Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
23andMe
|
35,013
|
1,129
|
C
|
Low
|
2
|
Clade
|
33,471
|
1,079
|
C
|
Mid
|
3
|
CRISPR
|
32,590
|
1,051
|
B
|
Top
|
4
|
Last universal common ancestor
|
30,121
|
971
|
GA
|
Mid
|
5
|
Receiver operating characteristic
|
26,695
|
861
|
B
|
Mid
|
6
|
Dynamic programming
|
21,896
|
706
|
B
|
Top
|
7
|
Systems theory
|
19,411
|
626
|
C
|
Mid
|
8
|
Bioinformatics
|
17,915
|
577
|
C
|
Top
|
9
|
Hidden Markov model
|
17,269
|
557
|
GA
|
Top
|
10
|
Phylogenetic tree
|
13,540
|
436
|
B
|
Top
|
11
|
Cellular automaton
|
13,009
|
419
|
B
|
Low
|
12
|
National Center for Biotechnology Information
|
12,362
|
398
|
C
|
Low
|
13
|
Genome
|
12,129
|
391
|
C
|
High
|
14
|
PubMed Central
|
12,109
|
390
|
B
|
Mid
|
15
|
Phylogenetics
|
12,090
|
390
|
B
|
Top
|
16
|
DNA sequencing
|
11,986
|
386
|
C
|
High
|
17
|
Ontology (information science)
|
11,053
|
356
|
C
|
High
|
18
|
Michaelis–Menten kinetics
|
10,285
|
331
|
B
|
Top
|
19
|
AlphaFold
|
10,215
|
329
|
C
|
High
|
20
|
Most recent common ancestor
|
9,601
|
309
|
B
|
High
|
21
|
Denis Noble
|
9,334
|
301
|
Start
|
Low
|
22
|
Phi coefficient
|
7,956
|
256
|
Start
|
Mid
|
23
|
Synthetic biology
|
7,820
|
252
|
B
|
Mid
|
24
|
Genomics
|
7,676
|
247
|
B
|
High
|
25
|
Cladistics
|
7,650
|
246
|
C
|
Mid
|
26
|
List of algorithms
|
7,187
|
231
|
List
|
Mid
|
27
|
FASTA format
|
7,046
|
227
|
B
|
High
|
28
|
Sanger sequencing
|
6,810
|
219
|
C
|
Mid
|
29
|
Heat map
|
6,538
|
210
|
Start
|
High
|
30
|
Compartmental models in epidemiology
|
6,464
|
208
|
C
|
Mid
|
31
|
Biostatistics
|
6,431
|
207
|
B
|
Top
|
32
|
Computational biology
|
6,255
|
201
|
C
|
Top
|
33
|
Whole genome sequencing
|
6,168
|
198
|
B
|
High
|
34
|
Illumina, Inc.
|
6,094
|
196
|
C
|
Low
|
35
|
FASTQ format
|
5,759
|
185
|
B
|
Mid
|
36
|
Global Biodiversity Information Facility
|
5,661
|
182
|
Start
|
Low
|
37
|
Medical Subject Headings
|
5,399
|
174
|
C
|
Mid
|
38
|
Mathematical and theoretical biology
|
5,390
|
173
|
C
|
Top
|
39
|
RNA-Seq
|
5,118
|
165
|
B
|
Top
|
40
|
Omics
|
5,027
|
162
|
C
|
Mid
|
41
|
Proteomics
|
4,945
|
159
|
C
|
High
|
42
|
Computational neuroscience
|
4,798
|
154
|
C
|
Top
|
43
|
PubChem
|
4,656
|
150
|
Start
|
Mid
|
44
|
Petri net
|
4,612
|
148
|
B
|
Low
|
45
|
Systems biology
|
4,506
|
145
|
C
|
Top
|
46
|
George Church (geneticist)
|
4,467
|
144
|
C
|
Mid
|
47
|
Protein Data Bank
|
4,202
|
135
|
C
|
High
|
48
|
Sequence alignment
|
4,184
|
134
|
C
|
High
|
49
|
Gene nomenclature
|
4,171
|
134
|
Start
|
Mid
|
50
|
Burrows–Wheeler transform
|
3,949
|
127
|
C
|
Mid
|
51
|
BLAST (biotechnology)
|
3,903
|
125
|
C
|
Top
|
52
|
Variant Call Format
|
3,803
|
122
|
Start
|
Mid
|
53
|
What Is Life?
|
3,766
|
121
|
C
|
Low
|
54
|
Folding@home
|
3,747
|
120
|
B
|
Mid
|
55
|
DNA microarray
|
3,742
|
120
|
B
|
Top
|
56
|
Junk DNA
|
3,734
|
120
|
B
|
Low
|
57
|
Europe PubMed Central
|
3,706
|
119
|
Start
|
Low
|
58
|
Baum–Welch algorithm
|
3,664
|
118
|
C
|
Mid
|
59
|
Genome-wide association study
|
3,622
|
116
|
GA
|
High
|
60
|
Needleman–Wunsch algorithm
|
3,581
|
115
|
Start
|
Mid
|
61
|
Bioconductor
|
3,551
|
114
|
C
|
Mid
|
62
|
Spurious relationship
|
3,520
|
113
|
Start
|
Low
|
63
|
Non-coding DNA
|
3,517
|
113
|
C
|
Low
|
64
|
Lineweaver–Burk plot
|
3,477
|
112
|
B
|
Low
|
65
|
Phred quality score
|
3,411
|
110
|
Start
|
Mid
|
66
|
Isomorphic Labs
|
3,400
|
109
|
Stub
|
Low
|
67
|
Single-cell sequencing
|
3,391
|
109
|
C
|
High
|
68
|
Michael Levitt (biophysicist)
|
3,381
|
109
|
C
|
Low
|
69
|
Wikispecies
|
3,363
|
108
|
Start
|
Mid
|
70
|
Biological computing
|
3,253
|
104
|
C
|
Mid
|
71
|
Similarity measure
|
3,208
|
103
|
Start
|
Mid
|
72
|
Docking (molecular)
|
3,187
|
102
|
B
|
High
|
73
|
Jmol
|
3,180
|
102
|
Start
|
Mid
|
74
|
Robert Gentleman (statistician)
|
3,154
|
101
|
Start
|
Mid
|
75
|
KNIME
|
3,141
|
101
|
Start
|
Low
|
76
|
Molecular clock
|
3,082
|
99
|
C
|
High
|
77
|
DNA barcoding
|
3,079
|
99
|
B
|
High
|
78
|
Exome sequencing
|
3,049
|
98
|
C
|
High
|
79
|
Metagenomics
|
2,967
|
95
|
GA
|
Mid
|
80
|
Smith–Waterman algorithm
|
2,912
|
93
|
B
|
Top
|
81
|
Broad Institute
|
2,902
|
93
|
Start
|
Low
|
82
|
Metabolomics
|
2,825
|
91
|
C
|
Mid
|
83
|
Data wrangling
|
2,803
|
90
|
Start
|
Low
|
84
|
Combined DNA Index System
|
2,774
|
89
|
GA
|
Low
|
85
|
STR analysis
|
2,769
|
89
|
Start
|
Low
|
86
|
Daphne Koller
|
2,758
|
88
|
C
|
Low
|
87
|
High-throughput screening
|
2,757
|
88
|
B
|
Low
|
88
|
Multiomics
|
2,752
|
88
|
C
|
High
|
89
|
Transcriptome
|
2,692
|
86
|
B
|
High
|
90
|
Protein structure prediction
|
2,650
|
85
|
B
|
High
|
91
|
Kabsch algorithm
|
2,641
|
85
|
Start
|
Mid
|
92
|
BED (file format)
|
2,635
|
85
|
C
|
Low
|
93
|
Intrinsically disordered proteins
|
2,624
|
84
|
Start
|
Mid
|
94
|
Gene set enrichment analysis
|
2,619
|
84
|
C
|
Mid
|
95
|
Genetic programming
|
2,594
|
83
|
B
|
Mid
|
96
|
KEGG
|
2,469
|
79
|
C
|
High
|
97
|
Nanopore sequencing
|
2,454
|
79
|
C
|
Low
|
98
|
SAM (file format)
|
2,418
|
78
|
Start
|
Mid
|
99
|
Multiple sequence alignment
|
2,416
|
77
|
Unknown
|
High
|
100
|
Ludwig von Bertalanffy
|
2,400
|
77
|
Start
|
Low
|
101
|
Gene Ontology
|
2,379
|
76
|
C
|
High
|
102
|
ATAC-seq
|
2,349
|
75
|
Start
|
Low
|
103
|
John Maynard Smith
|
2,335
|
75
|
C
|
Mid
|
104
|
BLOSUM
|
2,310
|
74
|
C
|
High
|
105
|
Polygenic score
|
2,281
|
73
|
C
|
Mid
|
106
|
Brain mapping
|
2,275
|
73
|
Start
|
Low
|
107
|
Volcano plot (statistics)
|
2,265
|
73
|
C
|
Mid
|
108
|
K-mer
|
2,180
|
70
|
B
|
Mid
|
109
|
Genetic distance
|
2,175
|
70
|
B
|
Mid
|
110
|
10x Genomics
|
2,164
|
69
|
Start
|
Mid
|
111
|
Molecular phylogenetics
|
2,147
|
69
|
C
|
High
|
112
|
Andrew Huxley
|
2,141
|
69
|
C
|
Low
|
113
|
Fitness function
|
2,100
|
67
|
Start
|
Mid
|
114
|
Superspreading event
|
2,085
|
67
|
C
|
High
|
115
|
Protein–protein interaction
|
2,074
|
66
|
C
|
High
|
116
|
UniProt
|
2,073
|
66
|
Start
|
High
|
117
|
Spatial transcriptomics
|
2,072
|
66
|
Start
|
Low
|
118
|
List of mass spectrometry software
|
2,036
|
65
|
List
|
Low
|
119
|
Environmental DNA
|
2,028
|
65
|
B
|
Low
|
120
|
Genome size
|
2,010
|
64
|
B
|
Mid
|
121
|
Reference genome
|
1,948
|
62
|
Start
|
Low
|
122
|
Schrödinger, Inc.
|
1,931
|
62
|
Start
|
Low
|
123
|
ChIP sequencing
|
1,929
|
62
|
C
|
Mid
|
124
|
Root mean square deviation of atomic positions
|
1,922
|
62
|
Start
|
Mid
|
125
|
List of biological databases
|
1,921
|
61
|
List
|
High
|
126
|
GenBank
|
1,920
|
61
|
Start
|
High
|
127
|
Catalogue of Life
|
1,898
|
61
|
C
|
Low
|
128
|
Illumina dye sequencing
|
1,885
|
60
|
C
|
Mid
|
129
|
Microarray
|
1,869
|
60
|
Start
|
Top
|
130
|
Biological network inference
|
1,864
|
60
|
C
|
Low
|
131
|
Gene regulatory network
|
1,828
|
58
|
B
|
High
|
132
|
Conserved sequence
|
1,826
|
58
|
C
|
High
|
133
|
Oxford Nanopore Technologies
|
1,810
|
58
|
Start
|
Low
|
134
|
Phylogeny
|
1,808
|
58
|
Redirect
|
NA
|
135
|
PyMOL
|
1,801
|
58
|
Start
|
Low
|
136
|
European Molecular Biology Laboratory
|
1,763
|
56
|
C
|
Low
|
137
|
Crossover (genetic algorithm)
|
1,752
|
56
|
B
|
Low
|
138
|
Aviv Regev
|
1,750
|
56
|
Start
|
Low
|
139
|
List of sequence alignment software
|
1,734
|
55
|
List
|
High
|
140
|
Online Mendelian Inheritance in Man
|
1,726
|
55
|
Start
|
Mid
|
141
|
Transcriptomics technologies
|
1,726
|
55
|
GA
|
High
|
142
|
Data curation
|
1,724
|
55
|
Start
|
Mid
|
143
|
David Baker (biochemist)
|
1,702
|
54
|
Start
|
Low
|
144
|
Monod equation
|
1,699
|
54
|
Start
|
Low
|
145
|
Cyberneticist
|
1,694
|
54
|
Stub
|
Low
|
146
|
N50, L50, and related statistics
|
1,667
|
53
|
Start
|
Low
|
147
|
Pan-genome
|
1,647
|
53
|
C
|
Mid
|
148
|
Protein Data Bank (file format)
|
1,621
|
52
|
Start
|
Mid
|
149
|
ChEMBL
|
1,591
|
51
|
Start
|
Mid
|
150
|
Approximate Bayesian computation
|
1,566
|
50
|
B
|
Low
|
151
|
Distance matrix
|
1,540
|
49
|
Start
|
High
|
152
|
Mathematical modelling of infectious diseases
|
1,529
|
49
|
C
|
Low
|
153
|
Proteome
|
1,445
|
46
|
C
|
High
|
154
|
Galaxy (computational biology)
|
1,427
|
46
|
Start
|
High
|
155
|
List of open-source bioinformatics software
|
1,406
|
45
|
List
|
High
|
156
|
Haldane's dilemma
|
1,395
|
45
|
B
|
Low
|
157
|
UK Biobank
|
1,385
|
44
|
B
|
Low
|
158
|
Pardis Sabeti
|
1,361
|
43
|
B
|
Low
|
159
|
List of protein structure prediction software
|
1,350
|
43
|
List
|
Mid
|
160
|
DNA sequencer
|
1,333
|
43
|
Start
|
Low
|
161
|
FishBase
|
1,332
|
42
|
Start
|
Low
|
162
|
Metabarcoding
|
1,329
|
42
|
B
|
Low
|
163
|
Lenia
|
1,324
|
42
|
Start
|
Unknown
|
164
|
Topologically associating domain
|
1,310
|
42
|
C
|
Low
|
165
|
C. H. Waddington
|
1,309
|
42
|
C
|
Low
|
166
|
Clustal
|
1,297
|
41
|
Start
|
Mid
|
167
|
Encyclopedia of Life
|
1,295
|
41
|
Start
|
Mid
|
168
|
DNA annotation
|
1,268
|
40
|
Start
|
Low
|
169
|
FitzHugh–Nagumo model
|
1,258
|
40
|
C
|
Low
|
170
|
Computational phylogenetics
|
1,254
|
40
|
C
|
High
|
171
|
UPGMA
|
1,252
|
40
|
C
|
Low
|
172
|
Martin Kulldorff
|
1,232
|
39
|
B
|
Low
|
173
|
DNA database
|
1,228
|
39
|
Start
|
Mid
|
174
|
Foundational Model of Anatomy
|
1,221
|
39
|
Start
|
Low
|
175
|
General feature format
|
1,203
|
38
|
Start
|
Low
|
176
|
Binary Alignment Map
|
1,199
|
38
|
Stub
|
Mid
|
177
|
Sequence motif
|
1,186
|
38
|
Start
|
High
|
178
|
1000 Genomes Project
|
1,161
|
37
|
B
|
Low
|
179
|
Maximum parsimony (phylogenetics)
|
1,155
|
37
|
C
|
High
|
180
|
Leroy Hood
|
1,151
|
37
|
B
|
Low
|
181
|
Consensus sequence
|
1,151
|
37
|
Start
|
High
|
182
|
ChEBI
|
1,149
|
37
|
Start
|
Low
|
183
|
Weighted correlation network analysis
|
1,142
|
36
|
B
|
Low
|
184
|
Indel
|
1,122
|
36
|
Start
|
Low
|
185
|
Synteny
|
1,115
|
35
|
Start
|
Low
|
186
|
Functional genomics
|
1,114
|
35
|
C
|
High
|
187
|
Alan Hodgkin
|
1,110
|
35
|
Start
|
Low
|
188
|
Amino acid replacement
|
1,103
|
35
|
Start
|
High
|
189
|
European Bioinformatics Institute
|
1,098
|
35
|
C
|
Low
|
190
|
Neighbor joining
|
1,087
|
35
|
C
|
High
|
191
|
Solvation shell
|
1,083
|
34
|
Start
|
Low
|
192
|
Celera Corporation
|
1,072
|
34
|
Start
|
Low
|
193
|
ENCODE
|
1,065
|
34
|
C
|
Mid
|
194
|
AMBER
|
1,062
|
34
|
C
|
Mid
|
195
|
GROMACS
|
1,058
|
34
|
Start
|
Low
|
196
|
Biochip
|
1,056
|
34
|
C
|
Low
|
197
|
Biobank
|
1,054
|
34
|
Start
|
High
|
198
|
Ukkonen's algorithm
|
1,047
|
33
|
Stub
|
Low
|
199
|
Haar-like feature
|
1,043
|
33
|
C
|
Low
|
200
|
Biological database
|
1,039
|
33
|
Start
|
High
|
201
|
Models of DNA evolution
|
1,028
|
33
|
B
|
Mid
|
202
|
Matthews correlation coefficient
|
1,026
|
33
|
Redirect
|
NA
|
203
|
Chromosome conformation capture
|
1,007
|
32
|
C
|
Low
|
204
|
Pfam
|
992
|
32
|
B
|
High
|
205
|
Wellcome Sanger Institute
|
991
|
31
|
C
|
Low
|
206
|
SNP array
|
990
|
31
|
Start
|
High
|
207
|
Sequence analysis
|
982
|
31
|
C
|
Top
|
208
|
Biochemical cascade
|
974
|
31
|
C
|
Mid
|
209
|
Sepp Hochreiter
|
968
|
31
|
Start
|
Low
|
210
|
Entrez
|
959
|
30
|
Start
|
Mid
|
211
|
FASTA
|
959
|
30
|
B
|
High
|
212
|
Protein family
|
954
|
30
|
Start
|
High
|
213
|
D'Arcy Wentworth Thompson
|
954
|
30
|
GA
|
Mid
|
214
|
Open Tree of Life
|
949
|
30
|
Start
|
Low
|
215
|
Knowledge engineering
|
948
|
30
|
Start
|
Low
|
216
|
Position weight matrix
|
947
|
30
|
C
|
Top
|
217
|
Biological systems engineering
|
945
|
30
|
Start
|
Low
|
218
|
Ensembl genome database project
|
937
|
30
|
B
|
High
|
219
|
List of RNA-Seq bioinformatics tools
|
937
|
30
|
List
|
Mid
|
220
|
Metabolome
|
931
|
30
|
C
|
High
|
221
|
Comparative genomics
|
914
|
29
|
C
|
Top
|
222
|
SAMtools
|
910
|
29
|
Start
|
Low
|
223
|
Microarray analysis techniques
|
898
|
28
|
B
|
Mid
|
224
|
Contig
|
897
|
28
|
C
|
High
|
225
|
Homology modeling
|
894
|
28
|
B
|
High
|
226
|
All of Us (initiative)
|
894
|
28
|
C
|
Low
|
227
|
Lior Pachter
|
886
|
28
|
Start
|
Mid
|
228
|
Substitution model
|
885
|
28
|
B
|
Mid
|
229
|
Manolis Kellis
|
874
|
28
|
C
|
Low
|
230
|
CASP
|
864
|
27
|
C
|
Mid
|
231
|
RNA integrity number
|
863
|
27
|
Stub
|
Low
|
232
|
CRISPR interference
|
861
|
27
|
B
|
Low
|
233
|
UCSC Genome Browser
|
858
|
27
|
Start
|
High
|
234
|
AutoDock
|
857
|
27
|
Start
|
Mid
|
235
|
Mutation (genetic algorithm)
|
855
|
27
|
Start
|
Low
|
236
|
Umbrella sampling
|
850
|
27
|
Start
|
Low
|
237
|
Virtual screening
|
842
|
27
|
Start
|
High
|
238
|
Rosetta@home
|
839
|
27
|
C
|
Mid
|
239
|
List of phylogenetics software
|
838
|
27
|
List
|
High
|
240
|
Gene family
|
837
|
27
|
C
|
High
|
241
|
DeCODE genetics
|
837
|
27
|
Start
|
Low
|
242
|
Machine learning in bioinformatics
|
833
|
26
|
C
|
High
|
243
|
Cable theory
|
825
|
26
|
C
|
Mid
|
244
|
Sequence logo
|
823
|
26
|
B
|
Mid
|
245
|
Population structure (genetics)
|
821
|
26
|
Start
|
Low
|
246
|
GeneCards
|
819
|
26
|
C
|
Mid
|
247
|
STRING
|
814
|
26
|
B
|
Low
|
248
|
List of bioinformatics journals
|
813
|
26
|
List
|
Low
|
249
|
MA plot
|
809
|
26
|
Start
|
Low
|
250
|
Bayesian inference in phylogeny
|
808
|
26
|
C
|
High
|
251
|
RefSeq
|
808
|
26
|
Start
|
Mid
|
252
|
Vito Volterra
|
804
|
25
|
C
|
Low
|
253
|
Outgroup (cladistics)
|
804
|
25
|
Start
|
Mid
|
254
|
Single-cell transcriptomics
|
801
|
25
|
C
|
Mid
|
255
|
Amplicon sequence variant
|
801
|
25
|
Start
|
Low
|
256
|
NanoString Technologies
|
792
|
25
|
Start
|
Low
|
257
|
Protein design
|
791
|
25
|
C
|
Mid
|
258
|
Boolean network
|
787
|
25
|
C
|
Mid
|
259
|
Bonnie Berger
|
784
|
25
|
Start
|
Low
|
260
|
Biological network
|
782
|
25
|
C
|
High
|
261
|
DbSNP
|
779
|
25
|
B
|
Mid
|
262
|
Robert Rosen (biologist)
|
776
|
25
|
Start
|
Low
|
263
|
MGI (company)
|
774
|
24
|
C
|
Low
|
264
|
DNA Data Bank of Japan
|
767
|
24
|
Stub
|
Low
|
265
|
HMMER
|
766
|
24
|
B
|
High
|
266
|
Cooperative binding
|
758
|
24
|
B
|
Mid
|
267
|
Cytoscape
|
758
|
24
|
B
|
High
|
268
|
Sequence assembly
|
756
|
24
|
Start
|
High
|
269
|
Margaret Oakley Dayhoff
|
751
|
24
|
B
|
High
|
270
|
Systems neuroscience
|
740
|
23
|
Stub
|
Mid
|
271
|
CHARMM
|
738
|
23
|
B
|
Mid
|
272
|
Point accepted mutation
|
738
|
23
|
B
|
High
|
273
|
List of protein-ligand docking software
|
735
|
23
|
List
|
Mid
|
274
|
CUT&RUN sequencing
|
732
|
23
|
C
|
Low
|
275
|
Theoretical ecology
|
730
|
23
|
B
|
High
|
276
|
Motoo Kimura
|
728
|
23
|
C
|
High
|
277
|
Cross-species transmission
|
716
|
23
|
C
|
Low
|
278
|
Interactome
|
715
|
23
|
C
|
Mid
|
279
|
PLOS Computational Biology
|
715
|
23
|
Start
|
High
|
280
|
De novo peptide sequencing
|
714
|
23
|
Start
|
Low
|
281
|
Gene expression profiling
|
705
|
22
|
B
|
High
|
282
|
Probabilistic context-free grammar
|
703
|
22
|
B
|
High
|
283
|
Ecosystem model
|
691
|
22
|
Start
|
Mid
|
284
|
Ion semiconductor sequencing
|
691
|
22
|
C
|
Low
|
285
|
List of RNA structure prediction software
|
686
|
22
|
List
|
Low
|
286
|
Institute of Genomics and Integrative Biology
|
686
|
22
|
C
|
Low
|
287
|
Fossilworks
|
671
|
21
|
Stub
|
Low
|
288
|
Structural Classification of Proteins database
|
667
|
21
|
Start
|
High
|
289
|
Protein superfamily
|
662
|
21
|
B
|
High
|
290
|
Computational genomics
|
653
|
21
|
Start
|
Mid
|
291
|
Protein contact map
|
649
|
20
|
Start
|
Mid
|
292
|
EBird
|
646
|
20
|
Start
|
Low
|
293
|
Avogadro (software)
|
646
|
20
|
Stub
|
Low
|
294
|
Co-occurrence network
|
645
|
20
|
Start
|
Low
|
295
|
Gene prediction
|
640
|
20
|
C
|
High
|
296
|
Synthetic biological circuit
|
639
|
20
|
Start
|
Low
|
297
|
Mathematical physiology
|
639
|
20
|
Stub
|
Mid
|
298
|
List of phylogenetic tree visualization software
|
633
|
20
|
List
|
Mid
|
299
|
Chromosome (genetic algorithm)
|
632
|
20
|
Start
|
Low
|
300
|
Chemical database
|
631
|
20
|
Start
|
Mid
|
301
|
List of neuroscience databases
|
631
|
20
|
List
|
Low
|
302
|
Eric Xing
|
626
|
20
|
Stub
|
Low
|
303
|
Michael Eisen
|
625
|
20
|
Start
|
Low
|
304
|
Molecular Evolutionary Genetics Analysis
|
619
|
19
|
Start
|
Low
|
305
|
Barry Smith (ontologist)
|
618
|
19
|
C
|
Low
|
306
|
Eadie–Hofstee diagram
|
617
|
19
|
Start
|
Low
|
307
|
Rob Knight (biologist)
|
617
|
19
|
Stub
|
Low
|
308
|
Attack rate
|
613
|
19
|
Start
|
Mid
|
309
|
UCSF Chimera
|
612
|
19
|
Start
|
Low
|
310
|
Pavel A. Pevzner
|
608
|
19
|
Start
|
Low
|
311
|
Mass spectrometry data format
|
598
|
19
|
Start
|
Low
|
312
|
Paradox of the plankton
|
598
|
19
|
Start
|
Low
|
313
|
Synthetic virology
|
598
|
19
|
Start
|
Mid
|
314
|
PROSITE
|
595
|
19
|
Start
|
High
|
315
|
Dot plot (bioinformatics)
|
591
|
19
|
Start
|
Mid
|
316
|
HUGO Gene Nomenclature Committee
|
591
|
19
|
Start
|
Mid
|
317
|
Tournament selection
|
587
|
18
|
Start
|
Low
|
318
|
BRENDA
|
585
|
18
|
Start
|
Mid
|
319
|
Evolutionary grade
|
584
|
18
|
Start
|
High
|
320
|
Batch effect
|
583
|
18
|
Stub
|
Low
|
321
|
Modelling biological systems
|
581
|
18
|
C
|
High
|
322
|
Gap penalty
|
578
|
18
|
C
|
High
|
323
|
Conservative replacement
|
576
|
18
|
Start
|
Low
|
324
|
MicroRNA sequencing
|
566
|
18
|
C
|
Low
|
325
|
Monod–Wyman–Changeux model
|
564
|
18
|
Start
|
Mid
|
326
|
Hirschberg's algorithm
|
558
|
18
|
B
|
Low
|
327
|
Trajectory inference
|
557
|
17
|
C
|
Low
|
328
|
Structural bioinformatics
|
553
|
17
|
B
|
High
|
329
|
Biopython
|
550
|
17
|
C
|
High
|
330
|
Template modeling score
|
549
|
17
|
Start
|
Low
|
331
|
Sarah Teichmann
|
548
|
17
|
C
|
Low
|
332
|
Tree of Life Web Project
|
546
|
17
|
Start
|
Low
|
333
|
454 Life Sciences
|
544
|
17
|
C
|
Low
|
334
|
Substitution matrix
|
533
|
17
|
C
|
High
|
335
|
DSSP (algorithm)
|
532
|
17
|
Start
|
Low
|
336
|
Genomic organization
|
532
|
17
|
Start
|
Low
|
337
|
List of sequenced animal genomes
|
528
|
17
|
List
|
Mid
|
338
|
Flux balance analysis
|
527
|
17
|
B
|
High
|
339
|
Centre for DNA Fingerprinting and Diagnostics
|
522
|
16
|
Start
|
Low
|
340
|
Ordinal priority approach
|
518
|
16
|
C
|
Unknown
|
341
|
Stephen Altschul
|
511
|
16
|
Start
|
Low
|
342
|
GeneDx
|
510
|
16
|
Stub
|
Low
|
343
|
Bioinformatics (journal)
|
508
|
16
|
Start
|
High
|
344
|
NK model
|
508
|
16
|
B
|
Low
|
345
|
List of biodiversity databases
|
507
|
16
|
List
|
Low
|
346
|
Dry lab
|
507
|
16
|
Start
|
High
|
347
|
Network motif
|
505
|
16
|
B
|
Low
|
348
|
CRAM (file format)
|
503
|
16
|
Start
|
Low
|
349
|
Visual Molecular Dynamics
|
501
|
16
|
Start
|
Low
|
350
|
World Community Grid
|
501
|
16
|
C
|
Low
|
351
|
ABI Solid Sequencing
|
500
|
16
|
Start
|
Low
|
352
|
Lipidomics
|
499
|
16
|
C
|
Low
|
353
|
Barcode of Life Data System
|
498
|
16
|
Stub
|
Low
|
354
|
Genomics England
|
498
|
16
|
Start
|
Low
|
355
|
List of molecular graphics systems
|
497
|
16
|
List
|
Mid
|
356
|
CATH database
|
491
|
15
|
Start
|
Mid
|
357
|
ARKive
|
491
|
15
|
C
|
Mid
|
358
|
Weasel program
|
489
|
15
|
B
|
Low
|
359
|
Polytomy
|
486
|
15
|
Start
|
Low
|
360
|
Uri Alon
|
481
|
15
|
Start
|
Low
|
361
|
Long branch attraction
|
479
|
15
|
Start
|
Low
|
362
|
Eugene Koonin
|
478
|
15
|
Start
|
Low
|
363
|
Phylogenetic comparative methods
|
476
|
15
|
C
|
Mid
|
364
|
Sequence database
|
472
|
15
|
Start
|
Mid
|
365
|
Swiss-model
|
472
|
15
|
Start
|
Mid
|
366
|
Accession number (bioinformatics)
|
469
|
15
|
Start
|
Low
|
367
|
Hanes–Woolf plot
|
462
|
14
|
Start
|
Low
|
368
|
Read (biology)
|
459
|
14
|
C
|
High
|
369
|
Nexus file
|
458
|
14
|
Start
|
Low
|
370
|
Metabolic network modelling
|
457
|
14
|
C
|
Mid
|
371
|
Scoring functions for docking
|
452
|
14
|
Start
|
Mid
|
372
|
List of omics topics in biology
|
445
|
14
|
List
|
Low
|
373
|
Phylogenetic Assignment of Named Global Outbreak Lineages
|
444
|
14
|
Start
|
Low
|
374
|
Sequence Read Archive
|
443
|
14
|
Start
|
High
|
375
|
List of human protein-coding genes 1
|
443
|
14
|
List
|
High
|
376
|
HomoloGene
|
434
|
14
|
Start
|
Low
|
377
|
De novo sequence assemblers
|
434
|
14
|
Start
|
Low
|
378
|
Protein tandem repeats
|
428
|
13
|
Start
|
Mid
|
379
|
Dryad (repository)
|
427
|
13
|
Start
|
Low
|
380
|
InterPro
|
421
|
13
|
B
|
High
|
381
|
Diseases Database
|
420
|
13
|
Start
|
Mid
|
382
|
Joseph DeRisi
|
419
|
13
|
Start
|
Low
|
383
|
Demographic and Health Surveys
|
419
|
13
|
B
|
Low
|
384
|
PLINK (genetic tool-set)
|
415
|
13
|
Stub
|
Low
|
385
|
Animal Diversity Web
|
413
|
13
|
C
|
Mid
|
386
|
Ancestral reconstruction
|
413
|
13
|
B
|
Low
|
387
|
McDonald–Kreitman test
|
413
|
13
|
C
|
Mid
|
388
|
Steven Salzberg
|
412
|
13
|
Start
|
Low
|
389
|
Marginal value theorem
|
410
|
13
|
C
|
Unknown
|
390
|
Ming Li
|
409
|
13
|
Start
|
Mid
|
391
|
Glycomics
|
405
|
13
|
Start
|
Low
|
392
|
BLAT (bioinformatics)
|
403
|
13
|
B
|
Low
|
393
|
DAVID
|
402
|
12
|
Start
|
Mid
|
394
|
David Botstein
|
397
|
12
|
Start
|
Low
|
395
|
List of alignment visualization software
|
396
|
12
|
List
|
Mid
|
396
|
FreeSurfer
|
394
|
12
|
Start
|
Mid
|
397
|
Nicolas Rashevsky
|
394
|
12
|
B
|
Mid
|
398
|
Tom Blundell
|
393
|
12
|
C
|
Low
|
399
|
Digital phenotyping
|
392
|
12
|
Start
|
Low
|
400
|
Eugene Myers
|
389
|
12
|
Start
|
Low
|
401
|
Quantum Aspects of Life
|
388
|
12
|
Stub
|
Low
|
402
|
Paradox of enrichment
|
384
|
12
|
Start
|
Low
|
403
|
List of sequenced eukaryotic genomes
|
382
|
12
|
List
|
Mid
|
404
|
FlowJo
|
382
|
12
|
Start
|
Low
|
405
|
Pyotr Anokhin
|
380
|
12
|
Start
|
Low
|
406
|
Allele frequency spectrum
|
374
|
12
|
Start
|
Low
|
407
|
List of MeSH codes
|
373
|
12
|
List
|
Mid
|
408
|
BMC Bioinformatics
|
373
|
12
|
C
|
Low
|
409
|
Binning (metagenomics)
|
373
|
12
|
Start
|
Low
|
410
|
Expasy
|
372
|
12
|
Start
|
Mid
|
411
|
MAFFT
|
370
|
11
|
Stub
|
Mid
|
412
|
Chemical library
|
367
|
11
|
Start
|
Low
|
413
|
Jay Shendure
|
367
|
11
|
Start
|
Low
|
414
|
Biclustering
|
366
|
11
|
B
|
Mid
|
415
|
Human Protein Atlas
|
366
|
11
|
Start
|
Low
|
416
|
Phylogenetic bracketing
|
362
|
11
|
Start
|
Low
|
417
|
Threading (protein sequence)
|
361
|
11
|
Start
|
High
|
418
|
Sequenom
|
361
|
11
|
Start
|
Low
|
419
|
List of genetic algorithm applications
|
359
|
11
|
List
|
Low
|
420
|
Ewan Birney
|
358
|
11
|
C
|
Low
|
421
|
MUSCLE (alignment software)
|
358
|
11
|
Start
|
Mid
|
422
|
UniFrac
|
356
|
11
|
Stub
|
Low
|
423
|
Robinson–Foulds metric
|
355
|
11
|
C
|
Low
|
424
|
EMBOSS
|
354
|
11
|
Start
|
Mid
|
425
|
100,000 Genomes Project
|
352
|
11
|
C
|
Low
|
426
|
Genome browser
|
349
|
11
|
List
|
High
|
427
|
Global distance test
|
349
|
11
|
Stub
|
Low
|
428
|
PHYLIP
|
346
|
11
|
Start
|
Low
|
429
|
Bernd Sturmfels
|
344
|
11
|
Stub
|
Low
|
430
|
Edward C. Holmes
|
343
|
11
|
Start
|
Low
|
431
|
ChIP-on-chip
|
342
|
11
|
C
|
Low
|
432
|
Anduril (workflow engine)
|
342
|
11
|
B
|
Low
|
433
|
Ehud Shapiro
|
337
|
10
|
Start
|
Low
|
434
|
Mouse Genome Informatics
|
336
|
10
|
Stub
|
Low
|
435
|
Consensus CDS Project
|
336
|
10
|
C
|
Low
|
436
|
Allen Brain Atlas
|
334
|
10
|
C
|
Mid
|
437
|
Genetic operator
|
334
|
10
|
Start
|
Low
|
438
|
RasMol
|
331
|
10
|
Start
|
Mid
|
439
|
Imaging informatics
|
330
|
10
|
Start
|
Low
|
440
|
Briefings in Bioinformatics
|
327
|
10
|
Start
|
Low
|
441
|
Pileup format
|
324
|
10
|
Start
|
Low
|
442
|
Atul Butte
|
323
|
10
|
Start
|
Mid
|
443
|
Taxonomic database
|
322
|
10
|
Start
|
Mid
|
444
|
Mona Singh (scientist)
|
321
|
10
|
Start
|
Mid
|
445
|
Journal of Theoretical Biology
|
319
|
10
|
Stub
|
Low
|
446
|
David S. Wishart
|
317
|
10
|
C
|
Low
|
447
|
Peter Donnelly
|
314
|
10
|
Start
|
Low
|
448
|
Fluxomics
|
314
|
10
|
Start
|
Low
|
449
|
Eran Segal
|
314
|
10
|
Start
|
Low
|
450
|
EMBRACE
|
312
|
10
|
Start
|
Low
|
451
|
Group size measures
|
310
|
10
|
Start
|
Low
|
452
|
Hindmarsh–Rose model
|
309
|
9
|
Stub
|
Low
|
453
|
David Goodsell
|
309
|
9
|
C
|
Low
|
454
|
Next-generation matrix
|
308
|
9
|
Start
|
Low
|
455
|
James D. Murray
|
307
|
9
|
Start
|
Low
|
456
|
De novo protein structure prediction
|
306
|
9
|
Start
|
High
|
457
|
CAZy
|
306
|
9
|
Start
|
Mid
|
458
|
List of gene prediction software
|
306
|
9
|
List
|
Mid
|
459
|
Dynamic energy budget theory
|
305
|
9
|
C
|
Low
|
460
|
Erez Lieberman Aiden
|
305
|
9
|
GA
|
Low
|
461
|
High-frequency oscillations
|
305
|
9
|
C
|
Low
|
462
|
Richard M. Durbin
|
303
|
9
|
C
|
Low
|
463
|
David J. Lipman
|
302
|
9
|
Start
|
Low
|
464
|
List of software for Monte Carlo molecular modeling
|
300
|
9
|
List
|
Mid
|
465
|
Dehaene–Changeux model
|
300
|
9
|
Start
|
Low
|
466
|
Metabolic flux analysis
|
299
|
9
|
Stub
|
Low
|
467
|
Evolutionary tree
|
297
|
9
|
Redirect
|
NA
|
468
|
Protein function prediction
|
295
|
9
|
Start
|
High
|
469
|
Digital organism
|
293
|
9
|
Stub
|
Low
|
470
|
David Haussler
|
293
|
9
|
C
|
Low
|
471
|
SBML
|
291
|
9
|
B
|
High
|
472
|
SNPedia
|
291
|
9
|
Start
|
Low
|
473
|
WPGMA
|
291
|
9
|
C
|
Low
|
474
|
Carl Bergstrom
|
289
|
9
|
Stub
|
Low
|
475
|
Haplotype estimation
|
288
|
9
|
Start
|
Low
|
476
|
Biological data visualization
|
287
|
9
|
Start
|
Mid
|
477
|
International Society for Computational Biology
|
286
|
9
|
B
|
High
|
478
|
Sequence clustering
|
285
|
9
|
Start
|
Mid
|
479
|
List of bioinformatics companies
|
285
|
9
|
List
|
Mid
|
480
|
European Nucleotide Archive
|
283
|
9
|
GA
|
Mid
|
481
|
Molecular models of DNA
|
281
|
9
|
B
|
Mid
|
482
|
Hypercycle (chemistry)
|
281
|
9
|
B
|
Low
|
483
|
Morris–Lecar model
|
279
|
9
|
Start
|
Low
|
484
|
Reactome
|
276
|
8
|
Start
|
Low
|
485
|
Velvet assembler
|
275
|
8
|
Start
|
Low
|
486
|
Viral phylodynamics
|
274
|
8
|
B
|
Low
|
487
|
GENESIS (software)
|
273
|
8
|
Start
|
Low
|
488
|
Structural genomics
|
270
|
8
|
Start
|
High
|
489
|
Codon Adaptation Index
|
270
|
8
|
Stub
|
Low
|
490
|
Consumer-resource model
|
270
|
8
|
B
|
Unknown
|
491
|
Ram Samudrala
|
269
|
8
|
Start
|
Mid
|
492
|
Bowtie (sequence analysis)
|
268
|
8
|
Start
|
Mid
|
493
|
Swiss Institute of Bioinformatics
|
264
|
8
|
Start
|
Low
|
494
|
Biodiversity informatics
|
262
|
8
|
C
|
Mid
|
495
|
Orphanet
|
261
|
8
|
C
|
Low
|
496
|
Brendan Frey
|
261
|
8
|
B
|
Low
|
497
|
Coot (software)
|
260
|
8
|
Start
|
Low
|
498
|
PANTHER
|
257
|
8
|
C
|
Low
|
499
|
Elasticity coefficient
|
256
|
8
|
C
|
Mid
|
500
|
Circular permutation in proteins
|
256
|
8
|
GA
|
Low
|