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 |
|---|---|---|---|---|---|---|---|---|
| Homo sapiens | ERX8012644 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | ERX8012645 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX2839356 | SRP107326 | 9606 | colon | phenotype: adjacent normal | adapter_trimmed | colorectal cancer | NA |
| Homo sapiens | ERX8012642 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | ERX8012643 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX2839354 | SRP107326 | 9606 | colon | phenotype: adjacent normal | adapter_trimmed | colorectal cancer | NA |
| Homo sapiens | ERX8012552 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX2154276 | SRP078144 | 9606 | PROSTATE | karyotype: This is a hypotriploid human cell line. Both 61 and 62 chromosome numbers had the highest rate of occurrence in 30 metaphase counts.The rate of higher ploidies was 3%. The t(11q12q), del(11)(q23), 16q+, del(9)(p11), del(1)(p32) and 6 other marker chromosomes were found in most cells. The N13 was usually absent. The Y chromosome is abnormal through translocation to an unidentified chromosomal segment. The X chromosome was present in single copy | Illumina | CARCINOMA | NA |
| Homo sapiens | ERX8012553 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX2154277 | SRP078144 | 9606 | COLON | tissue: COLON | Illumina | ADENOCARCINOMA | NA |
| Homo sapiens | ERX8012550 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX2154274 | SRP078144 | 9606 | OVARY | karyotype: This is a hypodiploid human cell line. The modal chromosome number was 43, occurring in 63.3% of cells. The range was 42 to 45. The rate of higher ploidies was 32%. The del(1)(q21), der(13)t(1;?;13) (q11;?;q34), der(11)t(11;?) (q12), del(10)(q22) and 3 other marker chromosomes were common to most cells, and 3 others were found only in some cells. One N11 had the HSR segment from p11 to the distal end. The normal N10, N12, N15, N17 and N19 were absent. Others were either single or paired. There were from 1 to 6 rearranged and unassignable chromosomes. The X chromosome was either single or paired | Illumina | ADENOCARCINOMA | NA |
| Homo sapiens | ERX8012551 | ERP135083 | 9606 | NA | INSDC status: public | adapter_trimmed | NA | NA |
| Homo sapiens | SRX2154275 | SRP078144 | 9606 | PANCREAS | karyotype: (P7) hypotriploid with abnormalities including dicentrics, breaks, acrocentric fragments, large submetacentric and subtelocentric chromosomes plus minute marker | Illumina | ADENOCARCINOMA | NA |
| Homo sapiens | SRX2154278 | SRP078144 | 9606 | COLON | karyotype: The stemline chromosome number is near diploid with the modal number at 45 (62%) and polyploids occurring at 6.8%. The markers 10q+ and t(?8p;18q) are present in all metaphases and t(9q;?16p-), in 80% of the cells karyotyped. N16 is monosomic in the presence of, but disomic in the absence of t(9q;?16p-). N10 and N18 are monosomic and other chromosomes from those mentioned above are disomic. Q-band observations revealed the presence of the Y chromosome, but not in all cells (50% of cells lacked the Y in G-band karyotypes) | Illumina | CARCINOMA | NA |