Class information for:
Level 1: COPY NUMBER VARIATION//CCL3L1//PENNCNV

Basic class information
ID Publications Average number
of references		 Avg. shr. active
ref. in WoS
5163 1594 39.7 88%


Bar chart of Publication_year

Last years might be incomplete

Classes in level above (level 2)


ID, lev.
above		 Publications Label for level above
1568 6715 NEXT GENERATION SEQUENCING//RNA SEQ//COPY NUMBER VARIATION

Terms with highest relevance score


Rank Term Type of term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 COPY NUMBER VARIATION Author keyword 29 20% 8% 134
2 CCL3L1 Author keyword 19 76% 1% 13
3 PENNCNV Author keyword 13 80% 1% 8
4 DNA COPY NUMBER Author keyword 10 37% 1% 22
5 CRLMM Author keyword 6 80% 0% 4
6 COPY NUMBER VARIATIONS Author keyword 6 20% 2% 25
7 CCL3L Author keyword 6 100% 0% 4
8 PARALOGUE RATIO TEST Author keyword 6 100% 0% 4
9 COPY NUMBER VARIATION CNV Author keyword 5 27% 1% 16
10 COPY NUMBER POLYMORPHISM Author keyword 4 36% 1% 9

Web of Science journal categories

Author Key Words


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class		 LCSH search Wikipedia search
1 COPY NUMBER VARIATION 29 20% 8% 134 Search COPY+NUMBER+VARIATION Search COPY+NUMBER+VARIATION
2 CCL3L1 19 76% 1% 13 Search CCL3L1 Search CCL3L1
3 PENNCNV 13 80% 1% 8 Search PENNCNV Search PENNCNV
4 DNA COPY NUMBER 10 37% 1% 22 Search DNA+COPY+NUMBER Search DNA+COPY+NUMBER
5 CRLMM 6 80% 0% 4 Search CRLMM Search CRLMM
6 COPY NUMBER VARIATIONS 6 20% 2% 25 Search COPY+NUMBER+VARIATIONS Search COPY+NUMBER+VARIATIONS
7 CCL3L 6 100% 0% 4 Search CCL3L Search CCL3L
8 PARALOGUE RATIO TEST 6 100% 0% 4 Search PARALOGUE+RATIO+TEST Search PARALOGUE+RATIO+TEST
9 COPY NUMBER VARIATION CNV 5 27% 1% 16 Search COPY+NUMBER+VARIATION+CNV Search COPY+NUMBER+VARIATION+CNV
10 COPY NUMBER POLYMORPHISM 4 36% 1% 9 Search COPY+NUMBER+POLYMORPHISM Search COPY+NUMBER+POLYMORPHISM

Key Words Plus


Rank Web of Science journal category Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 ARRAY CGH DATA 170 65% 10% 161
2 STRUCTURAL VARIATION 81 26% 17% 274
3 CIRCULAR BINARY SEGMENTATION 56 57% 4% 66
4 SEGMENTAL DUPLICATIONS 48 25% 10% 165
5 SNP GENOTYPING DATA 46 50% 4% 65
6 CGH DATA 44 59% 3% 50
7 GENOTYPING DATA 33 75% 2% 24
8 COPY NUMBER VARIATION 30 13% 13% 215
9 VARIANT ASSAYS 24 91% 1% 10
10 CCL3L1 22 66% 1% 21

Journals

Reviews


Title Publ. year Cit. Active references % act. ref.
to same field
A copy number variation map of the human genome 2015 3 90 39%
Copy number polymorphism in plant genomes 2014 14 91 29%
Correlating Multiallelic Copy Number Polymorphisms with Disease Susceptibility 2013 18 105 51%
Copy Number Variation in Human Health, Disease, and Evolution 2009 328 166 23%
Human Copy Number Variation and Complex Genetic Disease 2011 75 130 31%
Impacts of Variation in the Human Genome on Gene Regulation 2013 23 45 33%
Mechanisms of change in gene copy number 2009 362 145 17%
Copy number variation in the genomes of domestic animals 2012 28 90 48%
Phenotypic impact of genomic structural variation: insights from and for human disease 2013 47 145 16%
Structural variation in the human genome 2006 750 87 32%

Address terms


Rank Address term Relevance score
(tfidf)		 Class's shr.
of term's tot.
occurrences		 Shr. of publ.
in class containing
term		 Num. of
publ. in
class
1 SHANDONG PROV ANIM DIS CONTROL BREEDING 4 46% 0.4% 6
2 HLTH SOLUT GRP 3 43% 0.4% 6
3 INTEGRATED GENOME POLYMORPHISM 3 25% 0.7% 11
4 GENET GENOM ANAL 3 60% 0.2% 3
5 JNU HKUST JOINT 3 32% 0.4% 7
6 GRP MOL GENET SYST BIOL 2 67% 0.1% 2
7 JMP GENOM 2 67% 0.1% 2
8 BREAST CANC FUNCT GEN 1 100% 0.1% 2
9 COMMUNITY ENGAGED TRANSLAT 1 50% 0.1% 2
10 EPIDEMIOL PUBL HLTH MD3 1 100% 0.1% 2

Related classes at same level (level 1)


Rank Relatedness score Related classes
1 0.0000180362 SUBTELOMERIC REARRANGEMENTS//IDIOPATHIC MENTAL RETARDATION//MBD5
2 0.0000146051 ZNF804A//MCLAUGHLIN//MOL CLIN NEUROBIOL
3 0.0000104045 INTER SIMPLE SEQUENCE REPEAT PCR//BIOPHYS CYTOMETRY//HOSP UNIV SALAMANCA IBSAL
4 0.0000102895 GENOME ASSEMBLY//VARIANT CALLING//TARGET ENRICHMENT
5 0.0000088993 EVOLUT CANC//PETOS PARADOX//TRANSLAT CANC THER EUT
6 0.0000081933 COMPLEX CHROMOSOMAL REARRANGEMENT//COMPLEX CHROMOSOME REARRANGEMENT CCR//COMPLEX CHROMOSOMAL REARRANGEMENTS
7 0.0000065754 ZNF703//C8ORF4//8P12
8 0.0000061830 WHOLE GENOME AMPLIFICATION//MULTIPLE DISPLACEMENT AMPLIFICATION//PHI29 DNA POLYMERASE
9 0.0000061500 SMITH MAGENIS SYNDROME//RAI1//POTOCKI LUPSKI SYNDROME
10 0.0000055039 CLIN BREAST CARE PROJECT//16Q243//CHROMOSOMAL SCANNING