Multi-omics data of gastric cancer cell lines

Abstract Objectives Gastric cancer (GC) is the fourth most common cancer worldwide, with the highest incidence and mortality regardless of sex. Despite technological advances in diagnosing and treating gastric cancer, GC still has high incidence and mortality rates. Therefore, continuous research is...

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Main Authors: Eun-Hye Seo, Yun-Jae Shin, Hee-Jin Kim, Jeong-Hwan Kim, Yong Sung Kim, Seon-Young Kim
Format: Article
Language:English
Published: BMC 2023-04-01
Series:BMC Genomic Data
Subjects:
Online Access:https://doi.org/10.1186/s12863-023-01122-9
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author Eun-Hye Seo
Yun-Jae Shin
Hee-Jin Kim
Jeong-Hwan Kim
Yong Sung Kim
Seon-Young Kim
author_facet Eun-Hye Seo
Yun-Jae Shin
Hee-Jin Kim
Jeong-Hwan Kim
Yong Sung Kim
Seon-Young Kim
author_sort Eun-Hye Seo
collection DOAJ
description Abstract Objectives Gastric cancer (GC) is the fourth most common cancer worldwide, with the highest incidence and mortality regardless of sex. Despite technological advances in diagnosing and treating gastric cancer, GC still has high incidence and mortality rates. Therefore, continuous research is needed to overcome GC. In various studies, cell lines are used to find and verify the cause of specific diseases. Large-scale genomic studies such as ENCODE and Roadmap epigenomic projects provide multiomics data from various organisms and samples. However, few multi-omics data for gastric tissues and cell lines have been generated. Therefore, we performed RNA-seq, Exome-seq, and ChIP-seq with several gastric cell lines to generate a multi-omics data set in gastric cancer. Data description Multiomic data, such as RNA-seq, Exome-seq, and ChIP-seq, were produced in gastric cancer and normal cell lines. RNA-seq data were generated from nine GC and one normal gastric cell line, mapped to a human reference genome (hg38) using the STAR alignment tool, and quantified with HTseq. Exome sequence data were produced in nine GC and two normal gastric lines. Sequenced reads were mapped and processed using BWA-MEM and GATK, variants were called by stralka2, and annotation was performed using ANNOVAR. Finally, for the ChIP-seq, nine GC cell lines and four GC cell lines were used in two experimental sets; chip-seq was performed to confirm changes in H3K4me3 and H3K27me3. Data was mapped to human reference hg38 with BWA-MEM, and peak calling and annotation were performed using the Homer tool. Since these data provide multi-omics data for GC cell lines, it will be useful for researchers who use the GC cell lines to study.
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spelling doaj.art-93a8c24a3e994314bf177845992f0efd2023-04-23T11:29:40ZengBMCBMC Genomic Data2730-68442023-04-012411410.1186/s12863-023-01122-9Multi-omics data of gastric cancer cell linesEun-Hye Seo0Yun-Jae Shin1Hee-Jin Kim2Jeong-Hwan Kim3Yong Sung Kim4Seon-Young Kim5Korea Bioinformation Center, Korea Research Institute of Bioscience and BiotechnologyKorea Bioinformation Center, Korea Research Institute of Bioscience and BiotechnologyAging Convergence Research Center, Korea Research Institute of Bioscience and BiotechnologyAging Convergence Research Center, Korea Research Institute of Bioscience and BiotechnologyPersonalized Genomic Medicine Research Center, Korea Research Institute of Bioscience and BiotechnologyKorea Bioinformation Center, Korea Research Institute of Bioscience and BiotechnologyAbstract Objectives Gastric cancer (GC) is the fourth most common cancer worldwide, with the highest incidence and mortality regardless of sex. Despite technological advances in diagnosing and treating gastric cancer, GC still has high incidence and mortality rates. Therefore, continuous research is needed to overcome GC. In various studies, cell lines are used to find and verify the cause of specific diseases. Large-scale genomic studies such as ENCODE and Roadmap epigenomic projects provide multiomics data from various organisms and samples. However, few multi-omics data for gastric tissues and cell lines have been generated. Therefore, we performed RNA-seq, Exome-seq, and ChIP-seq with several gastric cell lines to generate a multi-omics data set in gastric cancer. Data description Multiomic data, such as RNA-seq, Exome-seq, and ChIP-seq, were produced in gastric cancer and normal cell lines. RNA-seq data were generated from nine GC and one normal gastric cell line, mapped to a human reference genome (hg38) using the STAR alignment tool, and quantified with HTseq. Exome sequence data were produced in nine GC and two normal gastric lines. Sequenced reads were mapped and processed using BWA-MEM and GATK, variants were called by stralka2, and annotation was performed using ANNOVAR. Finally, for the ChIP-seq, nine GC cell lines and four GC cell lines were used in two experimental sets; chip-seq was performed to confirm changes in H3K4me3 and H3K27me3. Data was mapped to human reference hg38 with BWA-MEM, and peak calling and annotation were performed using the Homer tool. Since these data provide multi-omics data for GC cell lines, it will be useful for researchers who use the GC cell lines to study.https://doi.org/10.1186/s12863-023-01122-9Gastric cancerGastric cancer cell linesRNA sequencingExome sequencingChIP-sequencing
spellingShingle Eun-Hye Seo
Yun-Jae Shin
Hee-Jin Kim
Jeong-Hwan Kim
Yong Sung Kim
Seon-Young Kim
Multi-omics data of gastric cancer cell lines
BMC Genomic Data
Gastric cancer
Gastric cancer cell lines
RNA sequencing
Exome sequencing
ChIP-sequencing
title Multi-omics data of gastric cancer cell lines
title_full Multi-omics data of gastric cancer cell lines
title_fullStr Multi-omics data of gastric cancer cell lines
title_full_unstemmed Multi-omics data of gastric cancer cell lines
title_short Multi-omics data of gastric cancer cell lines
title_sort multi omics data of gastric cancer cell lines
topic Gastric cancer
Gastric cancer cell lines
RNA sequencing
Exome sequencing
ChIP-sequencing
url https://doi.org/10.1186/s12863-023-01122-9
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AT jeonghwankim multiomicsdataofgastriccancercelllines
AT yongsungkim multiomicsdataofgastriccancercelllines
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