miSRA: search preprocessed public small-RNA data against your reference sequences (miRNA, tRNA, etc)
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| Name | Exp | Study | TaxonID | SampleTag | SampleTag2 | LibraryInf | Disease | Method |
|---|---|---|---|---|---|---|---|---|
| Rattus norvegicus | SRX9075446 | SRP280104 | 10116 | Kidney | treatment: Casein | Illumina | NA | NA |
| Homo sapiens | SRX2154279 | SRP078144 | 9606 | LUNG | karyotype: Modal number = 79; range = 71 to 83 This is a hypertriploid human cell line with the modal chromosome number of 79, occurring in 20% of cells. The rate of cells with a higher ploidy was 5.5%. Karyotypes were very complex. There were over 22 marker chromosomes commonly present in most cells, many with complex structural rearrangements. Among these markers were: double copies for t(10qter--10q11.2::?::13C--13qter) and der(9)t(3;9) (p12;p22?), and one copy each for del (1) (p22) and i (iq). There were two normal X chromosomes per cell. Normal chromosomes Y, N1, N5, N14, and N15 were not found. Chromosomes N20 and N22 generally had four or more copies per cell | Illumina | ADENOCARCINOMA | NA |
| Rattus norvegicus | SRX9075447 | SRP280104 | 10116 | Adipose | treatment: Casein | Illumina | NA | NA |
| Rattus norvegicus | SRX9075444 | SRP280104 | 10116 | Brain | treatment: Casein | Illumina | NA | NA |
| Rattus norvegicus | SRX9075445 | SRP280104 | 10116 | Liver | treatment: Casein | Illumina | NA | NA |
| Homo sapiens | SRX4029529 | SRP144441 | 9606 | Serum | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | SRX2154272 | SRP078144 | 9606 | SKIN | karyotype: (P6) hypodiploid to hypertetraploid with abnormalities including dicentrics, secondary constrictions and large telocentric marker. Note: Cytogenetic information is based on initial seed stock at ATCC. Cytogenetic instability has been reported in the literature for some cell lines | Illumina | MALIGNANT MELANOMA | NA |
| Homo sapiens | SRX2154273 | SRP078144 | 9606 | OVARY | tissue: OVARY | Illumina | ADENOCARCINOMA | NA |
| Homo sapiens | SRX2154270 | SRP078144 | 9606 | COLON | karyotype: modal number = 71; range = 68 to 72. The stemline chromosome number is hypertriploid with the 2S component occurring at 2.4%. Seventeen marker chromosomes are found in most metaphases, generally in single copy per chromosome. The marker designations are: M1p-(=t(3p-;?) with a deleted short arm), t(7q;?), t(10q;?), i(13q), 19q+a; M6, ?t(8q;9q-), ?Xp, M9, 6q+, t(13;?)a, t(13;?)b, 19q+b, M14, M15, 15p+, and Xq-. Chromosome 13 is nullisomic and chromosomes 8 and 14 are generally monosomic. No Y chromosome was detected by QM band analysis | Illumina | ADENOCARCINOMA | NA |
| Homo sapiens | SRX2154271 | SRP078144 | 9606 | SKIN | tissue: SKIN | Illumina | MALIGNANT MELANOMA | NA |
| Homo sapiens | SRX4029534 | SRP144441 | 9606 | Plasma | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | SRX4029535 | SRP144441 | 9606 | Plasma | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | SRX4029532 | SRP144441 | 9606 | Plasma | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | SRX4029533 | SRP144441 | 9606 | Serum | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | SRX4029538 | SRP144441 | 9606 | Plasma | condition: Healthy Subject | Illumina_2 | NA | NA |