Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
David Baker (biochemist)
|
153,701
|
4,958
|
Start
|
Low
|
2
|
AlphaFold
|
63,891
|
2,061
|
C
|
High
|
3
|
23andMe
|
41,260
|
1,330
|
C
|
Low
|
4
|
CRISPR
|
39,210
|
1,264
|
B
|
Top
|
5
|
Receiver operating characteristic
|
34,244
|
1,104
|
B
|
Mid
|
6
|
Last universal common ancestor
|
30,049
|
969
|
GA
|
Mid
|
7
|
Dynamic programming
|
26,049
|
840
|
B
|
Top
|
8
|
Clade
|
25,291
|
815
|
C
|
Mid
|
9
|
Hidden Markov model
|
22,185
|
715
|
GA
|
Top
|
10
|
Systems theory
|
21,223
|
684
|
C
|
Mid
|
11
|
Bioinformatics
|
19,232
|
620
|
C
|
Top
|
12
|
Protein structure prediction
|
18,458
|
595
|
B
|
High
|
13
|
PubMed Central
|
18,356
|
592
|
B
|
Mid
|
14
|
Michaelis–Menten kinetics
|
17,074
|
550
|
B
|
Top
|
15
|
Cellular automaton
|
15,942
|
514
|
B
|
Low
|
16
|
Phylogenetic tree
|
15,199
|
490
|
B
|
Top
|
17
|
DNA sequencing
|
15,015
|
484
|
C
|
High
|
18
|
National Center for Biotechnology Information
|
13,992
|
451
|
C
|
Low
|
19
|
Genome
|
13,793
|
444
|
C
|
High
|
20
|
Phylogenetics
|
13,786
|
444
|
B
|
Top
|
21
|
Ontology (information science)
|
12,627
|
407
|
C
|
High
|
22
|
Sanger sequencing
|
11,082
|
357
|
C
|
Mid
|
23
|
Compartmental models in epidemiology
|
10,514
|
339
|
C
|
Mid
|
24
|
FASTA format
|
9,747
|
314
|
B
|
High
|
25
|
Isomorphic Labs
|
9,350
|
301
|
Stub
|
Low
|
26
|
Synthetic biology
|
8,805
|
284
|
B
|
Mid
|
27
|
Most recent common ancestor
|
8,774
|
283
|
B
|
High
|
28
|
Protein design
|
8,028
|
258
|
C
|
Mid
|
29
|
Medical Subject Headings
|
7,976
|
257
|
C
|
Mid
|
30
|
Computational biology
|
7,916
|
255
|
C
|
Top
|
31
|
Cladistics
|
7,642
|
246
|
C
|
Mid
|
32
|
FASTQ format
|
7,638
|
246
|
B
|
Mid
|
33
|
Heat map
|
7,597
|
245
|
Start
|
High
|
34
|
Whole genome sequencing
|
7,549
|
243
|
B
|
High
|
35
|
List of algorithms
|
7,316
|
236
|
List
|
Mid
|
36
|
Genomics
|
7,172
|
231
|
B
|
High
|
37
|
PubChem
|
6,918
|
223
|
Start
|
Mid
|
38
|
Illumina, Inc.
|
6,850
|
220
|
C
|
Low
|
39
|
RNA-Seq
|
6,639
|
214
|
B
|
Top
|
40
|
Petri net
|
6,520
|
210
|
B
|
Low
|
41
|
Folding@home
|
6,453
|
208
|
B
|
Mid
|
42
|
Needleman–Wunsch algorithm
|
6,398
|
206
|
Start
|
Mid
|
43
|
Mathematical and theoretical biology
|
6,268
|
202
|
C
|
Top
|
44
|
Phi coefficient
|
6,212
|
200
|
Start
|
Mid
|
45
|
Lineweaver–Burk plot
|
6,126
|
197
|
B
|
Low
|
46
|
Proteomics
|
5,918
|
190
|
C
|
High
|
47
|
Biostatistics
|
5,884
|
189
|
B
|
Top
|
48
|
Burrows–Wheeler transform
|
5,871
|
189
|
C
|
Mid
|
49
|
Omics
|
5,722
|
184
|
C
|
Mid
|
50
|
Protein Data Bank
|
5,707
|
184
|
C
|
High
|
51
|
Computational neuroscience
|
5,692
|
183
|
C
|
Top
|
52
|
George Church (geneticist)
|
5,485
|
176
|
C
|
Mid
|
53
|
Sequence alignment
|
5,480
|
176
|
C
|
High
|
54
|
Spurious relationship
|
5,377
|
173
|
Start
|
Low
|
55
|
Rosetta@home
|
5,051
|
162
|
C
|
Mid
|
56
|
BLAST (biotechnology)
|
5,022
|
162
|
C
|
Top
|
57
|
Smith–Waterman algorithm
|
4,963
|
160
|
B
|
Top
|
58
|
DNA microarray
|
4,940
|
159
|
B
|
Top
|
59
|
Europe PubMed Central
|
4,854
|
156
|
Start
|
Low
|
60
|
DNA barcoding
|
4,799
|
154
|
B
|
High
|
61
|
Denis Noble
|
4,763
|
153
|
Start
|
Low
|
62
|
Systems biology
|
4,737
|
152
|
C
|
Top
|
63
|
Genome-wide association study
|
4,724
|
152
|
GA
|
High
|
64
|
Non-coding DNA
|
4,656
|
150
|
C
|
Low
|
65
|
Phred quality score
|
4,641
|
149
|
Start
|
Mid
|
66
|
Jmol
|
4,573
|
147
|
Start
|
Mid
|
67
|
Gene nomenclature
|
4,434
|
143
|
Start
|
Mid
|
68
|
Variant Call Format
|
4,323
|
139
|
Start
|
Mid
|
69
|
What Is Life?
|
4,198
|
135
|
C
|
Low
|
70
|
Single-cell sequencing
|
4,187
|
135
|
C
|
High
|
71
|
Junk DNA
|
4,015
|
129
|
B
|
Low
|
72
|
Global Biodiversity Information Facility
|
3,989
|
128
|
Start
|
Low
|
73
|
Daphne Koller
|
3,985
|
128
|
C
|
Low
|
74
|
CASP
|
3,942
|
127
|
C
|
Mid
|
75
|
STR analysis
|
3,903
|
125
|
Start
|
Low
|
76
|
Metagenomics
|
3,895
|
125
|
GA
|
Mid
|
77
|
Nanopore sequencing
|
3,805
|
122
|
C
|
Low
|
78
|
BLOSUM
|
3,787
|
122
|
C
|
High
|
79
|
Biological computing
|
3,772
|
121
|
C
|
Mid
|
80
|
Baum–Welch algorithm
|
3,729
|
120
|
C
|
Mid
|
81
|
Similarity measure
|
3,707
|
119
|
Start
|
Mid
|
82
|
High-throughput screening
|
3,454
|
111
|
B
|
Low
|
83
|
Molecular clock
|
3,450
|
111
|
C
|
High
|
84
|
Multiple sequence alignment
|
3,444
|
111
|
Unknown
|
High
|
85
|
Intrinsically disordered proteins
|
3,443
|
111
|
Start
|
Mid
|
86
|
KEGG
|
3,406
|
109
|
C
|
High
|
87
|
Broad Institute
|
3,404
|
109
|
Start
|
Low
|
88
|
Metabolomics
|
3,344
|
107
|
C
|
Mid
|
89
|
BED (file format)
|
3,310
|
106
|
C
|
Low
|
90
|
Exome sequencing
|
3,309
|
106
|
C
|
High
|
91
|
Gene set enrichment analysis
|
3,302
|
106
|
C
|
Mid
|
92
|
Docking (molecular)
|
3,296
|
106
|
B
|
High
|
93
|
KNIME
|
3,256
|
105
|
Start
|
Low
|
94
|
Illumina dye sequencing
|
3,135
|
101
|
C
|
Mid
|
95
|
Gene Ontology
|
3,064
|
98
|
C
|
High
|
96
|
ATAC-seq
|
3,044
|
98
|
Start
|
Low
|
97
|
Foundational Model of Anatomy
|
2,977
|
96
|
Start
|
Low
|
98
|
Data wrangling
|
2,949
|
95
|
Start
|
Low
|
99
|
ChIP sequencing
|
2,931
|
94
|
C
|
Mid
|
100
|
Robert Gentleman (statistician)
|
2,920
|
94
|
Start
|
Mid
|
101
|
SAM (file format)
|
2,916
|
94
|
Start
|
Mid
|
102
|
Ludwig von Bertalanffy
|
2,895
|
93
|
Start
|
Low
|
103
|
Multiomics
|
2,875
|
92
|
C
|
High
|
104
|
Bioconductor
|
2,837
|
91
|
C
|
Mid
|
105
|
Crossover (genetic algorithm)
|
2,833
|
91
|
B
|
Low
|
106
|
UniProt
|
2,824
|
91
|
Start
|
High
|
107
|
Genetic programming
|
2,817
|
90
|
B
|
Mid
|
108
|
Brendan Frey
|
2,816
|
90
|
B
|
Low
|
109
|
Root mean square deviation of atomic positions
|
2,793
|
90
|
Start
|
Mid
|
110
|
Andrew Huxley
|
2,751
|
88
|
C
|
Low
|
111
|
Cyberneticist
|
2,750
|
88
|
Stub
|
Low
|
112
|
Environmental DNA
|
2,720
|
87
|
B
|
Low
|
113
|
K-mer
|
2,718
|
87
|
B
|
Mid
|
114
|
Volcano plot (statistics)
|
2,709
|
87
|
C
|
Mid
|
115
|
Spatial transcriptomics
|
2,707
|
87
|
Start
|
Low
|
116
|
Michael Levitt (biophysicist)
|
2,706
|
87
|
C
|
Low
|
117
|
Brain mapping
|
2,697
|
87
|
Start
|
Low
|
118
|
Monod equation
|
2,683
|
86
|
Start
|
Low
|
119
|
10x Genomics
|
2,669
|
86
|
Start
|
Mid
|
120
|
Wikispecies
|
2,659
|
85
|
Start
|
Mid
|
121
|
Protein–protein interaction
|
2,600
|
83
|
C
|
High
|
122
|
Combined DNA Index System
|
2,576
|
83
|
GA
|
Low
|
123
|
Transcriptome
|
2,531
|
81
|
B
|
High
|
124
|
Microarray
|
2,516
|
81
|
Start
|
Top
|
125
|
Fitness function
|
2,457
|
79
|
Start
|
Mid
|
126
|
Biological network inference
|
2,450
|
79
|
C
|
Low
|
127
|
UK Biobank
|
2,414
|
77
|
B
|
Low
|
128
|
FitzHugh–Nagumo model
|
2,387
|
77
|
C
|
Low
|
129
|
Molecular phylogenetics
|
2,385
|
76
|
C
|
High
|
130
|
N50, L50, and related statistics
|
2,360
|
76
|
Start
|
Low
|
131
|
Oxford Nanopore Technologies
|
2,354
|
75
|
Start
|
Low
|
132
|
ChEMBL
|
2,336
|
75
|
Start
|
Mid
|
133
|
GenBank
|
2,327
|
75
|
Start
|
High
|
134
|
Kabsch algorithm
|
2,319
|
74
|
Start
|
Mid
|
135
|
John Maynard Smith
|
2,293
|
73
|
C
|
Mid
|
136
|
Gene regulatory network
|
2,240
|
72
|
B
|
High
|
137
|
Protein Data Bank (file format)
|
2,233
|
72
|
Start
|
Mid
|
138
|
UPGMA
|
2,221
|
71
|
C
|
Low
|
139
|
Online Mendelian Inheritance in Man
|
2,204
|
71
|
Start
|
Mid
|
140
|
Conserved sequence
|
2,164
|
69
|
C
|
High
|
141
|
Reference genome
|
2,163
|
69
|
Start
|
Low
|
142
|
Pan-genome
|
2,149
|
69
|
C
|
Mid
|
143
|
Genome size
|
2,087
|
67
|
B
|
Mid
|
144
|
PyMOL
|
2,085
|
67
|
Start
|
Low
|
145
|
European Molecular Biology Laboratory
|
2,059
|
66
|
C
|
Low
|
146
|
Martin Kulldorff
|
2,045
|
65
|
B
|
Low
|
147
|
Distance matrix
|
2,044
|
65
|
Start
|
High
|
148
|
Genetic distance
|
2,043
|
65
|
B
|
Mid
|
149
|
Transcriptomics technologies
|
2,010
|
64
|
GA
|
High
|
150
|
Schrödinger, Inc.
|
1,989
|
64
|
Start
|
Low
|
151
|
Metabarcoding
|
1,984
|
64
|
B
|
Low
|
152
|
Neighbor joining
|
1,982
|
63
|
C
|
High
|
153
|
Mathematical modelling of infectious diseases
|
1,899
|
61
|
C
|
Low
|
154
|
Topologically associating domain
|
1,895
|
61
|
C
|
Low
|
155
|
Polygenic score
|
1,892
|
61
|
C
|
Mid
|
156
|
ChEBI
|
1,877
|
60
|
Start
|
Low
|
157
|
Proteome
|
1,856
|
59
|
C
|
High
|
158
|
Superspreading event
|
1,856
|
59
|
C
|
High
|
159
|
Phylogeny
|
1,852
|
59
|
Redirect
|
NA
|
160
|
Pardis Sabeti
|
1,785
|
57
|
B
|
Low
|
161
|
Clustal
|
1,783
|
57
|
Start
|
Mid
|
162
|
List of sequence alignment software
|
1,761
|
56
|
List
|
High
|
163
|
Consensus sequence
|
1,755
|
56
|
Start
|
High
|
164
|
Synteny
|
1,747
|
56
|
Start
|
Low
|
165
|
List of biological databases
|
1,735
|
55
|
List
|
High
|
166
|
Alan Hodgkin
|
1,695
|
54
|
Start
|
Low
|
167
|
DNA sequencer
|
1,692
|
54
|
Start
|
Low
|
168
|
Aviv Regev
|
1,688
|
54
|
Start
|
Low
|
169
|
Approximate Bayesian computation
|
1,655
|
53
|
B
|
Low
|
170
|
Sepp Hochreiter
|
1,645
|
53
|
Start
|
Low
|
171
|
General feature format
|
1,629
|
52
|
Start
|
Low
|
172
|
Maximum parsimony (phylogenetics)
|
1,628
|
52
|
C
|
High
|
173
|
Models of DNA evolution
|
1,620
|
52
|
B
|
Mid
|
174
|
List of protein structure prediction software
|
1,617
|
52
|
List
|
Mid
|
175
|
Richard Bonneau
|
1,607
|
51
|
Start
|
Low
|
176
|
Computational phylogenetics
|
1,587
|
51
|
C
|
High
|
177
|
List of mass spectrometry software
|
1,558
|
50
|
List
|
Low
|
178
|
C. H. Waddington
|
1,550
|
50
|
C
|
Low
|
179
|
List of open-source bioinformatics software
|
1,524
|
49
|
List
|
High
|
180
|
Indel
|
1,521
|
49
|
Start
|
Low
|
181
|
Data curation
|
1,509
|
48
|
Start
|
Mid
|
182
|
Chromosome conformation capture
|
1,478
|
47
|
C
|
Low
|
183
|
Wellcome Sanger Institute
|
1,473
|
47
|
C
|
Low
|
184
|
Cable theory
|
1,448
|
46
|
C
|
Mid
|
185
|
Biochemical cascade
|
1,447
|
46
|
C
|
Mid
|
186
|
DNA annotation
|
1,446
|
46
|
Start
|
Low
|
187
|
FishBase
|
1,440
|
46
|
Start
|
Low
|
188
|
Catalogue of Life
|
1,436
|
46
|
C
|
Low
|
189
|
Biobank
|
1,417
|
45
|
Start
|
High
|
190
|
Encyclopedia of Life
|
1,413
|
45
|
Start
|
Mid
|
191
|
Binary Alignment Map
|
1,413
|
45
|
Stub
|
Mid
|
192
|
Sequence motif
|
1,412
|
45
|
Start
|
High
|
193
|
SNP array
|
1,407
|
45
|
Start
|
High
|
194
|
Contig
|
1,399
|
45
|
C
|
High
|
195
|
Haar-like feature
|
1,399
|
45
|
C
|
Low
|
196
|
European Bioinformatics Institute
|
1,396
|
45
|
C
|
Low
|
197
|
AMBER
|
1,386
|
44
|
C
|
Mid
|
198
|
Celera Corporation
|
1,364
|
44
|
Start
|
Low
|
199
|
Solvation shell
|
1,350
|
43
|
Start
|
Low
|
200
|
Weighted correlation network analysis
|
1,345
|
43
|
B
|
Low
|
201
|
GROMACS
|
1,342
|
43
|
Start
|
Low
|
202
|
Point accepted mutation
|
1,341
|
43
|
B
|
High
|
203
|
Lenia
|
1,340
|
43
|
Start
|
Unknown
|
204
|
Ensembl genome database project
|
1,335
|
43
|
B
|
High
|
205
|
1000 Genomes Project
|
1,327
|
42
|
B
|
Low
|
206
|
Amino acid replacement
|
1,319
|
42
|
Start
|
High
|
207
|
Substitution model
|
1,309
|
42
|
B
|
Mid
|
208
|
Leroy Hood
|
1,303
|
42
|
B
|
Low
|
209
|
Homology modeling
|
1,303
|
42
|
B
|
High
|
210
|
Position weight matrix
|
1,296
|
41
|
C
|
Top
|
211
|
Functional genomics
|
1,274
|
41
|
C
|
High
|
212
|
Outgroup (cladistics)
|
1,238
|
39
|
Start
|
Mid
|
213
|
Pfam
|
1,238
|
39
|
B
|
High
|
214
|
Sequence logo
|
1,237
|
39
|
B
|
Mid
|
215
|
DNA database
|
1,207
|
38
|
Start
|
Mid
|
216
|
Matthews correlation coefficient
|
1,189
|
38
|
Redirect
|
NA
|
217
|
Single-cell transcriptomics
|
1,188
|
38
|
C
|
Mid
|
218
|
Gene family
|
1,187
|
38
|
C
|
High
|
219
|
FASTA
|
1,182
|
38
|
B
|
High
|
220
|
Cooperative binding
|
1,165
|
37
|
B
|
Mid
|
221
|
UCSC Genome Browser
|
1,140
|
36
|
Start
|
High
|
222
|
Protein family
|
1,127
|
36
|
Start
|
High
|
223
|
Open Tree of Life
|
1,117
|
36
|
Start
|
Low
|
224
|
Tournament selection
|
1,101
|
35
|
Start
|
Low
|
225
|
Amplicon sequence variant
|
1,100
|
35
|
Start
|
Low
|
226
|
Metabolome
|
1,098
|
35
|
C
|
High
|
227
|
Mutation (genetic algorithm)
|
1,097
|
35
|
Start
|
Low
|
228
|
Eadie–Hofstee diagram
|
1,091
|
35
|
Start
|
Low
|
229
|
Hirschberg's algorithm
|
1,079
|
34
|
B
|
Low
|
230
|
RefSeq
|
1,079
|
34
|
Start
|
Mid
|
231
|
Biological database
|
1,076
|
34
|
Start
|
High
|
232
|
Gap penalty
|
1,072
|
34
|
C
|
High
|
233
|
Margaret Oakley Dayhoff
|
1,072
|
34
|
B
|
High
|
234
|
Knowledge engineering
|
1,065
|
34
|
Start
|
Low
|
235
|
Biochip
|
1,063
|
34
|
C
|
Low
|
236
|
ENCODE
|
1,060
|
34
|
C
|
Mid
|
237
|
Microarray analysis techniques
|
1,059
|
34
|
B
|
Mid
|
238
|
Entrez
|
1,055
|
34
|
Start
|
Mid
|
239
|
Sequence assembly
|
1,054
|
34
|
Start
|
High
|
240
|
Barcode of Life Data System
|
1,051
|
33
|
Stub
|
Low
|
241
|
D'Arcy Wentworth Thompson
|
1,050
|
33
|
GA
|
Mid
|
242
|
GeneDx
|
1,032
|
33
|
Stub
|
Low
|
243
|
Bayesian inference in phylogeny
|
1,021
|
32
|
C
|
High
|
244
|
STRING
|
1,021
|
32
|
B
|
Low
|
245
|
GeneCards
|
1,020
|
32
|
C
|
Mid
|
246
|
Vito Volterra
|
1,017
|
32
|
C
|
Low
|
247
|
Virtual screening
|
1,009
|
32
|
Start
|
High
|
248
|
MA plot
|
1,008
|
32
|
Start
|
Low
|
249
|
RNA integrity number
|
1,006
|
32
|
Stub
|
Low
|
250
|
Probabilistic context-free grammar
|
1,004
|
32
|
B
|
High
|
251
|
Comparative genomics
|
1,002
|
32
|
C
|
Top
|
252
|
Ukkonen's algorithm
|
1,001
|
32
|
Stub
|
Low
|
253
|
Avogadro (software)
|
997
|
32
|
Stub
|
Low
|
254
|
De novo peptide sequencing
|
984
|
31
|
Start
|
Low
|
255
|
Population structure (genetics)
|
973
|
31
|
Start
|
Low
|
256
|
CUT&RUN sequencing
|
971
|
31
|
C
|
Low
|
257
|
DbSNP
|
969
|
31
|
B
|
Mid
|
258
|
Umbrella sampling
|
951
|
30
|
Start
|
Low
|
259
|
List of bioinformatics journals
|
949
|
30
|
List
|
Low
|
260
|
MGI (company)
|
941
|
30
|
C
|
Low
|
261
|
Biological systems engineering
|
936
|
30
|
Start
|
Low
|
262
|
Eric Xing
|
936
|
30
|
Stub
|
Low
|
263
|
NanoString Technologies
|
930
|
30
|
Start
|
Low
|
264
|
List of RNA-Seq bioinformatics tools
|
914
|
29
|
List
|
Mid
|
265
|
AutoDock
|
913
|
29
|
Start
|
Mid
|
266
|
UCSF Chimera
|
911
|
29
|
Start
|
Low
|
267
|
List of protein-ligand docking software
|
908
|
29
|
List
|
Mid
|
268
|
Substitution matrix
|
907
|
29
|
C
|
High
|
269
|
Boolean network
|
905
|
29
|
C
|
Mid
|
270
|
DeCODE genetics
|
901
|
29
|
Start
|
Low
|
271
|
Gene expression profiling
|
900
|
29
|
B
|
High
|
272
|
Paradox of the plankton
|
900
|
29
|
Start
|
Low
|
273
|
Ion semiconductor sequencing
|
900
|
29
|
C
|
Low
|
274
|
CHARMM
|
893
|
28
|
B
|
Mid
|
275
|
Manolis Kellis
|
887
|
28
|
C
|
Low
|
276
|
HMMER
|
877
|
28
|
B
|
High
|
277
|
Sequence analysis
|
868
|
28
|
C
|
Top
|
278
|
CRISPR interference
|
864
|
27
|
B
|
Low
|
279
|
Cytoscape
|
856
|
27
|
B
|
High
|
280
|
List of sequenced animal genomes
|
854
|
27
|
List
|
Mid
|
281
|
Motoo Kimura
|
850
|
27
|
C
|
High
|
282
|
Galaxy (computational biology)
|
847
|
27
|
Start
|
High
|
283
|
Global distance test
|
846
|
27
|
Stub
|
Low
|
284
|
List of RNA structure prediction software
|
846
|
27
|
List
|
Low
|
285
|
Protein contact map
|
839
|
27
|
Start
|
Mid
|
286
|
Monod–Wyman–Changeux model
|
838
|
27
|
Start
|
Mid
|
287
|
Systems neuroscience
|
831
|
26
|
Stub
|
Mid
|
288
|
Michael Eisen
|
828
|
26
|
Start
|
Low
|
289
|
Bonnie Berger
|
828
|
26
|
Start
|
Low
|
290
|
Dot plot (bioinformatics)
|
820
|
26
|
Start
|
Mid
|
291
|
Theoretical ecology
|
805
|
25
|
B
|
High
|
292
|
Interactome
|
802
|
25
|
C
|
Mid
|
293
|
Robert Rosen (biologist)
|
800
|
25
|
Start
|
Low
|
294
|
Attack rate
|
798
|
25
|
Start
|
Mid
|
295
|
Hanes–Woolf plot
|
790
|
25
|
Start
|
Low
|
296
|
List of phylogenetics software
|
784
|
25
|
List
|
High
|
297
|
Mathematical physiology
|
783
|
25
|
Stub
|
Mid
|
298
|
Molecular Evolutionary Genetics Analysis
|
781
|
25
|
Start
|
Low
|
299
|
Lior Pachter
|
781
|
25
|
Start
|
Mid
|
300
|
Sarah Teichmann
|
780
|
25
|
C
|
Low
|
301
|
SAMtools
|
779
|
25
|
Start
|
Low
|
302
|
Ecosystem model
|
776
|
25
|
Start
|
Mid
|
303
|
Gene prediction
|
773
|
24
|
C
|
High
|
304
|
Phylogenetic Assignment of Named Global Outbreak Lineages
|
764
|
24
|
Start
|
Low
|
305
|
BRENDA
|
757
|
24
|
Start
|
Mid
|
306
|
Biological network
|
751
|
24
|
C
|
High
|
307
|
Conservative replacement
|
751
|
24
|
Start
|
Low
|
308
|
Structural Classification of Proteins database
|
747
|
24
|
Start
|
High
|
309
|
Synthetic biological circuit
|
741
|
23
|
Start
|
Low
|
310
|
Chemical database
|
740
|
23
|
Start
|
Mid
|
311
|
ABI Solid Sequencing
|
740
|
23
|
Start
|
Low
|
312
|
List of phylogenetic tree visualization software
|
740
|
23
|
List
|
Mid
|
313
|
PLOS Computational Biology
|
738
|
23
|
Start
|
High
|
314
|
All of Us (initiative)
|
737
|
23
|
C
|
Low
|
315
|
Eugene Koonin
|
734
|
23
|
Start
|
Low
|
316
|
DSSP (algorithm)
|
733
|
23
|
Start
|
Low
|
317
|
Stephen Altschul
|
722
|
23
|
Start
|
Low
|
318
|
Protein superfamily
|
722
|
23
|
B
|
High
|
319
|
Template modeling score
|
715
|
23
|
Start
|
Low
|
320
|
Marginal value theorem
|
714
|
23
|
C
|
Unknown
|
321
|
Network motif
|
700
|
22
|
B
|
Low
|
322
|
Dry lab
|
700
|
22
|
Start
|
High
|
323
|
List of sequenced eukaryotic genomes
|
699
|
22
|
List
|
Mid
|
324
|
Machine learning in bioinformatics
|
699
|
22
|
C
|
High
|
325
|
EBird
|
696
|
22
|
Start
|
Low
|
326
|
Polytomy
|
695
|
22
|
Start
|
Low
|
327
|
List of human protein-coding genes 1
|
694
|
22
|
List
|
High
|
328
|
Modelling biological systems
|
690
|
22
|
C
|
High
|
329
|
DNA Data Bank of Japan
|
686
|
22
|
Stub
|
Low
|
330
|
454 Life Sciences
|
682
|
22
|
C
|
Low
|
331
|
Biopython
|
681
|
21
|
C
|
High
|
332
|
Flux balance analysis
|
680
|
21
|
B
|
High
|
333
|
Co-occurrence network
|
678
|
21
|
Start
|
Low
|
334
|
CATH database
|
677
|
21
|
Start
|
Mid
|
335
|
HUGO Gene Nomenclature Committee
|
676
|
21
|
Start
|
Mid
|
336
|
List of genetic algorithm applications
|
672
|
21
|
List
|
Low
|
337
|
KiSAO
|
672
|
21
|
Start
|
Low
|
338
|
McDonald–Kreitman test
|
669
|
21
|
C
|
Mid
|
339
|
Tom Blundell
|
665
|
21
|
C
|
Low
|
340
|
Fossilworks
|
663
|
21
|
Stub
|
Low
|
341
|
Lipidomics
|
662
|
21
|
C
|
Low
|
342
|
Bioinformatics (journal)
|
652
|
21
|
Start
|
High
|
343
|
Accession number (bioinformatics)
|
649
|
20
|
Start
|
Low
|
344
|
InterPro
|
648
|
20
|
B
|
High
|
345
|
Centre for DNA Fingerprinting and Diagnostics
|
647
|
20
|
Start
|
Low
|
346
|
Batch effect
|
647
|
20
|
Stub
|
Low
|
347
|
Genomics England
|
645
|
20
|
Start
|
Low
|
348
|
World Community Grid
|
644
|
20
|
C
|
Low
|
349
|
Tree of Life Web Project
|
644
|
20
|
Start
|
Low
|
350
|
PROSITE
|
643
|
20
|
Start
|
High
|
351
|
Trajectory inference
|
642
|
20
|
C
|
Low
|
352
|
Structural bioinformatics
|
641
|
20
|
B
|
High
|
353
|
Mass spectrometry data format
|
638
|
20
|
Start
|
Low
|
354
|
De novo protein structure prediction
|
634
|
20
|
Start
|
High
|
355
|
Nexus file
|
624
|
20
|
Start
|
Low
|
356
|
List of molecular graphics systems
|
624
|
20
|
List
|
Mid
|
357
|
NK model
|
624
|
20
|
B
|
Low
|
358
|
Michael Laufer
|
621
|
20
|
Start
|
Unknown
|
359
|
List of neuroscience databases
|
620
|
20
|
List
|
Low
|
360
|
Institute of Genomics and Integrative Biology
|
617
|
19
|
C
|
Low
|
361
|
Sequence Read Archive
|
614
|
19
|
Start
|
High
|
362
|
Visual Molecular Dynamics
|
608
|
19
|
Start
|
Low
|
363
|
Allele frequency spectrum
|
606
|
19
|
Start
|
Low
|
364
|
Barry Smith (ontologist)
|
605
|
19
|
C
|
Low
|
365
|
De novo sequence assemblers
|
605
|
19
|
Start
|
Low
|
366
|
Haldane's dilemma
|
603
|
19
|
B
|
Low
|
367
|
HomoloGene
|
601
|
19
|
Start
|
Low
|
368
|
Evolutionary grade
|
600
|
19
|
Start
|
High
|
369
|
MicroRNA sequencing
|
596
|
19
|
C
|
Low
|
370
|
Biclustering
|
595
|
19
|
B
|
Mid
|
371
|
David Botstein
|
595
|
19
|
Start
|
Low
|
372
|
Synthetic virology
|
591
|
19
|
Start
|
Mid
|
373
|
Rob Knight (biologist)
|
591
|
19
|
Stub
|
Low
|
374
|
Uri Alon
|
590
|
19
|
Start
|
Low
|
375
|
Computational genomics
|
586
|
18
|
Start
|
Mid
|
376
|
Long branch attraction
|
585
|
18
|
Start
|
Low
|
377
|
Chou–Fasman method
|
583
|
18
|
B
|
Mid
|
378
|
Nicolas Rashevsky
|
574
|
18
|
B
|
Mid
|
379
|
Cross-species transmission
|
573
|
18
|
C
|
Low
|
380
|
David Goodsell
|
568
|
18
|
C
|
Low
|
381
|
CRAM (file format)
|
564
|
18
|
Start
|
Low
|
382
|
MAFFT
|
563
|
18
|
Stub
|
Mid
|
383
|
Weasel program
|
558
|
18
|
B
|
Low
|
384
|
Hiroaki Kitano
|
554
|
17
|
Start
|
Mid
|
385
|
Expasy
|
553
|
17
|
Start
|
Mid
|
386
|
Phylogenetic comparative methods
|
553
|
17
|
C
|
Mid
|
387
|
Swiss-model
|
552
|
17
|
Start
|
Mid
|
388
|
PLINK (genetic tool-set)
|
544
|
17
|
Stub
|
Low
|
389
|
PHYLIP
|
537
|
17
|
Start
|
Low
|
390
|
Ewan Birney
|
534
|
17
|
C
|
Low
|
391
|
ChIP-on-chip
|
530
|
17
|
C
|
Low
|
392
|
Group size measures
|
530
|
17
|
Start
|
Low
|
393
|
Read (biology)
|
522
|
16
|
C
|
High
|
394
|
Helen M. Berman
|
521
|
16
|
C
|
Low
|
395
|
Elasticity coefficient
|
514
|
16
|
C
|
Mid
|
396
|
Pileup format
|
507
|
16
|
Start
|
Low
|
397
|
Scoring functions for docking
|
506
|
16
|
Start
|
Mid
|
398
|
Metabolic network modelling
|
497
|
16
|
C
|
Mid
|
399
|
ARKive
|
496
|
16
|
C
|
Mid
|
400
|
Genomic organization
|
496
|
16
|
Start
|
Low
|
401
|
UniFrac
|
496
|
16
|
Stub
|
Low
|
402
|
Jay Shendure
|
496
|
16
|
Start
|
Low
|
403
|
Threading (protein sequence)
|
491
|
15
|
Start
|
High
|
404
|
DAVID
|
489
|
15
|
Start
|
Mid
|
405
|
Chromosome (genetic algorithm)
|
488
|
15
|
Start
|
Low
|
406
|
List of biodiversity databases
|
481
|
15
|
List
|
Low
|
407
|
Animal Diversity Web
|
479
|
15
|
C
|
Mid
|
408
|
Paradox of enrichment
|
470
|
15
|
Start
|
Low
|
409
|
David J. Lipman
|
470
|
15
|
Start
|
Low
|
410
|
Pyotr Anokhin
|
469
|
15
|
Start
|
Low
|
411
|
Crystallography Open Database
|
465
|
15
|
Stub
|
Low
|
412
|
Bernd Sturmfels
|
462
|
14
|
Stub
|
Low
|
413
|
Alston Scott Householder
|
461
|
14
|
Start
|
Low
|
414
|
MUSCLE (alignment software)
|
459
|
14
|
Start
|
Mid
|
415
|
Anduril (workflow engine)
|
457
|
14
|
B
|
Low
|
416
|
Demographic and Health Surveys
|
455
|
14
|
B
|
Low
|
417
|
Edward C. Holmes
|
455
|
14
|
Start
|
Low
|
418
|
Dryad (repository)
|
453
|
14
|
Start
|
Low
|
419
|
Digital phenotyping
|
451
|
14
|
Start
|
Low
|
420
|
Sequence database
|
450
|
14
|
Start
|
Mid
|
421
|
Ordinal priority approach
|
450
|
14
|
C
|
Unknown
|
422
|
List of alignment visualization software
|
449
|
14
|
List
|
Mid
|
423
|
Eugene Myers
|
448
|
14
|
Start
|
Low
|
424
|
RasMol
|
444
|
14
|
Start
|
Mid
|
425
|
List of MeSH codes
|
440
|
14
|
List
|
Mid
|
426
|
Cyrus Chothia
|
438
|
14
|
Start
|
Low
|
427
|
Human Protein Atlas
|
437
|
14
|
Start
|
Low
|
428
|
Dynamic energy budget theory
|
434
|
14
|
C
|
Low
|
429
|
Hindmarsh–Rose model
|
433
|
13
|
Stub
|
Low
|
430
|
Robinson–Foulds metric
|
432
|
13
|
C
|
Low
|
431
|
Binning (metagenomics)
|
432
|
13
|
Start
|
Low
|
432
|
FreeSurfer
|
431
|
13
|
Start
|
Mid
|
433
|
Morris–Lecar model
|
430
|
13
|
Start
|
Low
|
434
|
List of gene prediction software
|
428
|
13
|
List
|
Mid
|
435
|
Molecular models of DNA
|
426
|
13
|
B
|
Mid
|
436
|
Circular permutation in proteins
|
420
|
13
|
GA
|
Low
|
437
|
SNPedia
|
416
|
13
|
Start
|
Low
|
438
|
Taxonomic database
|
414
|
13
|
Start
|
Mid
|
439
|
Mikhail Gelfand
|
413
|
13
|
Stub
|
Mid
|
440
|
FlowJo
|
405
|
13
|
Start
|
Low
|
441
|
Steven Salzberg
|
402
|
12
|
Start
|
Low
|
442
|
Next-generation matrix
|
402
|
12
|
Start
|
Low
|
443
|
PSIPRED
|
401
|
12
|
Start
|
High
|
444
|
Ehud Shapiro
|
396
|
12
|
Start
|
Low
|
445
|
Genome browser
|
395
|
12
|
List
|
High
|
446
|
Structural genomics
|
394
|
12
|
Start
|
High
|
447
|
Codon Adaptation Index
|
394
|
12
|
Stub
|
Low
|
448
|
List of omics topics in biology
|
389
|
12
|
List
|
Low
|
449
|
Arthur Winfree
|
388
|
12
|
Start
|
Low
|
450
|
BMC Bioinformatics
|
388
|
12
|
C
|
Low
|
451
|
Haplotype estimation
|
387
|
12
|
Start
|
Low
|
452
|
Allen Brain Atlas
|
386
|
12
|
C
|
Mid
|
453
|
100,000 Genomes Project
|
386
|
12
|
C
|
Low
|
454
|
Protein function prediction
|
384
|
12
|
Start
|
High
|
455
|
Russ Altman
|
383
|
12
|
C
|
Mid
|
456
|
Phylogenetic bracketing
|
381
|
12
|
Start
|
Low
|
457
|
FlyBase
|
378
|
12
|
Start
|
Mid
|
458
|
Richard M. Durbin
|
372
|
12
|
C
|
Low
|
459
|
Orphanet
|
370
|
11
|
C
|
Low
|
460
|
Overton Prize
|
367
|
11
|
Start
|
Low
|
461
|
Consensus CDS Project
|
365
|
11
|
C
|
Low
|
462
|
Mouse Genome Informatics
|
362
|
11
|
Stub
|
Low
|
463
|
Briefings in Bioinformatics
|
360
|
11
|
Start
|
Low
|
464
|
Reactome
|
359
|
11
|
Start
|
Low
|
465
|
Genetic operator
|
356
|
11
|
Start
|
Low
|
466
|
Diseases Database
|
355
|
11
|
Start
|
Mid
|
467
|
Eran Segal
|
354
|
11
|
Start
|
Low
|
468
|
Low complexity regions in proteins
|
352
|
11
|
Start
|
Mid
|
469
|
Epitranscriptome
|
350
|
11
|
B
|
Low
|
470
|
BLAT (bioinformatics)
|
349
|
11
|
B
|
Low
|
471
|
Joseph DeRisi
|
347
|
11
|
Start
|
Low
|
472
|
Dana Pe'er
|
347
|
11
|
B
|
Mid
|
473
|
Direct coupling analysis
|
347
|
11
|
C
|
Low
|
474
|
CUT&Tag sequencing
|
347
|
11
|
Start
|
Low
|
475
|
High-frequency oscillations
|
346
|
11
|
C
|
Low
|
476
|
SPAdes (software)
|
344
|
11
|
C
|
Low
|
477
|
WPGMA
|
343
|
11
|
C
|
Low
|
478
|
Peter Donnelly
|
339
|
10
|
Start
|
Low
|
479
|
OBO Foundry
|
339
|
10
|
B
|
Mid
|
480
|
ADMIXTOOLS
|
339
|
10
|
Stub
|
Low
|
481
|
UGENE
|
336
|
10
|
C
|
Low
|
482
|
GENSCAN
|
335
|
10
|
Stub
|
Mid
|
483
|
Synthetic life
|
334
|
10
|
Redirect
|
NA
|
484
|
Consumer-resource model
|
333
|
10
|
B
|
Unknown
|
485
|
David Haussler
|
332
|
10
|
C
|
Low
|
486
|
Metabolic flux analysis
|
332
|
10
|
Stub
|
Low
|
487
|
Atul Butte
|
330
|
10
|
Start
|
Mid
|
488
|
Coot (software)
|
329
|
10
|
Start
|
Low
|
489
|
Metabolic control analysis
|
328
|
10
|
B
|
High
|
490
|
PANTHER
|
328
|
10
|
C
|
Low
|
491
|
Swiss Institute of Bioinformatics
|
327
|
10
|
Start
|
Low
|
492
|
Hypercycle (chemistry)
|
327
|
10
|
B
|
Low
|
493
|
Glycomics
|
326
|
10
|
Start
|
Low
|
494
|
Cellular model
|
324
|
10
|
Start
|
Mid
|
495
|
List of disorder prediction software
|
324
|
10
|
List
|
Low
|
496
|
Carl Bergstrom
|
322
|
10
|
Stub
|
Low
|
497
|
DNA adenine methyltransferase identification
|
320
|
10
|
Start
|
Low
|
498
|
Ancestral reconstruction
|
319
|
10
|
B
|
Low
|
499
|
SBML
|
318
|
10
|
B
|
High
|
500
|
Erez Lieberman Aiden
|
318
|
10
|
GA
|
Low
|