Các bài viết có thể truy cập công khai - Francisco M. De La VegaTìm hiểu thêm
Có tại một số nơi: 55
A global reference for human genetic variation
TGP Consortium
Nature 526, 68-74, 2015
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, Howard …
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, Howard …
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, Howard …
Pan-cancer analysis of whole genomes
Nature 578 (7793), 82-93, 2020
Các cơ quan ủy nhiệm: US National Institutes of Health, Cancer Research UK, UK Medical Research …
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1
J Hampe, A Franke, P Rosenstiel, A Till, M Teuber, K Huse, M Albrecht, ...
Nature genetics 39 (2), 207-211, 2007
Các cơ quan ủy nhiệm: German Research Foundation
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health, German Research Foundation
Organoid modeling of the tumor immune microenvironment
JT Neal, X Li, J Zhu, V Giangarra, CL Grzeskowiak, J Ju, IH Liu, SH Chiou, ...
Cell 175 (7), 1972-1988. e16, 2018
Các cơ quan ủy nhiệm: US National Science Foundation, US National Institutes of Health, Howard …
An Aboriginal Australian genome reveals separate human dispersals into Asia
M Rasmussen, X Guo, Y Wang, KE Lohmueller, S Rasmussen, ...
Science 334 (6052), 94-98, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
KJ McKernan, HE Peckham, GL Costa, SF McLaughlin, Y Fu, EF Tsung, ...
Genome research 19 (9), 1527-1541, 2009
Các cơ quan ủy nhiệm: US National Institutes of Health
Diversity of human copy number variation and multicopy genes
PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ...
Science 330 (6004), 641-646, 2010
Các cơ quan ủy nhiệm: US National Institutes of Health, Howard Hughes Medical Institute
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health
Variation in genome-wide mutation rates within and between human families
Nature genetics 43 (7), 712-714, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health, Genome Canada
Neratinib after trastuzumab-based adjuvant therapy in HER2-positive breast cancer (ExteNET): 5-year analysis of a randomised, double-blind, placebo-controlled, phase 3 trial
M Martin, FA Holmes, B Ejlertsen, S Delaloge, B Moy, H Iwata, ...
The lancet oncology 18 (12), 1688-1700, 2017
Các cơ quan ủy nhiệm: UK Medical Research Council, National Institute for Health Research, UK
Development of personalized tumor biomarkers using massively parallel sequencing
RJ Leary, I Kinde, F Diehl, K Schmidt, C Clouser, C Duncan, A Antipova, ...
Science translational medicine 2 (20), 20ra14-20ra14, 2010
Các cơ quan ủy nhiệm: US National Institutes of Health, Howard Hughes Medical Institute
Genomics for the world
CD Bustamante, FM De La Vega, EG Burchard
Nature 475 (7355), 163-165, 2011
Các cơ quan ủy nhiệm: US National Institutes of Health
Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America
R Kosoy, R Nassir, C Tian, PA White, LM Butler, G Silva, R Kittles, ...
Human mutation 30 (1), 69-78, 2009
Các cơ quan ủy nhiệm: US National Institutes of Health
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 3934, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health, UK Biotechnology and Biological Sciences …
Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort
SM Waszak, PA Northcott, I Buchhalter, GW Robinson, C Sutter, ...
The Lancet Oncology 19 (6), 785-798, 2018
Các cơ quan ủy nhiệm: US National Science Foundation, Swiss National Science Foundation, US …
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
Các cơ quan ủy nhiệm: US National Institutes of Health, Danish Council for Independent Research …
The 1000 Genomes Project: data management and community access
L Clarke, X Zheng-Bradley, R Smith, E Kulesha, C Xiao, I Toneva, ...
Nature methods 9 (5), 459-462, 2012
Các cơ quan ủy nhiệm: US National Institutes of Health
Chương trình máy tính sẽ tự động xác định thông tin xuất bản và thông tin về nhà tài trợ