SUPPLEMENTARY MATERIALS for Mitochondrial DNA genome variation in the Swedish population
SND-ID: 2024-357. Version: 1. DOI: https://doi.org/10.57804/mfyp-ea25
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Creator/Principal investigator(s)
Kimberly Sturk-Andreaggi - Uppsala University, Department of Immunology, Genetics and Pathology
Research principal
Description
The data consists of:
- Table S1. 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
- Table S1. 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. Show less..
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Genetics (Standard för svensk indelning av forskningsämnen 2011)
Forensic science (Standard för svensk indelning av forskningsämnen 2011)