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Data · dataset · 2022

SUPPLEMENTARY MATERIALS for Mitochondrial DNA genome variation in the Swedish population

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The data consists of: - Table S1.

Description

The haplogroup breakdown for the 934 SweGen haplotypes included in the final mitochondrial genome dataset. - Figure S1. Graphical description of the average read depths observed in the SweGen dataset. - Figure S2.

The distribution of read depth for the 16,569 positions of the mitochondrial genome based on the average observed in a subset of 100 representative SweGen haplotypes. - Figure S3. The box-and-whisker plot presents the distribution of average variant frequency for each coverage classification group. The dataset was originally published in DiVA and moved to SND in 2024.

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Inferred from text
Genetics 70% · Tabular 65%
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