miSRA: search preprocessed public small-RNA data against your reference sequences (miRNA, tRNA, etc)
Filter the database to select the samples
| Name | Exp | Study | TaxonID | SampleTag | SampleTag2 | LibraryInf | Disease | Method |
|---|---|---|---|---|---|---|---|---|
| Homo sapiens | SRX4029539 | SRP144441 | 9606 | Plasma | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | SRX4029536 | SRP144441 | 9606 | Plasma | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | SRX4029537 | SRP144441 | 9606 | Plasma | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | ERX8012558 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | ERX8012559 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | ERX8012556 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX4029530 | SRP144441 | 9606 | Plasma | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | ERX8012557 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX4029531 | SRP144441 | 9606 | Plasma | condition: Healthy Subject | Illumina_2 | NA | NA |
| Homo sapiens | ERX8012554 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | ERX8012555 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | ERX8012541 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX2154265 | SRP078144 | 9606 | OVARY | karyotype: The cell line is aneuploid human female, with chromosome counts in the sub to near-triploid range. Several normal chromosomes (N11, N13, N14, N15, N16, N17, and N22) are clearly under-represented. Many of these missing chromosomes are represented in the large number of cytogenetically altered chromosomes identified as marker chromosomes. In addition to the marker chromosomes, there are a large number of other structurally abnormal and unassignable chromosomes that are not recognized as markers. Random loss and gain of chromosomes from cell to cell are noted in the exact chromosome counts and in the analysis of the karyotypes | Illumina | ADENOCARCINOMA | NA |
| Homo sapiens | ERX8012542 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX2154266 | SRP078144 | 9606 | BREAST | karyotype: modal number = 82; range = 66 to 87. The stemline chromosome numbers ranged from hypertriploidy to hypotetraploidy, with the 2S component occurring at 1%. There were 29 to 34 marker chromosomes per S metaphase; 24 to 28 markers occurred in at least 30% of cells, and generally one large submetacentric (M1) and 3 large subtelocentric (M2, M3, and M4) markers were recognizable in over 80% of metaphases. No DM were detected. Chromosome 20 was nullisomic and X was disomic | Illumina | ADENOCARCINOMA | NA |