| Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
| 1
|
CRISPR
|
35,257
|
1,175
|
B
|
Top
|
| 2
|
Receiver operating characteristic
|
30,474
|
1,015
|
B
|
Mid
|
| 3
|
23andMe
|
28,248
|
941
|
C
|
Low
|
| 4
|
Last universal common ancestor
|
27,667
|
922
|
GA
|
Mid
|
| 5
|
Clade
|
24,012
|
800
|
C
|
Mid
|
| 6
|
PubMed Central
|
23,806
|
793
|
B
|
Mid
|
| 7
|
Dynamic programming
|
23,389
|
779
|
B
|
Top
|
| 8
|
Hidden Markov model
|
22,895
|
763
|
GA
|
Top
|
| 9
|
AlphaFold
|
22,857
|
761
|
C
|
High
|
| 10
|
Systems theory
|
19,124
|
637
|
C
|
Mid
|
| 11
|
Bioinformatics
|
18,133
|
604
|
C
|
Top
|
| 12
|
Phylogenetic tree
|
16,710
|
557
|
B
|
Top
|
| 13
|
Michaelis–Menten kinetics
|
15,793
|
526
|
B
|
Top
|
| 14
|
Cellular automaton
|
15,417
|
513
|
B
|
Low
|
| 15
|
Phylogenetics
|
13,674
|
455
|
B
|
Top
|
| 16
|
DNA sequencing
|
13,327
|
444
|
C
|
High
|
| 17
|
David Baker (biochemist)
|
12,941
|
431
|
Start
|
Low
|
| 18
|
Genome
|
12,336
|
411
|
C
|
High
|
| 19
|
Ontology (information science)
|
11,717
|
390
|
C
|
High
|
| 20
|
National Center for Biotechnology Information
|
10,100
|
336
|
C
|
Low
|
| 21
|
Compartmental models in epidemiology
|
10,071
|
335
|
C
|
Mid
|
| 22
|
Sanger sequencing
|
10,068
|
335
|
C
|
Mid
|
| 23
|
FASTA format
|
9,154
|
305
|
B
|
High
|
| 24
|
Most recent common ancestor
|
8,185
|
272
|
B
|
High
|
| 25
|
Martin Kulldorff
|
7,887
|
262
|
B
|
Low
|
| 26
|
Synthetic biology
|
7,832
|
261
|
B
|
Mid
|
| 27
|
Heat map
|
7,597
|
253
|
Start
|
High
|
| 28
|
Cladistics
|
7,492
|
249
|
C
|
Mid
|
| 29
|
Medical Subject Headings
|
7,426
|
247
|
C
|
Mid
|
| 30
|
List of algorithms
|
6,999
|
233
|
List
|
Mid
|
| 31
|
Genomics
|
6,889
|
229
|
B
|
High
|
| 32
|
FASTQ format
|
6,633
|
221
|
B
|
Mid
|
| 33
|
BLAST (biotechnology)
|
6,269
|
208
|
C
|
Top
|
| 34
|
Illumina, Inc.
|
6,241
|
208
|
C
|
Low
|
| 35
|
Petri net
|
6,166
|
205
|
B
|
Low
|
| 36
|
Computational biology
|
6,077
|
202
|
C
|
Top
|
| 37
|
PubChem
|
6,031
|
201
|
Start
|
Mid
|
| 38
|
Whole genome sequencing
|
6,023
|
200
|
B
|
High
|
| 39
|
Lineweaver–Burk plot
|
5,976
|
199
|
B
|
Low
|
| 40
|
RNA-Seq
|
5,959
|
198
|
B
|
Top
|
| 41
|
Phi coefficient
|
5,933
|
197
|
Start
|
Mid
|
| 42
|
Needleman–Wunsch algorithm
|
5,856
|
195
|
Start
|
Mid
|
| 43
|
Mathematical and theoretical biology
|
5,789
|
192
|
C
|
Top
|
| 44
|
Biostatistics
|
5,683
|
189
|
B
|
Top
|
| 45
|
Proteomics
|
5,677
|
189
|
C
|
High
|
| 46
|
Protein Data Bank
|
5,600
|
186
|
C
|
High
|
| 47
|
Sequence alignment
|
5,202
|
173
|
C
|
High
|
| 48
|
Omics
|
5,111
|
170
|
C
|
Mid
|
| 49
|
Computational neuroscience
|
5,052
|
168
|
C
|
Top
|
| 50
|
Protein structure prediction
|
4,744
|
158
|
B
|
High
|
| 51
|
DNA microarray
|
4,652
|
155
|
B
|
Top
|
| 52
|
Europe PubMed Central
|
4,579
|
152
|
Start
|
Low
|
| 53
|
Genome-wide association study
|
4,559
|
151
|
GA
|
High
|
| 54
|
George Church (geneticist)
|
4,547
|
151
|
C
|
Mid
|
| 55
|
Folding@home
|
4,534
|
151
|
B
|
Mid
|
| 56
|
Phred quality score
|
4,415
|
147
|
Start
|
Mid
|
| 57
|
Denis Noble
|
4,352
|
145
|
Start
|
Low
|
| 58
|
Smith–Waterman algorithm
|
4,304
|
143
|
B
|
Top
|
| 59
|
Baum–Welch algorithm
|
4,301
|
143
|
C
|
Mid
|
| 60
|
Jmol
|
4,258
|
141
|
Start
|
Mid
|
| 61
|
Systems biology
|
4,211
|
140
|
C
|
Top
|
| 62
|
Isomorphic Labs
|
4,203
|
140
|
Stub
|
Low
|
| 63
|
Variant Call Format
|
4,179
|
139
|
Start
|
Mid
|
| 64
|
Gene nomenclature
|
3,918
|
130
|
Start
|
Mid
|
| 65
|
Spurious relationship
|
3,900
|
130
|
Start
|
Low
|
| 66
|
Single-cell sequencing
|
3,871
|
129
|
C
|
High
|
| 67
|
DNA barcoding
|
3,832
|
127
|
B
|
High
|
| 68
|
STR analysis
|
3,827
|
127
|
Start
|
Low
|
| 69
|
Metagenomics
|
3,794
|
126
|
GA
|
Mid
|
| 70
|
Burrows–Wheeler transform
|
3,788
|
126
|
C
|
Mid
|
| 71
|
What Is Life?
|
3,771
|
125
|
C
|
Low
|
| 72
|
Non-coding DNA
|
3,727
|
124
|
C
|
Low
|
| 73
|
Similarity measure
|
3,684
|
122
|
Start
|
Mid
|
| 74
|
BLOSUM
|
3,633
|
121
|
C
|
High
|
| 75
|
Junk DNA
|
3,630
|
121
|
B
|
Low
|
| 76
|
Biological computing
|
3,579
|
119
|
C
|
Mid
|
| 77
|
Nanopore sequencing
|
3,485
|
116
|
C
|
Low
|
| 78
|
Molecular clock
|
3,353
|
111
|
C
|
High
|
| 79
|
Multiple sequence alignment
|
3,344
|
111
|
Unknown
|
High
|
| 80
|
Metabolomics
|
3,321
|
110
|
C
|
Mid
|
| 81
|
KEGG
|
3,301
|
110
|
C
|
High
|
| 82
|
Docking (molecular)
|
3,297
|
109
|
B
|
High
|
| 83
|
KNIME
|
3,283
|
109
|
Start
|
Low
|
| 84
|
High-throughput screening
|
3,183
|
106
|
B
|
Low
|
| 85
|
Intrinsically disordered proteins
|
3,085
|
102
|
Start
|
Mid
|
| 86
|
Daphne Koller
|
3,066
|
102
|
C
|
Low
|
| 87
|
Ludwig von Bertalanffy
|
3,035
|
101
|
Start
|
Low
|
| 88
|
Combined DNA Index System
|
2,955
|
98
|
GA
|
Low
|
| 89
|
Root mean square deviation of atomic positions
|
2,954
|
98
|
Start
|
Mid
|
| 90
|
Illumina dye sequencing
|
2,939
|
97
|
C
|
Mid
|
| 91
|
Broad Institute
|
2,915
|
97
|
Start
|
Low
|
| 92
|
ATAC-seq
|
2,912
|
97
|
Start
|
Low
|
| 93
|
Exome sequencing
|
2,903
|
96
|
C
|
High
|
| 94
|
Gene Ontology
|
2,878
|
95
|
C
|
High
|
| 95
|
FitzHugh–Nagumo model
|
2,795
|
93
|
C
|
Low
|
| 96
|
BED (file format)
|
2,794
|
93
|
C
|
Low
|
| 97
|
SAM (file format)
|
2,793
|
93
|
Start
|
Mid
|
| 98
|
Genetic programming
|
2,789
|
92
|
B
|
Mid
|
| 99
|
Multiomics
|
2,787
|
92
|
C
|
High
|
| 100
|
Crossover (genetic algorithm)
|
2,776
|
92
|
B
|
Low
|
| 101
|
Andrew Huxley
|
2,752
|
91
|
C
|
Low
|
| 102
|
Gene set enrichment analysis
|
2,745
|
91
|
C
|
Mid
|
| 103
|
UniProt
|
2,655
|
88
|
Start
|
High
|
| 104
|
Data wrangling
|
2,638
|
87
|
Start
|
Low
|
| 105
|
Monod equation
|
2,638
|
87
|
Start
|
Low
|
| 106
|
Wikispecies
|
2,599
|
86
|
Start
|
Mid
|
| 107
|
Bioconductor
|
2,588
|
86
|
C
|
Mid
|
| 108
|
ChIP sequencing
|
2,580
|
86
|
C
|
Mid
|
| 109
|
Environmental DNA
|
2,550
|
85
|
B
|
Low
|
| 110
|
Volcano plot (statistics)
|
2,516
|
83
|
C
|
Mid
|
| 111
|
Foundational Model of Anatomy
|
2,505
|
83
|
Start
|
Low
|
| 112
|
K-mer
|
2,503
|
83
|
B
|
Mid
|
| 113
|
Pardis Sabeti
|
2,474
|
82
|
B
|
Low
|
| 114
|
Fitness function
|
2,468
|
82
|
Start
|
Mid
|
| 115
|
Spatial transcriptomics
|
2,467
|
82
|
Start
|
Low
|
| 116
|
Oxford Nanopore Technologies
|
2,459
|
81
|
Start
|
Low
|
| 117
|
Protein–protein interaction
|
2,401
|
80
|
C
|
High
|
| 118
|
Robert Gentleman (statistician)
|
2,379
|
79
|
Start
|
Mid
|
| 119
|
Kabsch algorithm
|
2,371
|
79
|
Start
|
Mid
|
| 120
|
Transcriptome
|
2,332
|
77
|
B
|
High
|
| 121
|
John Maynard Smith
|
2,310
|
77
|
C
|
Mid
|
| 122
|
Microarray
|
2,278
|
75
|
Start
|
Top
|
| 123
|
GenBank
|
2,274
|
75
|
Start
|
High
|
| 124
|
Michael Levitt (biophysicist)
|
2,263
|
75
|
C
|
Low
|
| 125
|
Neighbor joining
|
2,257
|
75
|
C
|
High
|
| 126
|
Brain mapping
|
2,224
|
74
|
Start
|
Low
|
| 127
|
Global Biodiversity Information Facility
|
2,210
|
73
|
Start
|
Low
|
| 128
|
PyMOL
|
2,208
|
73
|
Start
|
Low
|
| 129
|
N50, L50, and related statistics
|
2,203
|
73
|
Start
|
Low
|
| 130
|
Cyberneticist
|
2,177
|
72
|
Stub
|
Low
|
| 131
|
10x Genomics
|
2,174
|
72
|
Start
|
Mid
|
| 132
|
ChEMBL
|
2,158
|
71
|
Start
|
Mid
|
| 133
|
Molecular phylogenetics
|
2,136
|
71
|
C
|
High
|
| 134
|
Protein Data Bank (file format)
|
2,116
|
70
|
Start
|
Mid
|
| 135
|
UPGMA
|
2,112
|
70
|
C
|
Low
|
| 136
|
Superspreading event
|
2,084
|
69
|
C
|
High
|
| 137
|
Gene regulatory network
|
2,069
|
68
|
B
|
High
|
| 138
|
Online Mendelian Inheritance in Man
|
2,032
|
67
|
Start
|
Mid
|
| 139
|
UK Biobank
|
2,027
|
67
|
B
|
Low
|
| 140
|
Schrödinger, Inc.
|
2,024
|
67
|
Start
|
Low
|
| 141
|
Polygenic score
|
2,002
|
66
|
C
|
Mid
|
| 142
|
C. H. Waddington
|
1,970
|
65
|
C
|
Low
|
| 143
|
Pan-genome
|
1,954
|
65
|
C
|
Mid
|
| 144
|
Reference genome
|
1,947
|
64
|
Start
|
Low
|
| 145
|
CASP
|
1,938
|
64
|
C
|
Mid
|
| 146
|
Distance matrix
|
1,925
|
64
|
Start
|
High
|
| 147
|
ENCODE
|
1,925
|
64
|
C
|
Mid
|
| 148
|
Genetic distance
|
1,898
|
63
|
B
|
Mid
|
| 149
|
Clustal
|
1,871
|
62
|
Start
|
Mid
|
| 150
|
Genome size
|
1,857
|
61
|
B
|
Mid
|
| 151
|
Proteome
|
1,851
|
61
|
C
|
High
|
| 152
|
Topologically associating domain
|
1,849
|
61
|
C
|
Low
|
| 153
|
Aviv Regev
|
1,820
|
60
|
Start
|
Low
|
| 154
|
Phylogenetic Assignment of Named Global Outbreak Lineages
|
1,819
|
60
|
Start
|
Low
|
| 155
|
Transcriptomics technologies
|
1,810
|
60
|
GA
|
High
|
| 156
|
Mathematical modelling of infectious diseases
|
1,804
|
60
|
C
|
Low
|
| 157
|
List of biological databases
|
1,795
|
59
|
List
|
High
|
| 158
|
Conserved sequence
|
1,792
|
59
|
C
|
High
|
| 159
|
European Molecular Biology Laboratory
|
1,791
|
59
|
C
|
Low
|
| 160
|
ChEBI
|
1,767
|
58
|
Start
|
Low
|
| 161
|
Metabarcoding
|
1,744
|
58
|
B
|
Low
|
| 162
|
Phylogeny
|
1,702
|
56
|
Redirect
|
NA
|
| 163
|
Rosetta@home
|
1,702
|
56
|
C
|
Mid
|
| 164
|
List of sequence alignment software
|
1,700
|
56
|
List
|
High
|
| 165
|
Computational phylogenetics
|
1,685
|
56
|
C
|
High
|
| 166
|
Approximate Bayesian computation
|
1,664
|
55
|
B
|
Low
|
| 167
|
Models of DNA evolution
|
1,621
|
54
|
B
|
Mid
|
| 168
|
Encyclopedia of Life
|
1,610
|
53
|
Start
|
Mid
|
| 169
|
Synteny
|
1,575
|
52
|
Start
|
Low
|
| 170
|
Alan Hodgkin
|
1,530
|
51
|
Start
|
Low
|
| 171
|
Maximum parsimony (phylogenetics)
|
1,519
|
50
|
C
|
High
|
| 172
|
Consensus sequence
|
1,513
|
50
|
Start
|
High
|
| 173
|
List of open-source bioinformatics software
|
1,495
|
49
|
List
|
High
|
| 174
|
DNA sequencer
|
1,486
|
49
|
Start
|
Low
|
| 175
|
Catalogue of Life
|
1,459
|
48
|
C
|
Low
|
| 176
|
General feature format
|
1,435
|
47
|
Start
|
Low
|
| 177
|
List of mass spectrometry software
|
1,419
|
47
|
List
|
Low
|
| 178
|
Haar-like feature
|
1,412
|
47
|
C
|
Low
|
| 179
|
Biological network inference
|
1,406
|
46
|
C
|
Low
|
| 180
|
Data curation
|
1,406
|
46
|
Start
|
Mid
|
| 181
|
Lenia
|
1,400
|
46
|
Start
|
Unknown
|
| 182
|
Ensembl genome database project
|
1,390
|
46
|
B
|
High
|
| 183
|
European Bioinformatics Institute
|
1,387
|
46
|
C
|
Low
|
| 184
|
FishBase
|
1,382
|
46
|
Start
|
Low
|
| 185
|
List of protein structure prediction software
|
1,355
|
45
|
List
|
Mid
|
| 186
|
Protein design
|
1,353
|
45
|
C
|
Mid
|
| 187
|
Manolis Kellis
|
1,336
|
44
|
C
|
Low
|
| 188
|
Position weight matrix
|
1,334
|
44
|
C
|
Top
|
| 189
|
Pfam
|
1,332
|
44
|
B
|
High
|
| 190
|
Chromosome conformation capture
|
1,331
|
44
|
C
|
Low
|
| 191
|
Indel
|
1,312
|
43
|
Start
|
Low
|
| 192
|
Binary Alignment Map
|
1,308
|
43
|
Stub
|
Mid
|
| 193
|
1000 Genomes Project
|
1,297
|
43
|
B
|
Low
|
| 194
|
DNA annotation
|
1,292
|
43
|
Start
|
Low
|
| 195
|
DNA database
|
1,289
|
42
|
Start
|
Mid
|
| 196
|
Contig
|
1,283
|
42
|
C
|
High
|
| 197
|
Point accepted mutation
|
1,282
|
42
|
B
|
High
|
| 198
|
FASTA
|
1,277
|
42
|
B
|
High
|
| 199
|
Wellcome Sanger Institute
|
1,271
|
42
|
C
|
Low
|
| 200
|
Substitution model
|
1,254
|
41
|
B
|
Mid
|
| 201
|
Biochemical cascade
|
1,242
|
41
|
C
|
Mid
|
| 202
|
SNP array
|
1,242
|
41
|
Start
|
High
|
| 203
|
Sarah Teichmann
|
1,210
|
40
|
C
|
Low
|
| 204
|
Cable theory
|
1,202
|
40
|
C
|
Mid
|
| 205
|
Amino acid replacement
|
1,201
|
40
|
Start
|
High
|
| 206
|
Biobank
|
1,199
|
39
|
Start
|
High
|
| 207
|
Open Tree of Life
|
1,199
|
39
|
Start
|
Low
|
| 208
|
Mutation (genetic algorithm)
|
1,197
|
39
|
Start
|
Low
|
| 209
|
AMBER
|
1,196
|
39
|
C
|
Mid
|
| 210
|
GROMACS
|
1,188
|
39
|
Start
|
Low
|
| 211
|
Sequence motif
|
1,187
|
39
|
Start
|
High
|
| 212
|
Homology modeling
|
1,186
|
39
|
B
|
High
|
| 213
|
Functional genomics
|
1,181
|
39
|
C
|
High
|
| 214
|
Single-cell transcriptomics
|
1,177
|
39
|
C
|
Mid
|
| 215
|
Celera Corporation
|
1,175
|
39
|
Start
|
Low
|
| 216
|
Solvation shell
|
1,173
|
39
|
Start
|
Low
|
| 217
|
Eadie–Hofstee diagram
|
1,140
|
38
|
Start
|
Low
|
| 218
|
STRING
|
1,116
|
37
|
B
|
Low
|
| 219
|
Sequence logo
|
1,111
|
37
|
B
|
Mid
|
| 220
|
Gene family
|
1,104
|
36
|
C
|
High
|
| 221
|
Protein family
|
1,091
|
36
|
Start
|
High
|
| 222
|
RefSeq
|
1,082
|
36
|
Start
|
Mid
|
| 223
|
Biological database
|
1,076
|
35
|
Start
|
High
|
| 224
|
Weighted correlation network analysis
|
1,076
|
35
|
B
|
Low
|
| 225
|
Leroy Hood
|
1,072
|
35
|
B
|
Low
|
| 226
|
Microarray analysis techniques
|
1,063
|
35
|
B
|
Mid
|
| 227
|
Sepp Hochreiter
|
1,057
|
35
|
Start
|
Low
|
| 228
|
Outgroup (cladistics)
|
1,053
|
35
|
Start
|
Mid
|
| 229
|
Entrez
|
1,050
|
35
|
Start
|
Mid
|
| 230
|
Probabilistic context-free grammar
|
1,047
|
34
|
B
|
High
|
| 231
|
Ukkonen's algorithm
|
1,047
|
34
|
Stub
|
Low
|
| 232
|
Bayesian inference in phylogeny
|
1,046
|
34
|
C
|
High
|
| 233
|
Knowledge engineering
|
1,045
|
34
|
Start
|
Low
|
| 234
|
Gap penalty
|
1,041
|
34
|
C
|
High
|
| 235
|
Matthews correlation coefficient
|
1,028
|
34
|
Redirect
|
NA
|
| 236
|
Biochip
|
1,022
|
34
|
C
|
Low
|
| 237
|
Cytoscape
|
1,019
|
33
|
B
|
High
|
| 238
|
MA plot
|
1,017
|
33
|
Start
|
Low
|
| 239
|
RNA integrity number
|
1,009
|
33
|
Stub
|
Low
|
| 240
|
Vito Volterra
|
1,002
|
33
|
C
|
Low
|
| 241
|
Sequence assembly
|
999
|
33
|
Start
|
High
|
| 242
|
Hirschberg's algorithm
|
992
|
33
|
B
|
Low
|
| 243
|
Tournament selection
|
980
|
32
|
Start
|
Low
|
| 244
|
Amplicon sequence variant
|
980
|
32
|
Start
|
Low
|
| 245
|
Sequence analysis
|
979
|
32
|
C
|
Top
|
| 246
|
Monod–Wyman–Changeux model
|
972
|
32
|
Start
|
Mid
|
| 247
|
AutoDock
|
965
|
32
|
Start
|
Mid
|
| 248
|
Motoo Kimura
|
960
|
32
|
C
|
High
|
| 249
|
Umbrella sampling
|
959
|
31
|
Start
|
Low
|
| 250
|
Avogadro (software)
|
957
|
31
|
Stub
|
Low
|
| 251
|
Biological network
|
953
|
31
|
C
|
High
|
| 252
|
De novo peptide sequencing
|
950
|
31
|
Start
|
Low
|
| 253
|
D'Arcy Wentworth Thompson
|
943
|
31
|
GA
|
Mid
|
| 254
|
Metabolome
|
932
|
31
|
C
|
High
|
| 255
|
Cooperative binding
|
922
|
30
|
B
|
Mid
|
| 256
|
List of bioinformatics journals
|
921
|
30
|
List
|
Low
|
| 257
|
GeneCards
|
920
|
30
|
C
|
Mid
|
| 258
|
Virtual screening
|
894
|
29
|
Start
|
High
|
| 259
|
NanoString Technologies
|
892
|
29
|
Start
|
Low
|
| 260
|
Population structure (genetics)
|
891
|
29
|
Start
|
Low
|
| 261
|
DbSNP
|
889
|
29
|
B
|
Mid
|
| 262
|
Boolean network
|
867
|
28
|
C
|
Mid
|
| 263
|
Comparative genomics
|
861
|
28
|
C
|
Top
|
| 264
|
Barcode of Life Data System
|
854
|
28
|
Stub
|
Low
|
| 265
|
Gene expression profiling
|
840
|
28
|
B
|
High
|
| 266
|
Mathematical physiology
|
837
|
27
|
Stub
|
Mid
|
| 267
|
List of phylogenetics software
|
835
|
27
|
List
|
High
|
| 268
|
UCSC Genome Browser
|
833
|
27
|
Start
|
High
|
| 269
|
Michael Eisen
|
832
|
27
|
Start
|
Low
|
| 270
|
Eric Xing
|
832
|
27
|
Stub
|
Low
|
| 271
|
List of RNA-Seq bioinformatics tools
|
831
|
27
|
List
|
Mid
|
| 272
|
Substitution matrix
|
827
|
27
|
C
|
High
|
| 273
|
Systems neuroscience
|
825
|
27
|
Stub
|
Mid
|
| 274
|
Biological systems engineering
|
821
|
27
|
Start
|
Low
|
| 275
|
Ion semiconductor sequencing
|
821
|
27
|
C
|
Low
|
| 276
|
CHARMM
|
813
|
27
|
B
|
Mid
|
| 277
|
Paradox of the plankton
|
806
|
26
|
Start
|
Low
|
| 278
|
EBird
|
804
|
26
|
Start
|
Low
|
| 279
|
Template modeling score
|
804
|
26
|
Start
|
Low
|
| 280
|
CUT&RUN sequencing
|
794
|
26
|
C
|
Low
|
| 281
|
Dot plot (bioinformatics)
|
793
|
26
|
Start
|
Mid
|
| 282
|
Bonnie Berger
|
793
|
26
|
Start
|
Low
|
| 283
|
CATH database
|
792
|
26
|
Start
|
Mid
|
| 284
|
DeCODE genetics
|
792
|
26
|
Start
|
Low
|
| 285
|
Structural Classification of Proteins database
|
789
|
26
|
Start
|
High
|
| 286
|
GeneDx
|
787
|
26
|
Stub
|
Low
|
| 287
|
Molecular Evolutionary Genetics Analysis
|
776
|
25
|
Start
|
Low
|
| 288
|
List of protein-ligand docking software
|
774
|
25
|
List
|
Mid
|
| 289
|
Hanes–Woolf plot
|
773
|
25
|
Start
|
Low
|
| 290
|
Theoretical ecology
|
767
|
25
|
B
|
High
|
| 291
|
Eugene Koonin
|
765
|
25
|
Start
|
Low
|
| 292
|
Protein contact map
|
764
|
25
|
Start
|
Mid
|
| 293
|
Interactome
|
756
|
25
|
C
|
Mid
|
| 294
|
MGI (company)
|
752
|
25
|
C
|
Low
|
| 295
|
Lior Pachter
|
744
|
24
|
Start
|
Mid
|
| 296
|
Robert Rosen (biologist)
|
741
|
24
|
Start
|
Low
|
| 297
|
ABI Solid Sequencing
|
741
|
24
|
Start
|
Low
|
| 298
|
HMMER
|
737
|
24
|
B
|
High
|
| 299
|
Flux balance analysis
|
731
|
24
|
B
|
High
|
| 300
|
Synthetic biological circuit
|
729
|
24
|
Start
|
Low
|
| 301
|
BRENDA
|
728
|
24
|
Start
|
Mid
|
| 302
|
UCSF Chimera
|
728
|
24
|
Start
|
Low
|
| 303
|
Polytomy
|
716
|
23
|
Start
|
Low
|
| 304
|
DNA Data Bank of Japan
|
715
|
23
|
Stub
|
Low
|
| 305
|
World Community Grid
|
708
|
23
|
C
|
Low
|
| 306
|
Weasel program
|
703
|
23
|
B
|
Low
|
| 307
|
Machine learning in bioinformatics
|
702
|
23
|
C
|
High
|
| 308
|
Attack rate
|
700
|
23
|
Start
|
Mid
|
| 309
|
Tree of Life Web Project
|
696
|
23
|
Start
|
Low
|
| 310
|
Protein superfamily
|
696
|
23
|
B
|
High
|
| 311
|
CRISPR interference
|
696
|
23
|
B
|
Low
|
| 312
|
DSSP (algorithm)
|
695
|
23
|
Start
|
Low
|
| 313
|
List of sequenced animal genomes
|
694
|
23
|
List
|
Mid
|
| 314
|
Margaret Oakley Dayhoff
|
678
|
22
|
B
|
High
|
| 315
|
List of RNA structure prediction software
|
677
|
22
|
List
|
Low
|
| 316
|
Co-occurrence network
|
677
|
22
|
Start
|
Low
|
| 317
|
Galaxy (computational biology)
|
666
|
22
|
Start
|
High
|
| 318
|
Lipidomics
|
664
|
22
|
C
|
Low
|
| 319
|
Chemical database
|
661
|
22
|
Start
|
Mid
|
| 320
|
PLOS Computational Biology
|
659
|
21
|
Start
|
High
|
| 321
|
Rob Knight (biologist)
|
658
|
21
|
Stub
|
Low
|
| 322
|
Gene prediction
|
656
|
21
|
C
|
High
|
| 323
|
InterPro
|
650
|
21
|
B
|
High
|
| 324
|
SAMtools
|
645
|
21
|
Start
|
Low
|
| 325
|
List of phylogenetic tree visualization software
|
644
|
21
|
List
|
Mid
|
| 326
|
All of Us (initiative)
|
642
|
21
|
C
|
Low
|
| 327
|
Nexus file
|
641
|
21
|
Start
|
Low
|
| 328
|
Ecosystem model
|
637
|
21
|
Start
|
Mid
|
| 329
|
Cross-species transmission
|
630
|
21
|
C
|
Low
|
| 330
|
Biopython
|
627
|
20
|
C
|
High
|
| 331
|
Trajectory inference
|
626
|
20
|
C
|
Low
|
| 332
|
Metabolic network modelling
|
625
|
20
|
C
|
Mid
|
| 333
|
Expasy
|
620
|
20
|
Start
|
Mid
|
| 334
|
Mass spectrometry data format
|
619
|
20
|
Start
|
Low
|
| 335
|
Stephen Altschul
|
616
|
20
|
Start
|
Low
|
| 336
|
PROSITE
|
614
|
20
|
Start
|
High
|
| 337
|
454 Life Sciences
|
611
|
20
|
C
|
Low
|
| 338
|
HUGO Gene Nomenclature Committee
|
609
|
20
|
Start
|
Mid
|
| 339
|
Scoring functions for docking
|
607
|
20
|
Start
|
Mid
|
| 340
|
Conservative replacement
|
605
|
20
|
Start
|
Low
|
| 341
|
Network motif
|
603
|
20
|
B
|
Low
|
| 342
|
Modelling biological systems
|
599
|
19
|
C
|
High
|
| 343
|
Institute of Genomics and Integrative Biology
|
596
|
19
|
C
|
Low
|
| 344
|
Evolutionary grade
|
593
|
19
|
Start
|
High
|
| 345
|
List of sequenced eukaryotic genomes
|
586
|
19
|
List
|
Mid
|
| 346
|
ARKive
|
585
|
19
|
C
|
Mid
|
| 347
|
CRAM (file format)
|
583
|
19
|
Start
|
Low
|
| 348
|
Accession number (bioinformatics)
|
581
|
19
|
Start
|
Low
|
| 349
|
List of molecular graphics systems
|
580
|
19
|
List
|
Mid
|
| 350
|
Dry lab
|
578
|
19
|
Start
|
High
|
| 351
|
List of biodiversity databases
|
571
|
19
|
List
|
Low
|
| 352
|
Batch effect
|
571
|
19
|
Stub
|
Low
|
| 353
|
Marginal value theorem
|
570
|
19
|
C
|
Unknown
|
| 354
|
Barry Smith (ontologist)
|
569
|
18
|
C
|
Low
|
| 355
|
Bioinformatics (journal)
|
567
|
18
|
Start
|
High
|
| 356
|
Genomic organization
|
563
|
18
|
Start
|
Low
|
| 357
|
Swiss-model
|
561
|
18
|
Start
|
Mid
|
| 358
|
Atul Butte
|
561
|
18
|
Start
|
Mid
|
| 359
|
MAFFT
|
560
|
18
|
Stub
|
Mid
|
| 360
|
Synthetic virology
|
558
|
18
|
Start
|
Mid
|
| 361
|
Chromosome (genetic algorithm)
|
555
|
18
|
Start
|
Low
|
| 362
|
List of neuroscience databases
|
554
|
18
|
List
|
Low
|
| 363
|
McDonald–Kreitman test
|
554
|
18
|
C
|
Mid
|
| 364
|
Structural bioinformatics
|
549
|
18
|
B
|
High
|
| 365
|
UniFrac
|
548
|
18
|
Stub
|
Low
|
| 366
|
Alston Scott Householder
|
545
|
18
|
Start
|
Low
|
| 367
|
Animal Diversity Web
|
540
|
18
|
C
|
Mid
|
| 368
|
Biclustering
|
539
|
17
|
B
|
Mid
|
| 369
|
NK model
|
538
|
17
|
B
|
Low
|
| 370
|
List of genetic algorithm applications
|
537
|
17
|
List
|
Low
|
| 371
|
Haldane's dilemma
|
534
|
17
|
B
|
Low
|
| 372
|
Brendan Frey
|
534
|
17
|
B
|
Low
|
| 373
|
De novo sequence assemblers
|
534
|
17
|
Start
|
Low
|
| 374
|
Global distance test
|
531
|
17
|
Stub
|
Low
|
| 375
|
PHYLIP
|
530
|
17
|
Start
|
Low
|
| 376
|
Computational genomics
|
529
|
17
|
Start
|
Mid
|
| 377
|
Sequence Read Archive
|
529
|
17
|
Start
|
High
|
| 378
|
Centre for DNA Fingerprinting and Diagnostics
|
528
|
17
|
Start
|
Low
|
| 379
|
Tom Blundell
|
526
|
17
|
C
|
Low
|
| 380
|
Uri Alon
|
521
|
17
|
Start
|
Low
|
| 381
|
List of MeSH codes
|
520
|
17
|
List
|
Mid
|
| 382
|
Read (biology)
|
520
|
17
|
C
|
High
|
| 383
|
Mascot (software)
|
516
|
17
|
C
|
High
|
| 384
|
David J. Lipman
|
515
|
17
|
Start
|
Low
|
| 385
|
Fossilworks
|
513
|
17
|
Stub
|
Low
|
| 386
|
Molecular models of DNA
|
513
|
17
|
B
|
Mid
|
| 387
|
De novo protein structure prediction
|
512
|
17
|
Start
|
High
|
| 388
|
Paradox of enrichment
|
510
|
17
|
Start
|
Low
|
| 389
|
DAVID
|
508
|
16
|
Start
|
Mid
|
| 390
|
PLINK (genetic tool-set)
|
506
|
16
|
Stub
|
Low
|
| 391
|
ChIP-on-chip
|
504
|
16
|
C
|
Low
|
| 392
|
Elasticity coefficient
|
497
|
16
|
C
|
Mid
|
| 393
|
Long branch attraction
|
493
|
16
|
Start
|
Low
|
| 394
|
Pyotr Anokhin
|
492
|
16
|
Start
|
Low
|
| 395
|
Robinson–Foulds metric
|
491
|
16
|
C
|
Low
|
| 396
|
MUSCLE (alignment software)
|
488
|
16
|
Start
|
Mid
|
| 397
|
Visual Molecular Dynamics
|
484
|
16
|
Start
|
Low
|
| 398
|
FreeSurfer
|
484
|
16
|
Start
|
Mid
|
| 399
|
Hindmarsh–Rose model
|
484
|
16
|
Stub
|
Low
|
| 400
|
Genomics England
|
477
|
15
|
Start
|
Low
|
| 401
|
Genetic operator
|
475
|
15
|
Start
|
Low
|
| 402
|
Ewan Birney
|
470
|
15
|
C
|
Low
|
| 403
|
Phylogenetic comparative methods
|
468
|
15
|
C
|
Mid
|
| 404
|
Carl Bergstrom
|
467
|
15
|
Stub
|
Low
|
| 405
|
Edward C. Holmes
|
462
|
15
|
Start
|
Low
|
| 406
|
Bernd Sturmfels
|
459
|
15
|
Stub
|
Low
|
| 407
|
Chou–Fasman method
|
459
|
15
|
B
|
Mid
|
| 408
|
David Goodsell
|
459
|
15
|
C
|
Low
|
| 409
|
Binning (metagenomics)
|
459
|
15
|
Start
|
Low
|
| 410
|
Michael Laufer
|
455
|
15
|
Start
|
Unknown
|
| 411
|
Allele frequency spectrum
|
453
|
15
|
Start
|
Low
|
| 412
|
RasMol
|
447
|
14
|
Start
|
Mid
|
| 413
|
HomoloGene
|
445
|
14
|
Start
|
Low
|
| 414
|
Steven Salzberg
|
445
|
14
|
Start
|
Low
|
| 415
|
Nicolas Rashevsky
|
445
|
14
|
B
|
Mid
|
| 416
|
List of human protein-coding genes 1
|
444
|
14
|
List
|
High
|
| 417
|
Morris–Lecar model
|
443
|
14
|
Start
|
Low
|
| 418
|
List of alignment visualization software
|
440
|
14
|
List
|
Mid
|
| 419
|
Phylogenetic bracketing
|
437
|
14
|
Start
|
Low
|
| 420
|
Human Protein Atlas
|
436
|
14
|
Start
|
Low
|
| 421
|
Threading (protein sequence)
|
429
|
14
|
Start
|
High
|
| 422
|
Anduril (workflow engine)
|
427
|
14
|
B
|
Low
|
| 423
|
WPGMA
|
424
|
14
|
C
|
Low
|
| 424
|
Dynamic energy budget theory
|
418
|
13
|
C
|
Low
|
| 425
|
OBO Foundry
|
418
|
13
|
B
|
Mid
|
| 426
|
Demographic and Health Surveys
|
418
|
13
|
B
|
Low
|
| 427
|
Reactome
|
410
|
13
|
Start
|
Low
|
| 428
|
GENSCAN
|
409
|
13
|
Stub
|
Mid
|
| 429
|
List of gene prediction software
|
404
|
13
|
List
|
Mid
|
| 430
|
Pileup format
|
400
|
13
|
Start
|
Low
|
| 431
|
Allen Brain Atlas
|
398
|
13
|
C
|
Mid
|
| 432
|
Holland's schema theorem
|
397
|
13
|
Start
|
Low
|
| 433
|
Sequence database
|
395
|
13
|
Start
|
Mid
|
| 434
|
Taxonomic database
|
394
|
13
|
Start
|
Mid
|
| 435
|
PSIPRED
|
392
|
13
|
Start
|
High
|
| 436
|
Orphanet
|
389
|
12
|
C
|
Low
|
| 437
|
European Nucleotide Archive
|
389
|
12
|
GA
|
Mid
|
| 438
|
List of omics topics in biology
|
388
|
12
|
List
|
Low
|
| 439
|
EMBOSS
|
387
|
12
|
Start
|
Mid
|
| 440
|
Next-generation matrix
|
386
|
12
|
Start
|
Low
|
| 441
|
BLAT (bioinformatics)
|
385
|
12
|
B
|
Low
|
| 442
|
SPAdes (software)
|
383
|
12
|
C
|
Low
|
| 443
|
David Botstein
|
382
|
12
|
Start
|
Low
|
| 444
|
Ehud Shapiro
|
378
|
12
|
Start
|
Low
|
| 445
|
Pavel A. Pevzner
|
376
|
12
|
Start
|
Low
|
| 446
|
Diseases Database
|
374
|
12
|
Start
|
Mid
|
| 447
|
100,000 Genomes Project
|
373
|
12
|
C
|
Low
|
| 448
|
Ordinal priority approach
|
372
|
12
|
C
|
Unknown
|
| 449
|
Rafael Irizarry (scientist)
|
371
|
12
|
Start
|
Mid
|
| 450
|
Group size measures
|
370
|
12
|
Start
|
Low
|
| 451
|
BMC Bioinformatics
|
369
|
12
|
C
|
Low
|
| 452
|
MicroRNA sequencing
|
369
|
12
|
C
|
Low
|
| 453
|
Jay Shendure
|
369
|
12
|
Start
|
Low
|
| 454
|
Mikhail Gelfand
|
369
|
12
|
Stub
|
Mid
|
| 455
|
Janet Thornton
|
368
|
12
|
C
|
Low
|
| 456
|
Dryad (repository)
|
367
|
12
|
Start
|
Low
|
| 457
|
CUT&Tag sequencing
|
365
|
12
|
Start
|
Low
|
| 458
|
Generic Model Organism Database
|
364
|
12
|
Start
|
High
|
| 459
|
Peter Donnelly
|
362
|
12
|
Start
|
Low
|
| 460
|
Coot (software)
|
360
|
12
|
Start
|
Low
|
| 461
|
SBML
|
359
|
11
|
B
|
High
|
| 462
|
Population viability analysis
|
354
|
11
|
C
|
Mid
|
| 463
|
Metabolic flux analysis
|
354
|
11
|
Stub
|
Low
|
| 464
|
Eugene Myers
|
352
|
11
|
Start
|
Low
|
| 465
|
Genome browser
|
351
|
11
|
List
|
High
|
| 466
|
Jim Kent
|
348
|
11
|
Start
|
Low
|
| 467
|
FlowJo
|
348
|
11
|
Start
|
Low
|
| 468
|
Richard M. Durbin
|
346
|
11
|
C
|
Low
|
| 469
|
Codon Adaptation Index
|
346
|
11
|
Stub
|
Low
|
| 470
|
Digital phenotyping
|
344
|
11
|
Start
|
Low
|
| 471
|
PDBsum
|
343
|
11
|
Start
|
Mid
|
| 472
|
Digital organism
|
342
|
11
|
Stub
|
Low
|
| 473
|
Russ Altman
|
342
|
11
|
C
|
Mid
|
| 474
|
Ancestral reconstruction
|
340
|
11
|
B
|
Low
|
| 475
|
GENESIS (software)
|
338
|
11
|
Start
|
Low
|
| 476
|
Circular permutation in proteins
|
338
|
11
|
GA
|
Low
|
| 477
|
Haplotype estimation
|
337
|
11
|
Start
|
Low
|
| 478
|
Joseph DeRisi
|
335
|
11
|
Start
|
Low
|
| 479
|
Swiss Institute of Bioinformatics
|
332
|
11
|
Start
|
Low
|
| 480
|
Hiroaki Kitano
|
330
|
11
|
Start
|
Mid
|
| 481
|
Crystallography Open Database
|
330
|
11
|
Stub
|
Low
|
| 482
|
Consensus CDS Project
|
329
|
10
|
C
|
Low
|
| 483
|
SNPedia
|
325
|
10
|
Start
|
Low
|
| 484
|
Structural genomics
|
324
|
10
|
Start
|
High
|
| 485
|
Mouse Genome Informatics
|
323
|
10
|
Stub
|
Low
|
| 486
|
Cyrus Chothia
|
323
|
10
|
Start
|
Low
|
| 487
|
Energy charge
|
322
|
10
|
Start
|
Low
|
| 488
|
FlyBase
|
322
|
10
|
Start
|
Mid
|
| 489
|
Protein Information Resource
|
321
|
10
|
Start
|
Low
|
| 490
|
Computational immunology
|
321
|
10
|
B
|
Mid
|
| 491
|
Epitranscriptome
|
321
|
10
|
B
|
Low
|
| 492
|
Low complexity regions in proteins
|
320
|
10
|
Start
|
Mid
|
| 493
|
Analysis of molecular variance
|
318
|
10
|
Stub
|
Low
|
| 494
|
De novo transcriptome assembly
|
317
|
10
|
C
|
Mid
|
| 495
|
David Haussler
|
316
|
10
|
C
|
Low
|
| 496
|
Erez Lieberman Aiden
|
315
|
10
|
GA
|
Low
|
| 497
|
Protein function prediction
|
315
|
10
|
Start
|
High
|
| 498
|
Consumer-resource model
|
314
|
10
|
B
|
Unknown
|
| 499
|
Glycomics
|
313
|
10
|
Start
|
Low
|
| 500
|
Sequence clustering
|
312
|
10
|
Start
|
Mid
|
