| 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
|
