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| Main Author: | |
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| Format: | Recurso digital |
| Language: | English |
| Published: |
Zenodo
2025
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| Online Access: | https://doi.org/10.5281/zenodo.16887275 |
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Table of Contents:
- <p>Unannotated whole-exome sequencing VCFs from two subjects with TANGO2 deficiency disorder. Files are separated into single nucleotide polymorphisms (SNP) and insertions/deletions (indels).</p> <p>SNP:</p> <p>TANGO2_Subject1.snp.vcf.gz</p> <p>TANGO2_Subject2.snp.vcf.gz</p> <p>Indels:</p> <p>TANGO2_Subject1.indel.vcf.gz</p> <p>TANGO2_Subject2.indel.vcf.gz</p>