| Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
| 1
|
23andMe
|
36,191
|
1,206
|
C
|
Low
|
| 2
|
Last universal common ancestor
|
34,734
|
1,157
|
GA
|
Mid
|
| 3
|
CRISPR
|
32,641
|
1,088
|
B
|
Top
|
| 4
|
Atul Butte
|
28,033
|
934
|
Start
|
Mid
|
| 5
|
UCSC Genome Browser
|
26,792
|
893
|
Start
|
High
|
| 6
|
Clade
|
24,180
|
806
|
C
|
Mid
|
| 7
|
Martin Kulldorff
|
22,938
|
764
|
B
|
Low
|
| 8
|
Receiver operating characteristic
|
22,281
|
742
|
B
|
Mid
|
| 9
|
Hidden Markov model
|
16,788
|
559
|
GA
|
Top
|
| 10
|
Cellular automaton
|
16,294
|
543
|
B
|
Low
|
| 11
|
Systems theory
|
16,203
|
540
|
C
|
Mid
|
| 12
|
Dynamic programming
|
15,818
|
527
|
B
|
Top
|
| 13
|
AlphaFold
|
15,263
|
508
|
C
|
High
|
| 14
|
Bioinformatics
|
13,903
|
463
|
C
|
Top
|
| 15
|
Ontology (information science)
|
13,286
|
442
|
C
|
High
|
| 16
|
Phylogenetic tree
|
13,254
|
441
|
B
|
Top
|
| 17
|
George Church (geneticist)
|
12,188
|
406
|
C
|
Mid
|
| 18
|
Most recent common ancestor
|
11,675
|
389
|
B
|
High
|
| 19
|
Genome
|
11,202
|
373
|
C
|
High
|
| 20
|
Cladistics
|
10,598
|
353
|
C
|
Mid
|
| 21
|
PubMed Central
|
10,384
|
346
|
B
|
Mid
|
| 22
|
DNA sequencing
|
10,216
|
340
|
B
|
High
|
| 23
|
Michaelis–Menten kinetics
|
9,732
|
324
|
B
|
Top
|
| 24
|
Phylogenetics
|
9,531
|
317
|
B
|
Top
|
| 25
|
Heat map
|
7,356
|
245
|
Start
|
High
|
| 26
|
National Center for Biotechnology Information
|
6,840
|
228
|
C
|
Low
|
| 27
|
Synthetic biology
|
6,695
|
223
|
B
|
Mid
|
| 28
|
David Baker (biochemist)
|
6,654
|
221
|
Start
|
Low
|
| 29
|
Genomics
|
6,569
|
218
|
B
|
High
|
| 30
|
PubChem
|
6,145
|
204
|
Start
|
Mid
|
| 31
|
Computational biology
|
6,028
|
200
|
C
|
Top
|
| 32
|
Sanger sequencing
|
6,010
|
200
|
C
|
Mid
|
| 33
|
FASTA format
|
5,764
|
192
|
B
|
High
|
| 34
|
Petri net
|
5,760
|
192
|
C
|
Low
|
| 35
|
Mathematical and theoretical biology
|
5,642
|
188
|
C
|
Top
|
| 36
|
Isomorphic Labs
|
5,538
|
184
|
Stub
|
Low
|
| 37
|
List of algorithms
|
5,476
|
182
|
List
|
Mid
|
| 38
|
Illumina, Inc.
|
5,466
|
182
|
C
|
Low
|
| 39
|
Burrows–Wheeler transform
|
5,384
|
179
|
C
|
Mid
|
| 40
|
Computational neuroscience
|
5,338
|
177
|
C
|
Top
|
| 41
|
Proteomics
|
5,333
|
177
|
C
|
High
|
| 42
|
RNA-Seq
|
5,312
|
177
|
B
|
Top
|
| 43
|
FASTQ format
|
5,141
|
171
|
B
|
Mid
|
| 44
|
Omics
|
5,057
|
168
|
C
|
Mid
|
| 45
|
Medical Subject Headings
|
5,004
|
166
|
C
|
Mid
|
| 46
|
Protein structure prediction
|
4,973
|
165
|
B
|
High
|
| 47
|
Phi coefficient
|
4,963
|
165
|
Start
|
Mid
|
| 48
|
Genome-wide association study
|
4,944
|
164
|
GA
|
High
|
| 49
|
Whole genome sequencing
|
4,853
|
161
|
B
|
High
|
| 50
|
Folding@home
|
4,631
|
154
|
B
|
Mid
|
| 51
|
Sequence alignment
|
4,566
|
152
|
C
|
High
|
| 52
|
Kseniia Petrova
|
4,525
|
150
|
B
|
Unknown
|
| 53
|
Systems biology
|
4,471
|
149
|
C
|
Top
|
| 54
|
DNA microarray
|
4,438
|
147
|
B
|
Top
|
| 55
|
Biostatistics
|
4,385
|
146
|
B
|
Top
|
| 56
|
Non-coding DNA
|
4,348
|
144
|
C
|
Low
|
| 57
|
Molecular clock
|
4,237
|
141
|
C
|
High
|
| 58
|
BLAST (biotechnology)
|
4,200
|
140
|
C
|
Top
|
| 59
|
Needleman–Wunsch algorithm
|
4,143
|
138
|
Start
|
Mid
|
| 60
|
Biological computing
|
4,010
|
133
|
C
|
Mid
|
| 61
|
DNA barcoding
|
3,953
|
131
|
B
|
High
|
| 62
|
Docking (molecular)
|
3,923
|
130
|
B
|
High
|
| 63
|
Smith–Waterman algorithm
|
3,890
|
129
|
B
|
Top
|
| 64
|
What Is Life?
|
3,822
|
127
|
C
|
Low
|
| 65
|
KNIME
|
3,666
|
122
|
Start
|
Low
|
| 66
|
Gene nomenclature
|
3,650
|
121
|
Start
|
Mid
|
| 67
|
Metabolomics
|
3,640
|
121
|
C
|
Mid
|
| 68
|
Similarity measure
|
3,619
|
120
|
Start
|
Mid
|
| 69
|
Denis Noble
|
3,615
|
120
|
Start
|
Low
|
| 70
|
Intrinsically disordered proteins
|
3,605
|
120
|
Start
|
Mid
|
| 71
|
Phred quality score
|
3,433
|
114
|
Start
|
Mid
|
| 72
|
Lineweaver–Burk plot
|
3,423
|
114
|
B
|
Low
|
| 73
|
Junk DNA
|
3,404
|
113
|
B
|
Low
|
| 74
|
Metagenomics
|
3,274
|
109
|
GA
|
Mid
|
| 75
|
Genetic programming
|
3,273
|
109
|
B
|
Mid
|
| 76
|
Wikispecies
|
3,265
|
108
|
Start
|
Mid
|
| 77
|
Spurious relationship
|
3,260
|
108
|
Start
|
Low
|
| 78
|
Protein Data Bank
|
3,215
|
107
|
C
|
High
|
| 79
|
Multiple sequence alignment
|
3,147
|
104
|
B
|
High
|
| 80
|
Exome sequencing
|
3,145
|
104
|
C
|
High
|
| 81
|
Single-cell sequencing
|
3,047
|
101
|
C
|
High
|
| 82
|
Baum–Welch algorithm
|
3,021
|
100
|
C
|
Mid
|
| 83
|
Gene regulatory network
|
2,991
|
99
|
B
|
High
|
| 84
|
Computational phylogenetics
|
2,982
|
99
|
C
|
High
|
| 85
|
Superspreading event
|
2,964
|
98
|
C
|
High
|
| 86
|
STR analysis
|
2,890
|
96
|
Start
|
Low
|
| 87
|
Biological network inference
|
2,834
|
94
|
C
|
Low
|
| 88
|
Nanopore sequencing
|
2,797
|
93
|
C
|
Low
|
| 89
|
Jmol
|
2,789
|
92
|
Start
|
Mid
|
| 90
|
Molecular phylogenetics
|
2,781
|
92
|
C
|
High
|
| 91
|
High-throughput screening
|
2,712
|
90
|
B
|
Low
|
| 92
|
Bioconductor
|
2,706
|
90
|
C
|
Mid
|
| 93
|
BLOSUM
|
2,704
|
90
|
C
|
High
|
| 94
|
Mathematical modelling of infectious diseases
|
2,688
|
89
|
C
|
Low
|
| 95
|
Transcriptome
|
2,688
|
89
|
B
|
High
|
| 96
|
Variant Call Format
|
2,680
|
89
|
Start
|
Mid
|
| 97
|
Broad Institute
|
2,588
|
86
|
Start
|
Low
|
| 98
|
ChIP sequencing
|
2,575
|
85
|
C
|
Mid
|
| 99
|
Andrew Huxley
|
2,553
|
85
|
C
|
Low
|
| 100
|
Kabsch algorithm
|
2,545
|
84
|
Start
|
Mid
|
| 101
|
Gene Ontology
|
2,471
|
82
|
C
|
High
|
| 102
|
UK Biobank
|
2,442
|
81
|
B
|
Low
|
| 103
|
Combined DNA Index System
|
2,358
|
78
|
GA
|
Low
|
| 104
|
Illumina dye sequencing
|
2,357
|
78
|
C
|
Mid
|
| 105
|
Polygenic score
|
2,354
|
78
|
C
|
Mid
|
| 106
|
Environmental DNA
|
2,346
|
78
|
B
|
Low
|
| 107
|
Maximum parsimony
|
2,340
|
78
|
C
|
High
|
| 108
|
Data wrangling
|
2,312
|
77
|
Start
|
Low
|
| 109
|
John Maynard Smith
|
2,310
|
77
|
C
|
Mid
|
| 110
|
FitzHugh–Nagumo model
|
2,270
|
75
|
C
|
Low
|
| 111
|
BED (file format)
|
2,263
|
75
|
C
|
Low
|
| 112
|
KEGG
|
2,197
|
73
|
C
|
High
|
| 113
|
Daphne Koller
|
2,183
|
72
|
C
|
Low
|
| 114
|
Gene set enrichment analysis
|
2,182
|
72
|
C
|
Mid
|
| 115
|
Transcriptomics technologies
|
2,165
|
72
|
GA
|
High
|
| 116
|
Crossover (evolutionary algorithm)
|
2,148
|
71
|
B
|
Low
|
| 117
|
N50, L50, and related statistics
|
2,146
|
71
|
Start
|
Low
|
| 118
|
Conserved sequence
|
2,130
|
71
|
C
|
High
|
| 119
|
Reference genome
|
2,122
|
70
|
Start
|
Low
|
| 120
|
Proteome
|
2,117
|
70
|
C
|
High
|
| 121
|
Multiomics
|
2,065
|
68
|
C
|
High
|
| 122
|
Root mean square deviation of atomic positions
|
2,006
|
66
|
Start
|
Mid
|
| 123
|
Oxford Nanopore Technologies
|
1,992
|
66
|
Start
|
Low
|
| 124
|
Fitness function
|
1,991
|
66
|
Start
|
Mid
|
| 125
|
Pardis Sabeti
|
1,983
|
66
|
B
|
Low
|
| 126
|
Ludwig von Bertalanffy
|
1,963
|
65
|
C
|
Low
|
| 127
|
Protein–protein interaction
|
1,934
|
64
|
C
|
High
|
| 128
|
ATAC-seq
|
1,929
|
64
|
C
|
Low
|
| 129
|
Biochemical cascade
|
1,928
|
64
|
C
|
Mid
|
| 130
|
Interactome
|
1,912
|
63
|
C
|
Mid
|
| 131
|
Global Biodiversity Information Facility
|
1,898
|
63
|
Start
|
Low
|
| 132
|
Monod equation
|
1,892
|
63
|
Start
|
Low
|
| 133
|
Volcano plot (statistics)
|
1,864
|
62
|
C
|
Mid
|
| 134
|
Solvation shell
|
1,862
|
62
|
Start
|
Low
|
| 135
|
Synteny
|
1,858
|
61
|
Start
|
Low
|
| 136
|
Approximate Bayesian computation
|
1,852
|
61
|
B
|
Low
|
| 137
|
SAM (file format)
|
1,849
|
61
|
Start
|
Mid
|
| 138
|
Phylogeny
|
1,825
|
60
|
Redirect
|
NA
|
| 139
|
Probabilistic context-free grammar
|
1,811
|
60
|
B
|
High
|
| 140
|
K-mer
|
1,802
|
60
|
B
|
Mid
|
| 141
|
Michael Levitt (biophysicist)
|
1,778
|
59
|
C
|
Low
|
| 142
|
ChEMBL
|
1,771
|
59
|
Start
|
Mid
|
| 143
|
1000 Genomes Project
|
1,764
|
58
|
B
|
Low
|
| 144
|
Theoretical ecology
|
1,744
|
58
|
B
|
High
|
| 145
|
Cathy Tie
|
1,741
|
58
|
C
|
Low
|
| 146
|
10x Genomics
|
1,739
|
57
|
Start
|
Mid
|
| 147
|
Genome size
|
1,733
|
57
|
B
|
Mid
|
| 148
|
UniProt
|
1,709
|
56
|
Start
|
High
|
| 149
|
Genetic distance
|
1,702
|
56
|
B
|
Mid
|
| 150
|
Schrödinger, Inc.
|
1,702
|
56
|
Start
|
Low
|
| 151
|
Sequence assembly
|
1,686
|
56
|
Start
|
High
|
| 152
|
HMMER
|
1,679
|
55
|
B
|
High
|
| 153
|
Evolutionary grade
|
1,668
|
55
|
Start
|
High
|
| 154
|
DNA database
|
1,668
|
55
|
Start
|
Mid
|
| 155
|
European Molecular Biology Laboratory
|
1,646
|
54
|
C
|
Low
|
| 156
|
CASP
|
1,628
|
54
|
C
|
Mid
|
| 157
|
PyMOL
|
1,626
|
54
|
Start
|
Low
|
| 158
|
Biological network
|
1,614
|
53
|
C
|
High
|
| 159
|
Encyclopedia of Life
|
1,607
|
53
|
Start
|
Mid
|
| 160
|
Online Mendelian Inheritance in Man
|
1,596
|
53
|
Start
|
Mid
|
| 161
|
Protein family
|
1,591
|
53
|
Start
|
High
|
| 162
|
Distance matrix
|
1,591
|
53
|
Start
|
High
|
| 163
|
Rosetta@home
|
1,578
|
52
|
C
|
Mid
|
| 164
|
SNP array
|
1,557
|
51
|
Start
|
High
|
| 165
|
Biobank
|
1,542
|
51
|
Start
|
High
|
| 166
|
Virtual screening
|
1,540
|
51
|
Start
|
High
|
| 167
|
Catalogue of Life
|
1,525
|
50
|
C
|
Low
|
| 168
|
Brain mapping
|
1,516
|
50
|
B
|
Low
|
| 169
|
Sequence motif
|
1,515
|
50
|
Start
|
High
|
| 170
|
Substitution model
|
1,495
|
49
|
B
|
Mid
|
| 171
|
Metabolome
|
1,483
|
49
|
C
|
High
|
| 172
|
Neighbor joining
|
1,476
|
49
|
C
|
High
|
| 173
|
Cross-species transmission
|
1,471
|
49
|
C
|
Low
|
| 174
|
UPGMA
|
1,463
|
48
|
C
|
Low
|
| 175
|
DNA annotation
|
1,462
|
48
|
Start
|
Low
|
| 176
|
Microarray
|
1,434
|
47
|
Start
|
Top
|
| 177
|
Weasel program
|
1,421
|
47
|
B
|
Low
|
| 178
|
Aviv Regev
|
1,417
|
47
|
Start
|
Low
|
| 179
|
Topologically associating domain
|
1,416
|
47
|
C
|
Low
|
| 180
|
Spatial transcriptomics
|
1,416
|
47
|
Start
|
Low
|
| 181
|
Functional genomics
|
1,412
|
47
|
C
|
High
|
| 182
|
C. H. Waddington
|
1,411
|
47
|
C
|
Low
|
| 183
|
Comparative genomics
|
1,401
|
46
|
C
|
Top
|
| 184
|
Wellcome Sanger Institute
|
1,400
|
46
|
C
|
Low
|
| 185
|
GenBank
|
1,399
|
46
|
Start
|
High
|
| 186
|
Alan Hodgkin
|
1,388
|
46
|
Start
|
Low
|
| 187
|
Haar-like feature
|
1,375
|
45
|
C
|
Low
|
| 188
|
Gene expression profiling
|
1,358
|
45
|
B
|
High
|
| 189
|
Pan-genome
|
1,357
|
45
|
C
|
Mid
|
| 190
|
General feature format
|
1,356
|
45
|
Start
|
Low
|
| 191
|
Network motif
|
1,350
|
45
|
B
|
Low
|
| 192
|
Gene family
|
1,347
|
44
|
C
|
High
|
| 193
|
Indel
|
1,344
|
44
|
Start
|
Low
|
| 194
|
FishBase
|
1,339
|
44
|
Start
|
Low
|
| 195
|
Metabarcoding
|
1,335
|
44
|
B
|
Low
|
| 196
|
Open Tree of Life
|
1,318
|
43
|
Start
|
Low
|
| 197
|
Eric Xing
|
1,314
|
43
|
Stub
|
Low
|
| 198
|
Point accepted mutation
|
1,291
|
43
|
B
|
High
|
| 199
|
Vito Volterra
|
1,290
|
43
|
C
|
Low
|
| 200
|
Foundational Model of Anatomy
|
1,284
|
42
|
Start
|
Low
|
| 201
|
Outgroup (cladistics)
|
1,283
|
42
|
Start
|
Mid
|
| 202
|
DNA sequencer
|
1,271
|
42
|
Start
|
Low
|
| 203
|
Leroy Hood
|
1,269
|
42
|
B
|
Low
|
| 204
|
Tournament selection
|
1,267
|
42
|
Start
|
Low
|
| 205
|
Sequence logo
|
1,265
|
42
|
B
|
Mid
|
| 206
|
Mathematical physiology
|
1,264
|
42
|
Stub
|
Mid
|
| 207
|
Consensus sequence
|
1,262
|
42
|
Start
|
High
|
| 208
|
Long branch attraction
|
1,259
|
41
|
Start
|
Low
|
| 209
|
Boolean network
|
1,259
|
41
|
C
|
Mid
|
| 210
|
Protein superfamily
|
1,245
|
41
|
B
|
High
|
| 211
|
Gap penalty
|
1,240
|
41
|
C
|
High
|
| 212
|
Gene prediction
|
1,235
|
41
|
C
|
High
|
| 213
|
Models of DNA evolution
|
1,225
|
40
|
B
|
Mid
|
| 214
|
Modelling biological systems
|
1,224
|
40
|
C
|
High
|
| 215
|
Ancestral reconstruction
|
1,224
|
40
|
B
|
Low
|
| 216
|
Position weight matrix
|
1,221
|
40
|
C
|
Top
|
| 217
|
Co-occurrence network
|
1,214
|
40
|
Start
|
Low
|
| 218
|
Celera Corporation
|
1,212
|
40
|
Start
|
Low
|
| 219
|
List of sequence alignment software
|
1,210
|
40
|
List
|
High
|
| 220
|
ChEBI
|
1,202
|
40
|
Start
|
Low
|
| 221
|
Circular permutation in proteins
|
1,195
|
39
|
GA
|
Low
|
| 222
|
Lenia
|
1,192
|
39
|
Start
|
Unknown
|
| 223
|
Protein–protein interaction prediction
|
1,177
|
39
|
Start
|
High
|
| 224
|
DeCODE genetics
|
1,168
|
38
|
Start
|
Low
|
| 225
|
Lipidomics
|
1,163
|
38
|
C
|
Low
|
| 226
|
Cable theory
|
1,156
|
38
|
C
|
Mid
|
| 227
|
Chromosome conformation capture
|
1,153
|
38
|
C
|
Low
|
| 228
|
Protein design
|
1,143
|
38
|
C
|
Mid
|
| 229
|
Homology modeling
|
1,134
|
37
|
B
|
High
|
| 230
|
Sequence analysis
|
1,130
|
37
|
C
|
Top
|
| 231
|
BAM (file format)
|
1,129
|
37
|
Start
|
Mid
|
| 232
|
European Bioinformatics Institute
|
1,126
|
37
|
C
|
Low
|
| 233
|
Motoo Kimura
|
1,123
|
37
|
C
|
High
|
| 234
|
Knowledge engineering
|
1,122
|
37
|
Start
|
Low
|
| 235
|
List of open-source bioinformatics software
|
1,118
|
37
|
List
|
High
|
| 236
|
GROMACS
|
1,112
|
37
|
Start
|
Low
|
| 237
|
Cooperative binding
|
1,104
|
36
|
B
|
Mid
|
| 238
|
CRISPR interference
|
1,098
|
36
|
B
|
Low
|
| 239
|
Synthetic biological circuit
|
1,095
|
36
|
Start
|
Low
|
| 240
|
Contig
|
1,090
|
36
|
C
|
High
|
| 241
|
Biclustering
|
1,072
|
35
|
B
|
Mid
|
| 242
|
Eugene Koonin
|
1,070
|
35
|
Start
|
Low
|
| 243
|
Brendan Frey
|
1,066
|
35
|
B
|
Low
|
| 244
|
D'Arcy Wentworth Thompson
|
1,064
|
35
|
GA
|
Mid
|
| 245
|
AMBER
|
1,063
|
35
|
C
|
Mid
|
| 246
|
List of mass spectrometry software
|
1,057
|
35
|
List
|
Low
|
| 247
|
List of biological databases
|
1,048
|
34
|
List
|
High
|
| 248
|
Substitution matrix
|
1,037
|
34
|
C
|
High
|
| 249
|
Population structure (genetics)
|
1,027
|
34
|
Start
|
Low
|
| 250
|
Monod–Wyman–Changeux model
|
1,024
|
34
|
Start
|
Mid
|
| 251
|
Microarray analysis techniques
|
1,023
|
34
|
B
|
Mid
|
| 252
|
De novo peptide sequencing
|
1,014
|
33
|
Start
|
Low
|
| 253
|
Entrez
|
1,009
|
33
|
Start
|
Mid
|
| 254
|
Mutation (evolutionary algorithm)
|
1,005
|
33
|
Start
|
Low
|
| 255
|
Michael Eisen
|
987
|
32
|
Start
|
Low
|
| 256
|
Metabolic network modelling
|
983
|
32
|
C
|
Mid
|
| 257
|
Structural genomics
|
979
|
32
|
Start
|
High
|
| 258
|
Data curation
|
977
|
32
|
Start
|
Mid
|
| 259
|
Sepp Hochreiter
|
974
|
32
|
Start
|
Low
|
| 260
|
SAMtools
|
974
|
32
|
Start
|
Low
|
| 261
|
Polytomy
|
972
|
32
|
Start
|
Low
|
| 262
|
Machine learning in bioinformatics
|
971
|
32
|
C
|
High
|
| 263
|
Clustal
|
965
|
32
|
Start
|
Mid
|
| 264
|
Ukkonen's algorithm
|
960
|
32
|
Stub
|
Low
|
| 265
|
Manolis Kellis
|
958
|
31
|
C
|
Low
|
| 266
|
Robert Gentleman (statistician)
|
955
|
31
|
Start
|
Mid
|
| 267
|
Ion semiconductor sequencing
|
945
|
31
|
C
|
Low
|
| 268
|
Single-cell transcriptomics
|
945
|
31
|
B
|
Mid
|
| 269
|
EBird
|
938
|
31
|
Start
|
Low
|
| 270
|
Dynamic energy budget theory
|
934
|
31
|
C
|
Low
|
| 271
|
MA plot
|
934
|
31
|
Start
|
Low
|
| 272
|
DSSP (algorithm)
|
933
|
31
|
Start
|
Low
|
| 273
|
Amino acid replacement
|
919
|
30
|
Start
|
High
|
| 274
|
FASTA
|
915
|
30
|
B
|
High
|
| 275
|
Matthews correlation coefficient
|
906
|
30
|
Redirect
|
NA
|
| 276
|
RNA integrity number
|
902
|
30
|
Stub
|
Low
|
| 277
|
CUT&RUN sequencing
|
901
|
30
|
C
|
Low
|
| 278
|
Paradox of enrichment
|
894
|
29
|
Start
|
Low
|
| 279
|
ENCODE
|
892
|
29
|
C
|
Mid
|
| 280
|
Umbrella sampling
|
890
|
29
|
Start
|
Low
|
| 281
|
Ensembl genome database project
|
887
|
29
|
B
|
High
|
| 282
|
Ecosystem model
|
883
|
29
|
Start
|
Mid
|
| 283
|
Robert Rosen (biologist)
|
879
|
29
|
Start
|
Low
|
| 284
|
ChIP-on-chip
|
878
|
29
|
C
|
Low
|
| 285
|
Population viability analysis
|
869
|
28
|
C
|
Mid
|
| 286
|
Pfam
|
855
|
28
|
B
|
High
|
| 287
|
Computational genomics
|
852
|
28
|
Start
|
Mid
|
| 288
|
List of RNA-Seq bioinformatics tools
|
840
|
28
|
List
|
Mid
|
| 289
|
Threading (protein sequence)
|
829
|
27
|
Start
|
High
|
| 290
|
GeneDx
|
828
|
27
|
Stub
|
Low
|
| 291
|
All of Us (initiative)
|
827
|
27
|
C
|
Low
|
| 292
|
Biochip
|
817
|
27
|
C
|
Low
|
| 293
|
Uri Alon
|
816
|
27
|
Start
|
Low
|
| 294
|
Flow cytometry bioinformatics
|
816
|
27
|
B
|
Low
|
| 295
|
Eadie–Hofstee diagram
|
814
|
27
|
Start
|
Low
|
| 296
|
Flux balance analysis
|
814
|
27
|
B
|
High
|
| 297
|
Glycomics
|
812
|
27
|
Start
|
Low
|
| 298
|
Allele frequency spectrum
|
805
|
26
|
Start
|
Low
|
| 299
|
DbSNP
|
803
|
26
|
B
|
Mid
|
| 300
|
Galaxy (computational biology)
|
798
|
26
|
Start
|
High
|
| 301
|
Chromosome (evolutionary algorithm)
|
797
|
26
|
Start
|
Low
|
| 302
|
Biodiversity informatics
|
796
|
26
|
C
|
Mid
|
| 303
|
Fusarium graminearum genome database
|
788
|
26
|
Stub
|
Low
|
| 304
|
List of RNA structure prediction software
|
785
|
26
|
List
|
Low
|
| 305
|
Macromolecular docking
|
782
|
26
|
B
|
Mid
|
| 306
|
CHARMM
|
781
|
26
|
B
|
Mid
|
| 307
|
Paradox of the plankton
|
781
|
26
|
Start
|
Low
|
| 308
|
Haldane's dilemma
|
775
|
25
|
B
|
Low
|
| 309
|
Dot plot (bioinformatics)
|
773
|
25
|
Start
|
Mid
|
| 310
|
NK model
|
773
|
25
|
B
|
Low
|
| 311
|
Cyberneticist
|
772
|
25
|
Redirect
|
Low
|
| 312
|
Biopython
|
769
|
25
|
C
|
High
|
| 313
|
Diseases Database
|
759
|
25
|
Start
|
Mid
|
| 314
|
UniFrac
|
756
|
25
|
Stub
|
Low
|
| 315
|
Chemical library
|
749
|
24
|
Start
|
Low
|
| 316
|
Biological systems engineering
|
744
|
24
|
Start
|
Low
|
| 317
|
Stephen Altschul
|
743
|
24
|
Start
|
Low
|
| 318
|
List of protein structure prediction software
|
740
|
24
|
List
|
Mid
|
| 319
|
Protein function prediction
|
734
|
24
|
Start
|
High
|
| 320
|
Cellular model
|
733
|
24
|
Start
|
Mid
|
| 321
|
Global distance test
|
726
|
24
|
Stub
|
Low
|
| 322
|
Conservative replacement
|
716
|
23
|
Start
|
Low
|
| 323
|
Protein contact map
|
714
|
23
|
Start
|
Mid
|
| 324
|
Viral phylodynamics
|
712
|
23
|
B
|
Low
|
| 325
|
STRING
|
709
|
23
|
B
|
Low
|
| 326
|
AutoDock
|
705
|
23
|
Start
|
Mid
|
| 327
|
International Society for Computational Biology
|
701
|
23
|
B
|
High
|
| 328
|
Scoring functions for docking
|
700
|
23
|
Start
|
Mid
|
| 329
|
RefSeq
|
699
|
23
|
Start
|
Mid
|
| 330
|
GeneCards
|
696
|
23
|
C
|
Mid
|
| 331
|
Mass spectrometry data format
|
692
|
23
|
Start
|
Low
|
| 332
|
List of neuroscience databases
|
687
|
22
|
List
|
Low
|
| 333
|
Biological database
|
682
|
22
|
Start
|
High
|
| 334
|
Robinson–Foulds metric
|
682
|
22
|
C
|
Low
|
| 335
|
McDonald–Kreitman test
|
680
|
22
|
C
|
Mid
|
| 336
|
List of protein-ligand docking software
|
678
|
22
|
List
|
Mid
|
| 337
|
DNA sequencing theory
|
677
|
22
|
B
|
High
|
| 338
|
Avogadro (software)
|
673
|
22
|
Stub
|
Low
|
| 339
|
Weighted correlation network analysis
|
673
|
22
|
B
|
Low
|
| 340
|
Bayesian inference in phylogeny
|
671
|
22
|
C
|
High
|
| 341
|
ARKive
|
669
|
22
|
C
|
Mid
|
| 342
|
DNA binding site
|
667
|
22
|
C
|
Mid
|
| 343
|
Barcode of Life Data System
|
666
|
22
|
Stub
|
Low
|
| 344
|
Hypercycle (chemistry)
|
665
|
22
|
B
|
Low
|
| 345
|
Phylogenetic bracketing
|
659
|
21
|
Start
|
Low
|
| 346
|
Chemical database
|
650
|
21
|
Start
|
Mid
|
| 347
|
Jacob Glanville
|
650
|
21
|
Stub
|
Low
|
| 348
|
Dry lab
|
648
|
21
|
Start
|
High
|
| 349
|
NanoString Technologies
|
643
|
21
|
Start
|
Low
|
| 350
|
Molecular Evolutionary Genetics Analysis
|
643
|
21
|
Start
|
Low
|
| 351
|
Margaret Oakley Dayhoff
|
642
|
21
|
B
|
High
|
| 352
|
Systems neuroscience
|
639
|
21
|
Stub
|
Mid
|
| 353
|
Barry Smith (ontologist)
|
636
|
21
|
C
|
Low
|
| 354
|
Animal Diversity Web
|
635
|
21
|
C
|
Mid
|
| 355
|
Template modeling score
|
634
|
21
|
Start
|
Low
|
| 356
|
Sequence database
|
632
|
21
|
Start
|
Mid
|
| 357
|
Multi-state modeling of biomolecules
|
631
|
21
|
B
|
Mid
|
| 358
|
Tree of Life Web Project
|
626
|
20
|
Start
|
Low
|
| 359
|
Amplicon sequence variant
|
625
|
20
|
Start
|
Low
|
| 360
|
List of phylogenetics software
|
624
|
20
|
List
|
High
|
| 361
|
Digital organism
|
623
|
20
|
Stub
|
Low
|
| 362
|
MGI (company)
|
623
|
20
|
C
|
Low
|
| 363
|
OBO Foundry
|
619
|
20
|
B
|
Mid
|
| 364
|
Genomics England
|
618
|
20
|
Start
|
Low
|
| 365
|
Sarah Teichmann
|
617
|
20
|
C
|
Low
|
| 366
|
Cytoscape
|
616
|
20
|
B
|
High
|
| 367
|
Eran Segal
|
615
|
20
|
Start
|
Low
|
| 368
|
David Botstein
|
612
|
20
|
Start
|
Low
|
| 369
|
Hirschberg's algorithm
|
612
|
20
|
B
|
Low
|
| 370
|
Carl Bergstrom
|
609
|
20
|
Stub
|
Low
|
| 371
|
2R hypothesis
|
606
|
20
|
B
|
Low
|
| 372
|
Computational immunology
|
602
|
20
|
B
|
Mid
|
| 373
|
Europe PubMed Central
|
589
|
19
|
Start
|
Low
|
| 374
|
List of sequenced animal genomes
|
586
|
19
|
List
|
Mid
|
| 375
|
Bonnie Berger
|
586
|
19
|
Start
|
Low
|
| 376
|
Marginal value theorem
|
581
|
19
|
C
|
Unknown
|
| 377
|
PLOS Computational Biology
|
580
|
19
|
Start
|
High
|
| 378
|
Ewan Birney
|
578
|
19
|
C
|
Low
|
| 379
|
LSID
|
578
|
19
|
Start
|
Low
|
| 380
|
Hindmarsh–Rose model
|
576
|
19
|
Stub
|
Low
|
| 381
|
HUGO Gene Nomenclature Committee
|
575
|
19
|
Start
|
Mid
|
| 382
|
World Community Grid
|
571
|
19
|
C
|
Low
|
| 383
|
Epitranscriptome
|
567
|
18
|
B
|
Low
|
| 384
|
Phred (software)
|
561
|
18
|
Start
|
Low
|
| 385
|
Minimum evolution
|
558
|
18
|
C
|
High
|
| 386
|
Virtual Physiological Human
|
557
|
18
|
C
|
Mid
|
| 387
|
Lior Pachter
|
549
|
18
|
Start
|
Mid
|
| 388
|
HomoloGene
|
548
|
18
|
Start
|
Low
|
| 389
|
De novo protein structure prediction
|
547
|
18
|
Start
|
High
|
| 390
|
List of bioinformatics journals
|
545
|
18
|
List
|
Low
|
| 391
|
Z curve
|
544
|
18
|
Start
|
Low
|
| 392
|
Protein Data Bank (file format)
|
543
|
18
|
Start
|
Mid
|
| 393
|
Erez Lieberman Aiden
|
541
|
18
|
GA
|
Low
|
| 394
|
MicroRNA sequencing
|
541
|
18
|
C
|
Low
|
| 395
|
Haplotype estimation
|
541
|
18
|
Start
|
Low
|
| 396
|
FreeSurfer
|
540
|
18
|
Start
|
Mid
|
| 397
|
Taxonomic database
|
540
|
18
|
Start
|
Mid
|
| 398
|
Bak–Sneppen model
|
538
|
17
|
Start
|
Low
|
| 399
|
InterPro
|
537
|
17
|
B
|
High
|
| 400
|
Phylogenetic comparative methods
|
537
|
17
|
C
|
Mid
|
| 401
|
CRAM (file format)
|
537
|
17
|
Start
|
Low
|
| 402
|
Accession number (bioinformatics)
|
532
|
17
|
Start
|
Low
|
| 403
|
Synthetic virology
|
530
|
17
|
Start
|
Mid
|
| 404
|
Bernd Sturmfels
|
529
|
17
|
Stub
|
Low
|
| 405
|
Genetic operator
|
528
|
17
|
Start
|
Low
|
| 406
|
List of molecular graphics systems
|
525
|
17
|
List
|
Mid
|
| 407
|
List of alignment visualization software
|
525
|
17
|
List
|
Mid
|
| 408
|
Rob Knight (biologist)
|
523
|
17
|
Stub
|
Low
|
| 409
|
Russ Altman
|
518
|
17
|
C
|
Mid
|
| 410
|
Inferring horizontal gene transfer
|
517
|
17
|
B
|
Low
|
| 411
|
List of biodiversity databases
|
514
|
17
|
List
|
Low
|
| 412
|
FlyBase
|
513
|
17
|
Start
|
Mid
|
| 413
|
Demographic and Health Surveys
|
512
|
17
|
B
|
Low
|
| 414
|
Chou–Fasman method
|
510
|
17
|
B
|
Mid
|
| 415
|
MEGAN
|
510
|
17
|
Start
|
High
|
| 416
|
Trajectory inference
|
510
|
17
|
C
|
Low
|
| 417
|
Peter Donnelly
|
509
|
16
|
Start
|
Low
|
| 418
|
List of MeSH codes
|
508
|
16
|
List
|
Mid
|
| 419
|
UCSF Chimera
|
508
|
16
|
Start
|
Low
|
| 420
|
Alston Scott Householder
|
507
|
16
|
Start
|
Low
|
| 421
|
Orphanet
|
505
|
16
|
C
|
Low
|
| 422
|
Gene Wiki
|
500
|
16
|
Start
|
Mid
|
| 423
|
Steven Salzberg
|
499
|
16
|
Start
|
Low
|
| 424
|
Pileup format
|
497
|
16
|
Start
|
Low
|
| 425
|
CATH database
|
496
|
16
|
Start
|
Mid
|
| 426
|
Structural Classification of Proteins database
|
492
|
16
|
Start
|
High
|
| 427
|
Apache Taverna
|
492
|
16
|
C
|
Low
|
| 428
|
Hanes–Woolf plot
|
491
|
16
|
Start
|
Low
|
| 429
|
FoldX
|
491
|
16
|
Start
|
Low
|
| 430
|
Automated species identification
|
481
|
16
|
Start
|
Low
|
| 431
|
Attack rate
|
477
|
15
|
Start
|
Mid
|
| 432
|
List of phylogenetic tree visualization software
|
477
|
15
|
List
|
Mid
|
| 433
|
Bioinformatics (journal)
|
477
|
15
|
Start
|
High
|
| 434
|
Anduril (workflow engine)
|
476
|
15
|
B
|
Low
|
| 435
|
FlowJo
|
475
|
15
|
Start
|
Low
|
| 436
|
Batch effect
|
475
|
15
|
Stub
|
Low
|
| 437
|
Holland's schema theorem
|
471
|
15
|
Start
|
Low
|
| 438
|
454 Life Sciences
|
467
|
15
|
C
|
Low
|
| 439
|
Codon Adaptation Index
|
462
|
15
|
Stub
|
Low
|
| 440
|
Arthur M. Lesk
|
460
|
15
|
C
|
Low
|
| 441
|
Jim Kent
|
458
|
15
|
Start
|
Low
|
| 442
|
Metabolic flux analysis
|
458
|
15
|
Stub
|
Low
|
| 443
|
BRENDA
|
456
|
15
|
Start
|
Mid
|
| 444
|
Next-generation matrix
|
456
|
15
|
Start
|
Low
|
| 445
|
Visual Molecular Dynamics
|
451
|
15
|
Start
|
Low
|
| 446
|
Institute of Genomics and Integrative Biology
|
451
|
15
|
C
|
Low
|
| 447
|
Dryad (repository)
|
451
|
15
|
Start
|
Low
|
| 448
|
Dehaene–Changeux model
|
451
|
15
|
Start
|
Low
|
| 449
|
Elasticity coefficient
|
449
|
14
|
C
|
Mid
|
| 450
|
Virtual karyotype
|
445
|
14
|
C
|
Low
|
| 451
|
Djungelskog (bacteriophage)
|
445
|
14
|
Stub
|
Low
|
| 452
|
Energy charge
|
443
|
14
|
Start
|
Low
|
| 453
|
MAFFT
|
443
|
14
|
Stub
|
Mid
|
| 454
|
DNA Data Bank of Japan
|
442
|
14
|
Stub
|
Low
|
| 455
|
David Goodsell
|
433
|
14
|
C
|
Low
|
| 456
|
Sequence profiling tool
|
432
|
14
|
Start
|
Mid
|
| 457
|
Bowtie (sequence analysis)
|
432
|
14
|
Start
|
Mid
|
| 458
|
Alzheimer's Disease Neuroimaging Initiative
|
430
|
14
|
Start
|
Low
|
| 459
|
Virtual Cell
|
430
|
14
|
B
|
Low
|
| 460
|
Nicolas Rashevsky
|
425
|
14
|
B
|
Mid
|
| 461
|
Short linear motif
|
424
|
14
|
B
|
Mid
|
| 462
|
Allen Brain Atlas
|
422
|
14
|
C
|
Mid
|
| 463
|
Sequest
|
422
|
14
|
Start
|
Mid
|
| 464
|
Nexus file
|
422
|
14
|
Start
|
Low
|
| 465
|
Structural bioinformatics
|
418
|
13
|
B
|
High
|
| 466
|
Ehud Shapiro
|
418
|
13
|
Start
|
Low
|
| 467
|
Centre for DNA Fingerprinting and Diagnostics
|
416
|
13
|
Start
|
Low
|
| 468
|
Narrow escape problem
|
416
|
13
|
C
|
Low
|
| 469
|
Eugene Myers
|
415
|
13
|
Start
|
Low
|
| 470
|
David S. Wishart
|
415
|
13
|
C
|
Low
|
| 471
|
Low complexity regions in proteins
|
414
|
13
|
Start
|
Mid
|
| 472
|
Binning (metagenomics)
|
413
|
13
|
Start
|
Low
|
| 473
|
Jay Shendure
|
412
|
13
|
Start
|
Low
|
| 474
|
Expasy
|
411
|
13
|
Start
|
Mid
|
| 475
|
Genomic organization
|
410
|
13
|
Start
|
Low
|
| 476
|
ABI Solid Sequencing
|
407
|
13
|
Start
|
Low
|
| 477
|
DAVID
|
407
|
13
|
Start
|
Mid
|
| 478
|
Phylogenetic Assignment of Named Global Outbreak Lineages
|
407
|
13
|
Start
|
Low
|
| 479
|
Daniel Gillespie
|
405
|
13
|
Start
|
Mid
|
| 480
|
Genome architecture mapping
|
401
|
13
|
C
|
Low
|
| 481
|
List of sequenced eukaryotic genomes
|
400
|
13
|
List
|
Mid
|
| 482
|
Biocuration
|
398
|
13
|
B
|
High
|
| 483
|
Felsenstein's tree-pruning algorithm
|
397
|
13
|
Stub
|
Low
|
| 484
|
List of omics topics in biology
|
397
|
13
|
List
|
Low
|
| 485
|
Reactome
|
394
|
13
|
Start
|
Low
|
| 486
|
ANOVA–simultaneous component analysis
|
394
|
13
|
Start
|
Low
|
| 487
|
BLAT (bioinformatics)
|
392
|
13
|
B
|
Low
|
| 488
|
De novo transcriptome assembly
|
392
|
13
|
C
|
Mid
|
| 489
|
Simulated growth of plants
|
391
|
13
|
Start
|
Low
|
| 490
|
Nucleic acid design
|
389
|
12
|
C
|
Mid
|
| 491
|
Microbial phylogenetics
|
389
|
12
|
Start
|
Low
|
| 492
|
Bioimage informatics
|
385
|
12
|
C
|
Mid
|
| 493
|
Tom Blundell
|
384
|
12
|
C
|
Low
|
| 494
|
Darwin Core
|
384
|
12
|
Start
|
Low
|
| 495
|
BMC Bioinformatics
|
382
|
12
|
C
|
Low
|
| 496
|
PLINK (genetic tool-set)
|
374
|
12
|
Stub
|
Low
|
| 497
|
MUSCLE (alignment software)
|
372
|
12
|
Start
|
Mid
|
| 498
|
Sequence Read Archive
|
369
|
12
|
Start
|
High
|
| 499
|
Read (biology)
|
369
|
12
|
C
|
High
|
| 500
|
WPGMA
|
368
|
12
|
C
|
Low
|
