Name | Exp | Study | TaxonID | SampleTag | SampleTag2 | LibraryInf | Disease | Method |
---|---|---|---|---|---|---|---|---|
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 |
Homo sapiens | SRX18106982 | SRP405648 | 9606 | NGN2-iNs | cell line: NGN2-iNs | Illumina | NA | NA |
Homo sapiens | SRX18106983 | SRP405648 | 9606 | NGN2-iNs | cell line: NGN2-iNs | Illumina | NA | NA |
Homo sapiens | SRX18106984 | SRP405648 | 9606 | NGN2-iNs | cell line: NGN2-iNs | Illumina | NA | NA |
Homo sapiens | SRX18106985 | SRP405648 | 9606 | NGN2-iNs | cell line: NGN2-iNs | Illumina | NA | NA |
Gallus gallus | SRX19911547 | SRP431634 | 9031 | IMHV | tissue: IMHV | NEB | NA | NA |