run_metadata: 60879
This data as json
| rowid | run.accession | experiment.accession | sample.accession | study.accession | bioproject | study.title | study.alias | study.type | study.abstract | study.attributes | study.PMIDs | sample.description | sample.title | sample.alias | sample.centername | sample.attributes | GEOsample.title | GEOsample.dataprocessing | GEOsample.source | GEOsample.treatmentprotocol | GEOsample.extractprotocol | GEOsample.growthprotocol | GEOsample.characteristics | GEOsample.accession | experiment.title | experiment.alias | experiment.library_name | experiment.design_description | experiment.library_construction_protocol | experiment.attributes | experiment.library_strategy | experiment.library_source | experiment.library_selection | experiment.library_layout | experiment.platform | experiment.instrument_model | experiment.spot_descriptor | experiment.study_ref | run.title | run.attributes | run.filename | run.semantic_name | run.total_bases | run.total_spots | run.alias | run.read_lengths | run.base_counts | run.r1_length | run.r2_length | run.r3_length | run.r4_length | run.Acount | run.Ccount | run.Gcount | run.Tcount | run.Ncount | run.experiment | run.pool_member | submission.accession | submission.srasource | submission.bioprojectsource | seqdetective.n_mates | seqdetective.mapping_rate.mate1 | seqdetective.mapping_rate.mate2 | seqdetective.nofeature_rate.mate1 | seqdetective.nofeature_rate.mate2 | seqdetective.sparsity.mate1 | seqdetective.sparsity.mate2 | seqdetective.pos_strand_rate.mate1 | seqdetective.pos_strand_rate.mate2 | seqdetective.readlen.mate1 | seqdetective.readlen.mate2 | seqdetective.judgement.mate1 | seqdetective.judgement.mate2 | seqdetective.judgement.reason | platform_family | instrument_generation | read_bias | selection_class | prep_kit | sc_or_bulk | tech_class | technology | tech_variant | submission.bioprojectsource.country | earliest_date | devstage_curation | devstage_curation_coarse | tissue_curation | tissue_curation_coarse |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 60879 | SRR12623498 | SRX9106224 | SRS7349641 | SRP282042 | PRJNA662909 | Nanoplastics and sunscreens contained in personal care products induce neurotoxicity in early zebrafish embryos | GSE157816 | Transcriptome Analysis | Nanoplastics with small particle size and high surface area/volume ratio make them easy to absorb environmental pollutants and affect their bioavailability. In this study polystyrene nanoplastic beads PS NPBs with a particle size of 100nm and sunscreen butyl methoxydibenzoylmethane BMDBM contained in personal care products were chosen as target pollutants to study their developmental toxicity and interactive effects on zebrafish embryo. The exposure period was 2 hpf 12 hpf. The BMDBM and PS NPBs significantly upregulated the genes related to antioxidant enzymes and downregulated the gene expression of aromatase and DNA methyltransferases but the influenced genes were not exactly the same and the combined exposure reduced the adverse effects on the expression of all genes. With the help of single cell RNA sequencing technology the neural mid cells were identified as the target cells of both pollutants and brain development head development and notch signaling pathway were the functions they commonly altered. The key genes and functions that are specifically affected by BMDBM and/or PS NPBs were identified. The BMDBM mainly affect the differentiation and fate of neurons in central nervous system through the regulation of her5 her6 her11 lfng pax2a and fgfr4. The PS NPBs regulated the expression of olig2 foxg1a fzd8b six3a rx1 lhx2b nkx2.1a and sfrp5 to alter nervous system development retinal development and stem cell differentiation. The phenotypic responses of zebrafish larvae at 120 hpf were tested and significant inhibition of locomotor activity was found indicating that early disrupting effect on central nervous system would have a sustained impact on the behavior of zebrafish. Overall design: mRNA profiles of 12 hpf wild type zebrafish embryos | MPs | GSM4775401 | tissue:emberyo|treatment:exposed to MPs|age:12 hpf|genotype:wild type | MPs | Seurat package in R version 3.5.2 was used to analyze the sequenced reads. Principal component analysis PCA was used for dimensionality reduction and a graph based clustering was applied to cluster in PCA space. UMAP was used for the visualization of the clusters. The marker genes of each cluster were identified by FindMarkers function in the Seurat package. The clusters were annotated to a known cell type according to the Zebrafish Information Network ZFIN database and current literature Genome build: mm10 Supplementary files format and content: Matrix table with raw gene counts for every gene and every cell | emberyo | post exposure forty embryos collected from each group were transferred to 1 mL phosphate buffer saline PBS with 1% bovine serum albumin BSA. post incubated in 0.5 mL Hank's balanced salt solution HBSS containing 0.6 U/mL of dispase Yuanye Biotechnology Shanghai China at 37 °C for 5 min 100 µL of fetal bovine serum FBS was added to stop digestion. The cell suspension was filtered through a 40 µm filter and washed by 1% BSA HBSS. The cells were finally transferred to 1 mL PBS in preparation for single cell sequencing. The obtained cells were loaded on a GemCode Single Cell Instrument 10× Genomics Pleasanton USA to generate single cell gel beads in the emulsion. ScRNA seq libraries were prepared using the GemCode Single Cell 3′ Gel Bead Chip and Library Kits 10× Genomics Pleasanton USA. | treatment:exposed to MPs|age:12 hpf|genotype:wild type | GSM4775401 | GSM4775401: MPs; Danio rerio; RNA Seq | GSM4775401 | 1 | post exposure forty embryos collected from each group were transferred to 1 mL phosphate buffer saline PBS with 1% bovine serum albumin BSA. post incubated in 0.5 mL Hank's balanced salt solution HBSS containing 0.6 U/mL of dispase Yuanye Biotechnology Shanghai China at 37 °C for 5 min 100 µL of fetal bovine serum FBS was added to stop digestion. The cell suspension was filtered through a 40 µm filter and washed by 1% BSA HBSS. The cells were finally transferred to 1 mL PBS in preparation for single cell sequencing. The obtained cells were loaded on a GemCode Single Cell Instrument 10× Genomics Pleasanton USA to generate single cell gel beads in the emulsion. ScRNA seq libraries were prepared using the GemCode Single Cell 3′ Gel Bead Chip and Library Kits 10× Genomics Pleasanton USA. | GEO Accession:GSM4775401 | RNA-Seq | TRANSCRIPTOMIC | cDNA | SINGLE | ILLUMINA | Illumina HiSeq 2500 | SRP282042 | MPs_S2_L006_R1_001.fastq.gz | fastq | 69080874938.0 | 457489238.0 | GSM4775401 r2 | 0:151 1:0 | A:16058446984;C:10537982472;G:9566377499;T:32913863031;N:4204952 | 151 | 0 | 16058446984 | 10537982472 | 9566377499 | 32913863031 | 4204952 | SRX9106224 | SRS7349641 | SRA1123780 | GEO | HOHAI | 1 | 0.10674 | 0.01242 | 0.96621 | 0.50529 | 151 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc_generic | single_cell_generic | generic-scrnaseq-only | China | 2020-09-11 | Segmentation | Embryo | Embryo Imprecise | All anatomical structures |