Class information for: |
Basic class information |
Hierarchy of classes |
The table includes all classes above and classes immediately below the current class. |
Cluster id | Level | Cluster label | #P |
---|---|---|---|
0 | 4 | ONCOLOGY//CELL BIOLOGY//BIOCHEMISTRY & MOLECULAR BIOLOGY | 2934640 |
304 | 3 | DNA METHYLATION//FRAGILE X SYNDROME//RETT SYNDROME | 41307 |
384 | 2 | DNA METHYLATION//EPIGENETICS//METHYLATION | 17479 |
1910 | 2 | LONG NONCODING RNAS//LNCRNA//LONG NONCODING RNA | 6239 |
2127 | 2 | RETT SYNDROME//MECP2//X CHROMOSOME INACTIVATION | 5430 |
2136 | 2 | FRAGILE X SYNDROME//FRAGILE X//FMR1 | 5383 |
2580 | 2 | GENOMIC IMPRINTING//IMPRINTING//SILVER RUSSELL SYNDROME | 3928 |
2979 | 2 | PRADER WILLI SYNDROME//ANGELMAN SYNDROME//UBE3A | 2848 |
Terms with highest relevance score |
rank | Category | termType | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|---|
1 | DNA METHYLATION | authKW | 1239981 | 10% | 39% | 4146 |
2 | FRAGILE X SYNDROME | authKW | 660729 | 3% | 80% | 1091 |
3 | RETT SYNDROME | authKW | 589235 | 2% | 86% | 901 |
4 | EPIGENETICS | authKW | 573480 | 7% | 25% | 2985 |
5 | PRADER WILLI SYNDROME | authKW | 469839 | 2% | 82% | 751 |
6 | LONG NONCODING RNAS | authKW | 462902 | 2% | 75% | 812 |
7 | LNCRNA | authKW | 379635 | 2% | 71% | 701 |
8 | GENOMIC IMPRINTING | authKW | 367891 | 2% | 67% | 719 |
9 | MECP2 | authKW | 267946 | 1% | 80% | 439 |
10 | ANGELMAN SYNDROME | authKW | 249623 | 1% | 86% | 383 |
Web of Science journal categories |
chi_square_rank | Category | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | Genetics & Heredity | 162452 | 27% | 2% | 11007 |
2 | Oncology | 33979 | 17% | 1% | 6854 |
3 | Cell Biology | 28722 | 15% | 1% | 6245 |
4 | Biochemistry & Molecular Biology | 27588 | 25% | 1% | 10153 |
5 | Developmental Biology | 8333 | 3% | 1% | 1323 |
6 | Neurosciences | 6039 | 10% | 0% | 3950 |
7 | Biotechnology & Applied Microbiology | 4145 | 6% | 0% | 2371 |
8 | Education, Special | 2459 | 1% | 1% | 365 |
9 | Medicine, Research & Experimental | 2048 | 4% | 0% | 1604 |
10 | Reproductive Biology | 1544 | 2% | 1% | 641 |
Address terms |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | EPIGENET | 83710 | 1% | 35% | 314 |
2 | MIND | 49013 | 1% | 22% | 299 |
3 | HUMAN GENET | 35443 | 4% | 3% | 1499 |
4 | DEV GENET IMPRINTING | 30884 | 0% | 54% | 76 |
5 | CANC EPIGENET | 28284 | 0% | 28% | 135 |
6 | MED GENET | 23441 | 3% | 3% | 1153 |
7 | EPIGENET PROGRAMME | 20136 | 0% | 48% | 55 |
8 | WESTERN SYDNEY GENET PROGRAM | 19652 | 0% | 39% | 66 |
9 | GENET | 19383 | 4% | 2% | 1521 |
10 | BIOCHEM MOL MED | 18953 | 1% | 12% | 212 |
Journals |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass |
---|---|---|---|---|---|
1 | EPIGENETICS | 123309 | 1% | 44% | 366 |
2 | EPIGENOMICS | 83292 | 1% | 46% | 241 |
3 | CLINICAL EPIGENETICS | 72827 | 1% | 45% | 214 |
4 | AMERICAN JOURNAL OF MEDICAL GENETICS | 71248 | 2% | 10% | 913 |
5 | HUMAN MOLECULAR GENETICS | 32902 | 2% | 7% | 674 |
6 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | 24919 | 1% | 8% | 450 |
7 | EPIGENETICS & CHROMATIN | 19872 | 0% | 29% | 92 |
8 | BRAIN & DEVELOPMENT | 15495 | 1% | 8% | 279 |
9 | ONCOTARGET | 15272 | 1% | 4% | 590 |
10 | JOURNAL OF MEDICAL GENETICS | 14452 | 1% | 6% | 340 |
Author Key Words |
chi_square_rank | term | chi_square | shrOfCwithTerm | shrOfTermInClass | termInClass | LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | DNA METHYLATION | 1239981 | 10% | 39% | 4146 | Search DNA+METHYLATION | Search DNA+METHYLATION |
2 | FRAGILE X SYNDROME | 660729 | 3% | 80% | 1091 | Search FRAGILE+X+SYNDROME | Search FRAGILE+X+SYNDROME |
3 | RETT SYNDROME | 589235 | 2% | 86% | 901 | Search RETT+SYNDROME | Search RETT+SYNDROME |
4 | EPIGENETICS | 573480 | 7% | 25% | 2985 | Search EPIGENETICS | Search EPIGENETICS |
5 | PRADER WILLI SYNDROME | 469839 | 2% | 82% | 751 | Search PRADER+WILLI+SYNDROME | Search PRADER+WILLI+SYNDROME |
6 | LONG NONCODING RNAS | 462902 | 2% | 75% | 812 | Search LONG+NONCODING+RNAS | Search LONG+NONCODING+RNAS |
7 | LNCRNA | 379635 | 2% | 71% | 701 | Search LNCRNA | Search LNCRNA |
8 | GENOMIC IMPRINTING | 367891 | 2% | 67% | 719 | Search GENOMIC+IMPRINTING | Search GENOMIC+IMPRINTING |
9 | MECP2 | 267946 | 1% | 80% | 439 | Search MECP2 | Search MECP2 |
10 | ANGELMAN SYNDROME | 249623 | 1% | 86% | 383 | Search ANGELMAN+SYNDROME | Search ANGELMAN+SYNDROME |
Core articles |
The table includes core articles in the class. The following variables is taken into account for the relevance score of an article in a cluster c: (1) Number of references referring to publications in the class. (2) Share of total number of active references referring to publications in the class. (3) Age of the article. New articles get higher score than old articles. (4) Citation rate, normalized to year. |
Classes with closest relation at Level 3 |