Applying Genomic Sequencing in Pediatrics (PediSeq)
Demographics (2)
- Age - Subject age (phv00251837.v1.p1)
- Sex - Gender of participant (phv00251832.v1.p1)
Disease Events (1)
- AFFECTION_STATUS - Case control status of the subject based on the DISEASE_COHORT variable in CSER_PediSeq_Subject_Phenotypes dataset table (phv00251827.v1.p1)
Race and Ethnicity (2)
- Ethnicity - Ethnicity of participant (phv00251834.v1.p1)
- Race - Race of participant (phv00251833.v1.p1)
Other (17)
- ANALYTE_TYPE - Analyte Type (phv00251840.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00251839.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00251824.v1.p1)
- Disease Cohort - Disease cohort (phv00251836.v1.p1)
- GENOTYPING_CENTER - Name of the center which conducted genotyping (phv00251843.v1.p1)
- HISTOLOGICAL_TYPE - Cell or tissue type or subtype of sample (phv00251842.v1.p1)
- IS_TUMOR - Tumor status (phv00251841.v1.p1)
- Other - Other ethnicity of participant (phv00251835.v1.p1)
- SAMPLE_ID - De-identified Sample ID (phv00251838.v1.p1)
- SAMPLE_ID - Sample ID (phv00251829.v1.p1)
- SAMPLE_USE - Sample use. Seq_DNA_SNP_CNV: SNP and CNV genotypes derived from sequence data; Seq_DNA_WholeExome: Whole exome sequencing (phv00251830.v1.p1)
- SEQUENCING_CENTER - Name of the center which conducted sequencing (phv00251844.v1.p1)
- SOURCE_SUBJECT_ID - Subject ID used in the Source Repository (phv00251826.v1.p1)
- SUBJECT_ID - De-identified Subject ID (phv00251831.v1.p1)
- SUBJECT_ID - Subject ID (phv00251823.v1.p1)
- SUBJECT_ID - Subject ID (phv00251828.v1.p1)
- SUBJECT_SOURCE - Source repository where subjects originate (phv00251825.v1.p1)