| The subject consent file includes subject IDs, consent information, and subject source. | Subject ID | phv00348650.v1.p1 |
| This sample attributes table contains sample IDs, tumor status, targeted exon region, tissue of origin, and analyte type. | Analyte Type | phv00348666.v1.p1 |
| This sample attributes table contains sample IDs, tumor status, targeted exon region, tissue of origin, and analyte type. | Tumor Status | phv00348663.v1.p1 |
| This subject phenotype table contains subject IDs, clinical diagnosis, sex, age, treatment, and WBC counts. | De-identified Subject ID | phv00348656.v1.p1 |
| This data table contains a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes sample use. | Subject ID | phv00348653.v1.p1 |
| The subject consent file includes subject IDs, consent information, and subject source. | Source repository where subjects originate | phv00348652.v1.p1 |
| This subject phenotype table contains subject IDs, clinical diagnosis, sex, age, treatment, and WBC counts. | Subject age | phv00348659.v1.p1 |
| This sample attributes table contains sample IDs, tumor status, targeted exon region, tissue of origin, and analyte type. | Tissue where DNA was collected | phv00348665.v1.p1 |
| This sample attributes table contains sample IDs, tumor status, targeted exon region, tissue of origin, and analyte type. | SAMPLE_ID | phv00348662.v1.p1 |
| The subject consent file includes subject IDs, consent information, and subject source. | Consent group as determined by DAC | phv00348651.v1.p1 |
| This subject phenotype table contains subject IDs, clinical diagnosis, sex, age, treatment, and WBC counts. | Clinical Diagnosis of T-cell acute lymphoblastic leukemia | phv00348657.v1.p1 |
| This data table contains a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes sample use. | Sample ID | phv00348654.v1.p1 |
| This subject phenotype table contains subject IDs, clinical diagnosis, sex, age, treatment, and WBC counts. | Treatment given to participant | phv00348660.v1.p1 |
| This subject phenotype table contains subject IDs, clinical diagnosis, sex, age, treatment, and WBC counts. | Sex of participant | phv00348658.v1.p1 |
| This subject phenotype table contains subject IDs, clinical diagnosis, sex, age, treatment, and WBC counts. | Peripheral white blood cell count at leukemia diagnosis | phv00348661.v1.p1 |
| This sample attributes table contains sample IDs, tumor status, targeted exon region, tissue of origin, and analyte type. | Targeted Exon Region | phv00348664.v1.p1 |
| This data table contains a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes sample use. | Sample use from https://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/projects/gap/cgi-bin/GetMolecularDataTypes.cgi Seq_DNA_Exome_Target: Targeted exome sequencing Seq_RNA: Whole transcriptome sequencing | phv00348655.v1.p1 |