Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
CRISPR
|
41,811
|
1,393
|
B
|
Top
|
2
|
Receiver operating characteristic
|
37,642
|
1,254
|
B
|
Mid
|
3
|
Dynamic programming
|
27,643
|
921
|
B
|
Top
|
4
|
Last universal common ancestor
|
25,529
|
850
|
GA
|
Mid
|
5
|
Hidden Markov model
|
24,756
|
825
|
GA
|
Top
|
6
|
National Center for Biotechnology Information
|
24,719
|
823
|
C
|
Low
|
7
|
Systems theory
|
24,518
|
817
|
C
|
Mid
|
8
|
Bioinformatics
|
24,392
|
813
|
C
|
Top
|
9
|
Clade
|
23,742
|
791
|
C
|
Mid
|
10
|
Genome
|
20,081
|
669
|
C
|
High
|
11
|
DNA sequencing
|
19,295
|
643
|
C
|
High
|
12
|
Phylogenetic tree
|
19,051
|
635
|
B
|
Top
|
13
|
23andMe
|
18,686
|
622
|
C
|
Low
|
14
|
Michaelis–Menten kinetics
|
18,458
|
615
|
B
|
Top
|
15
|
Cellular automaton
|
17,107
|
570
|
B
|
Low
|
16
|
Phylogenetics
|
14,849
|
494
|
C
|
Top
|
17
|
Ontology (information science)
|
13,779
|
459
|
C
|
High
|
18
|
Sanger sequencing
|
13,483
|
449
|
C
|
Mid
|
19
|
AlphaFold
|
13,291
|
443
|
C
|
High
|
20
|
PubMed Central
|
13,241
|
441
|
B
|
Mid
|
21
|
FASTA format
|
11,647
|
388
|
B
|
High
|
22
|
Heat map
|
11,354
|
378
|
Start
|
High
|
23
|
Most recent common ancestor
|
10,191
|
339
|
B
|
High
|
24
|
Compartmental models in epidemiology
|
9,807
|
326
|
C
|
Mid
|
25
|
Synthetic biology
|
9,515
|
317
|
B
|
Mid
|
26
|
Cladistics
|
9,504
|
316
|
C
|
Mid
|
27
|
BLAST (biotechnology)
|
9,325
|
310
|
C
|
Top
|
28
|
Genomics
|
9,242
|
308
|
B
|
High
|
29
|
Whole genome sequencing
|
8,690
|
289
|
B
|
High
|
30
|
FASTQ format
|
8,028
|
267
|
B
|
Mid
|
31
|
Biostatistics
|
8,026
|
267
|
B
|
Top
|
32
|
Sequence alignment
|
7,907
|
263
|
C
|
High
|
33
|
RNA-Seq
|
7,862
|
262
|
B
|
Top
|
34
|
List of algorithms
|
7,773
|
259
|
List
|
Mid
|
35
|
Computational biology
|
7,622
|
254
|
C
|
Top
|
36
|
Phi coefficient
|
7,348
|
244
|
Start
|
Mid
|
37
|
DNA microarray
|
7,332
|
244
|
B
|
Top
|
38
|
Lineweaver–Burk plot
|
6,939
|
231
|
B
|
Low
|
39
|
Petri net
|
6,881
|
229
|
B
|
Low
|
40
|
PubChem
|
6,799
|
226
|
Start
|
Mid
|
41
|
Proteomics
|
6,741
|
224
|
C
|
High
|
42
|
Illumina, Inc.
|
6,709
|
223
|
C
|
Low
|
43
|
Mathematical and theoretical biology
|
6,519
|
217
|
C
|
Top
|
44
|
Omics
|
6,511
|
217
|
C
|
Mid
|
45
|
Protein Data Bank
|
6,254
|
208
|
C
|
High
|
46
|
Needleman–Wunsch algorithm
|
6,203
|
206
|
Start
|
Mid
|
47
|
Metagenomics
|
6,047
|
201
|
GA
|
Mid
|
48
|
Variant Call Format
|
5,986
|
199
|
Start
|
Mid
|
49
|
Medical Subject Headings
|
5,871
|
195
|
C
|
Mid
|
50
|
DNA barcoding
|
5,695
|
189
|
B
|
High
|
51
|
Docking (molecular)
|
5,680
|
189
|
B
|
High
|
52
|
Folding@home
|
5,637
|
187
|
B
|
Mid
|
53
|
Smith–Waterman algorithm
|
5,421
|
180
|
B
|
Top
|
54
|
Single-cell sequencing
|
5,346
|
178
|
C
|
High
|
55
|
Multiple sequence alignment
|
5,259
|
175
|
Unknown
|
High
|
56
|
Gene nomenclature
|
5,251
|
175
|
Start
|
Mid
|
57
|
George Church (geneticist)
|
5,232
|
174
|
C
|
Mid
|
58
|
Systems biology
|
5,176
|
172
|
C
|
Top
|
59
|
Genome-wide association study
|
5,137
|
171
|
GA
|
High
|
60
|
Computational neuroscience
|
5,029
|
167
|
C
|
Top
|
61
|
Baum–Welch algorithm
|
4,785
|
159
|
C
|
Mid
|
62
|
Non-coding DNA
|
4,754
|
158
|
C
|
Low
|
63
|
Spurious relationship
|
4,732
|
157
|
Start
|
Low
|
64
|
Phred quality score
|
4,716
|
157
|
Start
|
Mid
|
65
|
STR analysis
|
4,618
|
153
|
Start
|
Low
|
66
|
Molecular clock
|
4,512
|
150
|
C
|
High
|
67
|
BLOSUM
|
4,500
|
150
|
C
|
High
|
68
|
High-throughput screening
|
4,494
|
149
|
B
|
Low
|
69
|
Exome sequencing
|
4,426
|
147
|
C
|
High
|
70
|
Metabolomics
|
4,337
|
144
|
C
|
Mid
|
71
|
Burrows–Wheeler transform
|
4,272
|
142
|
C
|
Mid
|
72
|
Combined DNA Index System
|
4,234
|
141
|
GA
|
Low
|
73
|
Multiomics
|
4,109
|
136
|
C
|
High
|
74
|
Junk DNA
|
4,097
|
136
|
B
|
Low
|
75
|
Nanopore sequencing
|
4,046
|
134
|
C
|
Low
|
76
|
Europe PubMed Central
|
4,041
|
134
|
Start
|
Low
|
77
|
Gene set enrichment analysis
|
3,984
|
132
|
C
|
Mid
|
78
|
Crossover (genetic algorithm)
|
3,947
|
131
|
B
|
Low
|
79
|
Similarity measure
|
3,940
|
131
|
Start
|
Mid
|
80
|
Protein structure prediction
|
3,919
|
130
|
B
|
High
|
81
|
KNIME
|
3,791
|
126
|
Start
|
Low
|
82
|
Gene Ontology
|
3,788
|
126
|
C
|
High
|
83
|
Illumina dye sequencing
|
3,762
|
125
|
C
|
Mid
|
84
|
List of mass spectrometry software
|
3,754
|
125
|
List
|
Low
|
85
|
ATAC-seq
|
3,730
|
124
|
Start
|
Low
|
86
|
Monod equation
|
3,702
|
123
|
Start
|
Low
|
87
|
What Is Life?
|
3,646
|
121
|
C
|
Low
|
88
|
K-mer
|
3,603
|
120
|
B
|
Mid
|
89
|
Brain mapping
|
3,587
|
119
|
Start
|
Low
|
90
|
Volcano plot (statistics)
|
3,529
|
117
|
C
|
Mid
|
91
|
Root mean square deviation of atomic positions
|
3,516
|
117
|
Start
|
Mid
|
92
|
N50, L50, and related statistics
|
3,494
|
116
|
Start
|
Low
|
93
|
Intrinsically disordered proteins
|
3,492
|
116
|
Start
|
Mid
|
94
|
Protein–protein interaction
|
3,474
|
115
|
C
|
High
|
95
|
Jmol
|
3,462
|
115
|
Start
|
Mid
|
96
|
Data wrangling
|
3,449
|
114
|
Start
|
Low
|
97
|
Bioconductor
|
3,442
|
114
|
C
|
Mid
|
98
|
Martin Kulldorff
|
3,396
|
113
|
B
|
Low
|
99
|
GenBank
|
3,363
|
112
|
Start
|
High
|
100
|
BED (file format)
|
3,363
|
112
|
C
|
Low
|
101
|
KEGG
|
3,356
|
111
|
C
|
High
|
102
|
Genetic programming
|
3,333
|
111
|
B
|
Mid
|
103
|
Transcriptome
|
3,323
|
110
|
B
|
High
|
104
|
Environmental DNA
|
3,312
|
110
|
B
|
Low
|
105
|
SAM (file format)
|
3,292
|
109
|
Start
|
Mid
|
106
|
Biological computing
|
3,241
|
108
|
C
|
Mid
|
107
|
Microarray
|
3,232
|
107
|
Start
|
Top
|
108
|
UniProt
|
3,166
|
105
|
Start
|
High
|
109
|
Daphne Koller
|
3,131
|
104
|
C
|
Low
|
110
|
Denis Noble
|
3,108
|
103
|
Start
|
Low
|
111
|
ChIP sequencing
|
3,106
|
103
|
C
|
Mid
|
112
|
Spatial transcriptomics
|
3,081
|
102
|
Start
|
Low
|
113
|
Clustal
|
3,073
|
102
|
Start
|
Mid
|
114
|
David Baker (biochemist)
|
3,053
|
101
|
Start
|
Low
|
115
|
Broad Institute
|
3,048
|
101
|
Start
|
Low
|
116
|
Robert Gentleman (statistician)
|
2,892
|
96
|
Start
|
Mid
|
117
|
Isomorphic Labs
|
2,871
|
95
|
Stub
|
Low
|
118
|
Conserved sequence
|
2,785
|
92
|
C
|
High
|
119
|
List of biological databases
|
2,733
|
91
|
List
|
High
|
120
|
10x Genomics
|
2,718
|
90
|
Start
|
Mid
|
121
|
Genome size
|
2,601
|
86
|
B
|
Mid
|
122
|
Protein Data Bank (file format)
|
2,594
|
86
|
Start
|
Mid
|
123
|
Ludwig von Bertalanffy
|
2,592
|
86
|
Start
|
Low
|
124
|
Transcriptomics technologies
|
2,576
|
85
|
GA
|
High
|
125
|
List of sequence alignment software
|
2,565
|
85
|
List
|
High
|
126
|
Molecular phylogenetics
|
2,536
|
84
|
C
|
High
|
127
|
John Maynard Smith
|
2,514
|
83
|
C
|
Mid
|
128
|
PyMOL
|
2,511
|
83
|
Start
|
Low
|
129
|
Distance matrix
|
2,502
|
83
|
Start
|
High
|
130
|
FitzHugh–Nagumo model
|
2,488
|
82
|
C
|
Low
|
131
|
Wikispecies
|
2,467
|
82
|
Start
|
Mid
|
132
|
Aviv Regev
|
2,429
|
80
|
Start
|
Low
|
133
|
Maximum parsimony (phylogenetics)
|
2,428
|
80
|
C
|
High
|
134
|
UPGMA
|
2,420
|
80
|
C
|
Low
|
135
|
Genetic distance
|
2,405
|
80
|
B
|
Mid
|
136
|
Kabsch algorithm
|
2,398
|
79
|
Start
|
Mid
|
137
|
Gene regulatory network
|
2,397
|
79
|
B
|
High
|
138
|
European Molecular Biology Laboratory
|
2,378
|
79
|
C
|
Low
|
139
|
Oxford Nanopore Technologies
|
2,365
|
78
|
Start
|
Low
|
140
|
Reference genome
|
2,305
|
76
|
Start
|
Low
|
141
|
Andrew Huxley
|
2,301
|
76
|
C
|
Low
|
142
|
Pan-genome
|
2,267
|
75
|
C
|
Mid
|
143
|
Polygenic score
|
2,266
|
75
|
C
|
Mid
|
144
|
List of protein structure prediction software
|
2,265
|
75
|
List
|
Mid
|
145
|
DNA annotation
|
2,264
|
75
|
Start
|
Low
|
146
|
Consensus sequence
|
2,217
|
73
|
Start
|
High
|
147
|
Synteny
|
2,159
|
71
|
Start
|
Low
|
148
|
Neighbor joining
|
2,134
|
71
|
C
|
High
|
149
|
Biological database
|
2,064
|
68
|
Start
|
High
|
150
|
Schrödinger, Inc.
|
2,058
|
68
|
Start
|
Low
|
151
|
Proteome
|
2,056
|
68
|
C
|
High
|
152
|
Topologically associating domain
|
2,040
|
68
|
C
|
Low
|
153
|
Catalogue of Life
|
2,039
|
67
|
C
|
Low
|
154
|
Global Biodiversity Information Facility
|
2,028
|
67
|
Start
|
Low
|
155
|
Biochip
|
1,998
|
66
|
C
|
Low
|
156
|
Metabarcoding
|
1,971
|
65
|
B
|
Low
|
157
|
Fitness function
|
1,957
|
65
|
Start
|
Mid
|
158
|
Online Mendelian Inheritance in Man
|
1,945
|
64
|
Start
|
Mid
|
159
|
Mathematical modelling of infectious diseases
|
1,926
|
64
|
C
|
Low
|
160
|
Approximate Bayesian computation
|
1,919
|
63
|
B
|
Low
|
161
|
Phylogeny
|
1,916
|
63
|
Redirect
|
NA
|
162
|
FASTA
|
1,901
|
63
|
B
|
High
|
163
|
Superspreading event
|
1,895
|
63
|
C
|
High
|
164
|
EBird
|
1,870
|
62
|
Start
|
Low
|
165
|
Sequence motif
|
1,868
|
62
|
Start
|
High
|
166
|
Contig
|
1,867
|
62
|
C
|
High
|
167
|
UCSC Genome Browser
|
1,864
|
62
|
Start
|
High
|
168
|
Data curation
|
1,859
|
61
|
Start
|
Mid
|
169
|
DNA sequencer
|
1,851
|
61
|
Start
|
Low
|
170
|
Homology modeling
|
1,836
|
61
|
B
|
High
|
171
|
DbSNP
|
1,835
|
61
|
B
|
Mid
|
172
|
Mutation (genetic algorithm)
|
1,831
|
61
|
Start
|
Low
|
173
|
ChEMBL
|
1,827
|
60
|
Start
|
Mid
|
174
|
UK Biobank
|
1,818
|
60
|
B
|
Low
|
175
|
SNP array
|
1,780
|
59
|
Start
|
High
|
176
|
Point accepted mutation
|
1,773
|
59
|
B
|
High
|
177
|
Binary Alignment Map
|
1,773
|
59
|
Stub
|
Mid
|
178
|
Outgroup (cladistics)
|
1,739
|
57
|
Start
|
Mid
|
179
|
Functional genomics
|
1,723
|
57
|
C
|
High
|
180
|
Michael Levitt
|
1,716
|
57
|
C
|
Low
|
181
|
STRING
|
1,708
|
56
|
B
|
Low
|
182
|
Haar-like feature
|
1,705
|
56
|
C
|
Low
|
183
|
Cyberneticist
|
1,701
|
56
|
Stub
|
Low
|
184
|
Indel
|
1,700
|
56
|
Start
|
Low
|
185
|
Chromosome conformation capture
|
1,692
|
56
|
C
|
Low
|
186
|
Computational phylogenetics
|
1,690
|
56
|
C
|
High
|
187
|
Models of DNA evolution
|
1,687
|
56
|
B
|
Mid
|
188
|
List of open-source bioinformatics software
|
1,683
|
56
|
List
|
High
|
189
|
Pfam
|
1,662
|
55
|
B
|
High
|
190
|
Amino acid replacement
|
1,646
|
54
|
Start
|
High
|
191
|
Position weight matrix
|
1,626
|
54
|
C
|
Top
|
192
|
European Bioinformatics Institute
|
1,623
|
54
|
C
|
Low
|
193
|
Gene family
|
1,562
|
52
|
C
|
High
|
194
|
General feature format
|
1,560
|
52
|
Start
|
Low
|
195
|
Pardis Sabeti
|
1,543
|
51
|
B
|
Low
|
196
|
AMBER
|
1,531
|
51
|
C
|
Mid
|
197
|
Ensembl genome database project
|
1,528
|
50
|
B
|
High
|
198
|
Substitution model
|
1,514
|
50
|
B
|
Mid
|
199
|
Population structure (genetics)
|
1,493
|
49
|
Start
|
Low
|
200
|
Alan Hodgkin
|
1,473
|
49
|
Start
|
Low
|
201
|
C. H. Waddington
|
1,469
|
48
|
C
|
Low
|
202
|
Ukkonen's algorithm
|
1,467
|
48
|
Stub
|
Low
|
203
|
Solvation shell
|
1,464
|
48
|
Start
|
Low
|
204
|
Weighted correlation network analysis
|
1,464
|
48
|
B
|
Low
|
205
|
Sequence analysis
|
1,462
|
48
|
C
|
Top
|
206
|
Foundational Model of Anatomy
|
1,455
|
48
|
Start
|
Low
|
207
|
1000 Genomes Project
|
1,452
|
48
|
B
|
Low
|
208
|
List of RNA-Seq bioinformatics tools
|
1,442
|
48
|
List
|
Mid
|
209
|
Biobank
|
1,438
|
47
|
Start
|
High
|
210
|
Rosetta@home
|
1,434
|
47
|
C
|
Mid
|
211
|
FishBase
|
1,428
|
47
|
Start
|
Low
|
212
|
Comparative genomics
|
1,427
|
47
|
C
|
Top
|
213
|
AutoDock
|
1,426
|
47
|
Start
|
Mid
|
214
|
Biochemical cascade
|
1,405
|
46
|
C
|
Mid
|
215
|
DNA database
|
1,395
|
46
|
Start
|
Mid
|
216
|
CASP
|
1,393
|
46
|
C
|
Mid
|
217
|
List of phylogenetics software
|
1,392
|
46
|
List
|
High
|
218
|
Single-cell transcriptomics
|
1,386
|
46
|
C
|
Mid
|
219
|
Metabolome
|
1,384
|
46
|
C
|
High
|
220
|
Encyclopedia of Life
|
1,384
|
46
|
Start
|
Mid
|
221
|
Sequence assembly
|
1,381
|
46
|
Start
|
High
|
222
|
Virtual screening
|
1,369
|
45
|
Start
|
High
|
223
|
Cable theory
|
1,366
|
45
|
C
|
Mid
|
224
|
Gene expression profiling
|
1,362
|
45
|
B
|
High
|
225
|
RefSeq
|
1,362
|
45
|
Start
|
Mid
|
226
|
RNA integrity number
|
1,351
|
45
|
Stub
|
Low
|
227
|
Wellcome Sanger Institute
|
1,347
|
44
|
C
|
Low
|
228
|
ChEBI
|
1,342
|
44
|
Start
|
Low
|
229
|
Gene prediction
|
1,341
|
44
|
C
|
High
|
230
|
Gap penalty
|
1,337
|
44
|
C
|
High
|
231
|
Cooperative binding
|
1,335
|
44
|
B
|
Mid
|
232
|
Protein family
|
1,330
|
44
|
Start
|
High
|
233
|
Microarray analysis techniques
|
1,326
|
44
|
B
|
Mid
|
234
|
Celera Corporation
|
1,313
|
43
|
Start
|
Low
|
235
|
MA plot
|
1,307
|
43
|
Start
|
Low
|
236
|
Matthews correlation coefficient
|
1,304
|
43
|
Redirect
|
NA
|
237
|
GROMACS
|
1,302
|
43
|
Start
|
Low
|
238
|
Sequence logo
|
1,301
|
43
|
B
|
Mid
|
239
|
Theoretical ecology
|
1,294
|
43
|
B
|
High
|
240
|
Entrez
|
1,289
|
42
|
Start
|
Mid
|
241
|
Manolis Kellis
|
1,279
|
42
|
C
|
Low
|
242
|
Margaret Oakley Dayhoff
|
1,278
|
42
|
B
|
High
|
243
|
GeneCards
|
1,278
|
42
|
C
|
Mid
|
244
|
Amplicon sequence variant
|
1,273
|
42
|
Start
|
Low
|
245
|
Tournament selection
|
1,269
|
42
|
Start
|
Low
|
246
|
ENCODE
|
1,247
|
41
|
C
|
Mid
|
247
|
Bayesian inference in phylogeny
|
1,234
|
41
|
C
|
High
|
248
|
NanoString Technologies
|
1,234
|
41
|
Start
|
Low
|
249
|
Knowledge engineering
|
1,213
|
40
|
Start
|
Low
|
250
|
Structural Classification of Proteins database
|
1,209
|
40
|
Start
|
High
|
251
|
Hirschberg's algorithm
|
1,202
|
40
|
B
|
Low
|
252
|
Molecular Evolutionary Genetics Analysis
|
1,197
|
39
|
Start
|
Low
|
253
|
List of protein-ligand docking software
|
1,192
|
39
|
List
|
Mid
|
254
|
Probabilistic context-free grammar
|
1,181
|
39
|
B
|
High
|
255
|
Vito Volterra
|
1,177
|
39
|
C
|
Low
|
256
|
DNA Data Bank of Japan
|
1,161
|
38
|
Stub
|
Low
|
257
|
DSSP (algorithm)
|
1,158
|
38
|
Start
|
Low
|
258
|
MGI (company)
|
1,137
|
37
|
C
|
Low
|
259
|
Eadie–Hofstee diagram
|
1,131
|
37
|
Start
|
Low
|
260
|
Biological systems engineering
|
1,130
|
37
|
Start
|
Low
|
261
|
Substitution matrix
|
1,120
|
37
|
C
|
High
|
262
|
D'Arcy Wentworth Thompson
|
1,108
|
36
|
GA
|
Mid
|
263
|
Leroy Hood
|
1,105
|
36
|
B
|
Low
|
264
|
Ion semiconductor sequencing
|
1,075
|
35
|
C
|
Low
|
265
|
Institute of Genomics and Integrative Biology
|
1,064
|
35
|
C
|
Low
|
266
|
Dot plot (bioinformatics)
|
1,056
|
35
|
Start
|
Mid
|
267
|
Open Tree of Life
|
1,049
|
34
|
Start
|
Low
|
268
|
Umbrella sampling
|
1,040
|
34
|
Start
|
Low
|
269
|
Sepp Hochreiter
|
1,038
|
34
|
Start
|
Low
|
270
|
CATH database
|
1,033
|
34
|
Start
|
Mid
|
271
|
Cytoscape
|
1,023
|
34
|
B
|
High
|
272
|
Protein contact map
|
1,012
|
33
|
Start
|
Mid
|
273
|
List of RNA structure prediction software
|
1,002
|
33
|
List
|
Low
|
274
|
Motoo Kimura
|
991
|
33
|
C
|
High
|
275
|
Structural bioinformatics
|
972
|
32
|
B
|
High
|
276
|
Conservative replacement
|
967
|
32
|
Start
|
Low
|
277
|
Attack rate
|
960
|
32
|
Start
|
Mid
|
278
|
Protein superfamily
|
960
|
32
|
B
|
High
|
279
|
Network motif
|
958
|
31
|
B
|
Low
|
280
|
Lior Pachter
|
957
|
31
|
Start
|
Mid
|
281
|
List of bioinformatics journals
|
953
|
31
|
List
|
Low
|
282
|
List of human protein-coding genes 1
|
951
|
31
|
List
|
High
|
283
|
List of phylogenetic tree visualization software
|
947
|
31
|
List
|
Mid
|
284
|
All of Us (initiative)
|
946
|
31
|
C
|
Low
|
285
|
Boolean network
|
935
|
31
|
C
|
Mid
|
286
|
HMMER
|
931
|
31
|
B
|
High
|
287
|
Biological network
|
924
|
30
|
C
|
High
|
288
|
Biopython
|
922
|
30
|
C
|
High
|
289
|
UCSF Chimera
|
913
|
30
|
Start
|
Low
|
290
|
Cross-species transmission
|
913
|
30
|
C
|
Low
|
291
|
Chromosome (genetic algorithm)
|
909
|
30
|
Start
|
Low
|
292
|
PROSITE
|
908
|
30
|
Start
|
High
|
293
|
Hanes–Woolf plot
|
904
|
30
|
Start
|
Low
|
294
|
Ecosystem model
|
892
|
29
|
Start
|
Mid
|
295
|
Co-occurrence network
|
889
|
29
|
Start
|
Low
|
296
|
RasMol
|
888
|
29
|
Start
|
Mid
|
297
|
Accession number (bioinformatics)
|
884
|
29
|
Start
|
Low
|
298
|
Interactome
|
882
|
29
|
C
|
Mid
|
299
|
List of sequenced animal genomes
|
879
|
29
|
List
|
Mid
|
300
|
Batch effect
|
879
|
29
|
Stub
|
Low
|
301
|
CUT&RUN sequencing
|
877
|
29
|
C
|
Low
|
302
|
Lipidomics
|
875
|
29
|
C
|
Low
|
303
|
Protein design
|
869
|
28
|
C
|
Mid
|
304
|
List of neuroscience databases
|
868
|
28
|
List
|
Low
|
305
|
Rob Knight (biologist)
|
866
|
28
|
Stub
|
Low
|
306
|
Template modeling score
|
848
|
28
|
Start
|
Low
|
307
|
Barry Smith (ontologist)
|
846
|
28
|
C
|
Low
|
308
|
ABI Solid Sequencing
|
845
|
28
|
Start
|
Low
|
309
|
CHARMM
|
843
|
28
|
B
|
Mid
|
310
|
McDonald–Kreitman test
|
839
|
27
|
C
|
Mid
|
311
|
Paradox of the plankton
|
837
|
27
|
Start
|
Low
|
312
|
DeCODE genetics
|
830
|
27
|
Start
|
Low
|
313
|
Avogadro (software)
|
820
|
27
|
Stub
|
Low
|
314
|
Scoring functions for docking
|
815
|
27
|
Start
|
Mid
|
315
|
Flux balance analysis
|
814
|
27
|
B
|
High
|
316
|
Machine learning in bioinformatics
|
812
|
27
|
C
|
High
|
317
|
Trajectory inference
|
808
|
26
|
C
|
Low
|
318
|
Expasy
|
803
|
26
|
Start
|
Mid
|
319
|
Synthetic biological circuit
|
795
|
26
|
Start
|
Low
|
320
|
Galaxy (computational biology)
|
779
|
25
|
Start
|
High
|
321
|
Monod–Wyman–Changeux model
|
775
|
25
|
Start
|
Mid
|
322
|
Protein tandem repeats
|
770
|
25
|
Start
|
Mid
|
323
|
Sarah Teichmann
|
769
|
25
|
C
|
Low
|
324
|
Paradox of enrichment
|
767
|
25
|
Start
|
Low
|
325
|
Read (biology)
|
763
|
25
|
C
|
High
|
326
|
Eric Xing
|
760
|
25
|
Stub
|
Low
|
327
|
Swiss-model
|
759
|
25
|
Start
|
Mid
|
328
|
Mass spectrometry data format
|
757
|
25
|
Start
|
Low
|
329
|
List of sequenced eukaryotic genomes
|
757
|
25
|
List
|
Mid
|
330
|
SAMtools
|
753
|
25
|
Start
|
Low
|
331
|
PHYLIP
|
749
|
24
|
Start
|
Low
|
332
|
Centre for DNA Fingerprinting and Diagnostics
|
743
|
24
|
Start
|
Low
|
333
|
Michael Eisen
|
737
|
24
|
Start
|
Low
|
334
|
Protein structure database
|
735
|
24
|
Start
|
Low
|
335
|
Computational genomics
|
731
|
24
|
Start
|
Mid
|
336
|
Polytomy
|
725
|
24
|
Start
|
Low
|
337
|
Modelling biological systems
|
719
|
23
|
C
|
High
|
338
|
Biological data visualization
|
718
|
23
|
Start
|
Mid
|
339
|
List of genetic algorithm applications
|
718
|
23
|
List
|
Low
|
340
|
Mathematical physiology
|
718
|
23
|
Stub
|
Mid
|
341
|
Systems neuroscience
|
714
|
23
|
Stub
|
Mid
|
342
|
454 Life Sciences
|
710
|
23
|
C
|
Low
|
343
|
HUGO Gene Nomenclature Committee
|
710
|
23
|
Start
|
Mid
|
344
|
De novo sequence assemblers
|
709
|
23
|
Start
|
Low
|
345
|
MAFFT
|
708
|
23
|
Stub
|
Mid
|
346
|
Bonnie Berger
|
704
|
23
|
Start
|
Low
|
347
|
Robert Rosen (biologist)
|
693
|
23
|
Start
|
Low
|
348
|
EMBOSS
|
693
|
23
|
Start
|
Mid
|
349
|
Dry lab
|
691
|
23
|
Start
|
High
|
350
|
Threading (protein sequence)
|
688
|
22
|
Start
|
High
|
351
|
Haldane's dilemma
|
686
|
22
|
B
|
Low
|
352
|
Sequence database
|
684
|
22
|
Start
|
Mid
|
353
|
InterPro
|
675
|
22
|
B
|
High
|
354
|
ChIP-on-chip
|
673
|
22
|
C
|
Low
|
355
|
Metabolic network modelling
|
672
|
22
|
C
|
Mid
|
356
|
PLOS Computational Biology
|
664
|
22
|
Start
|
High
|
357
|
Genomic organization
|
664
|
22
|
Start
|
Low
|
358
|
Chemical database
|
663
|
22
|
Start
|
Mid
|
359
|
Tree of Life Web Project
|
662
|
22
|
Start
|
Low
|
360
|
List of molecular graphics systems
|
653
|
21
|
List
|
Mid
|
361
|
Nexus file
|
651
|
21
|
Start
|
Low
|
362
|
Visual Molecular Dynamics
|
650
|
21
|
Start
|
Low
|
363
|
Long branch attraction
|
649
|
21
|
Start
|
Low
|
364
|
NK model
|
647
|
21
|
B
|
Low
|
365
|
Barcode of Life Data System
|
647
|
21
|
Stub
|
Low
|
366
|
Dana Pe'er
|
638
|
21
|
B
|
Mid
|
367
|
Binning (metagenomics)
|
636
|
21
|
Start
|
Low
|
368
|
Phylogenetic comparative methods
|
634
|
21
|
C
|
Mid
|
369
|
Biological network inference
|
630
|
21
|
C
|
Low
|
370
|
CRAM (file format)
|
629
|
20
|
Start
|
Low
|
371
|
Genome browser
|
624
|
20
|
List
|
High
|
372
|
Evolutionary grade
|
621
|
20
|
Start
|
High
|
373
|
Genetic operator
|
620
|
20
|
Start
|
Low
|
374
|
Jay Shendure
|
614
|
20
|
Start
|
Low
|
375
|
DAVID
|
612
|
20
|
Start
|
Mid
|
376
|
MUSCLE (alignment software)
|
611
|
20
|
Start
|
Mid
|
377
|
Eran Segal
|
608
|
20
|
Start
|
Low
|
378
|
Tom Blundell
|
604
|
20
|
C
|
Low
|
379
|
World Community Grid
|
603
|
20
|
C
|
Low
|
380
|
GENSCAN
|
603
|
20
|
Stub
|
Mid
|
381
|
Chou–Fasman method
|
601
|
20
|
B
|
Mid
|
382
|
Dryad (repository)
|
601
|
20
|
Start
|
Low
|
383
|
Sequence Read Archive
|
598
|
19
|
Start
|
High
|
384
|
HomoloGene
|
593
|
19
|
Start
|
Low
|
385
|
Biclustering
|
592
|
19
|
B
|
Mid
|
386
|
Uri Alon
|
591
|
19
|
Start
|
Low
|
387
|
List of alignment visualization software
|
590
|
19
|
List
|
Mid
|
388
|
Epitranscriptome
|
579
|
19
|
B
|
Low
|
389
|
PLINK (genetic tool-set)
|
577
|
19
|
Stub
|
Low
|
390
|
Reactome
|
573
|
19
|
Start
|
Low
|
391
|
List of biodiversity databases
|
573
|
19
|
List
|
Low
|
392
|
Bioinformatics (journal)
|
568
|
18
|
Start
|
High
|
393
|
MicroRNA sequencing
|
562
|
18
|
C
|
Low
|
394
|
List of gene prediction software
|
559
|
18
|
List
|
Mid
|
395
|
UniFrac
|
548
|
18
|
Stub
|
Low
|
396
|
Weasel program
|
543
|
18
|
B
|
Low
|
397
|
Mascot (software)
|
542
|
18
|
C
|
High
|
398
|
OBO Foundry
|
538
|
17
|
B
|
Mid
|
399
|
Eugene Koonin
|
535
|
17
|
Start
|
Low
|
400
|
Synthetic virology
|
532
|
17
|
Start
|
Mid
|
401
|
Genomics England
|
529
|
17
|
Start
|
Low
|
402
|
FreeSurfer
|
527
|
17
|
Start
|
Mid
|
403
|
Pileup format
|
526
|
17
|
Start
|
Low
|
404
|
Taxonomic database
|
518
|
17
|
Start
|
Mid
|
405
|
WPGMA
|
516
|
17
|
C
|
Low
|
406
|
MODELLER
|
509
|
16
|
Start
|
Mid
|
407
|
Global distance test
|
508
|
16
|
Stub
|
Low
|
408
|
Bernd Sturmfels
|
508
|
16
|
Stub
|
Low
|
409
|
GeneDx
|
501
|
16
|
Stub
|
Low
|
410
|
Structural genomics
|
499
|
16
|
Start
|
High
|
411
|
Human Protein Atlas
|
498
|
16
|
Start
|
Low
|
412
|
David Goodsell
|
489
|
16
|
C
|
Low
|
413
|
FlyBase
|
488
|
16
|
Start
|
Mid
|
414
|
Circular permutation in proteins
|
481
|
16
|
GA
|
Low
|
415
|
Crystallography Open Database
|
480
|
16
|
Stub
|
Low
|
416
|
List of omics topics in biology
|
478
|
15
|
List
|
Low
|
417
|
Stephen Altschul
|
477
|
15
|
Start
|
Low
|
418
|
Demographic and Health Surveys
|
475
|
15
|
B
|
Low
|
419
|
David Botstein
|
474
|
15
|
Start
|
Low
|
420
|
Allen Brain Atlas
|
472
|
15
|
C
|
Mid
|
421
|
Morris–Lecar model
|
471
|
15
|
Start
|
Low
|
422
|
Robinson–Foulds metric
|
469
|
15
|
C
|
Low
|
423
|
Elasticity coefficient
|
468
|
15
|
C
|
Mid
|
424
|
UniGene
|
465
|
15
|
Start
|
Low
|
425
|
100,000 Genomes Project
|
461
|
15
|
C
|
Low
|
426
|
Chemical library
|
459
|
15
|
Start
|
Low
|
427
|
IMGT
|
458
|
15
|
Start
|
Unknown
|
428
|
ARKive
|
456
|
15
|
C
|
Mid
|
429
|
De novo protein structure prediction
|
454
|
15
|
Start
|
High
|
430
|
Hypercycle (chemistry)
|
454
|
15
|
B
|
Low
|
431
|
Phylogenetic Assignment of Named Global Outbreak Lineages
|
450
|
15
|
Start
|
Low
|
432
|
List of MeSH codes
|
447
|
14
|
List
|
Mid
|
433
|
European Nucleotide Archive
|
447
|
14
|
GA
|
Mid
|
434
|
De novo transcriptome assembly
|
446
|
14
|
C
|
Mid
|
435
|
Steven Salzberg
|
441
|
14
|
Start
|
Low
|
436
|
Hindmarsh–Rose model
|
441
|
14
|
Stub
|
Low
|
437
|
Codon Adaptation Index
|
439
|
14
|
Stub
|
Low
|
438
|
Animal Diversity Web
|
438
|
14
|
C
|
Mid
|
439
|
Ewan Birney
|
433
|
14
|
Start
|
Low
|
440
|
CAZy
|
433
|
14
|
Start
|
Mid
|
441
|
SPAdes (software)
|
432
|
14
|
C
|
Low
|
442
|
Fossilworks
|
429
|
14
|
Stub
|
Low
|
443
|
Metabolic flux analysis
|
428
|
14
|
Stub
|
Low
|
444
|
Haplotype estimation
|
428
|
14
|
Start
|
Low
|
445
|
BRENDA
|
425
|
14
|
Start
|
Mid
|
446
|
Protein function prediction
|
424
|
14
|
Start
|
High
|
447
|
Energy charge
|
414
|
13
|
Start
|
Low
|
448
|
Dehaene–Changeux model
|
413
|
13
|
Start
|
Low
|
449
|
Diseases Database
|
412
|
13
|
Start
|
Mid
|
450
|
Pyotr Anokhin
|
410
|
13
|
Start
|
Low
|
451
|
FlowJo
|
409
|
13
|
Start
|
Low
|
452
|
Edward C. Holmes
|
405
|
13
|
Start
|
Low
|
453
|
Analysis of molecular variance
|
404
|
13
|
Stub
|
Low
|
454
|
Glycomics
|
402
|
13
|
Start
|
Low
|
455
|
Ehud Shapiro
|
401
|
13
|
Start
|
Low
|
456
|
PSIPRED
|
401
|
13
|
Start
|
High
|
457
|
BLAT (bioinformatics)
|
400
|
13
|
B
|
Low
|
458
|
BMC Bioinformatics
|
399
|
13
|
C
|
Low
|
459
|
CUT&Tag sequencing
|
398
|
13
|
Start
|
Low
|
460
|
Next-generation matrix
|
397
|
13
|
Start
|
Low
|
461
|
SBML
|
396
|
13
|
B
|
High
|
462
|
Joseph DeRisi
|
393
|
13
|
Start
|
Low
|
463
|
UGENE
|
392
|
13
|
C
|
Low
|
464
|
Ancestral reconstruction
|
390
|
13
|
B
|
Low
|
465
|
David Haussler
|
386
|
12
|
C
|
Low
|
466
|
Conserved Domain Database
|
385
|
12
|
Start
|
Low
|
467
|
Nicolas Rashevsky
|
379
|
12
|
B
|
Mid
|
468
|
Unique molecular identifier
|
378
|
12
|
Stub
|
Low
|
469
|
Epigenome-wide association study
|
378
|
12
|
C
|
Low
|
470
|
Saccharomyces Genome Database
|
377
|
12
|
Start
|
High
|
471
|
Putative gene
|
377
|
12
|
Start
|
Mid
|
472
|
Digital phenotyping
|
370
|
12
|
Start
|
Low
|
473
|
Fungal DNA barcoding
|
369
|
12
|
C
|
Low
|
474
|
Evolutionary tree
|
368
|
12
|
Redirect
|
NA
|
475
|
Sequence clustering
|
365
|
12
|
Start
|
Mid
|
476
|
High-frequency oscillations
|
363
|
12
|
C
|
Low
|
477
|
International Nucleotide Sequence Database Collaboration
|
362
|
12
|
Stub
|
Mid
|
478
|
Alston Scott Householder
|
362
|
12
|
Start
|
Low
|
479
|
Consensus CDS Project
|
362
|
12
|
C
|
Low
|
480
|
Protein–protein interaction prediction
|
358
|
11
|
Start
|
High
|
481
|
T-Coffee
|
357
|
11
|
Start
|
Mid
|
482
|
Maqsudul Alam
|
357
|
11
|
Stub
|
Low
|
483
|
Imaging informatics
|
356
|
11
|
Start
|
Low
|
484
|
Gaussian network model
|
350
|
11
|
C
|
Mid
|
485
|
Bowtie (sequence analysis)
|
350
|
11
|
Start
|
Mid
|
486
|
OpenAPS
|
348
|
11
|
Start
|
Low
|
487
|
Population viability analysis
|
347
|
11
|
C
|
Mid
|
488
|
Narrow escape problem
|
347
|
11
|
C
|
Low
|
489
|
Briefings in Bioinformatics
|
347
|
11
|
Start
|
Low
|
490
|
The Arabidopsis Information Resource
|
345
|
11
|
Stub
|
Low
|
491
|
Jim Kent
|
344
|
11
|
Start
|
Low
|
492
|
SNPedia
|
343
|
11
|
Start
|
Low
|
493
|
David J. Lipman
|
341
|
11
|
Start
|
Low
|
494
|
Richard M. Durbin
|
341
|
11
|
C
|
Low
|
495
|
Swiss Institute of Bioinformatics
|
340
|
11
|
Start
|
Low
|
496
|
Russ Altman
|
340
|
11
|
C
|
Mid
|
497
|
Journal of Theoretical Biology
|
339
|
11
|
Stub
|
Low
|
498
|
Dynamic energy budget theory
|
339
|
11
|
C
|
Low
|
499
|
List of software for Monte Carlo molecular modeling
|
339
|
11
|
List
|
Mid
|
500
|
Fluxomics
|
336
|
11
|
Start
|
Low
|