run_metadata: 39766
This data as json
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| 39766 | SRR2136165 | SRX1125641 | SRS1017713 | SRP061852 | PRJNA291530 | DNA methylome patterns of zebrafish cells under cold pressure | GSE71567 | Other | In this study MeDIP seq and RNA seq were performed to reveal a genome wide methylation profile of zebrafish Danio rerio embryonic fibroblast cell line ZF4 and its variation under cold environment.This study puts a new insight into the genome wide epigenetic regulation under cold environment. Overall design: ZF4 cells were cultured at 28 °C as control and at 18 °C for 5 days and 30 days seperately. Each condition has three biological replica. | ZF4 18d5dRNA2 | GSM1838564 | tissue:embryonic fibroblast cells|cell type:fibroblast cell line|growth:cultured at 18°C for 5 days|treatment:cold treatment for 5 days | ZF4 18d5dRNA2 | Illumina Casava1.7 software was used for basecalling. The fastx toolkit program was used to filter off low quality sequences from raw sequencing data. Sequences were aligned with Zebrafish genomeZR9/danRer7 downloaded from iGenome using Bowtie2. MeDIP seq peaks were called with the Model based Analysis of MeDIP Seq MACS software with default parameters with alignment results. The three peak sets generated by MACS were merged using Bedtools for peaks with at least 1bp overlap to get a reference peak set REF for following analysis. Genome build: ZR9/danRer7 Supplementary files format and content: .txt | embryonic fibroblast cells | For cold treatment cells were grown at 18 °C 5% CO2 in the same medium for up to 30 days. | For MeDIP seq genomic DNAs were isolated and sonicated. End repair adenylation adapter ligation methylated DNA enrichment and methylated DNA library construction were all performed with The NEXTflex™ Methyl Seq 1 Kit BIOO LIFE SCIENCE PRODUCTS Cat No. 5118 01 according to the manufacturer’s instruction. For RNA seq total RNA was isolated using TRlzol reagent Invitrogen life Technologies. | The zebrafish embryonic fibroblast cell line ZF4 was purchased from the American Type Culture Collection ATCC CRL 2050; Driever and Rangini 1993. The cells were grown at 28 °C 5% CO2 in Dulbecco's modified Eagle's medium/F12 nutrient mix DMEM/F12 supplemented with 10% FBS 1% l glutamine 100 u/ml penicillin 100 μg/ml streptomycin. For cold treatment cells were grown at 18 °C 5% CO2 in the same medium for up to 30 days. All cell culture medium components were purchased from Gibco BRL Life Technologies Ltd USA. | cell type:fibroblast cell line|growth:cultured at 18°C for 5 days|treatment:cold treatment for 5 days | GSM1838564 | GSM1838564: ZF4 18d5dRNA2; Danio rerio; RNA Seq | GSM1838564 | 1 | For MeDIP seq genomic DNAs were isolated and sonicated. End repair adenylation adapter ligation methylated DNA enrichment and methylated DNA library construction were all performed with The NEXTflex™ Methyl Seq 1 Kit BIOO LIFE SCIENCE PRODUCTS Cat No. 5118 01 according to the manufacturer’s instruction. For RNA seq total RNA was isolated using TRlzol reagent Invitrogen life Technologies. MeDIP DNA libraries were prepared with The NEXTflex™ Methyl Seq 1 Kit BIOO LIFE SCIENCE PRODUCTS Cat No. 5118 01 according to the manufacturer’s instruction. RNA libraries were prepared for sequencing using standard Illumina protocols. | GEO Accession:GSM1838564 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2000 | SRP061852 | 18_5_replica2_2.fastq.gz 18_5_replica2_1.fastq.gz | fastq fastq | 2948189798.0 | 14594999.0 | GSM1838564 r1 | 0:101 1:101 | A:784972120;C:694695628;G:681782943;T:786426712;N:312395 | 101 | 101 | 784972120 | 694695628 | 681782943 | 786426712 | 312395 | SRX1125641 | SRS1017713 | SRA281140 | GEO | College of fishery and life science, Shanghai Ocean University | 2 | 0.94304 | 0.94274 | 0.10665 | 0.10697 | 0.72383 | 0.72508 | 0.48863 | 0.4889 | 101 | 101 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | China | 2015-07-30 | Undetermined | Embryo | Embryo Imprecise | All anatomical structures |