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Status |
Public on Apr 19, 2023 |
Title |
HeLa RCA short reads |
Sample type |
SRA |
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Source name |
HeLa
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Organism |
Homo sapiens |
Characteristics |
cell line: HeLa treatment: Rolling circle amplification
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Extracted molecule |
other |
Extraction protocol |
DNA isolation by column separation(Plasmid Mini AX; A&A Biotechnology), removal of remaining linear DNA by exonuclease(Plasmid-Safe ATP-dependent DNase; Lucigen, PacI enzyme; NEB), and rolling-circle amplification by random hexamer. For short-reads, DNA were fragmented by sonication. For long-reads, DNA fragments were selected by the BluePippin system. Short-reads and long-reads libraries were constructed and sequenced following MGI’s and Nanopore standard protocol, respectively.
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Library strategy |
OTHER |
Library source |
other |
Library selection |
other |
Instrument model |
MGISEQ-2000RS |
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Data processing |
RNA-seq: The raw RNA-seq reads were aligned with HISAT2 then assembled and merged with StringTie (1.3.3b). All the transcripts and abundance data were analyzed with Ballgown. ChIP-seq: Raw sequencing data of ChIP-seq was evaluated with FastQC. Bowtie2 was used to map the ChIP-seq reads on the human GRCh38 genome. Reads with multiple hits were discarded to exclude false detection of non-specific repetitive sequences. Peak calling was carried out with MACS2 with a false discovery rate q-value of <0.01. Hi-C: The clean reads from FastQC of each cell line were aligned to GRCh38 plus correspond HPV genome through HiC-Pro. All valid pairs were converted to .hic file by Juicebox. WGS: We performed quality control on raw reads by FastQC in each cell line. The clean reads were aligned to GRCh38 plus correspond HPV genome by bwa and marked duplicates by picard. RCA: The long-reads were corrected by short-reads by Filtlong and mapped to GRCh38 plus correspond HPV genome by minimap2. Virus Capture: The virus integration were identified by VIPA pipeline using raw data. WGBS: The clean data generated from FastQC were subject to bismark, and the methylation were extracted with --CX option Assembly: hg38 Supplementary files format and content: RNA-seq_Processed: Reads counts, FPKM, and TPM table Supplementary files format and content: ChIP-seq_Processed: H3K4me3 and H3K27Ac peak and bigwig file Supplementary files format and content: Hi-C_Processed: The interaction matrices .hic file Supplementary files format and content: WGBS_Processed: Genome-wide cytosine methylation reports Library strategy: RCA
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Submission date |
Oct 19, 2022 |
Last update date |
Apr 19, 2023 |
Contact name |
yuyan wang |
E-mail(s) |
wangyy365@mail2.sysu.edu.cn
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Organization name |
The First Affiliated Hospital, Sun Yat-sen University
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Street address |
Zhongshan 2nd Road, Yuexiu
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City |
Guangzhou |
ZIP/Postal code |
510080 |
Country |
China |
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Platform ID |
GPL30209 |
Series (1) |
GSE195631 |
HPV integration generates cellular super enhancer and functions as ecDNA to regulate genome-wide transcription |
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Relations |
BioSample |
SAMN31370297 |
SRA |
SRX17960358 |
Supplementary data files not provided |
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Processed data not provided for this record |
Raw data are available in SRA |
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