miSRA: search preprocessed public small-RNA data against your reference sequences (miRNA, tRNA, etc)
ugr
miSRAdb automatic annotations
Experiments, taxonID and sample tag are searchable fields
Name Exp Study TaxonID SampleTag SampleTag2 LibraryInf Disease Method
Drosophila melanogaster SRX10238592 SRP309293 7227 sperm tissue: sperm NEB NA breeding_method: Flies were maintained on standard-diet at 25C. 0-4 days old flies were manually sorted to 15 males and 15 females per vial (or 45+45 in bottles) and allowed to lay eggs for 4 days. Flies were crossed on Thursday, flipped on Monday and virgins collected the following Monday. On Thursday flies were crossed again establishing a 2-week generation cycle. Genetic background was equalized between mutant and WT strains by crossing the mutant lines over double balancer lines where chromosomes were followed with a visible marker. This way crosses were generated in which all chromosomes were replaced with WT chromosomes, except the one carrying the mutation and the respective balancer. Flies from this cross were then crossed with WT, where offspring without the balancer chromosome was used for the hetrozygot mutant experiment.
Drosophila melanogaster SRX10238590 SRP309293 7227 sperm tissue: sperm NEB NA breeding_method: Flies were maintained on standard-diet at 25C. 0-4 days old flies were manually sorted to 15 males and 15 females per vial (or 45+45 in bottles) and allowed to lay eggs for 4 days. Flies were crossed on Thursday, flipped on Monday and virgins collected the following Monday. On Thursday flies were crossed again establishing a 2-week generation cycle. Genetic background was equalized between mutant and WT strains by crossing the mutant lines over double balancer lines where chromosomes were followed with a visible marker. This way crosses were generated in which all chromosomes were replaced with WT chromosomes, except the one carrying the mutation and the respective balancer. Flies from this cross were then crossed with WT, where offspring without the balancer chromosome was used for the hetrozygot mutant experiment.
Homo sapiens ERX1217538 ERP013193 9606 NA phenotype: Atopy (maternal) NEB NA NA
Homo sapiens ERX1217539 ERP013193 9606 NA phenotype: No atopy (maternal) NEB NA NA
Homo sapiens ERX1217536 ERP013193 9606 NA phenotype: No atopy (maternal) NEB NA NA
Homo sapiens ERX1217537 ERP013193 9606 NA phenotype: No atopy (maternal) NEB NA NA
Homo sapiens ERX1217534 ERP013193 9606 NA phenotype: Atopy (maternal) NEB NA NA
Homo sapiens ERX1217535 ERP013193 9606 NA phenotype: Atopy (maternal) NEB NA NA
Homo sapiens ERX1217532 ERP013193 9606 NA phenotype: No atopy (maternal) NEB NA NA
Homo sapiens ERX1217533 ERP013193 9606 NA phenotype: No atopy (maternal) NEB NA NA
Homo sapiens ERX1217530 ERP013193 9606 NA phenotype: No atopy (maternal) NEB NA NA
Homo sapiens ERX1217531 ERP013193 9606 NA phenotype: Atopy (maternal) NEB NA NA
Homo sapiens ERX1217540 ERP013193 9606 NA phenotype: No atopy (maternal) NEB NA NA
Haemonchus contortus SRX20276304 SRP436822 6289 polypide tissue: polypide NEB NA NA
Homo sapiens DRX325567 DRP010946 9606 NA NA Qiagen_UMI moyamoya dosease NA
Homo sapiens DRX325568 DRP010946 9606 NA NA Qiagen_UMI moyamoya dosease NA
Homo sapiens DRX325569 DRP010946 9606 NA NA Qiagen_UMI moyamoya dosease NA
Oryctolagus cuniculus SRX18249283 SRP407761 9986 femoral head genotype: Perthes disease adapter_trimmed NA NA
Oryctolagus cuniculus SRX18249284 SRP407761 9986 femoral head genotype: Perthes disease adapter_trimmed NA NA
Homo sapiens ERX1217549 ERP013193 9606 NA phenotype: Atopy (maternal) NEB NA NA
Oryctolagus cuniculus SRX18249281 SRP407761 9986 femoral head genotype: Perthes disease adapter_trimmed NA NA
Solanum lycopersicum SRX2213281 SRP090890 4081 root cultivar: Pusa Ruby Illumina NA NA
Oryctolagus cuniculus SRX18249282 SRP407761 9986 femoral head genotype: Perthes disease adapter_trimmed NA NA
Solanum lycopersicum SRX2213282 SRP090890 4081 root cultivar: Pusa Ruby Illumina NA NA
Homo sapiens ERX1217547 ERP013193 9606 NA phenotype: No atopy (maternal) NEB NA NA