Homo sapiens |
SRX21227343 |
SRP452991 |
9606 |
dermis |
genotype: vEDS |
Qiagen_UMI |
affected |
NA |
Sapindus mukorossi |
SRX13254617 |
SRP348415 |
57655 |
pericarp |
cultivar: not applicable |
NEB |
NA |
NA |
Homo sapiens |
SRX21227342 |
SRP452991 |
9606 |
dermis |
genotype: vEDS |
Qiagen_UMI |
affected |
NA |
Sapindus mukorossi |
SRX13254616 |
SRP348415 |
57655 |
pericarp |
cultivar: not applicable |
NEB |
NA |
NA |
Homo sapiens |
SRX21227341 |
SRP452991 |
9606 |
dermis |
genotype: healthy donors |
Qiagen_UMI |
unaffected |
NA |
Sapindus mukorossi |
SRX13254615 |
SRP348415 |
57655 |
pericarp |
cultivar: not applicable |
NEB |
NA |
NA |
Homo sapiens |
SRX21227340 |
SRP452991 |
9606 |
dermis |
genotype: healthy donors |
Qiagen_UMI |
unaffected |
NA |
Sapindus mukorossi |
SRX13254614 |
SRP348415 |
57655 |
pericarp |
cultivar: not applicable |
NEB |
NA |
NA |
Homo sapiens |
SRX21227347 |
SRP452991 |
9606 |
dermis |
genotype: vEDS |
Qiagen_UMI |
affected |
NA |
Sapindus mukorossi |
SRX13254613 |
SRP348415 |
57655 |
pericarp |
cultivar: not applicable |
Illumina_2 |
NA |
NA |
Homo sapiens |
SRX21227346 |
SRP452991 |
9606 |
dermis |
genotype: vEDS |
Qiagen_UMI |
affected |
NA |
Sapindus mukorossi |
SRX13254612 |
SRP348415 |
57655 |
pericarp |
cultivar: not applicable |
NEB |
NA |
NA |
Homo sapiens |
SRX21227345 |
SRP452991 |
9606 |
dermis |
genotype: vEDS |
Qiagen_UMI |
affected |
NA |
Sapindus mukorossi |
SRX13254611 |
SRP348415 |
57655 |
pericarp |
cultivar: not applicable |
NEB |
NA |
NA |
Homo sapiens |
SRX21227344 |
SRP452991 |
9606 |
dermis |
genotype: vEDS |
Qiagen_UMI |
affected |
NA |
Sapindus mukorossi |
SRX13254610 |
SRP348415 |
57655 |
pericarp |
cultivar: not applicable |
Illumina_2 |
NA |
NA |
Homo sapiens |
SRX4957494 |
SRP167242 |
9606 |
Urine |
condition: Nephrotic Syndrome |
Illumina_2 |
NA |
NA |
Homo sapiens |
SRX4957493 |
SRP167242 |
9606 |
Urine |
condition: Nephrotic Syndrome |
Illumina_2 |
NA |
NA |
Homo sapiens |
SRX4957492 |
SRP167242 |
9606 |
Urine |
condition: Nephrotic Syndrome |
Illumina_2 |
NA |
NA |
Homo sapiens |
SRX4957491 |
SRP167242 |
9606 |
Urine |
condition: Nephrotic Syndrome |
Illumina_2 |
NA |
NA |
Homo sapiens |
SRX4957490 |
SRP167242 |
9606 |
Urine |
condition: Nephrotic Syndrome |
Illumina_2 |
NA |
NA |
Rattus norvegicus |
SRX9709979 |
SRP298678 |
10116 |
Pancreatic islet cells |
cell type: Pancreatic islet cells |
NEB |
NA |
NA |
Rattus norvegicus |
SRX9709978 |
SRP298678 |
10116 |
Pancreatic islet cells |
cell type: Pancreatic islet cells |
NEB |
NA |
NA |
Rattus norvegicus |
SRX9709977 |
SRP298678 |
10116 |
Pancreatic islet cells |
cell type: Pancreatic islet cells |
NEB |
NA |
NA |
Homo sapiens |
SRX8132649 |
SRP256943 |
9606 |
Huh7 |
cell line: Huh7 |
Illumina |
infection: MER-CoV KNIH002 |
NA |