Chunk #106 — STAR★METHODS — DATA AND SOFTWARE AVAILABILITY — Data

Source

De Novo Coding Variants Are Strongly Associated with Tourette Disorder.

Embedded

yes

Text

We have deposited aligned whole exome sequencing data (.bam files) in the Sequence Read Archive (SRA; https://www.ncbi.nlm.nih.gov/sra/) under accession IDs SUB2101648 (Tic Genetics data) and YYY (TSAICG data).