Genetic variants from whole exome sequencing of female IVF patients

Jinchuan Xing; Karen Schindler

doi:10.7282/00000416

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Genetic variants from whole exome sequencing of female IVF patients

Dataset

Open access

Genetic variants from whole exome sequencing of female IVF patients

Jinchuan Xing and Karen Schindler

TBD

DOI:

https://doi.org/10.7282/00000416

Abstract

Genetics

Supplemental Data for: Maternal genetic variants in kinesin motor domains prematurely increase egg aneuploidy. Leelabati Biswas, Katarzyna M. Tyc, Mansour Aboelenain, Siqi Sun, Iva Dundović, Kruno Vukušić, Jason Liu, Vanessa Guo, Min Xu, Richard T. Scott, Jr., Xin Tao, Iva M. Tolić, Jinchuan Xing, Karen Schindler. Filename: SuppData1_VariantAF.vcf.gz Description: This VCF file contains 494,448 variants identified across 178 individuals by whole exome sequencing that were used in the study. Allele counts (AC), total allele number (AN), and allele frequencies (AF) for either Low Aneuploidy Rate group (LRG) or High Aneuploidy Rate group (HRG) were specified in the INFO tags.

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Details

Title: Subtitle: Genetic variants from whole exome sequencing of female IVF patients
Creators: Jinchuan Xing (Author) - Rutgers University, Genetics (SAS)
Karen Schindler (Author) - Rutgers University, Genetics (SAS)
Publisher: TBD
Grants: Understanding genetic risk for aneuploid conception, R01HD091331, Eunice Kennedy Shriver National Institute of Child Health and Human Development (United States, Bethesda) - NICHD
Academic Unit: Genetics (SAS)
Resource Type: Dataset
Identifiers: 991031964304104646