run_metadata
9 rows where experiment.library_selection = "other", experiment.library_strategy = "miRNA-Seq" and tissue_curation_coarse = "All anatomical structures"
This data as json, CSV (advanced)
| Link | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 39671 | 39671 | SRR2043046 | SRX1041307 | SRS947739 | SRP058729 | PRJNA284830 | MicroRNA expression changes during zebrafish Danio rerio development induced by hexabromocyclododecane | PRJNA284830 | Whole Genome Sequencing | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 and 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | HBCD 200nM sample3 | zebrafish at normal developmental age of 72hpf in the 200 nM HBCD rep3 | HBCD 200nM 3 | breed:zebrafish|strain:Wild type TU strain|age:72 hpf£¨hpf stage:embryo|sex:pooled male and female|tissue:whole zebrafish|treatment:HBCD 200nM 3|BioSampleModel:Model organism or animal | zebrafish at normal developmental age of 72hpf in the 200 nM HBCD rep3 | Sample HBCD 200nM 3 | 1 | 1 | miRNA-Seq | TRANSCRIPTOMIC | other | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>36</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP058729 | Sample_HBCD_200nM-3.fastq.tar.gz | fastq | 549695784.0 | 16657448.0 | Sample HBCD 200nM 3 | 0:33 | A:120885057;C:120386921;G:146939259;T:161323403;N:161144 | 33 | 120885057 | 120386921 | 146939259 | 161323403 | 161144 | SRX1041307 | SRS947739 | SRA269780 | MG | Xiamen University | 1 | 0.13819 | 0.03714 | 0.94968 | 0.52004 | 33 | B | usable mapping rate | illumina | early_illumina | unknown | small_rna | unknown | bulk | unknown | unknown | China | 2015-09-18 | Larval | Larval | Whole Organism | All anatomical structures | |||||||||||||||||||||||||
| 39672 | 39672 | SRR2043044 | SRX1041306 | SRS947738 | SRP058729 | PRJNA284830 | MicroRNA expression changes during zebrafish Danio rerio development induced by hexabromocyclododecane | PRJNA284830 | Whole Genome Sequencing | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 and 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | HBCD 200nM sample2 | zebrafish at normal developmental age of 72hpf in the 200 nM HBCD rep2 | HBCD 200nM 2 | breed:zebrafish|strain:Wild type TU strain|age:72 hpf£¨hpf stage:embryo|sex:pooled male and female|tissue:whole zebrafish|treatment:HBCD 200nM 2|BioSampleModel:Model organism or animal | zebrafish at normal developmental age of 72hpf in the 2 nM HBCD rep2 | Sample HBCD 200nM 2 | 1 | 1 | miRNA-Seq | TRANSCRIPTOMIC | other | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>36</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP058729 | Sample_HBCD_200nM-2.fastq.tar.gz | fastq | 566585217.0 | 17169249.0 | Sample HBCD 200nM 2 | 0:33 | A:119904892;C:129504656;G:159539041;T:157545273;N:91355 | 33 | 119904892 | 129504656 | 159539041 | 157545273 | 91355 | SRX1041306 | SRS947738 | SRA269780 | MG | Xiamen University | 1 | 0.07072 | 0.01837 | 0.96246 | 0.52439 | 33 | B | usable mapping rate | illumina | early_illumina | unknown | small_rna | unknown | bulk | unknown | unknown | China | 2015-05-27 | Larval | Larval | Whole Organism | All anatomical structures | |||||||||||||||||||||||||
| 39673 | 39673 | SRR2043035 | SRX1041305 | SRS947737 | SRP058729 | PRJNA284830 | MicroRNA expression changes during zebrafish Danio rerio development induced by hexabromocyclododecane | PRJNA284830 | Whole Genome Sequencing | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 and 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | HBCD 200nM sample1 | zebrafish at normal developmental age of 72hpf in the 200 nM HBCD rep1 | HBCD 200nM 1 | breed:zebrafish|strain:Wild type TU strain|age:72 hpf£¨hpf stage:embryo|sex:pooled male and female|tissue:whole zebrafish|treatment:HBCD 200nM 1|BioSampleModel:Model organism or animal | zebrafish at normal developmental age of 72hpf in the 200 nM HBCD rep1 | Sample HBCD 200nM 1 | 1 | 1 | miRNA-Seq | TRANSCRIPTOMIC | other | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>36</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP058729 | Sample_HBCD_200nM-1.fastq.tar.gz | fastq | 636936228.0 | 17692673.0 | Sample HBCD 200nM 1 | 0:36 | A:138321201;C:126054708;G:184822056;T:187709777;N:28486 | 36 | 138321201 | 126054708 | 184822056 | 187709777 | 28486 | SRX1041305 | SRS947737 | SRA269780 | MG | Xiamen University | 1 | 0.04374 | 0.0115 | 0.97839 | 0.29573 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | small_rna | unknown | bulk | unknown | unknown | China | 2015-09-18 | Larval | Larval | Whole Organism | All anatomical structures | |||||||||||||||||||||||||
| 39674 | 39674 | SRR2043030 | SRX1041276 | SRS947712 | SRP058729 | PRJNA284830 | MicroRNA expression changes during zebrafish Danio rerio development induced by hexabromocyclododecane | PRJNA284830 | Whole Genome Sequencing | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 and 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | HBCD 2nM sample3 | zebrafish at normal developmental age of 72hpf in the 2 nM HBCD rep3 | HBCD 2nM 3 | breed:zebrafish|strain:Wild type TU strain|age:72 hpf£¨hpf stage:embryo|sex:pooled male and female|tissue:whole zebrafish|treatment:HBCD 2nM 3|BioSampleModel:Model organism or animal | zebrafish at normal developmental age of 72hpf in the 200 nM HBCD rep3 | Sample HBCD 2nM 3 | 1 | 1 | miRNA-Seq | TRANSCRIPTOMIC | other | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>36</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP058729 | Sample_HBCD_2nM-3.fastq.tar.gz | fastq | 636936228.0 | 17692673.0 | Sample HBCD 2nM 3 | 0:36 | A:138321201;C:126054708;G:184822056;T:187709777;N:28486 | 36 | 138321201 | 126054708 | 184822056 | 187709777 | 28486 | SRX1041276 | SRS947712 | SRA269780 | MG | Xiamen University | 1 | 0.04377 | 0.01174 | 0.97812 | 0.30675 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | small_rna | unknown | bulk | unknown | unknown | China | 2015-05-27 | Larval | Larval | Whole Organism | All anatomical structures | |||||||||||||||||||||||||
| 39675 | 39675 | SRR2042999 | SRX1041271 | SRS947707 | SRP058729 | PRJNA284830 | MicroRNA expression changes during zebrafish Danio rerio development induced by hexabromocyclododecane | PRJNA284830 | Whole Genome Sequencing | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 and 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | HBCD 2nM sample2 | zebrafish at normal developmental age of 72hpf in the 2 nM HBCD rep2 | HBCD 2nM 2 | breed:zebrafish|strain:Wild type TU strain|age:72 hpf£¨hpf stage:embryo|sex:pooled male and female|tissue:whole zebrafish|treatment:HBCD 2nM 2|BioSampleModel:Model organism or animal | zebrafish at normal developmental age of 72hpf in the 2 nM HBCD rep2 | Sample HBCD 2nM 2 | 1 | 1 | miRNA-Seq | TRANSCRIPTOMIC | other | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>36</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP058729 | Sample_HBCD_2nM-2.fastq.tar.gz | fastq | 482176476.0 | 13393791.0 | Sample HBCD 2nM 2 | 0:36 | A:104565872;C:92998014;G:137403437;T:147164823;N:44330 | 36 | 104565872 | 92998014 | 137403437 | 147164823 | 44330 | SRX1041271 | SRS947707 | SRA269780 | MG | Xiamen University | 1 | 0.0759 | 0.02077 | 0.97025 | 0.33489 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | small_rna | unknown | bulk | unknown | unknown | China | 2015-09-18 | Larval | Larval | Whole Organism | All anatomical structures | |||||||||||||||||||||||||
| 39676 | 39676 | SRR2040574 | SRX1038901 | SRS945650 | SRP058729 | PRJNA284830 | MicroRNA expression changes during zebrafish Danio rerio development induced by hexabromocyclododecane | PRJNA284830 | Whole Genome Sequencing | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 and 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | HBCD 2nM sample1 | zebrafish at normal developmental age of 72hpf in the 2 nM HBCD rep1 | HBCD 2nM 1 | breed:zebrafish|strain:Wild type TU strain|age:72 hpf£¨hpf stage:embryo|sex:pooled male and female|tissue:whole zebrafish|treatment:HBCD 2nM 1|BioSampleModel:Model organism or animal | zebrafish at normal developmental age of 72hpf in the 2 nM HBCD rep1 | Sample HBCD 2nM 1 | 1 | 1 | miRNA-Seq | TRANSCRIPTOMIC | other | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>36</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP058729 | Sample_HBCD_2nM-1.fastq.tar.gz | fastq | 327925620.0 | 9109045.0 | Sample HBCD 2nM 1 | 0:36 | A:71167117;C:63917852;G:94874537;T:97936051;N:30063 | 36 | 71167117 | 63917852 | 94874537 | 97936051 | 30063 | SRX1038901 | SRS945650 | SRA269780 | MG | Xiamen University | 1 | 0.06484 | 0.01622 | 0.97459 | 0.35746 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | small_rna | unknown | bulk | unknown | unknown | China | 2015-05-27 | Larval | Larval | Whole Organism | All anatomical structures | |||||||||||||||||||||||||
| 39677 | 39677 | SRR2040573 | SRX1038898 | SRS945648 | SRP058729 | PRJNA284830 | MicroRNA expression changes during zebrafish Danio rerio development induced by hexabromocyclododecane | PRJNA284830 | Whole Genome Sequencing | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 and 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | HBCD 0nM sample3 | zebrafish at normal developmental age of 72hpf in the control rep3 | control 3 | breed:zebrafish|strain:Wild type TU strain|age:72 hpf£¨hpf stage:embryo|sex:pooled male and female|tissue:whole zebrafish|treatment:control 3|BioSampleModel:Model organism or animal | zebrafish at normal developmental age of 72hpf in the control rep3 | Sample control 3 | 1 | 1 | miRNA-Seq | TRANSCRIPTOMIC | other | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>33</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP058729 | Sample_control-3.fastq.tar.gz | fastq | 456812301.0 | 13842797.0 | Sample control 3 | 0:33 | A:99424011;C:100923631;G:121758068;T:134398048;N:308543 | 33 | 99424011 | 100923631 | 121758068 | 134398048 | 308543 | SRX1038898 | SRS945648 | SRA269780 | MG | Xiamen University | 1 | 0.14866 | 0.03878 | 0.95079 | 0.53781 | 33 | B | usable mapping rate | illumina | early_illumina | unknown | small_rna | unknown | bulk | unknown | unknown | China | 2015-09-18 | Larval | Larval | Whole Organism | All anatomical structures | |||||||||||||||||||||||||
| 39678 | 39678 | SRR2040572 | SRX1038893 | SRS945643 | SRP058729 | PRJNA284830 | MicroRNA expression changes during zebrafish Danio rerio development induced by hexabromocyclododecane | PRJNA284830 | Whole Genome Sequencing | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 and 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | HBCD 0nM sample2 | zebrafish at normal developmental age of 72hpf in the control rep2 | control 2 | breed:zebrafish|strain:Wild type TU strain|age:72 hpf£¨hpf stage:embryo|sex:pooled male and female|tissue:whole zebrafish|treatment:control 2|BioSampleModel:Model organism or animal | zebrafish at normal developmental age of 72hpf in the control rep2 | Sample control 2 | 1 | 1 | miRNA-Seq | TRANSCRIPTOMIC | other | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>33</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP058729 | 451846230.0 | 13692310.0 | Sample control 2 | 0:33 | A:100056403;C:97812076;G:121442936;T:132449348;N:85467 | 33 | 100056403 | 97812076 | 121442936 | 132449348 | 85467 | SRX1038893 | SRS945643 | SRA269780 | MG | Xiamen University | 1 | 0.06007 | 0.01901 | 0.96794 | 0.4743 | 33 | B | usable mapping rate | illumina | early_illumina | unknown | small_rna | unknown | bulk | unknown | unknown | China | 2015-05-27 | Larval | Larval | Whole Organism | All anatomical structures | |||||||||||||||||||||||||||
| 39679 | 39679 | SRR2040562 | SRX1038887 | SRS945623 | SRP058729 | PRJNA284830 | MicroRNA expression changes during zebrafish Danio rerio development induced by hexabromocyclododecane | PRJNA284830 | Whole Genome Sequencing | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 and 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | Hexabromocyclododecane HBCD one of the most widely used brominated flame retardants has been found to cause toxic effects on animals. Although microRNAs miRNAs play an important role in many biological and metabolic processes whether and how they are involved in the process of HBCD induced toxicity is largely unknown. In the present study zebrafish embryos were exposed to HBCD at low concentrations of 0 2 20 200 nM. Subsequently RNA was isolated from the embryo pool and the miRNAs expression profiles were analyzed using deep sequencing. | zebrafish at normal developmental age of 72hpf in the control rep1 | control 1 | breed:zebrafish|strain:Wild type TU strain|age:72 hpf£¨hpf stage:embryo|sex:pooled male and female|tissue:whole zebrafish|treatment:control 1|BioSampleModel:Model organism or animal | zebrafish at normal developmental age of 72hpf in the control rep1 | Sample control 1 | 1 | 1 | miRNA-Seq | TRANSCRIPTOMIC | other | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>33</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP058729 | Sample_control-1.fastq.tar.gz | fastq | 398024253.0 | 12061341.0 | Sample control 1 | 0:33 | A:90133666;C:86672655;G:103932053;T:117192591;N:93288 | 33 | 90133666 | 86672655 | 103932053 | 117192591 | 93288 | SRX1038887 | SRS945623 | SRA269780 | MG | Xiamen University | 1 | 0.08082 | 0.02367 | 0.96106 | 0.52033 | 33 | B | usable mapping rate | illumina | early_illumina | unknown | small_rna | unknown | bulk | unknown | unknown | China | 2015-05-27 | Larval | Larval | Whole Organism | All anatomical structures |
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CREATE TABLE run_metadata("run.accession" VARCHAR, "experiment.accession" VARCHAR, "sample.accession" VARCHAR, "study.accession" VARCHAR, bioproject VARCHAR, "study.title" VARCHAR, "study.alias" VARCHAR, "study.type" VARCHAR, "study.abstract" VARCHAR, "study.attributes" VARCHAR, "study.PMIDs" VARCHAR, "sample.description" VARCHAR, "sample.title" VARCHAR, "sample.alias" VARCHAR, "sample.centername" VARCHAR, "sample.attributes" VARCHAR, "GEOsample.title" VARCHAR, "GEOsample.dataprocessing" VARCHAR, "GEOsample.source" VARCHAR, "GEOsample.treatmentprotocol" VARCHAR, "GEOsample.extractprotocol" VARCHAR, "GEOsample.growthprotocol" VARCHAR, "GEOsample.characteristics" VARCHAR, "GEOsample.accession" VARCHAR, "experiment.title" VARCHAR, "experiment.alias" VARCHAR, "experiment.library_name" VARCHAR, "experiment.design_description" VARCHAR, "experiment.library_construction_protocol" VARCHAR, "experiment.attributes" VARCHAR, "experiment.library_strategy" VARCHAR, "experiment.library_source" VARCHAR, "experiment.library_selection" VARCHAR, "experiment.library_layout" VARCHAR, "experiment.platform" VARCHAR, "experiment.instrument_model" VARCHAR, "experiment.spot_descriptor" VARCHAR, "experiment.study_ref" VARCHAR, "run.title" VARCHAR, "run.attributes" VARCHAR, "run.filename" VARCHAR, "run.semantic_name" VARCHAR, "run.total_bases" DOUBLE, "run.total_spots" DOUBLE, "run.alias" VARCHAR, "run.read_lengths" VARCHAR, "run.base_counts" VARCHAR, "run.r1_length" BIGINT, "run.r2_length" BIGINT, "run.r3_length" BIGINT, "run.r4_length" BIGINT, "run.Acount" BIGINT, "run.Ccount" BIGINT, "run.Gcount" BIGINT, "run.Tcount" BIGINT, "run.Ncount" BIGINT, "run.experiment" VARCHAR, "run.pool_member" VARCHAR, "submission.accession" VARCHAR, "submission.srasource" VARCHAR, "submission.bioprojectsource" VARCHAR, "seqdetective.n_mates" BIGINT, "seqdetective.mapping_rate.mate1" DOUBLE, "seqdetective.mapping_rate.mate2" DOUBLE, "seqdetective.nofeature_rate.mate1" DOUBLE, "seqdetective.nofeature_rate.mate2" DOUBLE, "seqdetective.sparsity.mate1" DOUBLE, "seqdetective.sparsity.mate2" DOUBLE, "seqdetective.pos_strand_rate.mate1" DOUBLE, "seqdetective.pos_strand_rate.mate2" DOUBLE, "seqdetective.readlen.mate1" BIGINT, "seqdetective.readlen.mate2" BIGINT, "seqdetective.judgement.mate1" VARCHAR, "seqdetective.judgement.mate2" VARCHAR, "seqdetective.judgement.reason" VARCHAR, platform_family VARCHAR, instrument_generation VARCHAR, read_bias VARCHAR, selection_class VARCHAR, prep_kit VARCHAR, sc_or_bulk VARCHAR, tech_class VARCHAR, technology VARCHAR, tech_variant VARCHAR, "submission.bioprojectsource.country" VARCHAR, earliest_date DATE, devstage_curation VARCHAR, devstage_curation_coarse VARCHAR, tissue_curation VARCHAR, tissue_curation_coarse VARCHAR);;
CREATE INDEX idx_run_bioproject ON run_metadata(bioproject);;
CREATE INDEX idx_run_run_accession ON run_metadata("run.accession");;