Homo sapiens |
SRX11346536 |
SRP326792 |
9606 |
LCL |
genotype: FTSJ1 -/- |
Illumina |
NA |
NA |
Homo sapiens |
SRX4283794 |
SRP151126 |
9606 |
Peripheral blood mononuclear cell |
tissue: Peripheral blood mononuclear cell |
Illumina |
Type 2 Diabetes |
NA |
Homo sapiens |
SRX11346537 |
SRP326792 |
9606 |
LCL |
genotype: Wild Type |
Illumina |
NA |
NA |
Homo sapiens |
SRX4283795 |
SRP151126 |
9606 |
Peripheral blood mononuclear cell |
tissue: Peripheral blood mononuclear cell |
Illumina |
Type 2 Diabetes |
NA |
Homo sapiens |
SRX3675091 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Homo sapiens |
SRX3675092 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Pinus massoniana |
SRX8354102 |
SRP261990 |
88730 |
vegetative branch |
ecotype: WUYI |
NEB |
NA |
NA |
Homo sapiens |
SRX3675090 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Homo sapiens |
SRX11346530 |
SRP326791 |
9606 |
Plasma blood |
tissue: Plasma blood |
Illumina |
Hereditary hemorrhagic telangiectasia type 1 (HHT1) |
NA |
Homo sapiens |
SRX11346531 |
SRP326791 |
9606 |
Plasma blood |
tissue: Plasma blood |
Illumina |
Hereditary hemorrhagic telangiectasia type 1 (HHT1) |
NA |
Homo sapiens |
SRX3675099 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Homo sapiens |
SRX3675097 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Homo sapiens |
SRX3675098 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Homo sapiens |
SRX3675095 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Homo sapiens |
SRX3675096 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Homo sapiens |
SRX3675093 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Homo sapiens |
SRX3675094 |
SRP132519 |
9606 |
blood plasma |
NA |
other |
NA |
sequencing replicate: A |
Homo sapiens |
SRX11346529 |
SRP326791 |
9606 |
Plasma blood |
tissue: Plasma blood |
Illumina |
Hereditary hemorrhagic telangiectasia type 1 (HHT1) |
NA |
Homo sapiens |
SRX1099442 |
SRP061240 |
9606 |
plasma microvesicles |
disease status: Normal |
NEB |
Normal |
NA |
Homo sapiens |
SRX8026029 |
SRP254533 |
9606 |
Platelet |
molecule subtype: microRNA |
Illumina_2 |
Normal Young |
NA |
Homo sapiens |
SRX1099443 |
SRP061240 |
9606 |
plasma microvesicles |
disease status: Cancer |
NEB |
Cancer |
NA |
Homo sapiens |
SRX1099440 |
SRP061240 |
9606 |
plasma microvesicles |
disease status: Normal |
NEB |
Normal |
NA |
Homo sapiens |
SRX8026027 |
SRP254533 |
9606 |
Platelet |
molecule subtype: microRNA |
Illumina_2 |
Normal Young |
NA |
Homo sapiens |
SRX1099441 |
SRP061240 |
9606 |
plasma microvesicles |
disease status: Normal |
NEB |
Normal |
NA |
Homo sapiens |
SRX8026028 |
SRP254533 |
9606 |
Platelet |
molecule subtype: microRNA |
Illumina_2 |
Normal Young |
NA |