| Rank |
Page title |
Views |
Daily average |
Assessment |
Importance |
| 1 |
CRISPR |
43,873 |
1,462 |
B |
Top |
| 2 |
Receiver operating characteristic |
43,720 |
1,457 |
B |
Mid |
| 3 |
Dynamic programming |
31,631 |
1,054 |
B |
Top |
| 4 |
Bioinformatics |
27,098 |
903 |
C |
Top |
| 5 |
Systems theory |
26,195 |
873 |
C |
Mid |
| 6 |
DNA sequencing |
24,536 |
817 |
C |
High |
| 7 |
Clade |
24,106 |
803 |
C |
Mid |
| 8 |
Hidden Markov model |
22,405 |
746 |
GA |
Top |
| 9 |
Combined DNA Index System |
22,404 |
746 |
GA |
Low |
| 10 |
Last universal common ancestor |
21,333 |
711 |
B |
Mid |
| 11 |
Phylogenetic tree |
19,825 |
660 |
B |
Top |
| 12 |
Michaelis–Menten kinetics |
18,274 |
609 |
B |
Top |
| 13 |
23andMe |
18,182 |
606 |
C |
Low |
| 14 |
National Center for Biotechnology Information |
17,544 |
584 |
Start |
Low |
| 15 |
Genome |
17,269 |
575 |
C |
High |
| 16 |
Sanger sequencing |
13,667 |
455 |
C |
Mid |
| 17 |
Ontology (information science) |
13,595 |
453 |
C |
High |
| 18 |
Cellular automaton |
13,484 |
449 |
B |
Low |
| 19 |
DNA barcoding |
11,910 |
397 |
B |
High |
| 20 |
Compartmental models in epidemiology |
11,193 |
373 |
C |
Mid |
| 21 |
Phylogenetics |
10,958 |
365 |
C |
Top |
| 22 |
BLAST (biotechnology) |
10,945 |
364 |
C |
Top |
| 23 |
Heat map |
10,786 |
359 |
Start |
High |
| 24 |
FASTA format |
10,513 |
350 |
B |
High |
| 25 |
Most recent common ancestor |
10,103 |
336 |
B |
High |
| 26 |
Protein Data Bank |
10,075 |
335 |
C |
High |
| 27 |
PubMed Central |
9,994 |
333 |
B |
Mid |
| 28 |
Sequence alignment |
9,539 |
317 |
C |
High |
| 29 |
Genomics |
9,514 |
317 |
B |
High |
| 30 |
Whole genome sequencing |
9,273 |
309 |
B |
High |
| 31 |
Illumina, Inc. |
9,227 |
307 |
C |
Low |
| 32 |
DNA microarray |
9,061 |
302 |
B |
Top |
| 33 |
Cladistics |
9,055 |
301 |
C |
Mid |
| 34 |
Synthetic biology |
8,852 |
295 |
B |
Mid |
| 35 |
RNA-Seq |
8,778 |
292 |
B |
Top |
| 36 |
Medical Subject Headings |
8,713 |
290 |
C |
Mid |
| 37 |
FASTQ format |
8,693 |
289 |
B |
Mid |
| 38 |
List of algorithms |
8,366 |
278 |
List |
Mid |
| 39 |
Biostatistics |
8,351 |
278 |
B |
Top |
| 40 |
AlphaFold |
8,320 |
277 |
C |
High |
| 41 |
Computational biology |
8,152 |
271 |
C |
Top |
| 42 |
Reference genome |
8,099 |
269 |
Start |
Low |
| 43 |
Proteomics |
7,927 |
264 |
C |
High |
| 44 |
Phi coefficient |
7,677 |
255 |
Start |
Mid |
| 45 |
Mathematical and theoretical biology |
7,633 |
254 |
C |
Top |
| 46 |
Petri net |
7,339 |
244 |
B |
Low |
| 47 |
Lineweaver–Burk plot |
6,629 |
220 |
B |
Low |
| 48 |
Non-coding DNA |
6,531 |
217 |
C |
Low |
| 49 |
Consensus CDS Project |
6,384 |
212 |
C |
Low |
| 50 |
Omics |
6,349 |
211 |
C |
Mid |
| 51 |
Data wrangling |
5,965 |
198 |
Start |
Low |
| 52 |
Needleman–Wunsch algorithm |
5,827 |
194 |
Start |
Mid |
| 53 |
Protein–protein interaction |
5,532 |
184 |
C |
High |
| 54 |
Docking (molecular) |
5,493 |
183 |
B |
High |
| 55 |
Spurious relationship |
5,283 |
176 |
Start |
Low |
| 56 |
Gene nomenclature |
5,276 |
175 |
Start |
Mid |
| 57 |
Computational neuroscience |
5,167 |
172 |
C |
Top |
| 58 |
PubChem |
5,144 |
171 |
Start |
Mid |
| 59 |
High-throughput screening |
5,066 |
168 |
B |
Low |
| 60 |
Protein structure prediction |
4,980 |
166 |
C |
High |
| 61 |
Systems biology |
4,977 |
165 |
C |
Top |
| 62 |
Single cell sequencing |
4,943 |
164 |
C |
High |
| 63 |
Exome sequencing |
4,926 |
164 |
C |
High |
| 64 |
George Church (geneticist) |
4,887 |
162 |
C |
Mid |
| 65 |
Molecular clock |
4,837 |
161 |
C |
High |
| 66 |
Phred quality score |
4,795 |
159 |
Start |
Mid |
| 67 |
Smith–Waterman algorithm |
4,771 |
159 |
B |
Top |
| 68 |
Metabolomics |
4,712 |
157 |
C |
Mid |
| 69 |
BLOSUM |
4,576 |
152 |
C |
High |
| 70 |
Variant Call Format |
4,565 |
152 |
Start |
Mid |
| 71 |
ATAC-seq |
4,539 |
151 |
Start |
Low |
| 72 |
Genetic programming |
4,466 |
148 |
B |
Mid |
| 73 |
Folding@home |
4,359 |
145 |
B |
Mid |
| 74 |
Jmol |
4,246 |
141 |
Start |
Mid |
| 75 |
Baum–Welch algorithm |
4,132 |
137 |
C |
Mid |
| 76 |
Illumina dye sequencing |
4,115 |
137 |
C |
Mid |
| 77 |
ChIP sequencing |
4,106 |
136 |
C |
Mid |
| 78 |
Nanopore sequencing |
4,102 |
136 |
C |
Low |
| 79 |
Robert Gentleman (statistician) |
4,084 |
136 |
Start |
Mid |
| 80 |
Gene set enrichment analysis |
3,931 |
131 |
C |
Mid |
| 81 |
Gene Ontology |
3,914 |
130 |
C |
High |
| 82 |
Transcriptome |
3,898 |
129 |
B |
High |
| 83 |
K-mer |
3,891 |
129 |
B |
Mid |
| 84 |
Enzyme Commission number |
3,843 |
128 |
Start |
High |
| 85 |
Molecular phylogenetics |
3,830 |
127 |
C |
High |
| 86 |
Crossover (genetic algorithm) |
3,793 |
126 |
B |
Low |
| 87 |
KEGG |
3,726 |
124 |
C |
High |
| 88 |
Root-mean-square deviation of atomic positions |
3,713 |
123 |
Start |
Mid |
| 89 |
Similarity measure |
3,658 |
121 |
Start |
Mid |
| 90 |
BED (file format) |
3,650 |
121 |
Unknown |
Unknown |
| 91 |
Bioconductor |
3,639 |
121 |
C |
Mid |
| 92 |
Online Mendelian Inheritance in Man |
3,629 |
120 |
Start |
Mid |
| 93 |
Burrows–Wheeler transform |
3,617 |
120 |
C |
Mid |
| 94 |
KNIME |
3,554 |
118 |
Start |
Low |
| 95 |
What Is Life? |
3,530 |
117 |
C |
Low |
| 96 |
UniProt |
3,476 |
115 |
B |
High |
| 97 |
UPGMA |
3,442 |
114 |
C |
Low |
| 98 |
SAM (file format) |
3,380 |
112 |
Start |
Mid |
| 99 |
Ensembl genome database project |
3,335 |
111 |
B |
High |
| 100 |
Volcano plot (statistics) |
3,284 |
109 |
C |
Mid |
| 101 |
Broad Institute |
3,282 |
109 |
Start |
Low |
| 102 |
Monod equation |
3,263 |
108 |
Start |
Low |
| 103 |
STR analysis |
3,252 |
108 |
Stub |
Low |
| 104 |
Wikispecies |
3,251 |
108 |
Start |
Mid |
| 105 |
John Maynard Smith |
3,184 |
106 |
C |
Mid |
| 106 |
Mathematical modelling of infectious disease |
3,171 |
105 |
C |
Low |
| 107 |
FASTA |
3,136 |
104 |
B |
High |
| 108 |
List of biological databases |
3,042 |
101 |
List |
High |
| 109 |
GenBank |
3,039 |
101 |
Start |
High |
| 110 |
Clustal |
3,021 |
100 |
Start |
Mid |
| 111 |
Conserved sequence |
3,000 |
100 |
C |
High |
| 112 |
Data curation |
2,936 |
97 |
Start |
Mid |
| 113 |
Homology modeling |
2,932 |
97 |
B |
High |
| 114 |
Superspreading event |
2,879 |
95 |
C |
High |
| 115 |
Intrinsically disordered proteins |
2,842 |
94 |
C |
Mid |
| 116 |
Neighbor joining |
2,830 |
94 |
C |
High |
| 117 |
Daphne Koller |
2,830 |
94 |
C |
Low |
| 118 |
Multiomics |
2,817 |
93 |
C |
Mid |
| 119 |
Environmental DNA |
2,803 |
93 |
B |
Low |
| 120 |
Gene regulatory network |
2,803 |
93 |
B |
High |
| 121 |
Animal Diversity Web |
2,792 |
93 |
C |
Mid |
| 122 |
Microarray |
2,790 |
93 |
Start |
Top |
| 123 |
Distance matrix |
2,764 |
92 |
Start |
High |
| 124 |
Entrez |
2,762 |
92 |
B |
Mid |
| 125 |
Haar-like feature |
2,743 |
91 |
C |
Low |
| 126 |
Biological database |
2,739 |
91 |
Start |
High |
| 127 |
Functional genomics |
2,704 |
90 |
C |
High |
| 128 |
Foundational Model of Anatomy |
2,692 |
89 |
Start |
Low |
| 129 |
Ludwig von Bertalanffy |
2,645 |
88 |
Start |
Low |
| 130 |
Biological computing |
2,632 |
87 |
C |
Mid |
| 131 |
List of sequence alignment software |
2,632 |
87 |
List |
High |
| 132 |
List of open-source bioinformatics software |
2,591 |
86 |
List |
High |
| 133 |
List of protein structure prediction software |
2,583 |
86 |
List |
Mid |
| 134 |
Mutation (genetic algorithm) |
2,579 |
85 |
Start |
Low |
| 135 |
Encyclopedia of Life |
2,574 |
85 |
Start |
Mid |
| 136 |
Genetic distance |
2,551 |
85 |
B |
Mid |
| 137 |
Protein Data Bank (file format) |
2,512 |
83 |
C |
Mid |
| 138 |
Gene family |
2,508 |
83 |
C |
High |
| 139 |
ChEMBL |
2,502 |
83 |
Start |
Mid |
| 140 |
Brain mapping |
2,470 |
82 |
Start |
Low |
| 141 |
N50, L50, and related statistics |
2,452 |
81 |
Start |
Low |
| 142 |
European Molecular Biology Laboratory |
2,398 |
79 |
C |
Low |
| 143 |
Genome size |
2,394 |
79 |
B |
Mid |
| 144 |
Structural Classification of Proteins database |
2,351 |
78 |
Start |
High |
| 145 |
Maximum parsimony (phylogenetics) |
2,307 |
76 |
C |
High |
| 146 |
Kabsch algorithm |
2,293 |
76 |
Start |
Mid |
| 147 |
Sequence analysis |
2,279 |
75 |
C |
Top |
| 148 |
Fitness function |
2,279 |
75 |
Start |
Mid |
| 149 |
Martin Kulldorff |
2,265 |
75 |
Start |
Low |
| 150 |
Contig |
2,252 |
75 |
C |
High |
| 151 |
Topologically associating domain |
2,239 |
74 |
C |
Low |
| 152 |
DNA database |
2,219 |
73 |
Start |
Mid |
| 153 |
Point accepted mutation |
2,199 |
73 |
B |
High |
| 154 |
10x Genomics |
2,192 |
73 |
C |
Mid |
| 155 |
Schrödinger, Inc. |
2,177 |
72 |
Start |
Low |
| 156 |
PyMOL |
2,166 |
72 |
Start |
Low |
| 157 |
Biological network |
2,166 |
72 |
Start |
High |
| 158 |
Biochip |
2,161 |
72 |
C |
Low |
| 159 |
Pan-genome |
2,160 |
72 |
C |
Mid |
| 160 |
Spatial transcriptomics |
2,121 |
70 |
C |
Low |
| 161 |
DNA annotation |
2,109 |
70 |
Start |
Low |
| 162 |
Proteome |
2,073 |
69 |
C |
High |
| 163 |
Polygenic score |
2,058 |
68 |
C |
Mid |
| 164 |
Microarray analysis techniques |
2,035 |
67 |
B |
Mid |
| 165 |
Chromosome conformation capture |
2,027 |
67 |
C |
Low |
| 166 |
Isomorphic Labs |
2,021 |
67 |
Stub |
Low |
| 167 |
Oxford Nanopore Technologies |
2,016 |
67 |
Start |
Low |
| 168 |
Synteny |
2,007 |
66 |
Start |
Low |
| 169 |
SNP array |
2,002 |
66 |
Start |
High |
| 170 |
List of protein-ligand docking software |
1,998 |
66 |
List |
Mid |
| 171 |
Approximate Bayesian computation |
1,994 |
66 |
B |
Low |
| 172 |
Pfam |
1,981 |
66 |
B |
High |
| 173 |
Sequence motif |
1,950 |
65 |
Start |
High |
| 174 |
Consensus sequence |
1,949 |
64 |
Start |
High |
| 175 |
DNA sequencer |
1,945 |
64 |
Start |
Low |
| 176 |
Gene prediction |
1,920 |
64 |
C |
High |
| 177 |
Indel |
1,897 |
63 |
Start |
Low |
| 178 |
MA plot |
1,895 |
63 |
Start |
Low |
| 179 |
Phylogeny |
1,871 |
62 |
NA |
NA |
| 180 |
Michael Levitt |
1,868 |
62 |
C |
Low |
| 181 |
Position weight matrix |
1,809 |
60 |
C |
Top |
| 182 |
Andrew Huxley |
1,790 |
59 |
C |
Low |
| 183 |
Virtual screening |
1,788 |
59 |
Start |
High |
| 184 |
Matthews correlation coefficient |
1,754 |
58 |
NA |
NA |
| 185 |
Global Biodiversity Information Facility |
1,738 |
57 |
Start |
Low |
| 186 |
Pardis Sabeti |
1,734 |
57 |
B |
Low |
| 187 |
Metabarcoding |
1,684 |
56 |
B |
Low |
| 188 |
Sequence assembly |
1,683 |
56 |
Start |
High |
| 189 |
Comparative genomics |
1,669 |
55 |
C |
Top |
| 190 |
Gap penalty |
1,668 |
55 |
C |
High |
| 191 |
European Bioinformatics Institute |
1,655 |
55 |
C |
Low |
| 192 |
Knowledge engineering |
1,611 |
53 |
Start |
Low |
| 193 |
Ecosystem model |
1,607 |
53 |
Start |
Mid |
| 194 |
David Baker (biochemist) |
1,607 |
53 |
Start |
Low |
| 195 |
Ion semiconductor sequencing |
1,597 |
53 |
C |
Low |
| 196 |
GROMACS |
1,582 |
52 |
Start |
Low |
| 197 |
UCSC Genome Browser |
1,570 |
52 |
Start |
High |
| 198 |
Computational phylogenetics |
1,554 |
51 |
C |
High |
| 199 |
STRING |
1,541 |
51 |
B |
Low |
| 200 |
General feature format |
1,520 |
50 |
Start |
Low |
| 201 |
CASP |
1,497 |
49 |
C |
Mid |
| 202 |
Catalogue of Life |
1,489 |
49 |
C |
Low |
| 203 |
Models of DNA evolution |
1,484 |
49 |
B |
Mid |
| 204 |
ENCODE |
1,479 |
49 |
C |
Mid |
| 205 |
FitzHugh–Nagumo model |
1,475 |
49 |
Start |
Low |
| 206 |
Tournament selection |
1,463 |
48 |
Start |
Low |
| 207 |
Genetic operator |
1,462 |
48 |
Start |
Low |
| 208 |
Wellcome Sanger Institute |
1,462 |
48 |
C |
Low |
| 209 |
List of mass spectrometry software |
1,459 |
48 |
List |
Low |
| 210 |
Solvation shell |
1,455 |
48 |
Start |
Low |
| 211 |
Single-cell transcriptomics |
1,453 |
48 |
C |
Mid |
| 212 |
Substitution model |
1,452 |
48 |
B |
Mid |
| 213 |
RNA integrity number |
1,448 |
48 |
Stub |
Low |
| 214 |
Probabilistic context-free grammar |
1,447 |
48 |
B |
High |
| 215 |
Structural bioinformatics |
1,444 |
48 |
B |
High |
| 216 |
Gene expression profiling |
1,433 |
47 |
B |
High |
| 217 |
Aviv Regev |
1,430 |
47 |
Start |
Low |
| 218 |
FishBase |
1,428 |
47 |
Start |
Low |
| 219 |
UK Biobank |
1,425 |
47 |
B |
Low |
| 220 |
Substitution matrix |
1,423 |
47 |
C |
High |
| 221 |
ChEBI |
1,420 |
47 |
Start |
Low |
| 222 |
1000 Genomes Project |
1,410 |
47 |
Start |
Low |
| 223 |
Dot plot (bioinformatics) |
1,406 |
46 |
Start |
Mid |
| 224 |
Paradox of the plankton |
1,394 |
46 |
Start |
Low |
| 225 |
Sequence logo |
1,391 |
46 |
B |
Mid |
| 226 |
Weighted correlation network analysis |
1,351 |
45 |
B |
Low |
| 227 |
RefSeq |
1,341 |
44 |
Start |
Mid |
| 228 |
Metabolome |
1,325 |
44 |
C |
High |
| 229 |
Amino acid replacement |
1,312 |
43 |
Start |
High |
| 230 |
Protein superfamily |
1,312 |
43 |
B |
High |
| 231 |
List of phylogenetics software |
1,311 |
43 |
List |
High |
| 232 |
List of genetic algorithm applications |
1,310 |
43 |
List |
Low |
| 233 |
DNA Data Bank of Japan |
1,304 |
43 |
Start |
Low |
| 234 |
Cooperative binding |
1,302 |
43 |
B |
Mid |
| 235 |
Bayesian inference in phylogeny |
1,300 |
43 |
C |
High |
| 236 |
Outgroup (cladistics) |
1,299 |
43 |
Start |
Mid |
| 237 |
Computational genomics |
1,287 |
42 |
Start |
Mid |
| 238 |
AMBER |
1,284 |
42 |
C |
Mid |
| 239 |
Biobank |
1,264 |
42 |
C |
High |
| 240 |
Machine learning in bioinformatics |
1,255 |
41 |
B |
High |
| 241 |
Genomic organization |
1,252 |
41 |
Start |
Low |
| 242 |
Protein design |
1,246 |
41 |
C |
Mid |
| 243 |
Expasy |
1,242 |
41 |
Start |
Mid |
| 244 |
List of phylogenetic tree visualization software |
1,237 |
41 |
List |
Mid |
| 245 |
C. H. Waddington |
1,235 |
41 |
C |
Low |
| 246 |
CUT&RUN sequencing |
1,227 |
40 |
C |
Low |
| 247 |
Sequence database |
1,211 |
40 |
Start |
Mid |
| 248 |
Interactome |
1,200 |
40 |
C |
Mid |
| 249 |
Biological systems engineering |
1,187 |
39 |
Start |
Low |
| 250 |
ABI Solid Sequencing |
1,174 |
39 |
Start |
Low |
| 251 |
Threading (protein sequence) |
1,153 |
38 |
C |
High |
| 252 |
Protein family |
1,150 |
38 |
Start |
High |
| 253 |
Hirschberg's algorithm |
1,144 |
38 |
B |
Low |
| 254 |
Modelling biological systems |
1,143 |
38 |
C |
High |
| 255 |
Robinson–Foulds metric |
1,137 |
37 |
C |
Low |
| 256 |
CATH database |
1,131 |
37 |
Start |
Mid |
| 257 |
EBird |
1,115 |
37 |
Start |
Low |
| 258 |
Theoretical ecology |
1,106 |
36 |
B |
High |
| 259 |
PROSITE |
1,098 |
36 |
Start |
High |
| 260 |
CHARMM |
1,092 |
36 |
B |
Mid |
| 261 |
Cable theory |
1,088 |
36 |
C |
Mid |
| 262 |
DbSNP |
1,086 |
36 |
B |
Mid |
| 263 |
Network motif |
1,084 |
36 |
B |
Low |
| 264 |
AutoDock |
1,077 |
35 |
Start |
Mid |
| 265 |
Cytoscape |
1,068 |
35 |
B |
High |
| 266 |
Flux balance analysis |
1,063 |
35 |
B |
High |
| 267 |
List of RNA-Seq bioinformatics tools |
1,063 |
35 |
List |
Mid |
| 268 |
Systems neuroscience |
1,057 |
35 |
Stub |
Mid |
| 269 |
Protein structure database |
1,056 |
35 |
Start |
Low |
| 270 |
Umbrella sampling |
1,053 |
35 |
Start |
Low |
| 271 |
Scoring functions for docking |
1,050 |
35 |
Start |
Mid |
| 272 |
Celera Corporation |
1,041 |
34 |
Start |
Low |
| 273 |
List of bioinformatics journals |
1,041 |
34 |
List |
Mid |
| 274 |
Alan Hodgkin |
1,031 |
34 |
Start |
Low |
| 275 |
454 Life Sciences |
1,028 |
34 |
C |
Low |
| 276 |
D'Arcy Wentworth Thompson |
1,028 |
34 |
GA |
Mid |
| 277 |
Biochemical cascade |
1,027 |
34 |
C |
Mid |
| 278 |
World Community Grid |
1,025 |
34 |
C |
Low |
| 279 |
GeneCards |
1,019 |
33 |
C |
Mid |
| 280 |
Polytomy |
1,012 |
33 |
Start |
Low |
| 281 |
Tom Blundell |
1,005 |
33 |
C |
Low |
| 282 |
Molecular Evolutionary Genetics Analysis |
999 |
33 |
Start |
Low |
| 283 |
Cross-species transmission |
993 |
33 |
C |
Low |
| 284 |
Conservative replacement |
992 |
33 |
Start |
Low |
| 285 |
Attack rate |
976 |
32 |
Start |
Mid |
| 286 |
Boolean network |
966 |
32 |
C |
Mid |
| 287 |
InterPro |
963 |
32 |
B |
High |
| 288 |
RasMol |
963 |
32 |
Start |
Mid |
| 289 |
Vito Volterra |
959 |
31 |
C |
Low |
| 290 |
HMMER |
954 |
31 |
B |
High |
| 291 |
Stephen Altschul |
951 |
31 |
Start |
Low |
| 292 |
List of RNA structure prediction software |
949 |
31 |
List |
Low |
| 293 |
Sepp Hochreiter |
945 |
31 |
Start |
Low |
| 294 |
Eadie–Hofstee diagram |
940 |
31 |
Start |
Low |
| 295 |
Ukkonen's algorithm |
937 |
31 |
Stub |
Low |
| 296 |
Manolis Kellis |
933 |
31 |
C |
Low |
| 297 |
Leroy Hood |
915 |
30 |
B |
Low |
| 298 |
Lipidomics |
915 |
30 |
C |
Low |
| 299 |
Chou–Fasman method |
913 |
30 |
B |
Mid |
| 300 |
List of neuroscience databases |
913 |
30 |
List |
Low |
| 301 |
Batch effect |
910 |
30 |
Stub |
Low |
| 302 |
List of sequenced animal genomes |
901 |
30 |
List |
Mid |
| 303 |
Institute of Genomics and Integrative Biology |
888 |
29 |
C |
Low |
| 304 |
Read (biology) |
884 |
29 |
Stub |
High |
| 305 |
Denis Noble |
873 |
29 |
Start |
Low |
| 306 |
UCSF Chimera |
870 |
29 |
Start |
Low |
| 307 |
List of sequenced eukaryotic genomes |
869 |
28 |
List |
Mid |
| 308 |
De novo sequence assemblers |
868 |
28 |
Start |
Low |
| 309 |
Population viability analysis |
866 |
28 |
C |
Mid |
| 310 |
Galaxy (computational biology) |
862 |
28 |
Start |
High |
| 311 |
Centre for DNA Fingerprinting and Diagnostics |
860 |
28 |
Start |
Low |
| 312 |
Chemical database |
854 |
28 |
Start |
Mid |
| 313 |
Trajectory inference |
854 |
28 |
C |
Low |
| 314 |
Biopython |
847 |
28 |
C |
High |
| 315 |
List of alignment visualization software |
847 |
28 |
List |
Mid |
| 316 |
Co-occurrence network |
846 |
28 |
Start |
Low |
| 317 |
Avogadro (software) |
846 |
28 |
Stub |
Low |
| 318 |
SAMtools |
844 |
28 |
Start |
Low |
| 319 |
ChIP-on-chip |
833 |
27 |
C |
Low |
| 320 |
Diseases Database |
825 |
27 |
Start |
Mid |
| 321 |
Metabolic network modelling |
824 |
27 |
C |
Mid |
| 322 |
Hanes–Woolf plot |
821 |
27 |
Start |
Low |
| 323 |
Biclustering |
813 |
27 |
B |
Mid |
| 324 |
UniFrac |
809 |
26 |
Stub |
Low |
| 325 |
Accession number (bioinformatics) |
804 |
26 |
Start |
Low |
| 326 |
List of gene prediction software |
798 |
26 |
List |
Mid |
| 327 |
Rosetta@home |
795 |
26 |
C |
Mid |
| 328 |
Chromosome (genetic algorithm) |
792 |
26 |
Start |
Low |
| 329 |
Mass spectrometry data format |
782 |
26 |
Start |
Low |
| 330 |
Evolutionary grade |
782 |
26 |
Start |
High |
| 331 |
Protein contact map |
777 |
25 |
Start |
Mid |
| 332 |
Structural genomics |
772 |
25 |
Start |
High |
| 333 |
Swiss-model |
771 |
25 |
Start |
Mid |
| 334 |
All of Us (initiative) |
771 |
25 |
C |
Low |
| 335 |
List of bioinformatics companies |
768 |
25 |
List |
Mid |
| 336 |
Biological data visualization |
768 |
25 |
Start |
Mid |
| 337 |
Margaret Oakley Dayhoff |
754 |
25 |
B |
High |
| 338 |
HUGO Gene Nomenclature Committee |
749 |
24 |
Start |
Mid |
| 339 |
Monod-Wyman-Changeux model |
747 |
24 |
Start |
Mid |
| 340 |
Synthetic biological circuit |
740 |
24 |
Start |
Low |
| 341 |
Joseph DeRisi |
736 |
24 |
Start |
Low |
| 342 |
Weasel program |
725 |
24 |
B |
Low |
| 343 |
List of molecular graphics systems |
709 |
23 |
List |
Mid |
| 344 |
Long branch attraction |
696 |
23 |
Start |
Low |
| 345 |
Phylogenetic comparative methods |
694 |
23 |
C |
Mid |
| 346 |
Paradox of enrichment |
690 |
23 |
Start |
Low |
| 347 |
Dry lab |
680 |
22 |
Start |
High |
| 348 |
Binning (metagenomics) |
669 |
22 |
Start |
Low |
| 349 |
Visual Molecular Dynamics |
665 |
22 |
Start |
Low |
| 350 |
Motoo Kimura |
664 |
22 |
C |
High |
| 351 |
Eric Xing |
658 |
21 |
Stub |
Low |
| 352 |
PSIPRED |
658 |
21 |
Start |
High |
| 353 |
Robert Rosen (biologist) |
652 |
21 |
Start |
Low |
| 354 |
De novo transcriptome assembly |
651 |
21 |
C |
Mid |
| 355 |
DeCODE genetics |
651 |
21 |
Start |
Low |
| 356 |
PDBsum |
640 |
21 |
Start |
Mid |
| 357 |
MicroRNA sequencing |
633 |
21 |
C |
Low |
| 358 |
HomoloGene |
626 |
20 |
Start |
Low |
| 359 |
Macromolecular docking |
621 |
20 |
B |
Mid |
| 360 |
GOR method |
617 |
20 |
Start |
Mid |
| 361 |
Nexus file |
612 |
20 |
Start |
Low |
| 362 |
ARKive |
610 |
20 |
C |
Mid |
| 363 |
NK model |
604 |
20 |
B |
Low |
| 364 |
EMBOSS |
598 |
19 |
Start |
Mid |
| 365 |
FlowJo |
597 |
19 |
Start |
Low |
| 366 |
Synthetic life |
591 |
19 |
NA |
NA |
| 367 |
Sarah Teichmann |
590 |
19 |
C |
Low |
| 368 |
Pileup format |
588 |
19 |
Start |
Low |
| 369 |
MODELLER |
587 |
19 |
Start |
Mid |
| 370 |
Binary Alignment Map |
584 |
19 |
Stub |
Mid |
| 371 |
Next-generation matrix |
584 |
19 |
Start |
Low |
| 372 |
Haplotype estimation |
583 |
19 |
Start |
Low |
| 373 |
Nucleic acid design |
581 |
19 |
C |
Mid |
| 374 |
McDonald–Kreitman test |
579 |
19 |
C |
Mid |
| 375 |
CRAM (file format) |
577 |
19 |
Start |
Low |
| 376 |
BioPerl |
575 |
19 |
Start |
High |
| 377 |
MUSCLE (alignment software) |
574 |
19 |
Start |
Mid |
| 378 |
BRENDA |
570 |
19 |
Start |
Mid |
| 379 |
Genome browser |
567 |
18 |
List |
High |
| 380 |
Jay Shendure |
566 |
18 |
Start |
Low |
| 381 |
Bioinformatics (journal) |
563 |
18 |
Start |
High |
| 382 |
Protein Information Resource |
560 |
18 |
Start |
Low |
| 383 |
Europe PubMed Central |
560 |
18 |
Start |
Low |
| 384 |
Metabolic flux analysis |
559 |
18 |
Stub |
Low |
| 385 |
De novo protein structure prediction |
548 |
18 |
Start |
High |
| 386 |
Genomics England |
543 |
18 |
Start |
Low |
| 387 |
Eugene Koonin |
542 |
18 |
Start |
Low |
| 388 |
Template modeling score |
540 |
18 |
Start |
Low |
| 389 |
PHYLIP |
537 |
17 |
Start |
Low |
| 390 |
Cyberneticist |
534 |
17 |
Stub |
Low |
| 391 |
MAFFT |
534 |
17 |
Stub |
Mid |
| 392 |
GENSCAN |
533 |
17 |
Stub |
Mid |
| 393 |
BioJava |
528 |
17 |
Start |
High |
| 394 |
DAVID |
528 |
17 |
Start |
Mid |
| 395 |
Barry Smith (ontologist) |
527 |
17 |
Start |
Low |
| 396 |
List of MeSH codes |
525 |
17 |
List |
Mid |
| 397 |
Fossilworks |
522 |
17 |
Stub |
Low |
| 398 |
Microarray databases |
521 |
17 |
List |
Mid |
| 399 |
Erez Lieberman Aiden |
517 |
17 |
GA |
Low |
| 400 |
Sequence clustering |
516 |
17 |
Start |
Mid |
| 401 |
Evolutionary tree |
512 |
17 |
NA |
NA |
| 402 |
Phenome |
512 |
17 |
Start |
Low |
| 403 |
Barcode of Life Data System |
512 |
17 |
Stub |
Low |
| 404 |
Journal of Theoretical Biology |
507 |
16 |
Stub |
Mid |
| 405 |
T-Coffee |
505 |
16 |
Start |
Mid |
| 406 |
Codon Adaptation Index |
503 |
16 |
Stub |
Low |
| 407 |
Hypothetical protein |
494 |
16 |
Start |
Low |
| 408 |
WPGMA |
490 |
16 |
C |
Low |
| 409 |
Lior Pachter |
489 |
16 |
Start |
Mid |
| 410 |
Low complexity regions in proteins |
488 |
16 |
Start |
Mid |
| 411 |
Epitranscriptome |
487 |
16 |
B |
Low |
| 412 |
Mascot (software) |
485 |
16 |
C |
High |
| 413 |
Michael Eisen |
485 |
16 |
Start |
Low |
| 414 |
Allen Brain Atlas |
482 |
16 |
C |
Mid |
| 415 |
Hindmarsh–Rose model |
478 |
15 |
Stub |
Low |
| 416 |
Protein pKa calculations |
478 |
15 |
Start |
Low |
| 417 |
Uri Alon |
475 |
15 |
Start |
Low |
| 418 |
FreeSurfer |
473 |
15 |
Start |
Mid |
| 419 |
BLAT (bioinformatics) |
473 |
15 |
B |
Low |
| 420 |
PLOS Computational Biology |
472 |
15 |
Start |
High |
| 421 |
Circular permutation in proteins |
471 |
15 |
GA |
Low |
| 422 |
Phylogenetic bracketing |
471 |
15 |
Start |
Low |
| 423 |
Institute of Bioinformatics and Applied Biotechnology (IBAB) |
469 |
15 |
B |
Low |
| 424 |
International Nucleotide Sequence Database Collaboration |
468 |
15 |
Stub |
Mid |
| 425 |
Eran Segal |
468 |
15 |
Start |
Low |
| 426 |
SBML |
468 |
15 |
B |
High |
| 427 |
Protein function prediction |
468 |
15 |
Start |
High |
| 428 |
INSACOG |
468 |
15 |
Start |
High |
| 429 |
Heng Li |
467 |
15 |
Start |
Low |
| 430 |
GENESIS (software) |
466 |
15 |
Start |
Low |
| 431 |
Energy charge |
460 |
15 |
Start |
Low |
| 432 |
Global distance test |
458 |
15 |
Stub |
Low |
| 433 |
Taxonomic database |
457 |
15 |
Start |
Mid |
| 434 |
Group size measures |
457 |
15 |
Start |
Low |
| 435 |
List of biodiversity databases |
455 |
15 |
List |
Low |
| 436 |
100,000 Genomes Project |
455 |
15 |
Start |
Low |
| 437 |
UniGene |
454 |
15 |
Start |
Low |
| 438 |
SPAdes (software) |
451 |
15 |
C |
Low |
| 439 |
Holland's schema theorem |
447 |
14 |
Start |
Low |
| 440 |
Protein tandem repeats |
446 |
14 |
Start |
Mid |
| 441 |
National Institute of Biomedical Genomics |
443 |
14 |
Stub |
Mid |
| 442 |
Narrow escape problem |
442 |
14 |
C |
Low |
| 443 |
Tree of Life Web Project |
442 |
14 |
Start |
Low |
| 444 |
Mouse Genome Informatics |
441 |
14 |
Stub |
Low |
| 445 |
European Nucleotide Archive |
440 |
14 |
GA |
Mid |
| 446 |
Demographic and Health Surveys |
437 |
14 |
B |
Low |
| 447 |
Putative gene |
434 |
14 |
Start |
Mid |
| 448 |
Haldane's dilemma |
434 |
14 |
B |
Low |
| 449 |
Analysis of molecular variance |
433 |
14 |
Stub |
Low |
| 450 |
David J. Lipman |
428 |
14 |
Start |
Low |
| 451 |
Fungal DNA barcoding |
428 |
14 |
C |
Low |
| 452 |
PANTHER |
427 |
14 |
C |
Low |
| 453 |
Phyre |
425 |
14 |
B |
Low |
| 454 |
Unique molecular identifier |
423 |
14 |
Stub |
Low |
| 455 |
List of omics topics in biology |
423 |
14 |
List |
Low |
| 456 |
Protein–protein interaction prediction |
421 |
14 |
C |
High |
| 457 |
Carl Bergstrom |
414 |
13 |
Stub |
Low |
| 458 |
Arthur Winfree |
410 |
13 |
Start |
Low |
| 459 |
Pyotr Anokhin |
409 |
13 |
Start |
Low |
| 460 |
Human Protein Atlas |
408 |
13 |
Start |
Low |
| 461 |
Stockholm format |
408 |
13 |
Start |
Low |
| 462 |
Metabolic control analysis |
407 |
13 |
B |
Mid |
| 463 |
Bonnie Berger |
404 |
13 |
Start |
Low |
| 464 |
Reactome |
402 |
13 |
Start |
Low |
| 465 |
Ewan Birney |
401 |
13 |
Start |
Low |
| 466 |
UGENE |
401 |
13 |
C |
Low |
| 467 |
Warren Gish |
397 |
13 |
Start |
Low |
| 468 |
Velvet assembler |
397 |
13 |
Start |
Low |
| 469 |
Apache Taverna |
396 |
13 |
C |
Low |
| 470 |
Saccharomyces Genome Database |
395 |
13 |
Start |
High |
| 471 |
DECIPHER |
395 |
13 |
C |
Low |
| 472 |
David Goodsell |
391 |
13 |
C |
Low |
| 473 |
Chemical library |
390 |
13 |
Start |
Low |
| 474 |
Glycomics |
390 |
13 |
Start |
Low |
| 475 |
Sequenom |
389 |
12 |
Start |
Low |
| 476 |
Open Tree of Life |
388 |
12 |
Start |
Low |
| 477 |
High-frequency oscillations |
380 |
12 |
C |
Low |
| 478 |
Digital phenotyping |
379 |
12 |
Start |
Low |
| 479 |
FlyBase |
376 |
12 |
Start |
Mid |
| 480 |
LSID |
376 |
12 |
Start |
Low |
| 481 |
OpenAPS |
375 |
12 |
Start |
Low |
| 482 |
Morris–Lecar model |
374 |
12 |
Start |
Low |
| 483 |
Biomedical text mining |
373 |
12 |
Start |
High |
| 484 |
Maqsudul Alam |
373 |
12 |
Stub |
Low |
| 485 |
Edward C. Holmes |
372 |
12 |
Start |
Low |
| 486 |
Halbert L. Dunn |
371 |
12 |
Start |
Low |
| 487 |
Bernd Sturmfels |
371 |
12 |
Stub |
Low |
| 488 |
ZooBank |
371 |
12 |
Start |
Low |
| 489 |
SNV calling from NGS data |
371 |
12 |
B |
Low |
| 490 |
Wellcome Genome Campus |
369 |
12 |
Start |
Low |
| 491 |
COSMIC cancer database |
368 |
12 |
C |
Low |
| 492 |
HH-suite |
367 |
12 |
C |
Low |
| 493 |
Andrew Rambaut |
366 |
12 |
Stub |
Low |
| 494 |
PLINK (genetic tool-set) |
363 |
12 |
Stub |
Low |
| 495 |
Fluxomics |
360 |
12 |
Start |
Low |
| 496 |
Dynamic energy budget theory |
359 |
11 |
C |
Low |
| 497 |
David Botstein |
358 |
11 |
Start |
Low |
| 498 |
Hypercycle (chemistry) |
356 |
11 |
B |
Low |
| 499 |
Peter Donnelly |
353 |
11 |
Stub |
Low |
| 500 |
Human Genome Organisation |
348 |
11 |
Start |
Low |