X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (88) 88
genetics & heredity (37) 37
male (37) 37
research (35) 35
genetics (34) 34
genomes (34) 34
polymorphism, single nucleotide (34) 34
genome-wide association study (33) 33
female (32) 32
genetic aspects (32) 32
genomics (30) 30
genome-wide association (28) 28
medical and health sciences (26) 26
medicin och hälsovetenskap (26) 26
algorithms (23) 23
microbiology (23) 23
multidisciplinary sciences (23) 23
genotype (22) 22
biochemistry (21) 21
adult (20) 20
medicine (20) 20
biotechnology & applied microbiology (19) 19
genetic predisposition to disease (19) 19
studies (19) 19
disease (18) 18
gene expression (18) 18
beer (17) 17
chemistry (17) 17
compositions or test papers therefor (17) 17
condition-responsive control in microbiological orenzymological processes (17) 17
enzymology (17) 17
expression (17) 17
measuring or testing processes involving enzymes, nucleicacids or microorganisms (17) 17
metallurgy (17) 17
mutation or genetic engineering (17) 17
processes of preparing such compositions (17) 17
risk factors (17) 17
software (17) 17
spirits (17) 17
vinegar (17) 17
wine (17) 17
genome (16) 16
genome, human (16) 16
medical research (16) 16
biochemical research methods (15) 15
cohort studies (15) 15
single nucleotide polymorphisms (15) 15
epidemiology (14) 14
genetic variation (14) 14
population (14) 14
body mass index (13) 13
child (13) 13
haplotypes (13) 13
health aspects (13) 13
infant (13) 13
mathematical & computational biology (13) 13
research article (13) 13
risk (13) 13
biochemistry & molecular biology (12) 12
bioinformatics (12) 12
genes (12) 12
middle aged (12) 12
mutation (12) 12
obesity (12) 12
phenotype (12) 12
polymorphism (12) 12
adolescent (11) 11
alleles (11) 11
loci (11) 11
polymorphism, single nucleotide - genetics (11) 11
aged (10) 10
child, preschool (10) 10
children (10) 10
clinical medicine (10) 10
dna copy number variations (10) 10
klinisk medicin (10) 10
meta-analysis (10) 10
physiological aspects (10) 10
quantitative trait loci (10) 10
science (10) 10
variants (10) 10
analysis (9) 9
common variants (9) 9
endocrinology and diabetes (9) 9
endokrinologi och diabetes (9) 9
gene (9) 9
gene expression profiling (9) 9
genotype & phenotype (9) 9
infectious diseases (9) 9
proteins (9) 9
sequence analysis, dna - methods (9) 9
animals (8) 8
biology (8) 8
case-control studies (8) 8
copy number variation (8) 8
genetic loci (8) 8
identification (8) 8
medicin (8) 8
public health (8) 8
science & technology (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


JAMA : the journal of the American Medical Association, ISSN 0098-7484, 2016, Volume 316, Issue 8, pp. 835 - 845
Journal Article
BMC bioinformatics, ISSN 1471-2105, 2018, Volume 19, Issue 1, pp. 261 - 13
Detection of genomic inversions remains challenging. Many existing methods primarily target inzversions with a non repetitive breakpoint, leaving inverted... 
Inversion | Inverted repeat (IR) | Long read sequencing | Non allelic homologous recombination (NAHR) | Split read | NA12878 | Genotype | Humans | Chromosome Inversion - genetics | Inverted repeat | Homologous recombination | Inversions | Data processing | Homology | Genomes | Genotype & phenotype | Alignment | Genotyping | Simulation | Software | Bioinformatics | Chromosomes | Deoxyribonucleic acid--DNA
Journal Article
Nature communications, ISSN 2041-1723, 2018, Volume 9, Issue 1, pp. 4580 - 12
Journal Article
Journal Article
Scientific reports, ISSN 2045-2322, 2018, Volume 8, Issue 1, pp. 16616 - 9
... by analysis of BioNano and nanopore data Haojing Shao , Chenxi Zhou , Minh Duc Cao and Lachlan J. M. Coin The majority of human chromosome ends remain incompletely... 
TELOMERE | INSTABILITY | EVOLUTION | MULTIDISCIPLINARY SCIENCES | GENOME | SEQUENCE | Chromosome 7 | Gene duplication | Genomes | Nucleotide sequence | Chromosomes
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2009, Volume 41, Issue 2, pp. 157 - 159
Journal Article
by Freathy, Rachel and Mook-Kanamori, Dennis and Sovio, Ulla and Prokopenko, Inga and Timpson, Nicholas and Berry, Diane and Warrington, Nicole and Widen, Elisabeth and Hottenga, Jouke Jan and Kaakinen, Marika and Lange, Leslie and Bradfield, Jonathan and Kerkhof, Marjan and Marsh, Julie and Mägi, Reedik and Chen, Chao and Lyon, Helen and Kirin, Mirna and Adair, Linda and Aulchenko, Yurii and Bennett, Amanda and Borja, Judith and Bouatia-Naji, Nabila and Charoen, Pimphen and Coin, Lachlan and Cousminer, Diana and Geus, Eco and Deloukas, Panagiotis and Elliott, Paul and Evans, David and Froguel, Philippe and Glaser, Beate and Groves, Christopher and Hartikainen, A.L and Hassanali, Neelam and Hirschhorn, Joel and Hofman, Albert and Holly, Jeff and Hyppönen, Elina and Kanoni, Stavroula and Knight, Bridget and Laitinen, Jaana and Lindgren, Cecilia and McArdle, Wendy and O'Reilly, Paul and Pennell, Craig and Postma, Dirkje and Pouta, Anneli and Ramasamy, Adaikalavan and Rayner, Nigel William and Ring, Susan and Rivadeneira Ramirez, Fernando and Shields, Beverley and Strachan, David and Surakka, Ida and Taanila, Anja and Tiesler, Carla and Uitterlinden, Ané and Tikka-Kleemola, Päivi and Wijga, Alet and Willemsen, Gonneke and Zhang, Haitao and Zhao, Jing Hua and Wilson, James and Steegers-Theunissen, Régine and Hattersley, Anew and Hagen, Knut and Peltonen, Leena Johanna and Mohlke, Karen and Grant, Struan and Hakonarson, Hakon and Koppelman, Gerard and Dedoussis, George and Heinrich, Joachim and Gillman, Matthew W and Palmer, Cameron and Frayling, Timothy and Boomsma, Dorret and Smith, Davey and Power, Christopher and Jaddoe, Vincent and Jarvelin, Marjo-Riitta and McCarthy, Mark and EGG Consortium and MAGIC and WTCCC and GIANT Consortium and Wellcome Trust Case Control Consortium and Meta-Analyses of Glucose and Insulin-related traits Consortium and Early Growth Genetics (EGG) Consortium and Genetic Investigation of ANthropometric Traits (GIANT) Consortium and The Wellcome Trust Case Control Consortium (WTCCC) and the Early Growth Genetics (EGG) Consortium and The Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) and The Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature genetics, ISSN 1061-4036, 05/2010, Volume 42, Issue 5, pp. 430 - 435
Journal Article
Emerging infectious diseases, ISSN 1080-6059, 2019, Volume 25, Issue 3, pp. 406 - 415
In this retrospective study, we used whole-genome sequencing (WGS) to delineate transmission dynamics, characterize drug-resistance markers, and identify risk... 
INFECTIOUS DISEASES | TRANSMISSION | BEIJING STRAINS | MECHANISMS | IMMUNOLOGY | SPREAD | EMERGENCE | GENOME | Geography | History, 21st Century | Humans | Antitubercular Agents - pharmacology | Genotype | Mycobacterium tuberculosis - drug effects | Tuberculosis, Multidrug-Resistant - epidemiology | Australia - epidemiology | Mycobacterium tuberculosis - isolation & purification | Tuberculosis, Multidrug-Resistant - diagnosis | Whole Genome Sequencing | Microbial Sensitivity Tests | Tuberculosis, Multidrug-Resistant - microbiology | Bacterial Typing Techniques | Tuberculosis, Multidrug-Resistant - history | Papua New Guinea - epidemiology | Emigration and Immigration | Evolution, Molecular | Mycobacterium tuberculosis - genetics | Drug resistance in microorganisms | Tuberculosis | Genomics | Antitubercular agents | Genomes | Nucleotide sequencing | Drug therapy | DNA sequencing | Papua New Guinea | isoniazid | bacteria | whole-genome sequencing | tuberculosis | Torres Strait | mycobacteria | Cross-Border Movement of Highly Drug-Resistant | from Papua New Guinea to Australia through Torres Strait Protected Zone, 2010–2015 | ethionamide | transmission | Mycobacterium tuberculosis | antimicrobial resistance | tuberculosis and other mycobacteria | MDR TB | Beijing sublineage 2.2.1.1 | drug resistance | Australia | cross-border movement | MDR-TB
Journal Article
Journal Article