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Baby’s first genome

Nature Biotechnology volume 40, pages 636–640 (2022)Cite this article

Whole-genome sequencing may be the fastest way to diagnose rare complex diseases, but should it be incorporated into healthy newborn screening?

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Fig. 1: Cohort characteristics.

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  1. Los Angeles, CA, USA

    Caroline Seydel

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  1. Caroline Seydel
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Seydel, C. Baby’s first genome. Nat Biotechnol 40, 636–640 (2022). https://doi.org/10.1038/s41587-022-01306-1

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