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 SRX2154263 SRP078144 9606 BREAST karyotype: This is a hypotriploid human cell line. The modal chromosome number is 65 occurring at 50% and polyploidy at 0.8%. 18 marker chromosomes are common to most cells, of which 7 are paired and 11 are single-copied. The t(8q14q), t(9q17q), t(10q17p) are among 7 paired markers common to most cells. N7, N9, and N10 are absent and N11 is generally present in 4 copies. DMs occurred, but infrequently. Q-band examination did not show the presence of a Y chromosome Illumina DUCTAL CARCINOMA NA
Rattus norvegicus SRX9075439 SRP280104 10116 Adipose treatment: Casein Illumina NA NA
Homo sapiens ERX8012540 ERP135083 9606 NA INSDC status: public adapter_trimmed NA NA
Homo sapiens SRX2154264 SRP078144 9606 BRAIN karyotype: This is a hypodiploid human cell line with the modal chromosome number of 44 occurring in 48% of cells. The rate of higher ploidy was 5.9%., Twelve markers were common to all cells, including der(1)t(1;3) (p22;q21), der(16)t(1;16) (p22;p12), del(9) (p13) and nine others. The marker der(1) had two copies in most cells. There was only one copy of normal X. N1, N6 and N9 were not found Illumina GLIOBLASTOMA; ASTROCYTOMA NA
Homo sapiens SRX2154269 SRP078144 9606 COLON karyotype: The stemline modal chromosome number is 96, occurring at 16% with polyploidy at 3.2%. Ten common markers were detected i.e., t(1q;?), 10q-, t(11q17q) and 7 others. The t(1q17q) and M11 were found in a portion of cells. The ins(2), 10q-, and t(15q;?) were generally paired, and t(11q;17q) and t(21q;?) were mostly three-copied. Normal N9 was absent, and N21 was lost in some cells. One to 4 small acrocentric chromosomes were detected. No Y chromosome with bright distal q-band was detected by Q-observation Illumina ADENOCARCINOMA NA
Rattus norvegicus SRX9075437 SRP280104 10116 Liver treatment: Casein Illumina NA NA
Rattus norvegicus SRX9075438 SRP280104 10116 Kidney treatment: Casein Illumina NA NA
Homo sapiens SRX2154267 SRP078144 9606 COLON karyotype: The stemline chromosome number is hypotriploid and 11-12 marker chromosomes were common. Both double minutes and dicentrics were observed in 8% of each metaphase examined Illumina ADENOCARCINOMA NA
Homo sapiens SRX2154268 SRP078144 9606 BREAST tissue: BREAST Illumina ADENOCARCINOMA NA
Rattus norvegicus SRX9075436 SRP280104 10116 Brain treatment: Casein Illumina NA NA
Homo sapiens SRX4029518 SRP144441 9606 Serum condition: Healthy Subject Illumina_2 NA NA
Rattus norvegicus SRX9075431 SRP280104 10116 Adipose treatment: Casein Illumina NA NA
Gallus gallus SRX25146569 SRP500067 9031 Embryo-trachea tissue: Embryo-trachea NEB NA NA
Homo sapiens SRX4029519 SRP144441 9606 Plasma condition: Healthy Subject Illumina_2 NA NA
Homo sapiens SRX2154261 SRP078144 9606 BREAST karyotype: modal number = 93; range = 85 to 95. The cell line is aneuploid human female, with chromosome counts in the tetraploid range. Normal chromosomes N16 and N21 are least well represented, with from none to two copies per karyotype, while chromosome N7 tends to be over-represented, with four or five copies per karyotype, whereas two to four copies are found of most of the remaining normal chromosomes. Twenty-two marker chromosomes are found including: iso(1q), del(1)(q32), der(1)t(1;?)(p36;?), del(3)(q24), der(3)t(3;?)(q24;?), del(3)(p14p25), t(6q;21?) and others. Eight are identical to those reported or portrayed in the report by A.J. Langlois, et al Illumina CARCINOMA NA