X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2365) 2365
Publication (271) 271
Conference Proceeding (79) 79
Book Chapter (32) 32
Book Review (14) 14
Book / eBook (8) 8
Dissertation (8) 8
Data Set (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1724) 1724
humans (1341) 1341
variants (992) 992
genomes (981) 981
genetics & heredity (899) 899
genetics (877) 877
research (800) 800
genomics (738) 738
genetic aspects (723) 723
mutation (672) 672
female (632) 632
genes (601) 601
male (576) 576
research article (558) 558
multidisciplinary sciences (492) 492
polymorphism, single nucleotide (485) 485
medicine (465) 465
studies (441) 441
analysis (418) 418
disease (402) 402
gene expression (366) 366
science (359) 359
genome-wide association (354) 354
genome-wide association study (354) 354
genetic predisposition to disease (349) 349
genetic variation (340) 340
article (327) 327
bioinformatics (313) 313
genotype (307) 307
mutations (307) 307
dna sequencing (301) 301
biotechnology & applied microbiology (284) 284
deoxyribonucleic acid--dna (282) 282
risk factors (282) 282
cancer (281) 281
risk (280) 280
usage (280) 280
biology (274) 274
phenotype (274) 274
proteins (270) 270
adult (263) 263
nucleotide sequencing (262) 262
software (261) 261
computational biology (257) 257
single-nucleotide polymorphism (256) 256
single nucleotide polymorphisms (253) 253
biology and life sciences (249) 249
animals (246) 246
algorithms (244) 244
middle aged (244) 244
population (241) 241
alleles (238) 238
methods (238) 238
identification (233) 233
expression (213) 213
physiological aspects (212) 212
exome (210) 210
health aspects (205) 205
association (204) 204
genome-wide association studies (201) 201
molecular biology (196) 196
medical research (195) 195
genome (192) 192
loci (187) 187
gene (185) 185
high-throughput nucleotide sequencing (185) 185
gene frequency (179) 179
dna (177) 177
gene mutations (177) 177
aged (175) 175
genome, human (174) 174
human genetics (170) 170
medicine and health sciences (167) 167
gene sequencing (166) 166
polymorphism, single nucleotide - genetics (166) 166
genetic research (161) 161
pedigree (160) 160
research and analysis methods (159) 159
diagnosis (158) 158
sequence analysis, dna (153) 153
heredity (151) 151
case-control studies (150) 150
population genetics (147) 147
biotechnology (145) 145
framework (145) 145
common variants (142) 142
haplotypes (140) 140
next-generation sequencing (140) 140
discovery (136) 136
genetic loci (136) 136
biochemistry (135) 135
genetic diversity (135) 135
chromosomes (134) 134
biochemical research methods (131) 131
epidemiology (131) 131
quantitative trait loci (131) 131
sequence analysis, dna - methods (130) 130
high-throughput nucleotide sequencing - methods (128) 128
mathematical & computational biology (128) 128
child (122) 122
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2453) 2453
German (5) 5
Japanese (5) 5
Chinese (3) 3
French (2) 2
Arabic (1) 1
Portuguese (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Computer Vision and Image Understanding, ISSN 1077-3142, 04/2013, Volume 117, Issue 4, pp. 370 - 385
► Morphological operators acting on subgraphs of a graph are studied. ► Two dual adjunctions between edge and vertex sets of are considered. ► Classical... 
Graphs | Spatially variant morphology | Mathematical morphology | Adjunctions | Graphsm | CONNECTIVITY | SPACES | LATTICES | OPERATORS | COMPUTER SCIENCE, ARTIFICIAL INTELLIGENCE | WATERSHEDS | ENGINEERING, ELECTRICAL & ELECTRONIC | Image Processing | Computer Science
Journal Article
IEEE Transactions on Signal Processing, ISSN 1053-587X, 05/2019, Volume 67, Issue 9, pp. 2320 - 2333
Journal Article
Scientific Reports, ISSN 2045-2322, 09/2016, Volume 6, Issue 1, p. 33735
Sequencing large number of individuals, which is often needed for population genetics studies, is still economically challenging despite falling costs of Next... 
DISEASES | RARE VARIANTS | EXOMES | MULTIDISCIPLINARY SCIENCES | Filters | Genotyping | Gene frequency | Alleles | Population studies | Single-nucleotide polymorphism | Population genetics | Deoxyribonucleic acid--DNA | DNA sequencing
Journal Article
International Journal of Innovative Computing, Information and Control, ISSN 1349-4198, 2013, Volume 9, Issue 1, pp. 339 - 353
Journal Article
Human Mutation, ISSN 1059-7794, 08/2018, Volume 39, Issue 8, pp. 1051 - 1060
ClinVar Miner is a Web‐based suite that utilizes the data held in the National Center for Biotechnology Information's ClinVar archive. The goal is to render... 
expert panel | clinical domain working group | variant curation | ClinVar | variant archive | variant interpretation | VARIANTS | GENETICS & HEREDITY | AMERICAN-COLLEGE | MEDICAL GENETICS | CLINICAL GENOME RESOURCE | Conflict management | Web site management software | Biotechnology | Variant interpretation
Journal Article
Ecology and Evolution, ISSN 2045-7758, 07/2018, Volume 8, Issue 14, pp. 7002 - 7013
Journal Article
Human Mutation, ISSN 1059-7794, 02/2018, Volume 39, Issue 2, pp. 197 - 201
Journal Article