WES data

Unannotated whole-exome sequencing VCFs from two subjects with TANGO2 deficiency disorder. Files are separated into single nucleotide polymorphisms (SNP) and insertions/deletions (indels). SNP: TANGO2_Subject1.snp.vcf.gz TANGO2_Subject2.snp.vcf.gz Indels: TANGO2_Subject1.indel.vcf.gz TANGO2_Subject2.indel.vcf.gz

Institutions

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-08-16
DOI
https://doi.org/10.5281/zenodo.16887275
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

WES data

Zenodo (CERN European Organization for Nuclear Research)
Genomics and Rare Diseases
article

WES data

article en

Abstract

Unannotated whole-exome sequencing VCFs from two subjects with TANGO2 deficiency disorder. Files are separated into single nucleotide polymorphisms (SNP) and insertions/deletions (indels). SNP: TANGO2_Subject1.snp.vcf.gz TANGO2_Subject2.snp.vcf.gz Indels: TANGO2_Subject1.indel.vcf.gz TANGO2_Subject2.indel.vcf.gz

Zenodo (CERN European Organization for Nuclear Research)
University of Insubria (IT)
Openalex Percentile: Top 40%
Genomics and Rare Diseases
DOIOpen Access PDFOpenAlex
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

WES data · Zenodo (CERN European Organization for Nuclear Research) (2025) | TGRS Research Map | TGRS