miSRA: search preprocessed public small-RNA data against your reference sequences (miRNA, tRNA, etc)
ugr
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Name Exp Study TaxonID SampleTag SampleTag2 LibraryInf Disease Method
Homo sapiens SRX2839072 SRP107326 9606 colon phenotype: adjacent normal adapter_trimmed colorectal cancer NA
Homo sapiens SRX2839073 SRP107326 9606 colon phenotype: neoplastic adapter_trimmed colorectal cancer NA
Homo sapiens SRX2839070 SRP107326 9606 colon phenotype: adjacent normal adapter_trimmed colorectal cancer NA
Homo sapiens SRX2839071 SRP107326 9606 colon phenotype: neoplastic adapter_trimmed colorectal cancer NA
Drosophila melanogaster SRX10238591 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 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