2026-10-14 https://api.researchdata.se/oai-pmh

oai:researchdata.se:2024-357/1 2024-06-24 subject:ssif:10609 subject:ssif:30501 subject:ssif:106 subject:ssif:305 subject:ssif:1 subject:ssif:3 principal:slug:uppsala-university

info:eu-repo/semantics/other http://purl.org/dc/dcmitype/Dataset https://doi.org/10.57804/mfyp-ea25 SUPPLEMENTARY MATERIALS for Mitochondrial DNA genome variation in the Swedish population SUPPLEMENTARY MATERIALS for Mitochondrial DNA genome variation in the Swedish population https://orcid.org/0000-0001-6857-923X 0000-0003-4055-3163 0000-0001-6085-6749 Genetics and Genomics Genetik och genomik Forensic Science Rättsmedicin 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 coverage classification group. The dataset was originally published in DiVA and moved to SND in 2024. 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 coverage classification group. Datasetet har ursprungligen publicerats i DiVA och flyttades över till SND 2024. info:eu-repo/semantics/openAccess Uppsala University Uppsala universitet 2022-03-28T00:00:00Z eng