A reference catalog of DNA palindromes in the human genome and their variations in 1000 Genomes

A toolkit to detect DNA patterns has pinpointed millions of palindromes within the human genome, which could further the understanding of their association with disease. 

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Editor’s Selection on Splicing Variants and Copy Number Variation

Human Genome Variation is delighted to present its first Collection for the March 2019 issue. Coordinated by the Editor-in-Chief, Professor Katsushi Tokunaga, this Collection features the latest Data Reports and Articles on the identifications of disease-causing splicing variants and copy number variations.
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