Associated Papers
Analysis of Selective Pressure on Ancient Human Mitochondrial Genomes Reveals the Presence of Widespread Sequencing Artefacts.
Fernandes P et al.
International Journal of Molecular Sciences, 2025
40869060 (PubMed )
Supplement: ijms-26-07739-s001.zip › ijms-3768908-supplementary.pdf
Association of mitochondrial DNA content, heteroplasmies and inter-generational transmission with autism.
Wang Y et al.
Nature Communications, 2022
35778412 (PubMed )
Supplement: 41467_2022_30805_MOESM3_ESM.xlsx › all_heteroplasmies
Comprehensive profiling of 1015 patients' exomes reveals genomic-clinical associations in colorectal cancer.
Zhao Q et al.
Nature Communications, 2022
35487942 (PubMed )
Supplement: 41467_2022_30062_MOESM2_ESM.zip › Supplementary_Data › Supplementary_Data_8.xlsx › Supplementary_Data_8
Single-cell lineage tracing by endogenous mutations enriched in transposase accessible mitochondrial DNA.
Xu J et al.
Elife, 2019
30958261 (PubMed )
Supplement: elife-45105-supp2.xlsx › SU496
Site-specific selection reveals selective constraints and functionality of tumor somatic mtDNA mutations.
Li D et al.
Journal of Experimental & Clinical Cancer Research : Cr, 2017
29179728 (PubMed )
Supplement: 13046_2017_638_MOESM3_ESM.xlsx › Supplementary_table_5_Phylotree
Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy.
Ji Y et al.
Investigative Ophthalmology & Visual Science, 2016
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