m+Medelevator.RU
← Поиск публикаций
Nature · 2020

Telomere-to-telomere assembly of a complete human X chromosome.

СтатьяПоддержка NIH: внешняя программаResearch Support, N.I.H., IntramuralПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Miga Karen H, Koren Sergey, Rhie Arang, Vollger Mitchell R, Gershman Ariel, Bzikadze Andrey, Brooks Shelise, Howe Edmund, Porubsky David, Logsdon Glennis A, Schneider Valerie A, Potapova Tamara, Wood Jonathan, Chow William, Armstrong Joel, Fredrickson Jeanne, Pak Evgenia, Tigyi Kristof, Kremitzki Milinn, Markovic Christopher, Maduro Valerie, Dutra Amalia, Bouffard Gerard G, Chang Alexander M, Hansen Nancy F, Wilfert Amy B, Thibaud-Nissen Françoise, Schmitt Anthony D, Belton Jon-Matthew, Selvaraj Siddarth, Dennis Megan Y, Soto Daniela C, Sahasrabudhe Ruta, Kaya Gulhan, Quick Josh, Loman Nicholas J, Holmes Nadine, Loose Matthew, Surti Urvashi, Risques Rosa Ana, Graves Lindsay Tina A, Fulton Robert, Hall Ira, Paten Benedict, Howe Kerstin, Timp Winston, Young Alice, Mullikin James C, Pevzner Pavel A, Gerton Jennifer L, Sullivan Beth A, Eichler Evan E, Phillippy Adam M

Аннотация

After two decades of improvements, the current human reference genome (GRCh38) is the most accurate and complete vertebrate genome ever produced. However, no single chromosome has been finished end to end, and hundreds of unresolved gaps persist1,2. Here we present a human genome assembly that surpasses the continuity of GRCh382, along with a gapless, telomere-to-telomere assembly of a human chromosome. This was enabled by high-coverage, ultra-long-read nanopore sequencing of the complete hydatidiform mole CHM13 genome, combined with complementary technologies for quality improvement and validation. Focusing our efforts on the human X chromosome3, we reconstructed the centromeric satellite DNA array (approximately 3.1 Mb) and closed the 29 remaining gaps in the current reference, including new sequences from the human pseudoautosomal regions and from cancer-testis ampliconic gene families (CT-X and GAGE). These sequences will be integrated into future human reference genome releases. In addition, the complete chromosome X, combined with the ultra-long nanopore data, allowed us to map methylation patterns across complex tandem repeats and satellite arrays. Our results demonstrate that finishing the entire human genome is now within reach, and the data presented here will facilitate ongoing efforts to complete the other human chromosomes.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты