X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (65) 65
genetic variation (31) 31
genetics (31) 31
genomes (31) 31
genomics (29) 29
research (28) 28
genetics & heredity (25) 25
multidisciplinary sciences (24) 24
genotype (22) 22
genes (21) 21
polymorphism, single nucleotide (21) 21
mutation (20) 20
gene expression (19) 19
genetic aspects (19) 19
proteins (17) 17
computer science (16) 16
female (16) 16
male (16) 16
alleles (15) 15
genome, human (15) 15
genome-wide association study (15) 15
phenotype (15) 15
genome-wide association (14) 14
algorithms (13) 13
disease (13) 13
medical genetics (12) 12
genome (11) 11
mathematics (11) 11
parallel processing (11) 11
software engineering (11) 11
computational biology (10) 10
mathematics of computing (10) 10
medical and health sciences (10) 10
medicin och hälsovetenskap (10) 10
methods (10) 10
mutations (10) 10
risk factors (10) 10
variants (10) 10
algorithm analysis and problem complexity (9) 9
basic medicine (9) 9
biotechnology & applied microbiology (9) 9
computer software (9) 9
congresses (9) 9
epidemiology (9) 9
exome (9) 9
exome - genetics (9) 9
gene frequency (9) 9
genome, human - genetics (9) 9
haplotypes (9) 9
medicinsk genetik (9) 9
medicinska och farmaceutiska grundvetenskaper (9) 9
population (9) 9
studies (9) 9
association (8) 8
biochemistry & molecular biology (8) 8
biological sciences (8) 8
biology (8) 8
computer programming (8) 8
expression (8) 8
genetic diversity (8) 8
genetic predisposition to disease (8) 8
genetic research (8) 8
genetic variation - genetics (8) 8
health aspects (8) 8
medicine (8) 8
programming techniques (8) 8
transcriptome (8) 8
analysis (7) 7
binding sites (7) 7
computer communication networks (7) 7
databases, genetic (7) 7
gene (7) 7
gene expression profiling (7) 7
genetic variance (7) 7
informatics (7) 7
information systems applications (7) 7
middle aged (7) 7
natural sciences (7) 7
nucleotide sequencing (7) 7
physiological aspects (7) 7
polymorphism, single nucleotide - genetics (7) 7
population genetics (7) 7
tissues (7) 7
transcription factors (7) 7
adult (6) 6
autism (6) 6
bioinformatics (6) 6
cohort studies (6) 6
dna sequencing (6) 6
gene sequencing (6) 6
genetic loci (6) 6
genetics, population (6) 6
genotype & phenotype (6) 6
identification (6) 6
medical research (6) 6
models, genetic (6) 6
molecular sequence annotation (6) 6
pharmacogenetics (6) 6
physics (6) 6
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2013, ISBN 9780199644483, xi, 243 p., [8] p. of plates
This book provides a novel, inquiry-based approach to the understanding and interpretation of the practical, medical, physiological, and societal aspects of... 
Genetics, Medical | Genome | Individualized Medicine | Genomics | Genetics and Genomics | Evolutionary Biology | Research Methods in Life Sciences | Human genome | Personal Genome Project | Proteomics | Data processing | Genome, Human
Book
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2015, Volume 350, Issue 6265, pp. 1262 - 1266
Journal Article
by Dunham, Ian and Kundaje, Anshul and Aldred, Shelley F and Collins, Patrick J and Davis, Carrie A and Doyle, Francis and Epstein, Charles B and Frietze, Seth and Harrow, Jennifer and Kaul, Rajinder and Khatun, Jainab and Lajoie, Bryan R and Landt, Stephen G and Lee, Bum-Kyu and Pauli, Florencia and Rosenbloom, Kate R and Sabo, Peter and Safi, Alexias and Sanyal, Amartya and Shoresh, Noam and Simon, Jeremy M and Song, Lingyun and Trinklein, Nathan D and Altshuler, Robert C and Birney, Ewan and Brown, James B and Cheng, Chao and Djebali, Sarah and Dong, Xianjun and Ernst, Jason and Furey, Terrence S and Gerstein, Mark and Giardine, Belinda and Greven, Melissa and Hardison, Ross C and Harris, Robert S and Herrero, Javier and Hoffman, Michael M and Iyer, Sowmya and Kellis, Manolis and Kheradpour, Pouya and Lassmann, Timo and Li, Qunhua and Lin, Xinying and Marinov, Georgi K and Merkel, Angelika and Mortazavi, Ali and Parker, Stephen C. J and Reddy, Timothy E and Rozowsky, Joel and Schlesinger, Felix and Thurman, Robert E and Wang, Jie and Ward, Lucas D and Whitfield, Troy W and Wilder, Steven P and Wu, Weisheng and Xi, Hualin S and Yip, Kevin Y and Zhuang, Jiali and Bernstein, Bradley E and Green, Eric D and Gunter, Chris and Snyder, Michael and Pazin, Michael J and Lowdon, Rebecca F and Dillon, Laura A. L and Adams, Leslie B and Kelly, Caroline J and Zhang, Julia and Wexler, Judith R and Good, Peter J and Feingold, Elise A and Crawford, Gregory E and Dekker, Job and Elnitski, Laura and Farnham, Peggy J and Giddings, Morgan C and Gingeras, Thomas R and Guigó, Roderic and Hubbard, Timothy J and Kent, W. James and Lieb, Jason D and Margulies, Elliott H and Myers, Richard M and Stamatoyannopoulos, John A and Tenenbaum, Scott A and Weng, Zhiping and White, Kevin P and Wold, Barbara and Yu, Yanbao and Wrobel, John and Risk, Brian A and Gunawardena, Harsha P and Kuiper, Heather C and Maier, Christopher W and Xie, Ling and Chen, Xian and Mikkelsen, Tarjei S and Gillespie, Shawn and ... and The ENCODE Project Consortium and ENCODE Project Consortium
Nature (London), ISSN 1476-4687, 2012, Volume 489, Issue 7414, pp. 57 - 74
Journal Article
by Lek, Monkol and Karczewski, Konrad J and Minikel, Eric V and Samocha, Kaitlin E and Banks, Eric and Fennell, Timothy and O’Donnell-Luria, Anne H and Ware, James S and Hill, Andrew J and Cummings, Beryl B and Tukiainen, Taru and Birnbaum, Daniel P and Kosmicki, Jack A and Duncan, Laramie E and Estrada, Karol and Zhao, Fengmei and Zou, James and Pierce-Hoffman, Emma and Berghout, Joanne and Cooper, David N and Deflaux, Nicole and DePristo, Mark and Do, Ron and Flannick, Jason and Fromer, Menachem and Gauthier, Laura and Goldstein, Jackie and Gupta, Namrata and Howrigan, Daniel and Kiezun, Adam and Kurki, Mitja I and Moonshine, Ami Levy and Natarajan, Pradeep and Orozco, Lorena and Peloso, Gina M and Poplin, Ryan and Rivas, Manuel A and Ruano-Rubio, Valentin and Rose, Samuel A and Ruderfer, Douglas M and Shakir, Khalid and Stenson, Peter D and Stevens, Christine and Thomas, Brett P and Tiao, Grace and Tusie-Luna, Maria T and Weisburd, Ben and Won, Hong-Hee and Yu, Dongmei and Altshuler, David M and Ardissino, Diego and Boehnke, Michael and Danesh, John and Donnelly, Stacey and Elosua, Roberto and Florez, Jose C and Gabriel, Stacey B and Getz, Gad and Glatt, Stephen J and Hultman, Christina M and Kathiresan, Sekar and Laakso, Markku and McCarroll, Steven and McCarthy, Mark I and McGovern, Dermot and McPherson, Ruth and Neale, Benjamin M and Palotie, Aarno and Purcell, Shaun M and Saleheen, Danish and Scharf, Jeremiah M and Sklar, Pamela and Sullivan, Patrick F and Tuomilehto, Jaakko and Tsuang, Ming T and Watkins, Hugh C and Wilson, James G and Daly, Mark J and MacArthur, Daniel G and Exome Aggregation Consortium
Nature (London), ISSN 1476-4687, 2016, Volume 536, Issue 7616, pp. 285 - 291
...Author(s): Monkol Lek [1, 2, 3, 4]; Konrad J. Karczewski [1, 2]; Eric V. Minikel [1, 2, 5]; Kaitlin E. Samocha [1, 2, 5, 6]; Eric Banks [2]; Timothy Fennell [2... 
HUMAN-DISEASE | EVOLUTION | MULTIDISCIPLINARY SCIENCES | MUTATION | GUIDELINES | FRAMEWORK | SEQUENCE VARIANTS | NETWORKS | DISCOVERY | HUMAN-POPULATION HISTORY | Genetic aspects | Research | Man | Human beings | Genetic variation | Analysis | Datasets | Proteins | Databases | Disease | Genes | Principal components analysis | Genetics | Genomes
Journal Article
by Battle, Alexis and Brown, Christopher D and Engelhardt, Barbara E and Montgomery, Stephen B and Aguet, François and Ardlie, Kristin G and Cummings, Beryl B and Gelfand, Ellen T and Getz, Gad and Hadley, Kane and Handsaker, Robert E and Huang, Katherine H and Kashin, Seva and Karczewski, Konrad J and Lek, Monkol and Li, Xiao and MacArthur, Daniel G and Nedzel, Jared L and Nguyen, Duyen T and Noble, Michael S and Segrè, Ayellet V and Trowbridge, Casana A and Tukiainen, Taru and Abell, Nathan S and Balliu, Brunilda and Barshir, Ruth and Basha, Omer and Bogu, Gireesh K and Brown, Anew and Castel, Stephane E and Chen, Lin S and Chiang, Colby and Conrad, Donald F and Cox, Nancy J and Damani, Farhan N and Davis, Joe R and Delaneau, Olivier and Dermitzakis, Emmanouil T and Eskin, Eleazar and Ferreira, Peo G and Frésard, Laure and Gamazon, Eric R and Garrido-Martín, Diego and Gewirtz, Ariel D. H and Gliner, Genna and Gloudemans, Michael J and Guigo, Roderic and Hall, Ira M and Han, Buhm and He, Yuan and GTEx Consortium and Pathology and Laboratory Data Analysis and Lab Data Anal Coordinating Ct and Stat Methods Grps-Anal Working Grp and Biospecimen Collection Source Sit and Genome Browser Data Integration and Biospecimen Core Resource-Vari and Leidos Biomedical-Project and Genome Browser Data Integr and Enhancing Gtex Egtex Grps and Gtex Consortium and Biospecimen Collection Source and Brain Bank Repository-Univ M and Leidos Biomedical—Project Management and Laboratory, Data Analysis &Coordinating Center (LDACC) and NIH/NCI and Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group and Statistical Methods groups—Analysis Working Group and Biospecimen Collection Source Site—NDRI and NIH/NHGRI and Brain Bank Repository—University of Miami Brain Endowment Bank and Genome Browser Data Integration &Visualization—UCSC Genomics Institute, University of California Santa Cruz and NIH Common Fund and Enhancing GTEx (eGTEx) groups and NIH/NIMH and Genome Browser Data Integration &Visualization—EBI and Lead analysts and Biospecimen Collection Source Site—RPCI and Biospecimen collection and Biospecimen Core Resource—VARI and NIH program management and eQTL manuscript working group and ELSI Study and NIH/NIDA
Nature (London), ISSN 1476-4687, 2017, Volume 550, Issue 7675, pp. 204 - 213
Journal Article