X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (11118) 11118
Publication (1783) 1783
Book Chapter (195) 195
Book Review (89) 89
Conference Proceeding (61) 61
Newspaper Article (29) 29
Dissertation (24) 24
Web Resource (23) 23
Book / eBook (17) 17
Government Document (7) 7
Data Set (4) 4
Magazine Article (2) 2
Paper (1) 1
Reference (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (8284) 8284
humans (7325) 7325
copy number (3760) 3760
genetics & heredity (3484) 3484
female (3367) 3367
male (3042) 3042
genomics (2810) 2810
genetic aspects (2806) 2806
genomes (2520) 2520
genes (2502) 2502
dna copy number variations (2460) 2460
genetics (2360) 2360
mutation (2334) 2334
research (2307) 2307
analysis (1988) 1988
copy number variation (1954) 1954
polymorphism, single nucleotide (1937) 1937
cancer (1744) 1744
animals (1702) 1702
adult (1592) 1592
gene expression (1539) 1539
research article (1509) 1509
oncology (1496) 1496
middle aged (1408) 1408
article (1379) 1379
deoxyribonucleic acid--dna (1328) 1328
dna (1298) 1298
multidisciplinary sciences (1205) 1205
medicine (1202) 1202
comparative genomic hybridization (1184) 1184
dna copy number variations - genetics (1159) 1159
genetic research (1147) 1147
biochemistry & molecular biology (1139) 1139
expression (1136) 1136
chromosomes (1090) 1090
gene dosage (1086) 1086
genotype (1075) 1075
genetic variation (1061) 1061
phenotype (1035) 1035
aged (1024) 1024
tumors (978) 978
mutations (948) 948
gene (940) 940
genetic predisposition to disease (932) 932
science (918) 918
evolution (913) 913
biotechnology & applied microbiology (912) 912
child (912) 912
risk factors (903) 903
polymorphism (882) 882
single-nucleotide polymorphism (852) 852
genome (850) 850
studies (840) 840
polymerase chain reaction (813) 813
biology (812) 812
cell biology (800) 800
disease (789) 789
single nucleotide polymorphisms (782) 782
genome-wide association study (780) 780
genome, human (767) 767
identification (748) 748
copy-number variation (740) 740
association (723) 723
alleles (705) 705
adolescent (701) 701
health aspects (699) 699
proteins (699) 699
chromosome aberrations (691) 691
human genome (681) 681
genome-wide association (674) 674
physiological aspects (669) 669
copy number variations (666) 666
oligonucleotide array sequence analysis (653) 653
structural variation (641) 641
life sciences (630) 630
sequence analysis, dna (629) 629
variants (626) 626
polymorphism, single nucleotide - genetics (615) 615
usage (615) 615
gene deletion (610) 610
diagnosis (609) 609
pathology (606) 606
autism (599) 599
deletion (591) 591
child, preschool (585) 585
schizophrenia (582) 582
base sequence (579) 579
algorithms (567) 567
dna sequencing (566) 566
prognosis (564) 564
neurosciences (554) 554
development and progression (547) 547
case-control studies (546) 546
hybridization (544) 544
risk (543) 543
young adult (542) 542
cytogenetics (533) 533
bioinformatics (526) 526
deoxyribonucleic acid (524) 524
medical research (523) 523
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Collection Dvlpm't (Acquisitions) - Vendor file (3) 3
Gerstein Science - Stacks (3) 3
UofT at Scarborough - Stacks (3) 3
Law (Bora Laskin) - Stacks (2) 2
St. Michael's College (John M. Kelly) - 2nd Floor (2) 2
Trinity College (John W Graham) - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Dentistry (Harry R Abbott) - Stacks (1) 1
Engineering & Comp. Sci. - Stacks (1) 1
Law (Bora Laskin) - Searching (1) 1
Robarts - Stacks (1) 1
Royal Ontario Museum - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (11216) 11216
Chinese (39) 39
German (28) 28
Japanese (10) 10
Spanish (9) 9
Polish (7) 7
French (6) 6
Russian (6) 6
Korean (5) 5
Czech (2) 2
Hungarian (2) 2
Catalan (1) 1
Danish (1) 1
Dutch (1) 1
Norwegian (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Proceedings: Biological Sciences, ISSN 0962-8452, 11/2010, Volume 277, Issue 1698, pp. 3213 - 3221
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2017, Volume 12, Issue 1, p. e0170815
Journal Article
Journal Article
Genomics, ISSN 0888-7543, 2013, Volume 101, Issue 2, pp. 86 - 93
Genome structural variation shows remarkable complexity with respect to copy number, sequence content and distribution. While the discovery of copy number... 
Amplication | Copy number variation | Multiplex ligation-dependent probe | Paralogue ratio test | Multiplex ampliable probe hybridization | Southern blotting | Next generation sequencing | Qu