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排名必读论文期刊顶会热点AI 简史溯源树小脉星探人才迁徙塔尖人才国防情报追踪开源工具智慧手语
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论文共 109 篇作者统计合作学者相似作者

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P655: Performing long-read sequencing from dried blood spot cards
Sydney Ward, Joy Goffena, Sophie Storz,Miranda Galey, Alexandra Keefe,Cate Paschal,Anna Scott,Danny Miller
Genetics in Medicine Open (2024): 101560
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Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation
Jonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, Miranda Pg Zalusky, Kendra Hoekzema,David Twesigomwe,Lei Yang, Anthony A Snead, Phillip A Richmond,Wouter De Coster,Nathan D Olson,Andrea Guarracino,
medRxiv : the preprint server for health sciences (2024)
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3-hour genome sequencing and targeted analysis to rapidly assess genetic risk
Miranda Galey, Jonas Gustafson, Stephanie Bohaczuk, Ben Mallory, Paxton Reed,Tara Wenger,Erika Beckman,Irene J. Chang, Cate R. Paschal,Jillian G. Buchan,Christina M. Lockwood,Mihai Puia-Dumitrescu,
Genetics in Medicine Open (2024): 101833
引用5浏览0引用
5
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P630: Multi-modal testing, including long-read sequencing, to elucidate an unsolved case of dyskeratosis congenita
Ankita Jhuraney, Sarah Paolucci, Sophia Gibson, Nikhita Damaraju,Danny Miller, Jennifer Hayek, Bri Dingmann, Jillian Buchan
Genetics in Medicine Open (2024): 101536
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Long-Read DNA and RNA Sequencing to Streamline Clinical Genetic Testing and Reduce Barriers to Comprehensive Genetic Testing
Nikhita Damaraju, Angela L. Miller,Danny E. Miller
JOURNAL OF APPLIED LABORATORY MEDICINEno. 1 (2024): 138-150
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P214: SeqFirst DDi: Early whole genome sequencing improves access to early precise genetic diagnosis for children with developmental differences
Katrina Dipple,Daniel Doherty, Kailyn Anderson, Olivia Sommers,Tara Wenger, Kate MacDuffie, Alexandra Keefe,Abbey Scott, Lukas Kruidenier,Jamie Love-Nichols, Heidi Gildersleeve,Chayna Davis,
Genetics in Medicine Open (2024): 101111
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