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..
Data contains personal data
No
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Contributor(s)
Marie Allen (Data manager)
- Uppsala University, Department of Immunology, Genetics and Pathology
Adam Ameur (Data manager)
- Uppsala University, Department of Immunology, Genetics and Pathology
Identifiers
Research area
Genetics (Standard för svensk indelning av forskningsämnen 2011)
Forensic science (Standard för svensk indelning av forskningsämnen 2011)
