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18 results

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Page 1
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation.
Gustafson JA, Gibson SB, Damaraju N, Zalusky MP, Hoekzema K, Twesigomwe D, Yang L, Snead AA, Richmond PA, De Coster W, Olson ND, Guarracino A, Li Q, Miller AL, Goffena J, Anderson Z, Storz SH, Ward SA, Sinha M, Gonzaga-Jauregui C, Clarke WE, Basile AO, Corvelo A, Reeves C, Helland A, Musunuri RL, Revsine M, Patterson KE, Paschal CR, Zakarian C, Goodwin S, Jensen TD, Robb E; 1000 Genomes ONT Sequencing Consortium; University of Washington Center for Rare Disease Research (UW-CRDR); Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium; McCombie WR, Sedlazeck FJ, Zook JM, Montgomery SB, Garrison E, Kolmogorov M, Schatz MC, McLaughlin RN Jr, Dashnow H, Zody MC, Loose M, Jain M, Eichler EE, Miller DE. Gustafson JA, et al. Among authors: mclaughlin rn jr. medRxiv [Preprint]. 2024 Mar 7:2024.03.05.24303792. doi: 10.1101/2024.03.05.24303792. medRxiv. 2024. Update in: Genome Res. 2024 Nov 20;34(11):2061-2073. doi: 10.1101/gr.279273.124. PMID: 38496498 Free PMC article. Updated. Preprint.
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation.
Gustafson JA, Gibson SB, Damaraju N, Zalusky MPG, Hoekzema K, Twesigomwe D, Yang L, Snead AA, Richmond PA, De Coster W, Olson ND, Guarracino A, Li Q, Miller AL, Goffena J, Anderson ZB, Storz SHR, Ward SA, Sinha M, Gonzaga-Jauregui C, Clarke WE, Basile AO, Corvelo A, Reeves C, Helland A, Musunuri RL, Revsine M, Patterson KE, Paschal CR, Zakarian C, Goodwin S, Jensen TD, Robb E; 1000 Genomes ONT Sequencing Consortium; University of Washington Center for Rare Disease Research (UW-CRDR); Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium; McCombie WR, Sedlazeck FJ, Zook JM, Montgomery SB, Garrison E, Kolmogorov M, Schatz MC, McLaughlin RN Jr, Dashnow H, Zody MC, Loose M, Jain M, Eichler EE, Miller DE. Gustafson JA, et al. Among authors: mclaughlin rn jr. Genome Res. 2024 Nov 20;34(11):2061-2073. doi: 10.1101/gr.279273.124. Genome Res. 2024. PMID: 39358015 Free PMC article.
Stealing genes and facing consequences.
Del Valle RP, McLaughlin RN Jr. Del Valle RP, et al. Among authors: mclaughlin rn jr. Science. 2022 Oct 28;378(6618):356-357. doi: 10.1126/science.ade4942. Epub 2022 Oct 27. Science. 2022. PMID: 36302006
Genetic conflicts: the usual suspects and beyond.
McLaughlin RN Jr, Malik HS. McLaughlin RN Jr, et al. J Exp Biol. 2017 Jan 1;220(Pt 1):6-17. doi: 10.1242/jeb.148148. J Exp Biol. 2017. PMID: 28057823 Free PMC article. Review.
Predicting the functional effect of compound heterozygous genotypes from large scale variant effect maps.
Xie MJ, Cromie GA, Owens K, Timour MS, Tang M, Kutz JN, El-Hattab AW, McLaughlin RN, Dudley AM. Xie MJ, et al. Among authors: mclaughlin rn. bioRxiv [Preprint]. 2023 Jan 27:2023.01.11.523651. doi: 10.1101/2023.01.11.523651. bioRxiv. 2023. Update in: PLoS Genet. 2023 Oct 9;19(10):e1010972. doi: 10.1371/journal.pgen.1010972. PMID: 36711904 Free PMC article. Updated. Preprint.
LINE-1 Retroelements Get ZAPped!
McLaughlin RN Jr, Malik HS. McLaughlin RN Jr, et al. PLoS Genet. 2015 Jul 16;11(7):e1005364. doi: 10.1371/journal.pgen.1005364. eCollection 2015 Jul. PLoS Genet. 2015. PMID: 26182081 Free PMC article. No abstract available.
18 results