Bioinformatics AdvancesGenomicsPeer-reviewed journal article
XhetRel: A Pipeline for X Heterozygosity and Relatedness Analysis in Sequencing Data
Abstract
MotivationChecking sample sex is one of the preliminary controls performed in genetic studies. Comparing multiple individuals and families in terms of sex and relatedness allows us to eliminate systematic errors in downstream analyses. While developing the pipeline we further delved into the origins of X heterozygosity by analysing the chromosome X variants from the 1000 Genomes Project. ResultWe created an accessible and user-friendly notebook application for X heterozygosity analysis. XhetRel can serve as an initial quality control step in sequencing projects. Further investigating the source of X heterozygosity reveals the limitations of sequencing and variant calling methods in heterozygosity analysis. Our findings point to specific pseudogenes and gene clusters, such as SLC25A5 and GAGE cluster, as key contributors to erroneous variant allele fractions. Availability and implementationSource code is available https://github.com/barslmn/XhetRel. Collab notebook can be accessed at https://colab.research.google.com/drive/1ep69JvXLwK5ndHUQ8qIGTWvauzsTW9fi.
- assay: whole-genome sequencing
- research focus: variant calling
- research focus: variant effect prediction
- research focus: benchmarking
- approach: statistical model
- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 4th percentile
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