR and RNA-seq): Log2FCs for RNA-seq data have been calculated with DESeq2 on 9 samples (CAN1-3, EDU1-3, TRO1-3) and Log2FCs for RT-qPCRs have been calculated as follow for the 10 additional individuals (CAN7-11, EDU7-11): FC= efficiency of the qPCR mean of Ct of the 5 MtrBTN2-affected individuals - mean of Ct of the 5 MtrBTN2-free individuals

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Table S8: SNVs present in all MtrBTN2 samples and absent in MtrBTN2-free samples. VAF, variant allele frequency.

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Table S3: Samplings of Mytilus mussels used in the study.

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Figure S7: RDA on normalized read counts to analyze the impact of explanatory variables (“cell type”: hemocyte/MtrBTN2 cells, species: trossulus/edulis, “environment”: Barents Sea/Channel Sea) on response variables (gene expression) followed by ANOVA like permutation test (nperm=999, model=“full”). Both “cell type” and “environment” were retained as significant explanatory variables (p<0.05).

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Figure S6: Top-expressed transcripts of genes in whole flesh of MtrBTN2-affected additional samples (CAN 4–6).

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Table S4: List of the transcripts significantly differentially expressed with descriptions, Gene IDs, log2FC, mean normalised abundance, FDR, and QuantEval validation.

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Figure S3: Spearman's correlation between transcript and component (QuantEval) Log2FC. Orange points represent the 102 transcripts for which the significance of the differential expression obtained with DESeq2 v1.34 was not confirmed at the component level (FDR>0.05).

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    Authors: HAMMEL, M.; Touchard, F.; Burioli, E. A. V.; Paradis, L.; +9 Authors

    This document contains all raw data, environemental data sources, primers sequences, PCR results and statistical results. Each table is referred in the main document.

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Table S6: List of genes clustered by Gene Ontology (GO) terms comprised in enriched biological processes (p.adj<0.05).

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Table S1: Transcript annotation

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    Authors: Burioli, E. A. V.; Hammel, M.; Vignal, E.; Vidal-Dupiol, J.; +5 Authors

    Figure S1: Validation of the results obtained from RNAseq data by RT-qPCR quantification on 10 additional samples (cancerous: CAN7-11, healthy: EDU7-11). A) Normalised Ct values (mean of three replicates) of 17 selected genes with contrasting expression levels and oncogenic relevance. Normalisation was performed on the mean of the Ct of three constitutively expressed genes (GAPDH, RPS28 and UBE2D3) within each sample; B) Comparison of Log2FC values between the two quantification methods (RT-qPCR and RNA-seq): Log2FCs for RNA-seq data have been calculated with DESeq2 on 9 samples (CAN1-3, EDU1-3, TRO1-3) and Log2FCs for RT-qPCRs have been calculated as follow for the 10 additional individuals (CAN7-11, EDU7-11): FC= efficiency of the qPCR mean of Ct of the 5 MtrBTN2-affected individuals - mean of Ct of the 5 MtrBTN2-free individuals

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    Table S8: SNVs present in all MtrBTN2 samples and absent in MtrBTN2-free samples. VAF, variant allele frequency.

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    Table S3: Samplings of Mytilus mussels used in the study.

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    Figure S7: RDA on normalized read counts to analyze the impact of explanatory variables (“cell type”: hemocyte/MtrBTN2 cells, species: trossulus/edulis, “environment”: Barents Sea/Channel Sea) on response variables (gene expression) followed by ANOVA like permutation test (nperm=999, model=“full”). Both “cell type” and “environment” were retained as significant explanatory variables (p<0.05).

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    Figure S6: Top-expressed transcripts of genes in whole flesh of MtrBTN2-affected additional samples (CAN 4–6).

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    Table S4: List of the transcripts significantly differentially expressed with descriptions, Gene IDs, log2FC, mean normalised abundance, FDR, and QuantEval validation.

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    Figure S3: Spearman's correlation between transcript and component (QuantEval) Log2FC. Orange points represent the 102 transcripts for which the significance of the differential expression obtained with DESeq2 v1.34 was not confirmed at the component level (FDR>0.05).

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