Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
1159 | 2714 | 33.6 | 84% |
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 | GENOME ASSEMBLY | Author keyword | 17 | 36% | 1% | 39 |
2 | VARIANT CALLING | Author keyword | 11 | 57% | 0% | 13 |
3 | TARGET ENRICHMENT | Author keyword | 8 | 43% | 1% | 15 |
4 | SIMONS QUANTITAT BIOL | Address | 8 | 52% | 0% | 11 |
5 | GENOME FINISHING | Author keyword | 6 | 71% | 0% | 5 |
6 | EXOME | Author keyword | 6 | 18% | 1% | 30 |
7 | MASSIVELY PARALLEL SEQUENCING | Author keyword | 5 | 16% | 1% | 28 |
8 | WHOLE EXOME SEQUENCING | Author keyword | 5 | 11% | 1% | 38 |
9 | EXOME SEQUENCING | Author keyword | 4 | 10% | 2% | 41 |
10 | PERSONAL GENOME | Author keyword | 4 | 67% | 0% | 4 |
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 | GENOME ASSEMBLY | 17 | 36% | 1% | 39 | Search GENOME+ASSEMBLY | Search GENOME+ASSEMBLY |
2 | VARIANT CALLING | 11 | 57% | 0% | 13 | Search VARIANT+CALLING | Search VARIANT+CALLING |
3 | TARGET ENRICHMENT | 8 | 43% | 1% | 15 | Search TARGET+ENRICHMENT | Search TARGET+ENRICHMENT |
4 | GENOME FINISHING | 6 | 71% | 0% | 5 | Search GENOME+FINISHING | Search GENOME+FINISHING |
5 | EXOME | 6 | 18% | 1% | 30 | Search EXOME | Search EXOME |
6 | MASSIVELY PARALLEL SEQUENCING | 5 | 16% | 1% | 28 | Search MASSIVELY+PARALLEL+SEQUENCING | Search MASSIVELY+PARALLEL+SEQUENCING |
7 | WHOLE EXOME SEQUENCING | 5 | 11% | 1% | 38 | Search WHOLE+EXOME+SEQUENCING | Search WHOLE+EXOME+SEQUENCING |
8 | EXOME SEQUENCING | 4 | 10% | 2% | 41 | Search EXOME+SEQUENCING | Search EXOME+SEQUENCING |
9 | PERSONAL GENOME | 4 | 67% | 0% | 4 | Search PERSONAL+GENOME | Search PERSONAL+GENOME |
10 | SHORT READ ALIGNMENT | 4 | 67% | 0% | 4 | Search SHORT+READ+ALIGNMENT | Search SHORT+READ+ALIGNMENT |
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 | BURROWS WHEELER TRANSFORM | 66 | 45% | 4% | 112 |
2 | SHORT DNA SEQUENCES | 52 | 63% | 2% | 52 |
3 | READ ALIGNMENT | 46 | 34% | 4% | 110 |
4 | SHORT READ ALIGNMENT | 45 | 43% | 3% | 79 |
5 | EXON CAPTURE | 40 | 79% | 1% | 26 |
6 | SHORT READ | 39 | 63% | 1% | 40 |
7 | MILLIONS | 34 | 59% | 1% | 38 |
8 | EXOME | 34 | 38% | 3% | 70 |
9 | READS | 33 | 35% | 3% | 76 |
10 | DE BRUIJN GRAPHS | 32 | 56% | 1% | 39 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references |
% act. ref. to same field |
---|---|---|---|---|
APPLICATIONS OF NEXT-GENERATION SEQUENCING Sequencing technologies - the next generation | 2010 | 1743 | 91 | 49% |
Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing | 2015 | 6 | 37 | 43% |
One chromosome, one contig: complete microbial genomes from long-read sequencing and assembly | 2015 | 4 | 59 | 54% |
Field guide to next-generation DNA sequencers | 2011 | 294 | 12 | 75% |
Sequencing depth and coverage: key considerations in genomic analyses | 2014 | 56 | 96 | 35% |
Genotype and SNP calling from next-generation sequencing data | 2011 | 298 | 50 | 62% |
Toward better understanding of artifacts in variant calling from high-coverage samples | 2014 | 16 | 39 | 87% |
The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine | 2014 | 101 | 43 | 16% |
Sequence Artifacts in DNA from Formalin-Fixed Tissues: Causes and Strategies for Minimization | 2015 | 4 | 50 | 32% |
Exome sequencing as a tool for Mendelian disease gene discovery | 2011 | 466 | 78 | 36% |
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 | SIMONS QUANTITAT BIOL | 8 | 52% | 0.4% | 11 |
2 | HKU BGI BIOINFORMAT ALGORITHMS CORE TECHNOL | 4 | 56% | 0.2% | 5 |
3 | STANLEY COGNIT GENOM | 4 | 33% | 0.4% | 10 |
4 | BINA TECHNOL | 3 | 100% | 0.1% | 3 |
5 | HKU BGI BIOINFORMAT ALGORITHMS | 3 | 100% | 0.1% | 3 |
6 | GENOM PATHOL SERV | 3 | 60% | 0.1% | 3 |
7 | NIJMEGEN MOL LIFE SCI GENET METAB DIS | 3 | 60% | 0.1% | 3 |
8 | HLTH LAW EMERGING TECHNOL | 2 | 67% | 0.1% | 2 |
9 | IFM BIOINFORMAT SERC SWEDISH E SCI | 2 | 67% | 0.1% | 2 |
10 | INVEST CANC THER Y | 2 | 67% | 0.1% | 2 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000209785 | MAPPING BY SEQUENCING//RADSEQ//REDUCED REPRESENTATION LIBRARIES |
2 | 0.0000180168 | RNA SEQ//DE NOVO ASSEMBLY//TRANSCRIPTOME ASSEMBLY |
3 | 0.0000167807 | EPIDEMIOL PATHOPHYSIOL ONCOGEN VIRUS UNIT//LYSSAVIRUS DYNAM HOST AD TAT UNIT//VIRAL DISCOVERY |
4 | 0.0000129853 | METAGENOMICS//MICROBIAL GENOM METAGEN PROGRAM//BIOSCI RD |
5 | 0.0000114166 | EVOLUT CANC//PETOS PARADOX//TRANSLAT CANC THER EUT |
6 | 0.0000102895 | COPY NUMBER VARIATION//CCL3L1//PENNCNV |
7 | 0.0000100808 | NSSNP//POLYPHEN//NSSNPS |
8 | 0.0000094746 | UNIVARIATE OPTIMIZATION//UNIDIMENSIONAL SEARCH METHOD//INITIAL INTERVAL OF UNCERTAINTY |
9 | 0.0000078350 | RARE VARIANTS//GENETIC EPIDEMIOLOGY//RARE VARIANT ANALYSIS |
10 | 0.0000071918 | CHIP SEQ//PEAK CALLING//DNASE SEQ |