miSRA: search preprocessed public small-RNA data against your reference sequences (miRNA, tRNA, etc)
ugr
miSRAdb automatic annotations
Experiments, taxonID and sample tag are searchable fields
Name Exp Study TaxonID SampleTag SampleTag2 LibraryInf Disease Method
Homo sapiens SRX3671075 SRP132514 9606 Keratinocyte uvb treatment: none Illumina NA NA
Homo sapiens SRX10240722 SRP309361 9606 CD19+ B cells disease status: rheumatoid arthritis patient NEB rheumatoid arthritis patient NA
Homo sapiens SRX3671076 SRP132514 9606 Keratinocyte uvb treatment: none Illumina NA NA
Homo sapiens SRX10240723 SRP309361 9606 CD19+ B cells disease status: rheumatoid arthritis patient NEB rheumatoid arthritis patient NA
Homo sapiens SRX3671077 SRP132514 9606 Keratinocyte uvb treatment: none Illumina NA NA
Homo sapiens SRX10240724 SRP309361 9606 CD19+ B cells disease status: rheumatoid arthritis patient NEB rheumatoid arthritis patient NA
Homo sapiens SRX18106970 SRP405648 9606 NGN2-iNs cell line: NGN2-iNs Illumina NA NA
Homo sapiens SRX3671078 SRP132514 9606 Melanocyte uvb treatment: none Illumina NA NA
Homo sapiens SRX18106979 SRP405648 9606 NGN2-iNs cell line: NGN2-iNs Illumina NA NA
Gallus gallus SRX19911554 SRP431634 9031 IMHV tissue: IMHV NEB NA NA
Gallus gallus SRX19911555 SRP431634 9031 IMHV tissue: IMHV NEB NA NA
Gallus gallus SRX19911556 SRP431634 9031 IMHV tissue: IMHV NEB NA NA
Gallus gallus SRX19911557 SRP431634 9031 IMHV tissue: IMHV NEB NA NA
Homo sapiens SRX18106975 SRP405648 9606 NGN2-iNs cell line: NGN2-iNs Illumina NA NA
Gallus gallus SRX19911550 SRP431634 9031 IMHV tissue: IMHV NEB NA NA
Homo sapiens SRX18106976 SRP405648 9606 NGN2-iNs cell line: NGN2-iNs Illumina NA NA
Gallus gallus SRX19911551 SRP431634 9031 IMHV tissue: IMHV NEB NA NA
Homo sapiens SRX18106977 SRP405648 9606 NGN2-iNs cell line: NGN2-iNs Illumina NA NA
Gallus gallus SRX19911552 SRP431634 9031 IMHV tissue: IMHV NEB NA NA
Homo sapiens SRX18106978 SRP405648 9606 NGN2-iNs cell line: NGN2-iNs Illumina NA NA
Gallus gallus SRX19911553 SRP431634 9031 IMHV tissue: IMHV NEB NA NA
Homo sapiens SRX3876301 SRP136965 9606 T98G genotype/variation: EZH2-/- NEB NA NA
Homo sapiens SRX3876302 SRP136965 9606 T98G genotype/variation: EZH2-/- NEB NA NA
Homo sapiens SRX3876303 SRP136965 9606 T98G genotype/variation: WT NEB NA NA
Homo sapiens SRX3876304 SRP136965 9606 T98G genotype/variation: WT NEB NA NA