Whole Exome and Targeted Sequencing in Tourette Syndrome Multiplex Families
Demographics (2)
- sex - Gender of participant (phv00163339.v1.p1)
- SEX - Sex of subject (phv00163331.v1.p1)
Other (24)
- affecteds_fam - Number of affected individuals in pedigree (phv00163341.v1.p1)
- AFFECTION_STATUS - Affection status of the subject (phv00163326.v1.p1)
- ANALYTE_TYPE - Analyte Type (phv00163346.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00163345.v1.p1)
- Comments - Describes relationship between two families (phv00163332.v1.p1)
- CONSENT - Consent group (phv00163323.v1.p1)
- CT_affecteds_fam - Number of chronic tic disorder affected individuals in pedigree (phv00163343.v1.p1)
- DUPLICATE_SAMP - Duplicate sample (phv00163337.v1.p1)
- FAMID - Family ID (phv00163327.v1.p1)
- FATHER - Father's Subject ID (phv00163330.v1.p1)
- MOTHER - Mother's Subject ID (phv00163329.v1.p1)
- SAMP_SOURCE - Source repository where samples originate (phv00163335.v1.p1)
- SAMPID - Sample ID (phv00163334.v1.p1)
- SAMPID - De-identified Sample ID (phv00163344.v1.p1)
- SAMPLE_USE - Method applied to subject's sample. Array_SNP: SNP genotypes obtained using standard or custom microarrays; Seq_DNA_Target: Custom targeted DNA sequencing; Seq_DNA_WholeExome: Whole exome sequencing (phv00163347.v1.p1)
- SOURCE_SAMPID - Sample ID used in the Source Repository (phv00163336.v1.p1)
- SOURCE_SUBJID - Subject ID used in the Source Repository (phv00163325.v1.p1)
- SUBJ_SOURCE - Source repository where subjects originate (phv00163324.v1.p1)
- SUBJID - Unique Subject ID (phv00163328.v1.p1)
- SUBJID - Subject ID (phv00163333.v1.p1)
- SUBJID - De-identified Subject ID (phv00163338.v1.p1)
- SUBJID - Subject ID (phv00163322.v1.p1)
- Tic_Status - Affection status of participant (phv00163340.v1.p1)
- TS_affecteds_fam - Number of Tourette Syndrome affected individuals in pedigree (phv00163342.v1.p1)