Year |
Citation |
Score |
2022 |
Altemose N, Maslan A, Smith OK, Sundararajan K, Brown RR, Mishra R, Detweiler AM, Neff N, Miga KH, Straight AF, Streets A. DiMeLo-seq: a long-read, single-molecule method for mapping protein-DNA interactions genome wide. Nature Methods. PMID 35396487 DOI: 10.1038/s41592-022-01475-6 |
0.654 |
|
2022 |
Hoyt SJ, Storer JM, Hartley GA, Grady PGS, Gershman A, de Lima LG, Limouse C, Halabian R, Wojenski L, Rodriguez M, Altemose N, Rhie A, Core LJ, Gerton JL, Makalowski W, et al. From telomere to telomere: The transcriptional and epigenetic state of human repeat elements. Science (New York, N.Y.). 376: eabk3112. PMID 35357925 DOI: 10.1126/science.abk3112 |
0.507 |
|
2022 |
Nurk S, Koren S, Rhie A, Rautiainen M, Bzikadze AV, Mikheenko A, Vollger MR, Altemose N, Uralsky L, Gershman A, Aganezov S, Hoyt SJ, Diekhans M, Logsdon GA, Alonge M, et al. The complete sequence of a human genome. Science (New York, N.Y.). 376: 44-53. PMID 35357919 DOI: 10.1126/science.abj6987 |
0.641 |
|
2022 |
Gershman A, Sauria MEG, Guitart X, Vollger MR, Hook PW, Hoyt SJ, Jain M, Shumate A, Razaghi R, Koren S, Altemose N, Caldas GV, Logsdon GA, Rhie A, Eichler EE, et al. Epigenetic patterns in a complete human genome. Science (New York, N.Y.). 376: eabj5089. PMID 35357915 DOI: 10.1126/science.abj5089 |
0.579 |
|
2022 |
Altemose N, Logsdon GA, Bzikadze AV, Sidhwani P, Langley SA, Caldas GV, Hoyt SJ, Uralsky L, Ryabov FD, Shew CJ, Sauria MEG, Borchers M, Gershman A, Mikheenko A, Shepelev VA, et al. Complete genomic and epigenetic maps of human centromeres. Science (New York, N.Y.). 376: eabl4178. PMID 35357911 DOI: 10.1126/science.abl4178 |
0.649 |
|
2022 |
Gupta A, Shamsi F, Altemose N, Dorlhiac GF, Cypess AM, White AP, Yosef N, Patti ME, Tseng YH, Streets A. Characterization of transcript enrichment and detection bias in single-nucleus RNA-seq for mapping of distinct human adipocyte lineages. Genome Research. PMID 35042723 DOI: 10.1101/gr.275509.121 |
0.572 |
|
2020 |
Altemose N, Maslan A, Rios-Martinez C, Lai A, White JA, Streets A. μDamID: A Microfluidic Approach for Joint Imaging and Sequencing of Protein-DNA Interactions in Single Cells. Cell Systems. 11: 354-366.e9. PMID 33099405 DOI: 10.1016/j.cels.2020.08.015 |
0.616 |
|
2019 |
Li R, Bitoun E, Altemose N, Davies RW, Davies B, Myers SR. A high-resolution map of non-crossover events reveals impacts of genetic diversity on mammalian meiotic recombination. Nature Communications. 10: 3900. PMID 31467277 DOI: 10.1038/S41467-019-11675-Y |
0.421 |
|
2017 |
Altemose N, Noor N, Bitoun E, Tumian A, Imbeault M, Chapman JR, Aricescu AR, Myers SR. A map of human PRDM9 binding provides evidence for novel behaviors of PRDM9 and other zinc-finger proteins in meiosis. Elife. 6. PMID 29072575 DOI: 10.7554/Elife.28383 |
0.31 |
|
2015 |
Williams AL, Genovese G, Dyer T, Altemose N, Truax K, Jun G, Patterson N, Myers SR, Curran JE, Duggirala R, Blangero J, Reich D, Przeworski M. Non-crossover gene conversions show strong GC bias and unexpected clustering in humans. Elife. 4. PMID 25806687 DOI: 10.7554/Elife.04637 |
0.319 |
|
2014 |
Hinch AG, Altemose N, Noor N, Donnelly P, Myers SR. Recombination in the human Pseudoautosomal region PAR1. Plos Genetics. 10: e1004503. PMID 25033397 DOI: 10.1371/Journal.Pgen.1004503 |
0.393 |
|
2014 |
Altemose N, Miga KH, Maggioni M, Willard HF. Genomic Characterization of Large Heterochromatic Gaps in the Human Genome Assembly Plos Computational Biology. 10. PMID 24831296 DOI: 10.1371/Journal.Pcbi.1003628 |
0.583 |
|
2014 |
Miga KH, Newton Y, Jain M, Altemose N, Willard HF, Kent EJ. Centromere reference models for human chromosomes X and y satellite arrays Genome Research. 24: 697-707. PMID 24501022 DOI: 10.1101/Gr.159624.113 |
0.585 |
|
2013 |
Genovese G, Handsaker RE, Li H, Altemose N, Lindgren AM, Chambert K, Pasaniuc B, Price AL, Reich D, Morton CC, Pollak MR, Wilson JG, McCarroll SA. Using population admixture to help complete maps of the human genome. Nature Genetics. 45: 406-14, 414e1-2. PMID 23435088 DOI: 10.1038/Ng.2565 |
0.552 |
|
Low-probability matches (unlikely to be authored by this person) |
2016 |
Davies B, Hatton E, Altemose N, Hussin JG, Pratto F, Zhang G, Hinch AG, Moralli D, Biggs D, Diaz R, Preece C, Li R, Bitoun E, Brick K, Green CM, et al. Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice. Nature. PMID 26840484 DOI: 10.1038/Nature16931 |
0.267 |
|
2020 |
Nakatsuka N, Patterson N, Patsopoulos NA, Altemose N, Tandon A, Beecham AH, McCauley JL, Isobe N, Hauser S, De Jager PL, Hafler DA, Oksenberg JR, Reich D. Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans. Scientific Reports. 10: 16902. PMID 33037294 DOI: 10.1038/s41598-020-74035-7 |
0.15 |
|
2022 |
Altemose N. A classical revival: Human satellite DNAs enter the genomics era. Seminars in Cell & Developmental Biology. PMID 35487859 DOI: 10.1016/j.semcdb.2022.04.012 |
0.12 |
|
Hide low-probability matches. |