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pmid:33318985

RNA-Seq transcriptome data of human cells infected with influenza A/Puerto Rico/8/1934 (H1N1) virus.

Evgenii Zhuravlev · Mariia Sergeeva · Sergey Malanin · Rinat Amirkhanov · Dmitriy Semenov · Tatiana Grigoryeva · Andrey Komissarov · Grigory Stepanov

Data in brief · 2020 doi:10.1016/j.dib.2020.106604

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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title
RNA-Seq transcriptome data of human cells infected with influenza A/Puerto Rico/8/1934 (H1N1) virus.
doi
10.1016/j.dib.2020.106604
pmid
33318985
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[0]
Evgenii Zhuravlev
[1]
Mariia Sergeeva
[2]
Sergey Malanin
[3]
Rinat Amirkhanov
[4]
Dmitriy Semenov
[5]
Tatiana Grigoryeva
[6]
Andrey Komissarov
[7]
Grigory Stepanov
journal
Data in brief
year
2020
abstract
Human influenza remains a serious public health problem. This data article reports the transcriptome analysis data of human cell lines infected with influenza A/Puerto Rico/8/1934 (H1N1) virus. Mock-infected cells were included as controls. Human embryonic fibroblasts (MRC-5) and immortalized cell lines (A549, HEK293FT, WI-38 VA-13) were selected for RNA sequencing using Illumina NextSeq500 platform. Raw data were applied to the bioinformatic pipeline, which includes quality control with FastQC and MultiQC, adapter and quality trimming with Cutadapt, filtering to the genome of influenza A with STAR, transcript quantification with Salmon tool (GRCh38_RefSeq_Transcripts). Differential expressed genes were identified using R package DESeq2 with FDR-adjusted p-value < 0.001 and absolute value of log2(FC) > 1. Lists of differentially expressed genes is provided. The raw and processed RNA-seq data presented in this article were deposited to the European Nucleotide Archive via the ArrayExpress partner repository with the dataset accession number E-MTAB-9511 .
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To study genes involved in cellular response to influenza A virus infection, differential expressed genes were identified using R package DESeq2 with a FDR-adjusted p-value < 0.001 and the absolute value of a log2(FC) > 1 [9]. The raw data (FASTQ files) were deposited to the European Nucleotide Archive via the ArrayExpress partner repository with the dataset accession number E-MTAB-9511 [1].
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To study genes involved in cellular response to influenza A virus infection, differential expressed genes were identified using R package DESeq2 with a FDR-adjusted p-value < 0.001 and the absolute value of a log2(FC) > 1 [9].
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MRC-5, WI-38 VA-13, A549 and HEK293FT human cells were infected with influenza A/Puerto Rico/8/1934 virus at a dose of 1 TCID50/cell and incubated at 37°С for 48 h. Mock-infected cells were included as controls.
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Following the incubation period, the cell monolayer was directly lysed. Total RNA was extracted, then polyA RNA fraction was enriched and used for construction cDNA libraries using a NEBNext Ultra II Directional RNA library preparation kit and NEBNext mRNA Magnetic Isolation Module. Massive parallel sequencing was performed on a NextSeq Illumina 500 platform using NextSeq 500/550 High Output v2.5 Kit (75 cycles).
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Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia
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Both raw and processed RNA-seq data were deposited to the European Nucleotide Archive via the ArrayExpress partner repository with the dataset accession number E-MTAB-9511.Repository name: ArrayExpressData identification number: E-MTAB-9511Direct URL to data: https://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-9511/
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Number of raw, trimmed and filtered reads of 16 cDNA libraries of mock-infected (0h) and infected with influenza A virus (48h) cell lines (MRC-5, WI-38 VA-13, A549 and HEK293FT).
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To study genes involved in cellular response to influenza A virus infection, differential expressed genes were identified using R package DESeq2 with a FDR-adjusted p-value < 0.001 and the absolute value of a log2(FC) > 1 [9]. The raw data (FASTQ files) were deposited to the European Nucleotide Archive via the ArrayExpress partner repository with the dataset accession number E-MTAB-9511 [1].
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Complete file
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This data article reports the transcriptome analysis data of human cell lines infected with influenza A/Puerto Rico/8/1934 (H1N1) virus. Mock-infected cells were included as controls. Human embryonic fibroblasts (MRC-5) and immortalized cell lines (A549, HEK293FT, WI-38 VA-13) were selected for RNA sequencing using Illumina NextSeq500 platform. Raw data were applied to the bioinformatic pipeline, which includes quality control with FastQC and MultiQC, adapter and quality trimming with Cutadapt, filtering to the genome of influenza A with STAR, transcript quantification with Salmon tool (GRCh38_RefSeq_Transcripts). Differential expressed genes were identified using R package DESeq2 with FDR-adjusted p-value < 0.001 and absolute value of log2(FC) > 1. Lists of differentially expressed genes is provided. 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Mock-infected cells were included as controls."], ["Description of data collection", "Following the incubation period, the cell monolayer was directly lysed. Total RNA was extracted, then polyA RNA fraction was enriched and used for construction cDNA libraries using a NEBNext Ultra II Directional RNA library preparation kit and NEBNext mRNA Magnetic Isolation Module. Massive parallel sequencing was performed on a NextSeq Illumina 500 platform using NextSeq 500/550 High Output v2.5 Kit (75 cycles)."], ["Data source location", "Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia"], ["Data accessibility", "Both raw and processed RNA-seq data were deposited to the European Nucleotide Archive via the ArrayExpress partner repository with the dataset accession number E-MTAB-9511.Repository name: ArrayExpressData identification number: E-MTAB-9511Direct URL to data: https://www.ebi.ac.uk/arrayexpress/experiments/E-MTAB-9511/"]], "row_count": 9, "column_count": 2, "numeric_cells": 4, "header_rows": 0, "locator": "section[1]/table-wrap[1]#utbl0001"}}, {"id": "asset:table:pmid:33318985:2", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:5b36a41d5591bd831b014a490ad43d7e8fef2fd5861f9847307d5066f236d14c", "bytes": 1016, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[3]/table-wrap[1]#tbl0001", "version": null, "note": "Number of raw, trimmed and filtered reads of 16 cDNA libraries of mock-infected (0h) and infected with influenza A virus (48h) cell lines (MRC-5, WI-38 VA-13, A549 and HEK293FT).", "structure": {"pmcid": "PMC7725734", "section_index": 3, "section_title": "Data Description", "row_count": 17, "column_count": 5}, "table": {"label": "Table 1", "caption": "Number of raw, trimmed and filtered reads of 16 cDNA libraries of mock-infected (0h) and infected with influenza A virus (48h) cell lines (MRC-5, WI-38 VA-13, A549 and HEK293FT).", "rows": [["Sample name", "Biological replicate", "M Reads (Raw)", "M Reads(after trimming)", "M Seqs(after filtering)"], ["MRC-5_0h", "M01", "11.3", "11.3", "11.3"], ["M02", "11.6", "11.6", "11.6"], ["MRC-5_48h", "M481", "11.4", "11.3", "10.0"], ["M482", "11.5", "11.4", "10.1"], ["WI-38 VA-13_0h", "W01", "13.8", "13.8", "13.8"], ["W02", "13.9", "13.9", "13.9"], ["WI-38 VA-13_48h", "W481", "13.9", "13.9", "12.6"], ["W482", "14.1", "14.1", "12.4"], ["A549_0h", "A01", "12.7", "12.7", "12.7"], ["A02", "10.6", "10.6", "10.6"], ["A549_48h", "A481", "11.4", "11.4", "8.9"], ["A482", "11.6", "11.5", "8.9"], ["HEK293FT_0h", "H01", "13.0", "13.0", "13.0"], ["H02", "13.6", "13.6", "13.6"], ["HEK293FT_48h", "H481", "14.1", "14.1", "13.7"], ["H482", "13.5", "13.4", "12.7"]], "row_count": 17, "column_count": 5, "numeric_cells": 72, "header_rows": 1, "locator": "section[3]/table-wrap[1]#tbl0001"}}], "gaps": ["asset:data:geo:E-MTAB-9511 not downloaded", "asset:data:geo:E-MTAB-9511 licence not read"]}, "analysis": {"state": "complete", "methods": [{"id": "method-1", "family": "differential_expression", "specific": "deseq2", "label": "Differential expression analysis", "dsl_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["count_matrix_with_condition"], "evidence": {"score": 1.0, "band": "reordered", "quote": "To study genes involved in cellular response to influenza A virus infection, differential expressed genes were identified using R package DESeq2 with a FDR-adjusted p-value < 0.001 and the absolute value of a log2(FC) > 1 [9]. 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