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DES Y3 + KiDS-1000: Consistent cosmology combining cosmic shear surveys

Autor: Dark Energy Survey, Kilo-Degree Survey Collaboration, T. M. C. Abbott, M. Aguena, A. Alarcon, O. Alves, A. Amon, F. Andrade-Oliveira, M. Asgari, S. Avila, D. Bacon, K. Bechtol, M. R. Becker, G. M. Bernstein, E. Bertin, M. Bilicki, J. Blazek, S. Bocquet, D. Brooks, P. Burger, D. L. Burke, H. Camacho, A. Campos, A. Carnero Rosell, M. Carrasco Kind, J. Carretero, F. J. Castander, R. Cawthon, C. Chang, R. Chen, A. Choi, C. Conselice, J. Cordero, M. Crocce, L. N. da Costa, M. E. da Silva Pereira, R. Dalal, C. Davis, J. T. A. deJong, J. DeRose, S. Desai, H. T. Diehl, S. Dodelson, P. Doel, C. Doux, A. Drlica-Wagner, A. Dvornik, K. Eckert, T. F. Eifler, J. Elvin-Poole, S. Everett, X. Fang, I. Ferrero, A. Ferté, B. Flaugher, O. Friedrich, J. Frieman, J. García-Bellido, M. Gatti, G. Giannini, B. Giblin, D. Gruen, R. A. Gruendl, G. Gutierrez, I. Harrison, W. G. Hartley, K. Herner, C. Heymans, H. Hildebrandt, S. R. Hinton, H. Hoekstra, D. L. Hollowood, K. Honscheid, H. Huang, E. M. Huff, D. Huterer, D. J. James, M. Jarvis, N. Jeffrey, T. Jeltema, B. Joachimi, S. Joudaki, A. Kannawadi, E. Krause, K. Kuehn, K. Kuijken, N. Kuropatkin, O. Lahav, P. -F. Leget, P. Lemos, S. Li, X. Li, A. R. Liddle, M. Lima, C. -A Lin, H. Lin, N. MacCrann, C. Mahony, J. L. Marshall, J. McCullough, J. Mena-Fernández, F. Menanteau, R. Miquel, J. J. Mohr, J. Muir, J. Myles, N. Napolitano, A. Navarro-Alsina, R. L. C. Ogando, A. Palmese, S. Pandey, Y. Park, M. Paterno, J. A. Peacock, D. Petravick, A. Pieres, A. A. Plazas Malagón, A. Porredon, J. Prat, M. Radovich, M. Raveri, R. Reischke, N. C. Robertson, R. P. Rollins, A. K. Romer, A. Roodman, E. S. Rykoff, S. Samuroff, C. Sánchez, E. Sanchez, J. Sanchez, P. Schneider, L. F. Secco, I. Sevilla-Noarbe, H.-Y. Shan, E. Sheldon, T. Shin, C. Sifón, M. Smith, M. Soares-Santos, B. Stölzner, E. Suchyta, M. E. C. Swanson, G. Tarle, D. Thomas, C. To, M. A. Troxel, T. Tröster, I. Tutusaus, J. L. van den Busch, T. N. Varga, A. R. Walker, N. Weaverdyck, R. H. Wechsler, J. Weller, P. Wiseman, A. H. Wright, B. Yanny, B. Yin, M. Yoon, Y. Zhang, J. Zuntz

Publikováno v: The Open Journal of Astrophysics, Vol 6 (2023)

We present a joint cosmic shear analysis of the Dark Energy Survey (DES Y3) and the Kilo-Degree Survey (KiDS-1000) in a collaborative effort between the two survey teams. We find consistent cosmological parameter constraints between DES Y3 and KiDS-1

Externí odkaz: https://doaj.org/article/9d120fead68546f7b5be9c92e04af1a4

Comprehensive sequencing of PALB2 in patients with breast cancer suggests PALB2 mutations explain a subset of hereditary breast cancer

Autor: Rajesh R. Kaldate, Benjamin B. Roa, Shelly Cummings, Elisha Hughes, Sonia Chen, Jeffrey T. Trost, Aaron Theisen, Priscilla H. Fernandes, Jenny Peterson, Jennifer Saam

Publikováno v: Cancer. 120:963-967

BACKGROUND This study sought to determine the prevalence of PALB2 mutations in a cohort referred for diagnostic testing for hereditary breast cancer. METHODS Sanger sequencing was used to analyze the entire coding region and flanking introns of PALB2

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cc44767baaa8ec2e76f224db6e3c444e
https://doi.org/10.1002/cncr.28504

Clinical significance of large rearrangements in BRCA1 and BRCA2

Autor: Jeffrey T. Trost, Eric Rosenthal, Benjamin B. Roa, Richard J. Wenstrup, Jeremy Schoenberger, Christopher Arnell, Thaddeus Judkins, Wade Geary, Toby Barrus, Lynn Anne Burbidge

Publikováno v: Cancer

BACKGROUND: Current estimates of the contribution of large rearrangement (LR) mutations in the BRCA1 (breast cancer 1, early onset) and BRCA2 (breast cancer 2, early onset) genes responsible for hereditary breast and ovarian cancer are based on limit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e6aaa8a5c0f1ba76b7d8805427a815f
http://europepmc.org/articles/PMC3532625

Development and analytical validation of a 25-gene next generation sequencing panel that includes the BRCA1 and BRCA2 genes to assess hereditary cancer risk

Autor: Mark Bastian, Jian Chen, James McCulloch, Thanh Tran, J.T. Mitchell, Karla R. Bowles, Natalia Gutin, Srikanth Jammulapati, Deborah Williams, Jeffrey T. Trost, Bryan Wardell, Kirsten Timms, Adam Murray, Jonathan Craft, Jennifer Potter, Benoît Leclair, Michael C. Perry, Benjamin B. Roa, Brian Morris, Thaddeus Judkins, Satish Bhatnagar

Publikováno v: BMC Cancer

Background Germline DNA mutations that increase the susceptibility of a patient to certain cancers have been identified in various genes, and patients can be screened for mutations in these genes to assess their level of risk for developing cancer. T

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fabeba990a046057c3186b9159120ac
https://doi.org/10.1186/s12885-015-1224-y