Long-read sequencing identified a causal structural variant in an exome-negative case and enabled preimplantation genetic diagnosis https://t.co/rh3gVvEDMY
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GrandOmics results:The first examples of using long-read sequencing ( on Oxford @nanopore platform) to identify causal yet complex SVs in exome-negative patients, which subsequently enabled successful personalized PGD.The results was pulished on Hereditas.
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Long-read sequencing identified a causal structural variant in an exome-negative case and enabled preimplantation genetic diagnosis. https://t.co/gsRxUiRU6C https://t.co/6IU9hoF6Wq
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Long-read sequencing identified a causal structural variant in an exome-negative case and enabled preimplantation genetic diagnosis. https://t.co/DYcQOhB1nL